Monitoring the incidence and causes of diseases potentially transmitted by food in Australia: Annual report of the OzFoodNet Network, 2008

OzFoodNet conducts surveillance on foodborne disease to investigate, describe and understand foodborne disease at the national level to provide better evidence of how to prevent foodborne illness. This page contains the annual report for 2008.

Page last updated: 22 February 2010

The OzFoodNet Working Group

Abstract

In 2008, OzFoodNet sites reported 25,260 notifications of 9 diseases or conditions that are commonly transmitted by food. The most frequently notified infections were Campylobacter (15,535 notifications) and Salmonella (8,310 notifications). Public health authorities provided complete serotype and phage type information on 94% of all Salmonella infections in 2008. The most common Salmonella serotype notified in Australia during 2008 was Salmonella Typhimurium, and the most common phage type was S. Typhimurium 135. During 2008, OzFoodNet sites reported 1,545 outbreaks of gastrointestinal illness; affecting 25,555 people and resulting in 691 people being hospitalised. There were 99 deaths during these outbreaks. The majority (83%, 1,276/1,545) of outbreaks were due to personto-person spread, but 7% (104/1,545) were transmitted by contaminated food. Foodborne outbreaks affected 1,454 persons including 96 hospitalisations. Eleven deaths were reported during these outbreaks. For these foodborne outbreaks, Salmonella was the most common aetiological agent and restaurants were the most common setting where foods were prepared. Twenty of these foodborne outbreaks were related to the consumption of eggs; the majority (n=18) of these outbreaks were due to various phage types of S. Typhimurium. This report summarises the incidence of disease potentially transmitted by food in Australia and details outbreaks associated with various food vehicles in 2008. These data assist agencies to identify emerging disease, develop food safety policies, and prevent foodborne illness. Commun Dis Intell 2009;33(4):389–413.

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Introduction

In Australia, an estimated 5.4 million cases of foodborne disease occur annually, costing an estimated $1.2 billion dollars per year.1 Many of these illnesses are preventable by appropriate interventions and surveillance helps to identify control measures.2 Health departments conduct surveillance for foodborne diseases and diseases potentially transmitted by food to monitor trends in illness, detect outbreaks, inform preventative measures and to evaluate the efficacy of intervention efforts.3,4

In Australia, state and territory health departments conduct surveillance for between 10 and 15 different diseases that may be transmitted through food. Most of these diseases are transmitted by the faecal–oral route and as such may also be transmitted by contact with infected animals or people, or through consumption of contaminated water. In addition, health departments collect summary data on all outbreaks of foodborne diseases, which provides robust surveillance information on contaminated foods causing illness in Australia.

Most foodborne diseases manifest as mild self-limiting gastroenteritis, with only around 20% of affected people seeking medical attention. Consequently, surveillance data collected by health departments underestimate the true burden of disease. In Australia, for every case of salmonellosis notified to a health department there are an estimated 7 infections that occur in the community, while there are approximately 10 and 8 cases in the community for every notified case of campylobacteriosis and infection with Shiga-toxin producing Escherichia coli (STEC), respectively.5,6

The Australian Government established OzFoodNet—Australia’s enhanced foodborne disease surveillance system—in 2000 to improve national surveillance and conduct applied research into the causes of foodborne illness.7 OzFoodNet aggregates and analyses national information on the incidence of diseases caused by pathogens commonly transmitted by food, as well as foodborne disease outbreaks. The OzFoodNet network includes collaborators from the National Centre for Epidemiology and Population Health at the Australian National University, the Public Health Laboratory Network, Food Standards Australia New Zealand (FSANZ), and the Department of Agriculture Fisheries and Forestry. OzFoodNet is a member of the Communicable Diseases Network Australia, which is Australia’s peak body for communicable disease control.8 This is the 8th annual report for the OzFoodNet network and summarises 2008 surveillance data, which includes a comparison with data from previous years.

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Methods

Population under surveillance

In 2008, the network covered the whole of the Australian population, which was estimated to be 21,373,998 persons.9

Data sources

Notified infections

All Australian states and territories have public health legislation requiring doctors and pathology laboratories to notify cases of infectious diseases that are important to public health. State and territory health departments record details of notified patients on surveillance databases. These surveillance datasets are aggregated into a national database—the National Notifiable Diseases Surveillance System (NNDSS)—under the auspices of the National Health Security Act 2007 and the National Health Securities Agreement 2008. OzFoodNet aggregated and analysed data from NNDSS and enhanced surveillance data from OzFoodNet sites on the following 9 diseases or conditions, a proportion of which are commonly transmitted by food:

  • non-typhoidal Salmonella infections;
  • Campylobacter infections (except in New South Wales);
  • Listeria infections;
  • Shigella infections;
  • Salmonella Typhi;
  • hepatitis A
  • botulism
  • STEC infections; and
  • haemolytic uraemic syndrome (HUS).

Data for this report were extracted from NNDSS in July 2009 and were analysed by the date of diagnosis within the reporting period 1 January to 31 December 2008. Date of diagnosis was derived from the earliest date supplied from the date of onset of the case’s illness, the date a specimen was collected or the date that a health department received the notification. Estimated resident populations for each state or territory as at June 2008 were used to calculate rates of notified infections.

Enhanced surveillance

OzFoodNet sites collected supplementary data on infections commonly transmitted by foods. Information on travel status was collected for cases of Salmonella Enteritidis, hepatitis A and typhoid. We compared the incidence of infection in returned travellers with the number of travellers to that region using customs data derived from incoming passenger cards.10 The field ‘country where you spent the most time abroad’ was used as the numerator.

To examine the quality of surveillance data collected across Australia, OzFoodNet sites provided data on the completeness of serotype and phage type for Salmonella notifications. Data from Western Australia were excluded from the analysis, as isolates have not been routinely sent for phage typing since June 2007. To assess completeness, data were analysed using the date a notification was received by the health department.

OzFoodNet sites supplied data on listeriosis cases, which included whether a case was materno–foetal or not, and whether the case died. Many cases have severe chronic illnesses prior to their Listeria infection so it is difficult to determine if listeriosis is the cause of death for fatal cases, or one of many contributing factors. We did not validate deaths and all cases reported to have died were considered a listeriosis fatality. Maternofoetal pairs (mother and neonate) were counted as a single case with the mother being counted as the primary case. This affects age-specific notification rates for listeriosis and the proportion of reported cases that were female.

Gastrointestinal and foodborne disease outbreaks

OzFoodNet sites collected summary information on gastrointestinal and foodborne disease outbreaks that occurred in Australia during 2008. An outbreak of foodborne disease was defined as two or more people with a particular infection or illness whose common exposure was associated with a specific food or meal. A cluster was defined as an increase in infections that were epidemiologically related in time, place or person where investigators were unable to implicate a vehicle or determine a mode of transmission.

For foodborne and suspected foodborne outbreaks, the summary information collected on each outbreak included the setting where the outbreak occurred, where food was prepared, the month the outbreak occurred, the aetiological agent, the number of persons affected, the type of investigation conducted, the level of evidence obtained, and the food vehicle responsible for the outbreak. To summarise the data, outbreaks were categorised by aetiological agents, food vehicles and settings where the implicated food was prepared. Data on outbreaks due to waterborne transmission and data from clusters investigated by jurisdictional health departments were also summarised. The number of outbreaks and documented causes reported here may vary from summaries previously published by individual jurisdictions as these can take time to finalise.

Data analysis

We used Microsoft Excel and Stata version 10.1 for all analyses. Where appropriate we compared proportions using χ2 tests.

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Results

Rates of notified infections

In 2008, OzFoodNet sites reported 25,260 notifications of 9 diseases or conditions that are commonly transmitted by food (Table 1), similar to the mean of 25,054 notifications per year for the previous 5 years (2003–2007). There were no cases of botulism in 2008.

Table 1: Number of notified cases, crude rate and 5-year mean (2003–2007) rate per 100,000 population of diseases or infections commonly transmitted by food, Australia, 2008, by disease and state or territory

Disease
  State or territory  
ACT NSW NT Qld SA Tas Vic WA Aust
Salmonella Notified cases, 2008
132
2,261
497
2,047
661
206
1,651
855
8,310
Rate 2008
38.3
32.5
226.0
47.8
41.3
41.4
31.2
39.5
38.9
Mean rate, 2003–2007
31.2
31.9
200.3
63.4
38.6
40.4
28.3
37.8
40.1
Campylobacter* Notified cases, 2008
381
257
4,821
1,992
475
5,780
1,829
15,535
Rate 2008
110.7
116.8
112.7
124.4
95.4
109.1
84.5
107.8
Mean rate, 2003–2007
121.3
125.3
103.9
153.3
136.4
119.2
102.9
116.9
Listeria Notified cases, 2008
1
34
0
12
1
1
11
8
68
Rate 2008
0.3
0.5
0.0
0.3
0.1
0.2
0.2
0.4
0.3
Mean rate, 2003–2007
0.4
0.4
0.1
0.2
0.3
0.2
0.3
0.3
0.3
Shigella Notified cases, 2008
3
109
175
97
137
4
134
169
828
Rate 2008
0.9
1.6
79.6
2.3
8.6
0.8
2.5
7.8
3.9
Mean rate, 2003–2007
0.9
1.3
71.9
1.9
3.1
0.7
1.6
6.0
2.8
Typhoid Notified cases, 2008
0
43
1
18
3
0
33
8
106
Rate 2008
0.0
0.6
0.5
0.4
0.2
0.0
0.6
0.4
0.5
Mean rate, 2003–2007
0.1
0.5
0.6
0.2
0.2
0.2
0.4
0.4
0.3
Hepatitis A Notified cases, 2008
5
69
3
71
20
1
85
22
276
Rate 2008
1.5
1.0
1.4
1.7
1.2
0.2
1.6
1.0
1.3
Mean rate, 2003–2007
0.7
1.5
15.3
0.9
0.6
1.0
1.2
2.9
1.5
Shiga toxin-producing Escherichia coli Notified cases, 2008
0
19
0
37
39
0
11
0
106
Rate 2008
0.0
0.3
0.0
0.9
2.4
0.0
0.2
0.0
0.5
Mean rate, 2003–2007
0.1
0.2
0.5
0.3
2.3
0.1
0.1
0.2
0.4
Haemolytic uraemic syndrome Notified cases, 2008
0
17
1
7
2
0
4
0
31
Rate 2008
0.00
0.24
0.45
0.16
0.12
0.00
0.08
0.00
0.15
Mean rate, 2003–2007
0.06
0.14
0.20
0.03
0.12
0.08
0.05
0.03
0.08

* Campylobacter is not a notifiable disease in New South Wales.

