Skip to main content Accessibility help
×
Home
Hostname: page-component-6c8bd87754-dzvvk Total loading time: 0.505 Render date: 2022-01-21T00:27:08.630Z Has data issue: true Feature Flags: { "shouldUseShareProductTool": true, "shouldUseHypothesis": true, "isUnsiloEnabled": true, "metricsAbstractViews": false, "figures": true, "newCiteModal": false, "newCitedByModal": true, "newEcommerce": true, "newUsageEvents": true }

The effects of ambient temperature and heatwaves on daily Campylobacter cases in Adelaide, Australia, 1990–2012

Published online by Cambridge University Press:  11 July 2017

A. MILAZZO*
Affiliation:
School of Public Health, The University of Adelaide, Adelaide 5000, South Australia, Australia
L. C. GILES
Affiliation:
School of Public Health, The University of Adelaide, Adelaide 5000, South Australia, Australia
Y. ZHANG
Affiliation:
School of Public Health, The University of Adelaide, Adelaide 5000, South Australia, Australia School of Public Health, The University of Sydney, Sydney 2006, New South Wales, Australia
A. P. KOEHLER
Affiliation:
Communicable Disease Control Branch, Department for Health and Ageing, Adelaide 5000, South Australia, Australia
J. E. HILLER
Affiliation:
School of Public Health, The University of Adelaide, Adelaide 5000, South Australia, Australia School of Health Sciences, Swinburne University of Technology, Melbourne 3122, Victoria, Australia
P. BI
Affiliation:
School of Public Health, The University of Adelaide, Adelaide 5000, South Australia, Australia
*
*Author for correspondence: A. Milazzo, School of Public Health, Level 9, AHMS Building, North Terrace, Adelaide, South Australia 5000, MAIL DROP DX 650 550, Australia. (Email: adriana.milazzo@adelaide.edu.au)
Rights & Permissions[Opens in a new window]

Summary

Campylobacter spp. is a commonly reported food-borne disease with major consequences for morbidity. In conjunction with predicted increases in temperature, proliferation in the survival of microorganisms in hotter environments is expected. This is likely to lead, in turn, to an increase in contamination of food and water and a rise in numbers of cases of infectious gastroenteritis. This study assessed the relationship of Campylobacter spp. with temperature and heatwaves, in Adelaide, South Australia.

We estimated the effect of (i) maximum temperature and (ii) heatwaves on daily Campylobacter cases during the warm seasons (1 October to 31 March) from 1990 to 2012 using Poisson regression models.

There was no evidence of a substantive effect of maximum temperature per 1 °C rise (incidence rate ratio (IRR) 0·995, 95% confidence interval (95% CI) 0·993–0·997) nor heatwaves (IRR 0·906, 95% CI 0·800–1·026) on Campylobacter cases. In relation to heatwave intensity, which is the daily maximum temperature during a heatwave, notifications decreased by 19% within a temperature range of 39–40·9 °C (IRR 0·811, 95% CI 0·692–0·952). We found little evidence of an increase in risk and lack of association between Campylobacter cases and temperature or heatwaves in the warm seasons. Heatwave intensity may play a role in that notifications decreased with higher temperatures. Further examination of the role of behavioural and environmental factors in an effort to reduce the risk of increased Campylobacter cases is warranted.

Type
Original Papers
Copyright
Copyright © Cambridge University Press 2017 

INTRODUCTION

Changes in climatic conditions, such as warmer ambient temperature and increased frequency in heatwaves, are considered to be contributing factors to the emergence and re-emergence of infectious diseases [Reference Wu1]. Infectious gastrointestinal diseases, including those that are foodborne, are influenced by weather conditions, and this has been evident with increased cases and outbreaks of salmonellosis linked to elevated ambient temperature [Reference Grjibovski2Reference Zhang, Bi and Hiller5]. While the relationship with ambient warmer temperature and increased numbers of cases of Salmonella infection has been established, Campylobacter infections have a less clear relationship with temperature and climate variability. Some studies report a positive association of increasing temperature and incidence of cases [Reference Allard6Reference Yun13] and others an inverse or no relationship [Reference Bi14Reference Lal16]. Of the studies, most have been reported from Europe, England and Wales [Reference Lake8Reference Tam11, Reference Yun13, Reference Kovats15], the USA and Canada [Reference Allard6, Reference Fleury7, Reference White12]. Two studies have examined data from Australasia: one was a multi-city study [Reference Kovats15], and the other compared Adelaide (capital city of South Australia (SA)) and Brisbane (capital city of Queensland) [Reference Bi14].