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Salmonella infections

In 2008, OzFoodNet sites reported 8,310 cases of Salmonella infection, a rate of 39 cases per 100,000 population (Table 1). Notification rates among jurisdictions ranged from 31 cases per 100,000 population in Victoria to 226 cases per 100,000 population in the Northern Territory, which usually has the highest rate of salmonellosis. Approximately half (49%) of Salmonella notifications were in males. The highest age-specific rate of Salmonella infection was 300 cases per 100,000 population in children aged 0–4 years (Figure 1). The notification rate increased dramatically in children aged 2 years or under, with rates in children aged 3 or 4 years being similar to the 5–9 year age group.

Figure 1: Salmonellosis notifications, Australia, 2008, by age group and sex

Salmonellosis notifications, Australia, 2008, by age group and sex

Nationally during 2008, the most commonly notified Salmonella serotype was S. Typhimurium, which was responsible for approximately 42% of all notified infections (Tables 2 and 3). During 2008, S. Typhimurium phage types 135, 44, 170/108 and 9 were commonly reported, representing four of the top 5 infections nationally. All serotypes in the Northern Territory exceeded 12 cases per 100,000 population, with Salmonella Ball being the highest at 20 cases per 100,000 population. Tasmania recorded a high rate for S. Mississippi notifications, which was 14.9 cases per 100,000 population. S. Mississippi is endemic in Tasmania and is thought to be transmitted from exposure to environments and drinking water that have been contaminated by native animals.11

Table 2: Numbers, rates and proportions of the top 5 Salmonella infections, Australia (excluding Western Australia), 2007 to 2008,* by OzFoodNet site

OzFoodNet site
Sero/phage type
2008 Proportion 2007 2008/2007 ratio§
n Rate (%) n Rate
Australian Capital Territory S. Typhimurium 44
23
6.7
17
6
1.8
3.8
S. Typhimurium 9
19
5.5
14
6
1.8
3.2
S. Typhimurium 135
12
3.5
9
8
2.4
1.5
S. Typhimurium 170/108
11
3.2
8
5
1.5
2.2
S. Infantis
5
1.5
4
3
0.9
1.7
New South Wales S. Typhimurium 135
256
3.7
11
232
3.4
1.1
S. Typhimurium 170/108
240
3.4
11
138
2.0
1.7
S. Typhimurium 9
146
2.1
6
363
5.3
0.4
S. Typhimurium 44
70
1.0
3
86
1.2
0.8
S. Birkenhead
68
1.0
3
105
1.5
0.6
Northern Territory S. Ball
44
20.0
9
38
17.7
1.2
S. Saintpaul
38
17.3
8
32
14.9
1.2
S. Weltevreden
31
14.1
6
16
7.4
1.9
S. Virchow 8
29
13.2
6
15
7.0
1.9
S. Lansing
27
12.3
5
10
4.7
2.7
Queensland S. Typhimurium 135
159
3.7
8
154
3.7
1.0
S. Saintpaul
155
3.6
8
219
5.2
0.7
S. Birkenhead
119
2.8
6
116
2.8
1.0
S. Virchow 8
99
2.3
5
183
4.4
0.5
S. Aberdeen
72
1.7
4
121
2.9
0.6
South Australia S. Typhimurium 135
93
5.8
14
66
4.2
1.4
S. Typhimurium 9
75
4.7
11
124
7.8
0.6
S. Infantis
39
2.4
6
42
2.7
0.9
S. Typhimurium 29
36
2.2
5
77
4.9
0.5
S. Typhimurium 193
27
1.7
4
22
1.4
1.2
Tasmania S. Mississippi
74
14.9
36
118
23.9
0.6
S. Typhimurium 135
58
11.6
28
43
8.7
1.3
S. Typhimurium 44
11
2.2
5
2
0.4
5.5
S. Virchow 8
5
1.0
2
2
0.4
2.5
S. Typhimurium 9
4
0.8
2
4
0.8
1.0
S. Enteritidis 6a
4
0.8
2
0
Victoria S. Typhimurium 135
272
5.1
16
214
4.1
1.3
S. Typhimurium 44
196
3.7
12
283
5.4
0.7
S. Typhimurium 9
154
2.9
9
141
2.7
1.1
S. Typhimurium 170/108
130
2.5
8
112
2.2
1.2
S. Stanley
40
0.8
2
44
0.8
0.9

* Where there were multiple 5th ranking Salmonella types all data have been shown; Western Australia data not included due to incomplete phage typing of S. Typhimurium, S. Enteritidis, and S. Virchow in 2008.

† Rate per 100,000 population.

‡ Proportion of total Salmonella notified for this jurisdiction in 2008.

§ Ratio of the number of cases in 2008 compared to the number in 2007.

Table 3: Numbers, rates, and proportions of top 5 Salmonella infections, Western Australia, 2007 to 2008

OzFoodNet site
Serotype
2008 Proportion 2007 2008/2007 ratio
n Rate* (%) n Rate
Western Australia S. Typhimurium
302
14.0
35
392
18.6
0.8
S. Enteritidis
139
6.4
16
105
5.0
1.3
S. Saintpaul
25
1.2
3
48
2.3
0.5
S. Chester
24
1.1
3
26
1.2
0.9
S. Kiambu
20
0.9
2
9
0.4
2.2
S. Muenchen
20
0.9
2
23
1.1
0.9

* Rate per 100,000 population.

† Proportion of total Salmonella notified for this jurisdiction in 2008.

‡ Ratio of the number of cases in 2008 compared to the number in 2007.

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Salmonella Enteritidis

Salmonella Enteritidis is a globally important Salmonella serotype that can infect the internal contents of eggs, but is not endemic in Australian egg layer flocks. To monitor the emergence of this strain in Australia, OzFoodNet conducts enhanced surveillance of locally-acquired infections of S. Enteritidis. The majority of cases in Australia are associated with overseas travel.

During 2008, OzFoodNet sites reported 511 cases of S. Enteritidis infection (Table 4). Of those cases where travel status was reported, 83% (399/480) had travelled overseas and cases often reported visiting several countries. A travel history could not be obtained for 6% (31/511) of cases in 2008, compared with 18% of cases (73/396) in 2007 and 24% (72/305) of cases in 2006.

Table 4: Number of Salmonella Enteritidis infections, Australia, 2008, by travel history and state or territory

State or territory
History of overseas travel
Yes No Unknown Total
Australian Capital Territory
8
0
1
9
New South Wales
72
29
0
101
Northern Territory
4
2
0
6
Queensland
59
37
19
115
South Australia
34
2
2
38
Tasmania
6
2
0
8
Victoria
89
1
5
95
Western Australia
127
8
4
139
Total
399
81
31
511

Of the cases that were known to have been acquired overseas, 80% (321/399) reported travel to South East Asia. This compares with only 13% (714,000 of 5,551,600) of returning travellers coming from South East Asia in 2008 (relative risk [RR] 28, 95% confidence interval [CI] 22–36).10 Similar to previous years, the most common country of acquisition for overseas-acquired cases was Indonesia, with 43% (173/399) of cases reporting travel there, while comprising only 2% (94,000 of 5,551,600) of travel undertaken in 2008 (RR 44, 95% CI 36–54). Thailand was the 2nd most common country of acquisition with 16% (63/399) of all notifications that were known to have been acquired overseas, followed by Malaysia with 10% (40/399) and Singapore with 6% (25/399). The most common infecting phage types amongst overseas-acquired cases were 6a (17.5%) and 1 (11.3%) (Table 5).

Table 5: Number and percentage of each phage type for of overseas-acquired cases of Salmonella Enteritidis, Australia, 2008

Phage type
Total
  n %
6a
70
17.5
1
45
11.3
4
20
5.0
1b
19
4.8
21
19
4.8
Reactions do not conform
17
4.3
Untypable
10
2.5
21b var
8
2.0
8
7
1.8
21c
7
1.8
26
6
1.5
Other phage types
32
8.0
No phage type was provided
139
34.8
Total
399
100.0

* The number of overseas-acquired cases with no phage type available includes 123 cases from Western Australia, where phage typing ceased in June 2007.

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All states and territories except the Australian Capital Territory reported locally acquired S. Enteritidis cases in 2008. In total, 16% (81/511) of S. Enteritidis infections were locally-acquired, which was higher than previous years. There was an average of 44 locally-acquired cases per year between 2003 and 2007. In 2008, 30% (24/81) of locally-acquired infections were due to S. Enteritidis 26, while 16% (13/81) were due to S. Enteritidis 6a. No phage type was recorded for 22% (18/81) of locally-acquired cases, the majority of which were reported from New South Wales. Queensland reported 90% (19/21) of S. Enteritidis 26 cases with infections occurring throughout the year, except during winter months. In contrast, S. Enteritidis 6a occurred mainly in the last half of 2008 and affected 3 jurisdictions; Queensland, New South Wales and Tasmania.

Completeness of Salmonella serotyping and phage typing

Overall, 94% (6,983/7,464) of Salmonella notifications on state and territory databases contained information about serotype and/or phage type (excluding Western Australia). In Australia, 6 serotypes are routinely phage typed: Bovismorbificans; Enteritidis; Hadar; Heidelberg; Typhimurium; and Virchow. In 2008, phage typing was greater than 90% complete for serotypes Typhimurium, Virchow and Enteritidis (Table 6). There was an overall decline in the percentage of notifications with phage type reported in 2008 compared with previous years, with 94.1% containing complete information on phage type during 2008 (excluding Western Australia where routine phage typing ceased after June 2007).

Table 6: Percentage of Salmonella notifications for 6 serotypes notified to state and territory health departments with phage type information available, Australia,* 2003 to 2008

Salmonella serotype
2003 2004 2005 2006 2007 2008
S. Bovismorbificans
94.7
95.9
95
96.9
97.4
83.5
S. Enteritidis
97.6
95.2
97.6
98.1
94.1
92.3
S. Hadar
100.0
90.0
87.0
100.0
90.0
81.3
S. Heidelberg
96.3
89.5
88.4
95.0
90.0
80.5
S. Typhimurium
98.8
98.7
98.6
98.3
98.3
94.8
S. Virchow
98.9
99.8
98.7
99.2
95.4
93.4

* 2007 to 2008 data excluding Western Australia, where phage typing ceased in June 2007.

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Campylobacter infections

In 2008, OzFoodNet sites (excluding New South Wales) reported 15,535 cases of Campylobacter infection; a rate of 108 cases per 100,000 population (Table 1). The lowest and highest rates of Campylobacter notification were in Western Australia (84.5 cases per 100,000 population) and in South Australia (124 cases per 100,000 population) respectively. Fifty-four per cent of notified cases were male, which is consistent with previous years. Notification rates were highest among males in nearly all age groups and particularly in males aged less than 5 years and greater than 65 years. The highest age-specific rate of notifications was in 1-year-old infants for both males and females (233 and 180 cases per 100,000 population, respectively) with additional peaks in the 20–29 year age group (Figure 2).

Figure 2: Campylobacteriosis notification rates and sex, Australia, 2008, by age group

Campylobacteriosis notification rates and sex, Australia, 2008, by age group

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Listeria infections

OzFoodNet sites reported 65 cases of Listeria monocytogenes infection in 2008 representing a crude rate of 0.3 per 100,000 population; the same as the 5-year historical mean (Table 1).

Similar to previous years, 18% (12/65) of cases were pregnancy-associated infections. In 2008, 47% (25/53) of the non-pregnancy related cases were female. Fifty-one per cent (33/65) of notifications were in people aged 60 years or over. The highest age-specific notification rate was in people aged 85 years or over (1.9 cases per 100,000 population, 7 cases) (Figure 3). Eight per cent (1/12) of pregnancy related cases and 21% (11/53) of non-pregnancy associated cases in 2008 were fatal (Figure 4).

Figure 3: Listeriosis notifications, Australia, 2008, by age group

Listeriosis notifications, Australia, 2008, by age group

Figure 4: Notifications and case fatality ratio (CFR %) for fatal and surviving listeriosis cases, Australia, 2003 to 2008, by pregnancy status

Notifications and case fatality ratio (CFR %) for fatal and surviving listeriosis cases, Australia, 2003 to 2008, by pregnancy status

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Shigella infections

There were 828 notifications of shigellosis in Australia in 2008; a rate of 3.9 notifications per 100,000 population compared with a mean of 568 cases (2.8 notifications per 100,000 population) per year between 2003 and 2008 (Table 1). As in previous years, the Northern Territory reported the highest notification rate with 79.6 cases per 100,000 population compared with a mean of 71.9 cases per 100,000 population between the years 2003 and 2007.

The increased notification rate of shigellosis in 2008 compared with previous years is in part explained by an outbreak of S. sonnei biotype g with matching antibiotic resistance profiles amongst men who have sexual contact with other men (MSM), with cases in New South Wales (n = 12), Queensland (n = 4), Victoria (n = 29) and Western Australia (n = 2). Victoria also reported an outbreak of S. sonnei biotype g with matching antibiotic resistance profiles (different to the MSM cluster) amongst members of the Jewish community in Melbourne, with 12 cases and a further 2 cases from the same geographical area, although no source for the outbreak was identified. South Australia reported clusters of S. flexneri 6 with 3 cases and S. sonnei biotype a with 8 cases.

In 2008, notification rates for shigellosis were highest in males and females aged 0–4 years, with 12.5 and 13.9 notifications per 100,000 population respectively. Secondary peaks were observed in children aged 5–9 years and in males aged 30–44 years (Figure 5). Amongst children aged less than 5 years, the highest notification rates were in children aged 1 year. In 2008, 50% of all shigellosis cases were male. In 2008, 38.4% (318/828) of infections occurred in people of Aboriginal or Torres Strait Island origin and this proportion varied by state or territory.

Figure 5: Age and sex specific notification rates of shigellosis, Australia 2008

Age and sex specific notification rates of shigellosis, Australia 2008

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The most frequently reported Shigella biotype in 2008 was S. sonnei biotype a, followed by S. sonnei biotype g. Together these biotypes accounted for 50% of all Shigella infections reported in 2008 (Table 7).

Table 7: Number, percentage and ratio of the top 10 Shigella infections, Australia, 2006 to 2008

Biotype
2006 2007 2008 2008/2006 ratio* 2008/2007 ratio*
n % n % n %
Shigella sonnei biotype a
80
14.7
134
22.3
232
28.0
1.9
1.3
Shigella sonnei biotype g
76
13.9
98
16.3
185
22.3
1.6
1.4
Shigella flexneri 2a
54
9.9
64
10.6
55
6.6
0.7
0.6
Shigella flexneri 4a mannitol neg
94
17.2
69
11.5
103
12.4
0.7
1.1
Shigella sonnei untyped
31
5.7
37
6.1
48
5.8
1.0
0.9
Shigella flexneri 4
84
15.4
49
8.1
35
4.2
0.3
0.5
Shigella flexneri untyped
15
2.7
20
3.3
21
2.5
0.9
0.8
Shigella flexneri 6
16
2.9
3
0.5
16
1.9
0.7
3.9
Shigella flexneri 3a
18
3.3
37
6.1
41
5.0
1.5
0.8
Shigella
22
4.0
21
3.5
27
3.3
0.8
0.9

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Typhoid

In Australia during 2008, there were 106 cases of typhoid due to Salmonella serotype Typhi infection. This equated to a rate of 0.5 cases per 100,000 population compared with a mean of 0.3 cases per 100,000 between 2003 and 2007 (Table 1). Cases were reported from all Australian states and territories except for the Australian Capital Territory and Tasmania.

Notification rates for typhoid in 2008 were highest in young adults, with 1.4 cases per 100,000 (21 cases) and 1.1 cases per 100,000 (16 cases) amongst the 20–24 year and 25–29 year age groups, respectively (Figure 6). Overseas travel was the primary risk factor for typhoid in Australia in 2008 with 92.5% (98/106) of cases known to have been acquired overseas. In 2008, 59.4% (63/106) of cases were male.

Figure 6: Age specific notification rates for typhoid, Australia, 2008

Age specific notification rates for typhoid, Australia, 2008

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India was the most frequently reported country of travel for overseas-acquired cases of typhoid in 2008, with 50% (49/98) of cases, followed by Bangladesh, Indonesia, and Pakistan, each reported as a travel destination by 9% (9/98) of overseas-acquired cases (Table 8). The most common phage type of S. Typhi isolated from cases was E1 (36.8%, 39/106), and the majority of cases infected with E1 (79%, 30/39) reported travel to India (including cases who also reported travel to Bangladesh and Thailand). This was consistent with previous years, with approximately half of overseas-acquired cases in 2007 (51%, 42/83) reporting travel to India and 40% (19/48) being phage type E1.12

Table 8: Salmonella Typhi phage types isolated from cases (n=106), Australia, 2008

Country where travelled
Phage type (n)
Number of cases
India E1(29), 36(2), A (3), D2 (2), degraded (2), E9 (2) J1(5), untypeable (2)
47
Bangladesh E7 (1), E9 (2), non-typeable(6)
9
Indonesia D2 (2), degraded(1), E2(1), E2 var(1), M1(1), non-typeable (2), unknown(1)
9
Pakistan E9 (6), T(1), non-typeable(1), 51(1)
9
Samoa E1 (4), E7 (1)E9 (1)
6
Papua New Guinea D2 (2), G3 (1)
3
Philippines A (1), B1 var 1(1), degraded (1)
3
Thailand and Burma O var (3)
3
Cambodia E1 (1)
1
China and India 36 (1)
1
India and Bangladesh E1 (1)
1
India or Thailand D2 (1)
1
Malaysia E1 (1)
1
Malaysia and Thailand D1 (1)
1
Nepal E1 (1)
1
Sudan Degraded (1)
1
Thailand and China Untypeable (1)
1
No travel reported E1 (2), untypeable (1), degraded (1), A (2), 40 (1), C4 (1)
8

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Hepatitis A

Hepatitis A notifications declined in 2008, with 276 cases reported compared with a mean of 306 cases per year between 2003 and 2007 (Table 1 and Figure 7).13 This decline may have been due to increased uptake of vaccine amongst high risk groups such as travellers, and targeted vaccination programs for Indigenous children.13

Figure 7: Trends in notifications of hepatitis A, Australia, 1991 to 2008, by month of diagnosis and inset, notifications of hepatitis A, 2008, by month and state or territory

Trends in notifications of hepatitis A, Australia, 1991 to 2008, by month of diagnosis and inset, notifications of hepatitis A, 2008, by month and state or territory

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In 2008, the median age of notified cases was 24 years old (range 1–97 years) and 57% (158/276) of cases were male. Indigenous status was known for 88.8% of cases in 2008. The proportion of cases of hepatitis A among Indigenous persons declined from a mean of 14% (167/1,193) of cases for the years 2003 to 2006 to 1.2% (3/245) of cases in 2008. This marked decrease in the number and proportion of cases that were Indigenous may have been due to targeted vaccination programs for Indigenous children in Queensland commencing in 199914 as well as free vaccine for Indigenous children in South Australia, Western Australia and the Northern Territory from 2006.