Human infection with Campylobacter spp. is an important cause of food-borne illness, with major consequences for morbidity in individuals and populations [Reference Havelaar17]. In 2010, of the 550 million infectious gastroenteritis cases reported in the world, 96 million were attributed to Campylobacter spp. the most common bacterial infectious agent [Reference Havelaar17]. In Australia, of the estimated 16·6 million cases of acute gastroenteritis, 4·7% of cases was caused by Campylobacter spp. [Reference Gibney18]. In SA, around 2000 Campylobacter notifications occur each year. Heatwaves, with longer and higher temperatures, may increase the development pace of the pathogen, affect the reservoirs and also impact people's behaviour, including food storage and transportation. With temperature and the frequency of heatwaves predicted to rise, it is important to assess whether these climatic variables have an impact on Campylobacter notifications.

The aim of this study was to assess the relationship between reported cases of Campylobacter spp., and temperature and heatwaves. The findings will inform the design of public health messages and interventions aimed at improvements in food safety, prevention and control in an effort to reduce burden associated with warmer ambient temperature due to climate change.

METHODS

Adelaide experiences a Mediterranean climate with cool wet winters and hot dry summers with high temperatures in the warm season and heatwaves becoming more frequent, intense and of longer duration [Reference Deo19]. The average ambient temperature in SA has increased by 0·96 °C in the last 95 years. This increase in maximum temperature is occurring more rapidly than that observed nationally [Reference Suppiah20].

Data collection

Notifiable cases

Laboratory-confirmed Campylobacter cases notified to the Communicable Disease Control Branch (CDCB), SA Department for Health and Ageing between 1 January 1990 and 31 December 2012 were obtained from their notifiable disease surveillance system. Cases were included if they were a resident of metropolitan Adelaide. Information on demographic characteristics and illness was extracted for each case.

Temperature data

Recordings of daily maximum temperature (T max) in degrees Celsius (°C) from 1990 to 2012 were obtained from an Australian Bureau of Meteorology (BOM) weather monitoring station close to the Adelaide city centre. We used T max as our exposure variable because it is considered to be a better index of exposure than average or minimum temperature [Reference Milazzo3, Reference Xiang21]. This was also in keeping with previous studies in Adelaide, in which T max was used as a predictor of health outcomes related to heat exposure [Reference Hansen22, Reference Nitschke, Tucker and Bi23].

Heatwave definition

In this study, a heatwave was defined to have occurred when the daily T max reached or exceeded 35 °C for 3 or more consecutive days in a given period. This definition has been applied in previous heat-health studies conducted in Adelaide [Reference Milazzo4, Reference Hansen22Reference Xiang25]. Because of the uncertainty about the characteristics that make heatwaves hazardous to health [Reference Tryhorn and Risbey26], we assessed the role of intensity (T max of ⩾35 °C during a heatwave event), duration (the length of a heatwave, in number of days) and timing (occurrence of a heatwave according to timing within the season, e.g. first, second and so on) on daily Campylobacter notifications.

Analysis

Temperature effects

A time-series Poisson regression model was fit to estimate the effect of T max on daily Campylobacter cases. The analysis dataset was restricted to the warm season from 1 October to 31 March, to control for the potential confounding effects of seasonal fluctuations [Reference Bhaskaran27].

We used Spearman's correlation coefficient to examine the relationship between T max and the daily number of Campylobacter notifications in the warm season. To identify any delayed effects of T max on daily Campylobacter notifications, we performed cross-correlation analyses and examined different lags in time. Sensitivity analyses of different lag times up to 28 days were conducted based on the cross-correlation results and were taken into account in the regression models. We controlled for autocorrelation (AC) of daily Campylobacter notifications based on the autocorrelation function (ACF) and partial ACF so as to identify the most appropriate autoregressive (AR) order.

To take into account potential confounders of temperature effects, we included day of the week (as a categorical variable with Sunday as the reference day), public holidays (as an indicator variable), and linear and quadratic terms for year to adjust for long-term trends. Lag values were also included to estimate the delayed effects of temperature on daily Campylobacter notifications. In the case of overdispersion, a negative binomial model was fitted. Goodness-of-fit tests were used to assess model fit.