Overseas travel was found to be the most frequently reported risk factor for infection amongst cases of hepatitis A in 2008, with 54.7% (151/276) reporting overseas travel (Table 9). The most commonly reported overseas travel destinations were India (29 cases), Indonesia (11 cases) and Pakistan (8 cases). Household contact with confirmed cases was identified as a risk factor for 4.3% (12/276) of cases, highlighting the importance of post-exposure prophylaxis for contacts. In 2008, 3.6% (10/276) of notified hepatitis A cases were suspected to be associated with foodborne transmission.

Table 9: Risk factors identified for cases of hepatitis A, Australia, 2008

Risk factor
Number of cases Percentage of cases
Overseas travel
151
54.7
Household contact with confirmed cases
12
4.3
Associated with foodborne outbreak
10
3.6
Contact with confirmed cases
3
1.1
Overseas travel and contact with cases
2
0.7
Contact with injecting drug users
1
0.4
Contact with possible cases
1
0.4
Injecting drug use
1
0.4
Overseas travel and male-to-male sexual contact
1
0.4
Recent migrant from endemic area
1
0.4
No known risk factors
73
26.4
Unknown
20
7.2
Total
276
100

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Shiga toxin-producing Escherichia coli infections

In 2008, there were 106 notifications of STEC in Australia, equating to a rate of 0.5 cases per 100,000 population. This was an increase over a mean of 0.4 cases per 100,000 population between 2003 and 2007 (Table 1). Cases were reported from South Australia (39), Queensland (37), New South Wales (19) and Victoria (11). There were no cases in the Australian Capital Territory, the Northern Territory, Tasmania or Western Australia in 2008. Rates of STEC infection are strongly influenced by jurisdictional practices regarding the screening of stool specimens.15 In particular, South Australia routinely tests all bloody stools by polymerase chain reaction (PCR) for gene coding for Shiga toxins and other virulence factors, making rates for this State the highest in the country.

In 2008, 51.9% of cases were female. The median age of cases was 24 years (range 0–89 years). Notification rates were highest in people aged 85 years or older, young people aged 10–14 years and children aged 4 years or under (Figure 8).

Figure 8: Age specific notification rates of Shiga toxin-producing Escherichia coli, Australia, 2008

Age specific notification rates of Shiga toxin-producing Escherichia coli, Australia, 2008

* Low case numbers make rates unstable and only age specific rates (not age and sex) have been calculated for Shiga toxin-producing Escherichia coli, with counts of less than 20 in all groups.

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The number of STEC notifications has increased over the past 5 years, from an average of 5 cases per month between 2003 and 2006 to 9 cases per month between 2007 and 2008 (Figure 9). Seven cases of STEC in 2008 were associated with an outbreak due to waterborne transmission at a camp in Queensland. STEC notifications have a seasonal association, tending to increase during the warmer months (November to April).

Figure 9: Shiga toxin-producing Escherichia coli notifications, Australia, 2003 to 2008, by month and year of diagnosis

Shiga toxin-producing Escherichia coli notifications, Australia, 2003 to 2008, by month and year of diagnosis

The most commonly identified serogroups of STEC cases in 2008 were O157, with 27 cases (25.5%), followed by O111 (8 cases, 7.5%) and O26 (7 cases, 6.6%). No organism was isolated or the serogroup was reported for 33.0% (35/106) of cases.

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Haemolytic uraemic syndrome

In 2008, OzFoodNet sites reported 31 cases of HUS; a rate of 0.15 cases per 100,000 population (Table 1), compared with a mean of 0.08 cases per 100,000 population for the years 2003 to 2007. New South Wales reported the largest number of cases (17 cases), followed by Queensland (7 cases) and Victoria (4 cases). Similar to previous years, the highest notification rate in 2008 was in children aged 0–4 years (Figure 10), with 35.5% (11/31) of cases notified in this age group.

Figure 10: Age specific notifications of haemolytic uraemic syndrome, Australia, 2008

Age specific notifications of haemolytic uraemic syndrome, Australia, 2008

HUS may be due to causes other than Shiga toxin-producing E. coli, including other non-foodborne pathogens and genetic predisposition. In 2008, an antecedent STEC infection was reported for 52% (16/31) of cases, with serogroup information reported for 56% (9/16) of these cases. E. coli O111 was reported in 5 instances, while serogroup O157 and O166 were reported for 1 case each. In 2008, 1 case of HUS was known to be due to a non-bacterial cause, 2 cases resulted from Streptococcus pneumoniae infection, and in the remaining 11 cases no aetiology was reported.

In Australia, HUS cases are more common during late spring and early summer,12 with 37.4% (58/155) of cases occurring in the months of November, December or January for the years 2003 to 2008 (Figure 11). This was significantly more than expected (P = 0.01).

Figure 11: Notifications of haemolytic uraemic syndrome by month and year of diagnosis, Australia, 2003 to 2008

Notifications of haemolytic uraemic syndrome by month and year of diagnosis, Australia, 2003 to 2008

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Gastrointestinal and foodborne disease outbreaks

During 2008, OzFoodNet sites reported 1,545 outbreaks of gastroenteritis, including foodborne disease, which affected 25,555 people and hospitalised 691 (Table 10). There were 99 deaths during these outbreaks. This compares with 1,882 and 1,544 outbreaks reported across Australia in 2007 and 2006, respectively.

Table 10: Outbreaks of gastroenteritis including foodborne disease reported to state and territory health departments, Australia, 2008

Mode of transmission
Number of outbreaks Number affected Hospitalised Fatalities
Foodborne
104
1,454
96
11
Person-to-person
1,276
22,508
502
81
Unknown mode (Salmonella cluster)
22
309
46
0
Unknown mode (other pathogen)
22
157
19
1
Unknown mode (unknown aetiology)
118
1,085
26
6
Waterborne
1
7
1
0
Total
1,545
25,555
691
99

* Two outbreaks are included that commenced in December 2007, but were notified and investigated in 2008, one of them foodborne transmission and the other person-to-person.

Outbreaks due to person-to-person spread

In 2008, 83% (1,276/1,545) of all gastroenteritis outbreaks were due to person-to-person spread. There were 22,508 people affected in these outbreaks and 81 deaths. These outbreaks were most common in aged care homes, with 61% (784/1,276) of outbreaks occurring in this setting, followed by 17% (211/1,276) and 15% (189/1,276) in hospitals and child care centres respectively. Approximately 40% (513/1,276) of outbreaks spread from person-to-person were caused by norovirus, followed by only 3% of outbreaks caused by rotavirus. Forty-two per cent (531/1,276) of outbreaks due to person-to-person spread were of unknown aetiology. Late winter and early spring were the peak seasons for person-to-person outbreaks, with 38% (487/1,276) of outbreaks reported in the months of August to October 2008.

Waterborne outbreaks

There was 1 outbreak due to waterborne transmission; an outbreak of E. coli (multiple serotypes) associated with the consumption of tank water, affecting 7 people at a camp.

Outbreaks with unknown mode of transmission

There were 162 outbreaks where the mode of transmission was not determined, affecting a total of 1,551 people. There were 22 investigations of Salmonella and 22 investigations of other pathogens that were clustered in time, place or person where investigators were unable to develop an adequate hypothesis for the source of illness. There were 118 outbreaks where investigators were unable to determine the mode of transmission or the aetiology.

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Foodborne outbreaks

In 2008, there were 104 outbreaks of foodborne disease affecting 1,454 people, compared with 149 and 115 foodborne outbreaks in 2007 and 2006, respectively (Appendix). There were 96 people hospitalised and 11 deaths reported during these outbreaks.

The overall rate of reported foodborne disease outbreaks for Australia was 4.9 outbreaks per million population in 2008 (Table 11). The highest rates of foodborne outbreak reporting were from the Northern Territory with 22.7 per million population and New South Wales with 7.6 per million population. Outbreaks were more common in warmer months (Figure 12).

Table 11: Outbreaks of foodborne disease, Australia, 2008, by OzFoodNet site

State
Number of outbreaks People affected Mean size (persons) Hospitalised Outbreaks per million population
ACT
1
24
24.0
2
2.9
NSW
53
632
11.9
31
7.6
NT
5
36
7.2
7
22.7
Qld
14
137
9.8
3
3.3
SA
4
66
16.5
14
2.5
Tas
2
81
40.5
9
4.0
Vic
21
328
15.6
27
4.0
WA
4
150
37.5
3
1.8
Australia
104
1454
14.0
96
4.9

Figure 12: Outbreaks of foodborne Salmonella infections and other aetiological agents (n=687) reported to state and territory health departments, Australia, 2003–2008, by month and year of outbreak

Outbreaks of foodborne <em>Salmonella</em> infections and other aetiological agents (n=687) reported to state and territory health departments, Australia, 2003-2008, by month and year of outbreak

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Aetiological agents

The mostly commonly implicated aetiological agent in outbreaks of foodborne illness was Salmonella, which caused 34% (35/104) of outbreaks; 89% (31/35) of these being due to S. Typhimurium (Table 12).

Table 12: Aetiological agents responsible for foodborne disease outbreaks, number of outbreaks and persons affected, Australia, 2008

Agent category
Number of outbreaks People affected Mean size (people) Hospitalised
Salmonella Typhimurium
31
443
14
67
Foodborne intoxication
13
348
27
6
Viral
8
238
30
4
Ciguatera/histamine poisoning
6
22
4
2
Campylobacter
4
16
4
0
Other Salmonella serotypes
4
43
11
4
Unknown
38
344
9
13
Total
104
1,454
14
96

Toxin-mediated outbreaks comprised 18% (19/104) of all foodborne outbreaks, with 32% (6/19) of these due to fish toxins (5 outbreaks of ciguatera fish poisoning, and 1 outbreak of histamine poisoning) and 68% (13/19) due to foodborne intoxications with Bacillus cereus, Clostridium perfringens or Staphylococcus aureus.

There were also 4 foodborne outbreaks of Campylobacter, and 8 outbreaks were caused by viral agents. In 2008, 37% (38/104) of foodborne outbreaks were of unknown aetiology compared with 38% in the previous year.

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Food vehicles

A wide variety of food vehicles were implicated in outbreaks of foodborne disease in 2008. Investigators were unable to identify a food vehicle in 28% (29/104) of outbreaks (Table 13).

Table 13: Categories of food vehicles implicated in foodborne disease outbreaks, Australia, 2008

Vehicle category
Number of outbreaks Number affected Mean size (persons) Hospitalised
Mixed dishes
17
300
6
8
Egg-containing desserts
9
98
9
10
Chicken and chicken-containing dishes
9
104
12
7
Meat and meat-containing dishes
7
90
13
2
Fish
6
22
4
2
Salads and/or sandwiches
6
68
11
6
Molluscs
4
19
5
0
Egg-based sauces and dressings
5
133
27
12
Eggs
3
26
9
8
Pasta dish
3
43
14
3
Vitamised foods
2
45
23
7
Egg-containing dish
1
3
3
1
Rice based dish
1
3
3
0
Sauces and gravies
1
31
31
0
Suspected chicken and/or eggs
1
14
14
2
Unknown
29
455
16
28
Total
104
1,454
14
96

There were 20 outbreaks associated with eggs; these comprised 19% of all foodborne outbreaks and included all outbreaks that investigators considered to be egg-associated (Table 14). Nine of these outbreaks involved desserts that commonly contain raw egg (such as chocolate mousse and tiramisu), five were due to egg-based sauces or dressings (such as aioli or hollandaise sauce), three were due to eggs as a whole food and 1 outbreak each was due to mixed dishes, a dish containing eggs and suspected chicken and/or eggs. These outbreaks affected a total of 289 people and hospitalised 36 people.

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Table 14: Outbreaks of foodborne illness associated with egg-based dishes (n=20), Australia, 2008

State
Setting prepared
Agent responsible
Number affected Evidence
Responsible vehicles
ACT Restaurant S. Typhimurium 44
24
A
Hollandaise sauce and poached eggs
NSW Private residence S. Typhimurium
20
D
Eggs
Private residence S. Typhimurium 170
17
D
Eggs used to make cake filling
Restaurant S. Typhimurium 126
3
D
Chicken salad made with raw egg dressing
Unknown Unknown
14
D
Suspected chicken and/or eggs
Aged care facility S. Typhimurium 144
10
M
Chocolate mousse with raw eggs
Bakery S. Typhimurium
10
A
Chocolate mousse cake
Bakery S. Typhimurium
16
D
Chocolate mousse cake
Restaurant S. Typhimurium 170 var
24
A
Raw eggs in Caesar salad dressing
National franchised fast food S. Typhimurium 44
3
D
Bacon and egg sandwich
Restaurant Unknown
5
D
Aioli made with raw eggs
NT Restaurant S. Typhimurium 9
2
D
Suspected raw egg mayonnaise/Caesar salad dressing
SA Bakery S. Typhimurium 9
15
A
Sweet bakery products
Tas Restaurant S. Typhimurium 135a
78
AM
Aioli
Private residence S. Typhimurium 135a
3
D
Cake mix containing raw egg
Vic Private residence S. Typhimurium 135a
7
M
Ice cream cake made with raw eggs
Private residence S. Typhimurium 44
12
D
Lemon dessert made with raw eggs
Restaurant Unknown
4
D
Desserts suspected
Restaurant S. Typhimurium 44
4
D
Desserts suspected
Restaurant S. Typhimurium 170
4
D
Tiramisu

D Descriptive evidence implicating the vehicle

A Analytical epidemiological association between illness and vehicle

M Microbiological confirmation of aetiology in vehicle and cases.

Fifteen per cent (16/104) of outbreaks were due to mixed dishes, including buffets where a variety of dishes were served, and investigators were unable to implicate a particular ingredient (1 outbreak was suspected to be egg-associated). Nine per cent (9/104) of outbreaks were due to chicken or dishes containing chicken and 7% (7/104) were due to meat or dishes containing meat, 6% (6/104) due to fish and 6% (6/104) due to salads and/or sandwiches and 4% (4/104) due to molluscs. The remaining outbreaks were due to pasta dishes (3), vitamised foods (2), a rice-based dish (1) and a non-egg-based sauce or gravy (1).

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Settings where food was prepared

In 2008, foods implicated in outbreaks were most commonly prepared in restaurants (43%, 45/104), by commercial caterers (12%, 12/104) or in private residences (12%, 12/104). Outbreaks were less frequently reported as being associated with foods prepared in aged care facilities (7%, 7/104), takeaway premises (6%, 6/104) or primary produce (5%, 5/104) (Table 15). In 2008 the only implicated foods that were contaminated in primary produce environments were fish involved in ciguatera fish poisoning outbreaks. The species of fish involved in these outbreaks included yellowtail kingfish, black kingfish, red throat emperor/reef snapper, yellow king/Samson fish and cod.

Table 15: Food preparation settings implicated in disease outbreaks, Australia, 2008

Setting prepared
Number of outbreaks Proportion of all outbreaks (%)* Number affected (persons)
Restaurant
45
43
530
Commercial caterer
12
12
259
Private residence
12
12
107
Aged care facility
7
7
178
Takeaway
6
6
77
Primary produce
5
5
21
Bakery
4
4
42
Institution
4
4
101
Camp
2
2
29
Grocery store/delicatessen
1
1
2
Institution – other
1
1
15
Military
1
1
45
National franchised fast food
1
1
3
School
1
1
26
Unknown
2
2
19
Total
104
1,454

* Percentages do not add up to 100% due to rounding.

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Investigative methods and levels of evidence

To investigate these foodborne outbreaks, state and territory investigators conducted 28 retrospective cohort studies and 4 case control studies. Descriptive case series were obtained for 62 outbreaks. No individual data were collected on patients in 10 outbreaks. An analytical association between illness and the implicated food as well as microbiological evidence of the aetiological agent in the implicated food was obtained for 3 outbreaks. Analytical evidence alone was obtained for 14 outbreaks and microbiological evidence alone for 9 outbreaks. These confirmed outbreaks comprised 25% (26/104) of all outbreaks compared with 46% in 2007 and 41% in 2006. Investigators relied on descriptive evidence implicating the food vehicle in 54 outbreaks, and there were no data available on the evidence obtained for 24 outbreaks (many of these were not attributed to a specific food vehicle).

Significant outbreaks

In 2008 there were 8 outbreaks of foodborne illness affecting 40 or more people: 2 outbreaks of C. perfringens; 1 mixed outbreak of C. perfringens and B. cereus; 3 outbreaks of norovirus; one of S. Typhimurium 135a; and one of unknown aetiology. In total, these outbreaks affected 481 people, with a range of 41 to 78 people affected per outbreak. Nine people were hospitalised, all of them associated with a Salmonella outbreak.

Tasmania reported the largest of these outbreaks; an outbreak of S. Typhimurium 135a affecting 78 people who dined at the same restaurant over a 4-day period. A cohort study of 212 restaurant patrons showed a very strong association between the consumption of aioli and illness (odds ratio [OR] = 511, 95% CI 90–4,709), P < 0.000). S. Typhimurium 135a was isolated from 4 food items collected from the food premises; the aioli, 2 foods containing the aioli, and a guacamole, which was considered by the investigators likely to have been cross-contaminated. Eggs supplied to the food business were from the same producer who was implicated in outbreaks of this Salmonella strain in 2005 and 2007.16,17

New South Wales reported 3 outbreaks of foodborne intoxication affecting more than 40 people:

an outbreak of gastrointestinal illness affecting all 75 guests of a birthday party where food had been supplied by an unregistered catering business. Several foods contained C. perfringens and B. cereus enterotoxins, and the proprietor was advised to cease preparing any foods for sale until the premises used for food preparation was brought up to a satisfactory standard.

an outbreak of gastroenteritis affecting 45 of 100 people at an army training facility. A cohort study found an association between a curry meal and illness. Seven stool specimens were positive for C. perfringens enterotoxin type A. Temperature abuse of foods and inadequate equipment were considered by investigators to have been contributing factors in this outbreak.

an outbreak of gastrointestinal illness affected 69 of 131 residents of an aged care facility over a 1 month period beginning in June. The outbreak may have involved two or more smaller peaks of illness accounting for the long time period of the outbreak. Seven out of 10 stool specimens were positive for C. perfringens enterotoxin type A. Consumption of vitamised or pureed diets and living in the high dependency unit were found to increase the risk of illness, although these 2 factors were not independent. Food handling and hygiene practices were found to be satisfactory.