Different temperature thresholds were examined to ascertain if a differential relationship across the temperature spectrum existed for a number of Campylobacter cases. A lowess smoother at a bandwidth of 0·8 was used to assess the shape of the exposure–response relationship between T max and counts of Campylobacter. Piecewise linear regression models were fitted with a single breakpoint at the identified temperature thresholds using the ‘hockey-stick’ nl command in Stata [Reference Muggeo28].

Heatwave effects

Poison regression models were used to examine the effect of heatwaves on daily Campylobacter cases. Generalized estimating equations were used to account for the clustering of observations within a heatwave. We accepted an exchangeable correlation structure within each cluster of heatwave days and used the quasi-likelihood under the independence model criterion to select the best working correlation structure. Similar to the models we used to assess the effect of T max on daily Campylobacter notifications, we included day of the week, public holidays and year and year2 in our statistical models.

Heatwave characteristics

As well as examining each of the three heatwave characteristics (intensity, duration and timing, as described earlier), we also estimated the overall effects of heatwaves on daily notifications by including a binary variable (heatwave and non-heatwave days). Separate models were fitted to examine the effects of each heatwave characteristic on number of daily Campylobacter cases. Heatwave day (e.g. days 3, 4 or 5) was used to examine the day which produced a greater risk of Campylobacter infection. Intensity was defined as daily T max recorded within heatwaves with four temperature ranges (35–36·9, 37–38·9, 39–40·9 and ⩾41 °C) included in the model. We examined duration by length of 3, 4 and 5 or more days. We also considered whether the duration was short (3 days) compared with long (4 or more days). We considered two different characteristics of timing. We defined timing by the first, second and third heatwave events within each warm season denoting the order of occurrence. We then examined whether timing differed by the occurrence of a heatwave event in the early part of the warm season (October to December) or later (January to March).

We report incidence rate ratios (IRRs) with 95% confidence intervals (CIs) with results interpreted as per cent (%) change in the number of daily Campylobacter counts per °C increase in T max and during heatwave periods compared with non-heatwave periods. A significance level of 0·05 was used for all statistical tests. Analyses were conducted using StataSE 13 (StataCorp LP, College Station, Texas, USA).

Ethics approval

Ethics approval was given by the Human Research Ethics Committees of the University of Adelaide (H-202–2011) and the SA Department for Health and Ageing (463/07/2014).

RESULTS

Descriptive statistics

In Adelaide, from 1990 to 2012, 35 601 Campylobacter cases were notified, with 18 570 (52%) reporting onset of illness in the warm season. During this period, there were no outbreaks detected, and hence no records were excluded from the analyses. Figure 1 shows the temporal distribution of daily Campylobacter spp. notifications over the entire study period with no obvious peaks occurring in the warmer months. Temperature summary statistics for the entire study period, by season, and by heatwaves are displayed in Table 1. The mean daily T max during the warm seasons was 26·5 °C (standard deviation (s.d.) = 6·1) and 38·4 °C (s.d. = 2·2) during heatwaves. Over the study period, 213 heatwave days across 50 distinct episodes were recorded. The length of heatwaves ranged from 3 to 15 days with a mean of 3·17 (s.d. = 2·40) days. During the study period, there were no recorded heatwaves in 1990, 1996 and 2005, and none occurred outside of the warm season. The proportion of days during the warm season with a recorded T max over 40 °C was 1%.

Fig. 1. Annual distribution of monthly notifications of Campylobacter infection, 1990–2012, Adelaide, South Australia.

Table 1. Daily maximum temperature (Tmax) by season, 1990 to 2012, Adelaide, South Australia

a Campylobacter cases (n=35,601) notified in the study period.

b Campylobacter cases (n=17,031) notified in the cool season (April to September).

c Campylobacter cases (n=18,570) notified in the warm season (October to March).

d Campylobacter cases (n=908) notified during heatwaves (within the warm season).

The final time-series Poisson regression model included an AR structure of order three and daily T max, based on the maximum correlation coefficients. We examined the data for overdispersion, and as there was none, negative binominal models were not fitted.

Effects of maximum temperature on Campylobacter infections

Correlation of T max with Campylobacter notifications was negligible. There was no lagged effect of T max on the number of daily Campylobacter cases. A third-order AC of the number of campylobacteriosis notifications was detected (IRR 1·037, 95% CI 1·032–1·042, P = <0·01). There was no substantiative effect of T max per 1 °C rise (IRR 0·995, 95% CI 0·993–0·997, P = <0·01) on Campylobacter cases.