A large outbreak of norovirus affected 56 of 138 attendees on a 5-day training course at a Brisbane academy in March. A retrospective cohort study identified an association between a cold meat and salad dish, provided by an outside caterer, and illness (RR = 2.0, 95% CI 1.5–2.7, P = 0.004). Eight stool specimens were positive for norovirus.18

An outbreak of norovirus gastroenteritis affected 75 of 366 people eating a buffet meal at a Western Australian restaurant. A Thai fish curry was the only food significantly associated with illness (RR=1.30, P < 0.05), however this food was consumed by only 28% of cases. Six faecal specimens obtained were positive for norovirus. An inspection of the premises did not identify any major deficiencies and there were no reports of staff illness.19

An outbreak of norovirus at an aged care facility in Western Australia affected 42 people including residents and staff. The index case was a chef who had prepared food while he was ill with gastroenteritis. Other staff and residents subsequently became ill over a 24 hour period. No single food was identified as the vehicle in this outbreak, and some person-to-person spread may have been possible.

Victoria reported an outbreak of unknown aetiology affecting 41 people from 3 different groups who ate at a large buffet restaurant in October. While C. perfringens enterotoxin was suspected as the cause of this outbreak, it was detected in only one out of 13 stool specimens collected. Univariate analysis showed that illness was associated with consumption of lamb tenderloin (RR 4.0; 95% CI 2.3–7.0), chicken cacciatore (RR 2.0; 95% CI 1.4–2.8) and roast pork (RR 2.4; 95% CI 1.4–4.0).20

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Discussion

This report documents changes in the incidence of gastrointestinal diseases commonly transmitted by food in Australia. There was a decrease in the number of notifications of Salmonella and Campylobacter compared with previous years. Despite these declines, these 2 infections continue to be reported at higher rates than in other developed countries.2,21 This is the first time hepatitis A has been included in the annual report. While the proportion of hepatitis A infections that may be foodborne is thought to be less than 10%, it is important to keep this infection under surveillance as it can cause large outbreaks of foodborne disease.22,23

Similar to 2007, higher rates of campylobacteriosis were observed in males than in females, particularly those over the age of 45 years.12 The reasons for this were unclear, but may relate to higher susceptibility of males in this age group due to the use of acid suppressive medications.24 In Australia, the primary source of Campylobacter infection is thought to be chicken consumption, causing an estimated 29.3% of all infections.25 This is consistent with findings from other countries, although recent work in New Zealand highlights that the fraction of campylobacteriosis due to chicken meat consumption may be considerably higher.26 The New Zealand Food Safety Authority recently announced that the poultry industry had successfully reduced the prevalence of Campylobacter on chicken meat, which had lead to a marked decline in human cases.27

In 2008, the proportion of Salmonella isolates that contained appropriate information on serotype and/or phage type decreased by 3% compared with 2007. Typing is vital for outbreak detection and monitoring trends. Western Australia ceased phage typing isolates in 2007 in favour of pulsed field gel electrophoresis, which is a discriminatory technique for typing Salmonella but not routinely used by other Australian laboratories.28 Other jurisdictions used multi-locus variable number of tandem repeats analysis to compare strains during outbreaks, which proved rapid and very useful. The use of these different typing schemes caused some complexity during multi-jurisdictional investigations. Despite this there is increasing harmonisation in typing schemes used by Australian laboratories.

Despite travel warnings and vaccine recommendations, travellers continue to acquire infections abroad, the risk being higher for long-term travellers and people who visit friends or relatives.29 In this report, we summarised data on 3 infections that are commonly acquired overseas; typhoid (96% of cases), hepatitis A (54.7% of cases) and S. Enteritidis (83% of cases). A large proportion of hepatitis A infections are likely to be acquired while visiting friends or relatives, with a recent study in New South Wales showing travellers who were born in endemic areas were at higher risk of infection.30 Travellers visiting friends or relatives may be less likely than other travellers to seek advice from a website such as the Department of Foreign Affairs’ Smartraveller (http://www.smartraveller.gov.au), or from a travel clinic or general practitioner prior to travel, due to a perception of lower risk and lack of access to culturally and linguistically appropriate advice. It is important that prevention information is targeted at these groups. We compared the reported country and region of acquisition for S. Enteritidis infections with the proportion of all returning travellers who had nominated that place as their primary destination and observed that cases were more likely to have travelled to the South East Asian region.

In 2008, OzFoodNet sites reported 1,545 outbreaks of gastrointestinal disease, which was less than that reported in 2007.12 Similar to previous years, the majority of outbreaks in 2008 were transmitted from person to person (83%), with 61% of these reported from aged care facilities, reflecting the frequency with which outbreaks of gastrointestinal illness occur, the ease of transmission in this setting and the improved reporting practices of these facilities. Outbreaks transmitted person-to-person were most frequently of unknown aetiology (42%) followed by norovirus (40%). Norovirus outbreaks peaked in late winter and early spring in 2008.

In 2008, OzFoodNet sites reported 104 foodborne or suspected foodborne outbreaks, a rate of 4.9 outbreaks per million people, with a mean outbreak size of 14 people affected per outbreak. This compares with 7.1 outbreaks per million in Australia in 2007, and an estimated 4.2 outbreaks per million in the United States in 2006.31 Salmonella continues to be the leading cause of reported outbreaks of foodborne illness in Australia, with 34% of outbreaks due to this pathogen, the majority of them due to S. Typhimurium. In 2008, there were 8 large outbreaks of foodborne illness (affecting 40 or more people). The largest of these was due to S. Typhimurium 135a, which affected 78 people who dined at the same restaurant over a 4-day period. Eggs used at the restaurant were supplied by a producer who had been implicated in previous foodborne outbreaks.

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Eggs were suspected as the cause of 27% (20/75) of foodborne outbreaks where investigators were able to identify a food vehicle. Eggs are a commonly consumed food, and as an ingredient of many dishes, and may be served raw or lightly cooked in dishes such as aioli, sauces and desserts. It is important that egg safety continues to be improved in Australia. During 2009, FSANZ continued developing a primary production and processing standard for eggs and egg products that is considering safety of the whole production chain from farm through to retail.32

Since the commencement of OzFoodNet in 2000, the network has successfully enhanced surveillance and conducted applied research into foodborne diseases in Australia. In 2008, OzFoodNet and the New South Wales Food Authority conducted the National Gastroenteritis Survey II (NGSII), which repeated the original survey in 2001–2002.33 The NGSII survey was completed in early 2009 and is currently being analysed. OzFoodNet continues to be engaged in regional capacity building activities through the World Health Organization’s Global Foodborne infections network, and has sent epidemiologists as trainers to 2 training workshops (held in Papua New Guinea and Thailand) in 2008.

It is important to recognise some of the limitations of the data used in this report. Where there are small numbers of notifications, caution must be used in comparisons between jurisdictions and over time. Some of the most common enteric pathogens are not notifiable, particularly norovirus and C. perfringens, which is why surveillance of outbreaks is so important. A limitation of the outbreak data provided by OzFoodNet sites for this report is the potential for variation in categorising features of outbreaks depending on investigator interpretation and circumstances. States and territories are working towards harmonising surveillance and outbreak data to address some of these issues.

Foodborne disease surveillance provides information to assist in not only immediate public health action and the prevention of these diseases, but also to the assessment of food safety policies and campaigns. A national program of surveillance for foodborne diseases and outbreak investigation has many benefits including identifying foods that cause human illness by identifying outbreaks that occur across state and territory borders. Continuing efforts to strengthen the quality of these data will ensure their use by agencies to develop food safety policy and thereby help prevent foodborne illness.

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Acknowledgements

We thank the many epidemiologists, project officers, interviewers and research assistants at each of the OzFoodNet sites who contributed to this report. We acknowledge the work of various public health professionals and laboratory staff around Australia who interviewed patients, tested specimens, typed isolates and investigated outbreaks. We would particularly like to thank jurisdictional laboratories, the Microbiological Diagnostic Unit Public Health Laboratory, the Australian Salmonella Reference Centre at the Institute of Medical and Veterinary Science, and the National Enteric Pathogen Surveillance Scheme for their help with foodborne disease surveillance in 2008. The quality of their work was the foundation of this report. OzFoodNet is an initiative of the Australian Government.

In 2008, the OzFoodNet Working Group and additional contributors were (in alphabetical order): Robert Bell (Qld), Therese Carroll (NSW), Barry Combs (WA), Craig Dalton (HNE Health), Gerard Fitzsimmons (DoHA), Lindy Fritsche (NSW), Kathleen Fullerton (DoHA), Robyn Gibbs (WA), Joy Gregory (Vic), Jenine Gunn (NT) Gillian Hall (NCEPH), Michelle Harlock (NT), Geoff Hogg (MDU), Rebecca Hundy (ACT), Cameron Moffatt (ACT), Katina Kardamanidas (NSW), Martyn Kirk (DoHA), Katrina Knope (DoHA), Karin Lalor (Vic), Mark Salter (FSANZ), Lisa McCallum (SA), Charlotte McKercher (Tas), Michelle McPherson (SA), Tony Merritt (HNE Health), Sally Munnoch (HNE Health), Jennie Musto (NSW), Lillian Mwanri (SA), Nevada Pingault (WA), Jane Raupach (SA), Michelle Robertson (FSANZ), April Roberts-Witeveen (HNE Health), Mark Salter (FSANZ), Cameron Sault (Tas), Craig Shadbolt (NSWFA), Russell Stafford (Qld), Nicola Stephens (Tas), Dayna Swiatek (DoHA), Barbara Telfer (NSW), Hassan Vally (NCEPH, WA), Tory Worgan (HNE Health).