Temperature thresholds

Figure 2 demonstrates the exposure–response relationship between T max and daily Campylobacter cases during the warm season. The relationship between temperature and Campylobacter notifications changed across the observed temperature range – as T max increased, the number of cases decreased. However, a clear temperature threshold was not detected.

Fig. 2. Exposure–response relationship between maximum temperature and daily Campylobacter notifications, reported in the warm season (October to March), 1990–2012, Adelaide, South Australia.

Effect of heatwaves and heatwave characteristics on Campylobacter notifications

As illustrated in Table 2, no association between heatwaves and an overall increase in daily Campylobacter cases was identified (IRR 0·906, 95% CI 0·800–1·026, P = 0·126). When examining heatwave characteristics, a 3-day heatwave compared with a heatwave with a duration of 4 and 5 days decreased the risk of infection on daily Campylobacter counts by 21% (IRR 0·795, 95% CI 0·689–0·918, P = 0·002). A 19% decrease in cases (IRR 0·818, 95% CI 0·679–0·987, P = 0·036) was estimated with the first heatwave in the season, thus reducing the risk compared with subsequent heatwaves in the season. The number of cases was lower in the early months of the warm seasons compared with the later months. Heatwave intensity within a temperature range of 39–40·9 °C on daily cases decreased the risk of infection (IRR 0·811, 95% CI 0·692–0·952, P = 0·010) by 19%.

Table 2. Effect estimates of heatwave characteristics on daily Campylobacter cases

IRR, incidence rate ratio; CI, confidence interval; P-value (0·05 significance level).

Adjusted for long-term trends, day of the week (reference day is Sunday) and public holidays. The reference group are non-heatwave days.

DISCUSSION

Our study found that there is no substantiative effect of T max on daily Campylobacter cases in the warm seasons. When examining the effect of heatwaves on daily Campylobacter notifications, there was little evidence of an effect of an increased risk of infection. These findings indicate that Campylobacter incidence in Adelaide may not be affected by temperature in the warm seasons or during heatwaves.

Few studies have examined the relationship between temperature and Campylobacter spp. in the warm seasons and none so far have considered the effects of heatwaves on cases. Among those studies that have been conducted, a positive association of increasing temperature and incidence of cases have been reported in studies from Europe [Reference Patrick10, Reference Yun13], the UK [Reference Lake8, Reference Louis9, Reference Tam11], the USA [Reference White12] and Canada [Reference Allard6, Reference Fleury7].

Our findings that temperature and heatwaves did not increase the risk of infection concur with a study in Australia comparing temperature effects and Campylobacter cases in Adelaide that has a temperate climate, with Brisbane a sub-tropical climate [Reference Bi14]. The study in Adelaide found an inverse relationship with temperature and Campylobacter cases, yet in Brisbane the effect was positive [Reference Bi14]. It is postulated that this difference could be associated with weather conditions specific to that area, which could have an impact on animal reservoirs or proccesses along the food chain [Reference Bi14]. Likewise a multi-jurisdictional study that compared the effects of temperature on Campylobacter infection across multiple continents of Europe, Canada, Australia and New Zealand did not find a strong effect of temperature on Campylobacter cases [Reference Kovats15]. This suggests that the impact of temperature on cases varies within and between geographical regions, thereby affecting disease transmission and environmental routes.

We found no lagged effect of temperature in the warm seasons on cases. Contrary to this, previous studies found lags ranged from 1 to 6 weeks. A positive association was found between Campylobacter and temperature in the current and previous weeks in a UK study [Reference Lake8]. Studies that identified long lags of 8 weeks or more were those that had a null effect of temperature on Campylobacter cases [Reference Bi14Reference Lal16]. Bi et al. reported no discernible lag effect of temperature on Campylobacter cases in Adelaide but a lag of up to 6 weeks on cases in Brisbane [Reference Bi14]. The lack of a lag effect in Bi et al. and our study suggests that the main route of transmission may not be foodborne [Reference Bi14]. Generally, lag effects indicate when and where food contamination could have occurred, with short time lags pointing to food contamination closer to the time of consumption, and long lags indicating effects at the production processing stages [Reference Lake8]. In our study, we found that the number of campylobacteriosis notifications was related to the number occurring in the previous 3 days. As there was little evidence in our study of a lagged effect of temperature on daily counts in our study, we did not further explore this association with heatwaves.