Author details

Correspondence: Ms Katrina Knope, A/Coordinating Epidemiologist, OzFoodNet, Office of Health Protection, Australian Government Department of Health and Ageing, GPO Box 9848, MDP 14, CANBERRA ACT 2601. Telephone: +61 2 6289 2751. Facsimile: +61 2 6289 2500. Email: ozfoodnet@health.gov.au

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References

1. Hall G, Kirk MD, Becker N, Gregory JE, Unicomb L, Millard G, et al. Estimating foodborne gastroenteritis, Australia. Emerg Infect Dis 2005;11(8):1257–1264.

2. Centers for Disease Control and P. Preliminary FoodNet Data on the incidence of infection with pathogens transmitted commonly through food—10 States, 2008. MMWR Morb Mortal Wkly Rep 2009;58(13):333–337.

3. Allos BM, Moore MR, Griffin PM, Tauxe RV. Surveillance for sporadic foodborne disease in the 21st century: the FoodNet perspective. Clin Infect Dis 2004;38 Suppl 3:S115–S120.

4. Hocking AD, ed. Foodborne microorganisms of public health significance. 6th edn: Australian Institute of Food Science and Technology Incorporated; 2003.

5. Majowicz SE, Edge VL, Fazil A, McNab WB, Doré KA, Sockett PN, et al. Estimating the under-reporting rate for infectious gastrointestinal illness in Ontario. Can J Public Health 2005;96(3):178–181.

6. Hall G, Raupach J, Yohannes K, Halliday L, Unicomb L, Kirk M. An estimate of under-reporting of foodborne notifiable diseases: Salmonella, Campylobacter, Shiga toxin-like Escherichia coli (STEC). National Centre for Epidemiology and Population Health Working Paper No. 52, 2006.

7. Kirk MD, McKay I, Hall GV, Dalton CB, Stafford R, Unicomb L, et al. Food safety: foodborne disease in Australia: The OzFoodNet experience. Clin Infect Dis 2008;47(3):392–400.

8. Lindenmayer P. Networking for health protection: the Communicable Diseases Network Australia. Commun Dis Intell 2001;25(4):266–269.

9. Australian Bureau of Statistics. Population by age and sex, Australian states and territories, June 2008. ABS Cat. no. 3101.0. Canberra; 2008.

10. Australian Government Department of Customs. Check-in ports 2007.

11. Ashbolt R, Kirk MD. Salmonella Mississippi infections in Tasmania: the role of native Australian animals and untreated drinking water. Epidemiol Infect 2006;134(6):1257–1265.

12. OzFoodNet Working Group. Monitoring the incidence and causes of diseases potentially transmitted by food in Australia: annual report of the OzFoodNet Network, 2007. Commun Dis Intell 2008;32(4):400–424.

13. National Health and Medical Research Council. The Australian Immunisation Handbook. 7th edn. Canberra: Australian Government Publishing Service; 2000.

14. Hanna JN, Hills SL, Humphreys JL. Impact of hepatitis A vaccination of Indigenous children on notifications of hepatitis A in north Queensland. Med J Aust 2004;181(9):482–485.

15. Combs BG, Raupach JC, Kirk MD. Surveillance of Shiga toxigenic Escherichia coli in Australia. Commun Dis Intell 2005;29(4):366–369.

16. Stephens N, Sault C, Firestone SM, Lightfoot D, Bell C. Large outbreaks of Salmonella Typhimurium phage type 135 infections associated with the consumption of products containing raw egg in Tasmania. Commun Dis Intell 2007;31(1):118–124.

17. Stephens N, Coleman D, Shaw K. Recurring outbreaks of Salmonella Typhimurium phage type 135 associated with the consumption of products containing raw egg in Tasmania. Commun Dis Intell 2008;32(4):466–468.

18. OzFoodNet Working Group. OzFoodNet quarterly report, 1 January to 31 March 2008. Commun Dis Intell 2008;32:267–271.

19. OzFoodNet Working Group. OzFoodNet quarterly report, 1 April to 30 June 2008. Commun Dis Intell 2008;32(3):335–340.

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20. OzFoodNet Working Group. OzFoodNet quarterly report, 1 October to 31 December 2008. Commun Dis Intell 2009;33(1):53–58.

21. Vally H, Hall G, Scallan E, Kirk MD, Angulo FJ. Higher rate of culture-confirmed Campylobacter infections in Australia than in the USA: is this due to differences in healthcare-seeking behaviour or stool culture frequency? Epidemiol Infect 2009;137(12):1751–1758.

22. Conaty S, Bird P, Bell G, Kraa E, Grohmann G, McAnulty JM. Hepatitis A in New South Wales, Australia from consumption of oysters: the first reported outbreak. Epidemiol Infect 2000;124(1):121–130.

23. Hall G, Kirk M, Department of Health and Ageing. Foodborne illness in Australia : annual incidence circa 2000. Canberra: Department of Health and Ageing; 2005.

24. Tam CC, Higgins CD, Neal KR, Rodrigues LC, Millership SE, O’Brien SJ. Chicken consumption and use of acid-suppressing medications as risk factors for Campylobacter enteritis, England. Emerg Infect Dis 2009;15(9):1402–1408.

25. Stafford RJ, Schluter PJ, Wilson AJ, Kirk MD, Hall G, Unicomb L, et al. Population-attributable risk estimates for risk factors associated with Campylobacter infection, Australia. Emerg Infect Dis 2008;14(6):895–901.

26. Mullner P, Jones G, Noble A, Spencer SE, Hathaway S, French NP. Source attribution of food-borne zoonoses in New Zealand: a modified Hald model. Risk Anal 2009;29(7):970–984.

27. New Zealand Food and Safety Authority. Media release. New Zealand leads world on controlling dangerous bacteria. Available from: http://www.nzfsa.govt.nz/publications/media-releases/2009/2009-10-15-campy-codex-work.htm Accessed on 27 November 2008.

28. Swaminathan B, Gerner-Smidt P, Ng LK, Lukinmaa S, Kam KM, Rolando S, et al. Building PulseNet International: an interconnected system of laboratory networks to facilitate timely public health recognition and response to foodborne disease outbreaks and emerging foodborne diseases. Foodborne Pathog Dis 2006;3(1):36–50.

29. Chen LH, Wilson ME, Davis X, Loutan L, Schwartz E, Keystone J, et al. Illness in long-term travelers visiting GeoSentinel clinics. Emerg Infect Dis 2009;15(11):1773–1782.

30. Ward K, McAnulty J. Hepatitis A: who in NSW is most at risk of infection? N S W Public Health Bull 2008;19(1–2):32–35.

31. Lynch MF, Tauxe RV, Hedberg CW. The growing burden of foodborne outbreaks due to contaminated fresh produce: risks and opportunities. Epidemiol Infect 2009;137(3):307–315.

32. Food Standards Australia New Zealand. Media release. Primary production and processing standard for eggs. Available from: http://www.foodstandards.gov.au/thecode/primaryproductionprocessingstandards/eggstandard/index.cfm Accessed on 27 November 2009.

33. Hall GV, Kirk MD, Ashbolt R, Stafford R, Lalor K. Frequency of infectious gastrointestinal illness in Australia, 2002: regional, seasonal and demographic variation. Epidemiol Infect 2006;134(1):111–118.

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Appendix: Foodborne outbreak summary for OzFoodNet sites, Australia, 2008

State
Month of outbreak
Setting prepared
Aetiology
Number affected Hospitalised Fatalities Evidence Epidemiological study
Responsible vehicles
Food vehicle category
ACT November Restaurant Salmonella Typhimurium 44
24
2
0
A
CCS
Hollandaise sauce and poached eggs Egg-based sauces and dressings
NSW December Aged care facility Salmonella Typhimurium
6
2
0
D
Unknown Unknown
  February Commercial caterer Bacillus cereus and Clostridium perfringens
75
0
0
M
D
Curry pumpkin, curry chicken, rice with lamb Mixed dishes
  June Institution Unknown
14
0
0
D
D
Lasagne Pasta dish
  January Institution Unknown
6
0
0
D
Unknown Unknown
  January Private residence Unknown
3
0
0
D
Mussels - fresh Bivalves and molluscs
  March Private residence Salmonella Typhimurium 170
17
2
0
D
D
Eggs used to make cake filling Egg-containing desserts
  January Private residence Salmonella Typhimurium
20
6
0
D
D
Eggs Eggs
  July Restaurant Unknown
4
0
0
D
D
Oysters Bivalves and molluscs
  September Restaurant Staphylococcus aureus
7
1
0
M
D
Chicken Chicken & chicken-containing dishes
  May Restaurant Salmonella Anatum
11
0
0
D
D
Chicken meal Chicken & chicken-containing dishes
  December Restaurant Unknown
5
0
0
D
D
Aioli made with raw eggs Egg-based sauces and dressings
  March Restaurant Salmonella Typhimurium 126
3
1
0
D
Chicken salad with raw egg dressing Egg-containing dish
  January Restaurant Unknown
2
0
0
D
D
Suspected ham Meat and meat-containing dishes
  April Restaurant Salmonella Typhimurium U290
7
0
0
D
Most likely chilli beef Meat and meat-containing dishes
  April Restaurant Salmonella Typhimurium U290
4
1
0
M
D
Variety of Chinese foods Mixed dishes
  December Restaurant Unknown
5
0
0
D
Unknown - suspected Indian takeaway food Mixed dishes
  December Restaurant Unknown
3
0
0
D
Rice, naan, butter chicken and lamb sabjwala Mixed dishes
  May Restaurant Unknown
4
0
0
D
Stir fry beef with dried hot chilli and peanut Mixed dishes
  April Restaurant Unknown
7
0
0
D
Rice or salt and pepper prawn Mixed dishes
  March Restaurant Unknown
3
0
0
D
D
Spring roll, suspected Mixed dishes
  September Restaurant Unknown
5
1
0
D
Barramundi, lamb, salad Mixed dishes
  July Restaurant Unknown
3
0
0
D
Fried rice Rice based dish
  November Restaurant Unknown
3
0
0
D
Unknown, possibly pizza Unknown
  April Restaurant Unknown
25
3
0
D
Unknown Unknown
  December Restaurant Unknown
3
0
0
D
Unknown Unknown
  February Restaurant Unknown
4
0
0
D
Unknown Unknown
  January Restaurant Unknown
7
0
0
D
D
Unknown Unknown
  November Restaurant Unknown
6
0
0
D
Unknown Unknown
  October Restaurant Unknown
6
1
0
D
Unknown Unknown
  September Takeaway Unknown
5
0
0
D
Lamb kebab suspected Meat and meat-containing dishes
  November Takeaway Unknown
4
0
0
D
Pasta with tomato sauce (suspected) Pasta dish
  December Takeaway Unknown
25
1
0
D
D
Unknown Unknown
  January Takeaway Unknown
3
0
0
D
Unknown Unknown
  May Unknown Unknown
14
2
0
D
Unknown but likely chicken and or eggs Suspected chicken and/or eggs
  January Bakery Scombroid
1
1
0
D
N
Tuna from can used to prepare tuna salad roll in hot bread shop Fish
  November Camp Campylobacter
6
0
0
N
Unknown Unknown
  November Grocery store/ delicatessen Salmonella Typhimurium
2
1
0
N
Cabanossi and pepperoni sausages Meat and meat-containing dishes
  December National franchised fast food Salmonella Typhimurium 44
3
2
0
D
N
Bacon and egg sandwich - likely eggs Eggs
  January Private residence Unknown
2
0
0
N
Mussels - fresh Bivalves and molluscs
  November Restaurant Salmonella Typhimurium 170 var
24
1
0
A
N
Raw eggs in Caesar salad dressing Egg-based sauces and dressings
  August Aged care facility Salmonella Typhimurium 144
10
0
0
M
C
Chocolate mousse with raw eggs Egg-containing desserts
  June Aged care facility Clostridium perfringens
69
0
7
AM
C
Unknown possibly pureed food Unknown
  November Bakery Salmonella Typhimurium
10
1
0
A
C
Chocolate mousse cake Egg-containing desserts
  November Bakery Salmonella Typhimurium
16
0
0
D
C
Chocolate mousse cake Egg-containing desserts
  August Commercial caterer Viral
8
0
0
D
C
Mixed sandwiches Salads and/or sandwiches
  April Commercial caterer Clostridium perfringens
31
0
0
A
C
Gravy Sauces and gravies
  August Institution Clostridium perfringens
25
3
0
AM
C
Macaroni bolognaise Pasta dish
  March Military Clostridium perfringens
45
0
0
D
C
Curry Meat and meat-containing dishes
  July Restaurant Unknown
10
0
0
A
C
Oysters Bivalves and molluscs
  May Restaurant Unknown
17
0
0
A
C
Fattouch salad Salads and/or sandwiches
  November Restaurant Unknown
4
0
0
M
C
Unknown Unknown
  October Restaurant Unknown
5
0
0
D
C
Unknown Unknown
  December Takeaway Unknown
25
1
0
D
C
Unknown Unknown
NT November Restaurant Salmonella Typhimurium 9
2
0
0
D
N
Suspect raw egg mayonnaise/ Caesar salad dressing Egg-based sauces and dressings
  November Restaurant Unknown
3
0
0
D
N
Unknown Unknown
  June Takeaway Salmonella Weltevreden
15
3
0
D
N
Unknown Unknown
  January unknown Salmonella Typhimurium 182
5
1
0
D
N
Unknown Unknown
  March Restaurant Unknown
11
3
0
D
C
Steak and/ or fried rice Mixed dishes
Qld March Commercial caterer Unknown
6
0
0
D
CCS
Unknown Unknown
  October Camp Staphylococcus aureus
23
2
0
D
D
Roast chicken Chicken & chicken-containing dishes
  December Primary produce Ciguatera fish Poisoning
3
0
0
D
D
Cod Fish
  July Primary produce Ciguatera fish Poisoning
4
Unknown
0
D
D
'Yellow king' - Samson fish Fish
  July Primary produce Ciguatera fish Poisoning
6
1
0
D
D
Red throat emperor/ reef snapper Fish
  March Primary produce Ciguatera fish Poisoning
6
Unknown
0
D
D
Black kingfish Fish
  March Primary produce Ciguatera fish Poisoning
2
0
0
D
D
Yellowtail kingfish Fish
  October Private residence Salmonella Virchow 8
3
0
0
D
D
Chicken curry Chicken & chicken-containing dishes
  February Restaurant Campylobacter
4
0
0
D
D
Chicken liver pate Chicken & chicken-containing dishes
  February Restaurant Campylobacter
2
0
0
D
D
Chicken Chicken & chicken-containing dishes
  April Restaurant Clostridium perfringens
2
0
0
M
D
Refried Mexican beans Mixed dishes
  November Restaurant Staphylococcus aureus
4
0
0
D
D
Unknown Unknown
  November Commercial caterer Staphylococcus aureus
16
Unknown
0
M
C
Multiple foods Mixed dishes
  March Institution Norovirus
56
0
0
A
C
Deli meat & salad dish Mixed dishes
SA December Bakery Salmonella Typhimurium 9
15
3
0
A
CCS
Sweet bakery products Mixed dishes
  January Private residence Salmonella Typhimurium 9
15
6
0
D
D
Unknown Unknown
  June Aged care facility Salmonella Typhimurium 135
31
5
3
A
C
Unspecified vitamised food Vitamised foods
  September Commercial caterer Norovirus
5
0
0
D
C
No specific food identified Unknown
Tas March Private residence Salmonella Typhimurium 135a
3
0
0
D
D
Raw egg Eggs
  January Restaurant Salmonella Typhimurium 135a
78
9
0
AM
C
Aioli Egg-based sauces and dressings
Vic February Aged care facility Clostridium perfringens
6
0
0
D
D
Unknown Unknown
  September Aged care facility Salmonella Typhimurium 44
14
2
1
D
D
Vitamised food Vitamised foods
  March Commercial caterer Salmonella Typhimurium 44
24
10
0
D
D
Unknown Unknown
  August Institution – other Clostridium perfringens
15
0
0
D
D
Savoury mince Meat and meat-containing dishes
  January Private residence Salmonella Typhimurium 135a
7
1
0
M
D
Ice cream cake made with raw eggs Egg-containing desserts
  June Private residence Salmonella Typhimurium 135a
4
3
0
D
D
Suspect egg/custard dessert Egg-containing desserts
  April Restaurant Salmonella Typhimurium 44
4
1
0
D
D
Desserts suspected Egg-containing desserts
  October Restaurant Salmonella Typhimurium 170
18
1
0
D
D
Tiramisu Egg-containing desserts
  May Restaurant Salmonella Johannesburg
14
1
0
M
D
Roast pork Meat and meat-containing dishes
  May Restaurant Norovirus
14
0
0
D
D
Breakfast meals Mixed dishes
  June Restaurant Unknown
9
unknown
0
D
D
Ready to eat uncooked foods such as salads Salads and/or sandwiches
  May Restaurant Hepatitis A
12
4
0
D
D
Ready to eat foods such as salads and sandwiches Salads and/or sandwiches
  December Restaurant Norovirus
26
0
0
D
D
Unknown Unknown
  May Commercial caterer Unknown
21
1
0
A
C
Chicken curry Chicken & chicken-containing dishes
  February Commercial caterer Unknown
21
0
0
A
C
Continental custard cake Mixed foods
  February Commercial caterer Salmonella Typhimurium 170
18
2
0
A
C
Chicken and pasta salad and ham Salads and/or sandwiches
  February Commercial caterer Campylobacter
4
0
0
A
C
Chicken and pasta salad Salads and/or sandwiches
  January Private residence Salmonella Typhimurium 44
12
1
0
D
C
Lemon dessert made with raw eggs Egg-containing desserts
  January Private residence Salmonella Typhimurium 135a
18
0
0
D
C
Several foods had statistically significant associations with illness. Mixed dishes
  October Restaurant Unknown
41
0
0
A
C
Lamb tenderloin and gravy or roast pork or chicken cacciatore Mixed dishes
  May School Salmonella Typhimurium 44
26
0
0
D
C
Unknown Unknown
WA July Commercial caterer Clostridium perfringens
30
0
0
D
CCS
BBQ Asian chicken Chicken & chicken-containing dishes
  April Aged care facility Norovirus
42
0
0
D
D
Unknown Unknown
  January Private residence Salmonella Typhimurium 9
3
3
0
D
D
Chicken Chicken & chicken-containing dishes
  April Restaurant Norovirus
75
0
0
D
C
Unknown Unknown

Evidence
D Descriptive evidence implicating the vehicle
A Analytical epidemiological association between illness and vehicle
M Microbiological confirmation of aetiology in vehicle and cases.

Epidemiological study
C Cohort study
D Descriptive case series
CCS Case-control study
N Individual patient data not collected


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This issue - Vol 33 No 4, December 2009