We were unable to discern a temperature threshold, although by visually inspecting the plot, we observed a decrease in cases with a rise in T max above approximately 36 °C. These results need to be interpreted with caution and warrant further investigation. It may be that ambient temperature in the warm seasons and heatwaves are not linked to an increase in the risk of infection as indicated by daily Campylobacter notifications as the bacteria is sensitive to high temperature. The relationship between pathogen growth and temperature is non-linear [Reference Basu29], and there could be a temperature above which proliferation and survival of Campylobacter spp. in the environment will begin to decline. Campylobacter spp. does not multiply at temperatures below 30 °C; hence, the bacteria do not increase in foods kept at usual room temperatures in temperate regions [Reference Bronowski, James and Winstanley30].

Limitations in this study are similar to those reported in our related work concerned with effects of temperature and heatwaves on Salmonella cases [Reference Milazzo3, Reference Milazzo4]. Passive disease surveillance systems are likely to result in an under-reporting of Campylobacter notifications [Reference Hall31], but this is not likely to affect the estimates of the association between temperature and heatwaves in the warm seasons and the risk of Campylobacter infection. We did not exclude cases that travelled prior to becoming unwell because of the incomplete data recorded in the disease notification surveillance system. Only a small proportion of cases are expected to travel, and inclusion of cases that travelled is unlikely to affect the results [Reference Kovats32].

It remains unclear as to why Campylobacter infections have a less obvious relationship than Salmonella with temperature and climate variability. Transmission of campylobacteriosis is complex, as there are many routes and exposure pathways including environmental paths [Reference Domingues33, Reference Whiley34]. The seasonality with campylobacteriosis peaking in spring is not fully understood, but the environment is credited to play a role in this [Reference Bronowski, James and Winstanley30].

Campylobacter spp. is ubiquitous in the environment, and hosts include wild domestic animals and birds. It can be found in the gastrointestinal tract of cattle, sheep, goats, dogs, rabbits, cats, chickens, turkey, duck and pigs [Reference Craig and Batholomaeus35]. It is hypothesised that flies can act as a vector for the transmission of Campylobacter spp. to humans [Reference Ekdahl, Normann and Andersson36]. Food-borne transmission is another route as the primary source for Campylobacter infection in humans is the consumption of poultry meat [Reference Newell37]. A case–control study in Australia identified chicken consumption as the main risk factor for Campylobacter infection, with a population-attributable risk estimate of >50 000 cases each year [Reference Stafford38]. Although Campylobacter spp. is sensitive to high temperatures and dry environments, the bacteria survive well in poultry processing production stages [Reference Craig and Batholomaeus35] further supporting poultry meat as a high-risk food for Campylobacter transmission to humans.

Environmental transmission of Campylobacter infection via birds, farm and other wild animals to humans is multi-factorial. These many routes of transmission, some which may not be temperature-dependent, are multi-faceted. From our study, as well as those conducted previously, we know that varying environmental and climatic conditions prevail between continents, countries and regions, and may have an impact on disease transmission and case incidence [Reference Bi14]. This calls for further studies from different countries with different climatic conditions to ascertain a truer picture of the role of temperature in the incidence of Campylobacter infection.

Our study suggests that temperature has a limited role in increased incidence of Campylobacter notifications in the warm season, and we also found little evidence for an effect of heatwaves on cases. Limited understanding about the reservoirs and transmission routes for Campylobacter infection make it difficult to determine the role of ambient temperature in the warm season on disease incidence. Notwithstanding this, previous studies have established that there is a relationship with temperature and consequently the role of the environment, especially warmer temperature should not be ignored with the emerging evidence of climate change and predicted increase in the frequency of warmer days.

ACKNOWLEDGEMENTS

The authors thank staff from the Disease Surveillance and Investigation Section, Communicable Disease Control Branch, Department for Health and Ageing (SA Health) for their support in conducting this study.

DECLARATION OF INTEREST

We confirm that there is no conflict of interest.

References

1. Wu, X, et al. Impact of climate change on human infectious diseases: empirical evidence and human adaptation. Environment International 2016; 86: 1423.CrossRefGoogle ScholarPubMed
2. Grjibovski, AM, et al. Climate variations and salmonellosis in northwest Russia: a time-series analysis. Epidemiology and Infection 2013; 141: 269276.CrossRefGoogle ScholarPubMed
3. Milazzo, A, et al. The effect of temperature on different Salmonella serotypes during warm seasons in a Mediterranean climate city, Adelaide, Australia. Epidemiology and Infection 2016; 144: 12311240.CrossRefGoogle Scholar
4. Milazzo, A, et al. Heatwaves differentially affect risk of Salmonella serotypes. Journal of Infection 2016; 73: 231240.CrossRefGoogle ScholarPubMed
5. Zhang, Y, Bi, P, Hiller, JE. Climate variations and Salmonella infection in Australian subtropical and tropical regions. Science of the Total Environment 2010; 408: 524530.CrossRefGoogle ScholarPubMed
6. Allard, R, et al. The reported incidence of campylobacteriosis modelled as a function of earlier temperatures and numbers of cases, Montreal, Canada, 1990–2006. International Journal of Biometeorology 2010; 55: 353360.CrossRefGoogle Scholar
7. Fleury, M, et al. A time series analysis of the relationship of ambient temperature and common bacterial enteric infections in two Canadian provinces. International Journal of Biometeorology 2006; 50: 385391.CrossRefGoogle Scholar
8. Lake, IR, et al. A re-evaluation of the impact of temperature and climate change on foodborne illness. Epidemiology and Infection 2009; 137: 15381547.CrossRefGoogle ScholarPubMed
9. Louis, VR, et al. Temperature-driven Campylobacter seasonality in England and Wales. Applied and Environmental Microbiology 2005; 71: 8592.CrossRefGoogle Scholar
10. Patrick, ME, et al. Effects of climate on incidence of Campylobacter spp. in humans and prevalence in broiler flocks in Denmark. Applied and Environmental Microbiology 2004; 70: 74747480.CrossRefGoogle Scholar
11. Tam, CC, et al. Temperature dependence of reported Campylobacter infection in England, 1989–1999. Epidemiology and Infection 2006; 134: 119125.CrossRefGoogle Scholar
12. White, AN, et al. Environmental determinants of campylobacteriosis risk in Philadelphia from 1994 to 2007. EcoHealth 2009; 6: 200208.CrossRefGoogle Scholar
13. Yun, J, et al. Association between the ambient temperature and the occurrence of human Salmonella and Campylobacter infections. Scientific Reports 2016; 6: 28442.CrossRefGoogle ScholarPubMed
14. Bi, P, et al. Weather and notified Campylobacter infections in temperate and sub-tropical regions of Australia: an ecological study. Journal of Infection 2008; 57: 317323.CrossRefGoogle Scholar
15. Kovats, RS, et al. Climate variability and campylobacter infection: an international study. International Journal of Biometeorology 2005; 49: 207214.CrossRefGoogle ScholarPubMed
16. Lal, A, et al. Climate variability, weather and enteric disease incidence in New Zealand: time series analysis. PLoS ONE 2013; 8: e83484.CrossRefGoogle Scholar
17. Havelaar, AH, et al. World Health Organization global estimates and regional comparisons of the burden of foodborne disease in 2010. PLoS Medicine 2015; 12: e1001923.CrossRefGoogle Scholar
18. Gibney, KB, et al. Disease burden of selected gastrointestinal pathogens in Australia, 2010. International Journal of Infectious Diseases 2014; 28: 176185.CrossRefGoogle ScholarPubMed
19. Deo, RC, et al. On Australian heat waves: time series analysis of extreme temperature events in Australia, 1950–2005. In: Oxley L, Kulasari D, eds. MODSIM 2007 International Congress on Modelling and Simulation. New Zealand: The Modelling and Simulation Society of Australia and NZ Inc., 2007, p. 10.Google Scholar
20. Suppiah, R, et al. Climate Change Under Enhanced Greenhouse Conditions in South Australia. Adelaide, South Australia: CSIRO, 2006.Google Scholar
21. Xiang, J, et al. Association between high temperature and work-related injuries in Adelaide, South Australia, 2001–2010. Journal of Occupational and Environmental Medicine 2014; 71: 246252.CrossRefGoogle Scholar
22. Hansen, A, et al. The effect of heat waves on hospital admissions for renal disease in a temperate city of Australia. International Journal of Epidemiology 2008; 37: 13591365.CrossRefGoogle Scholar
23. Nitschke, M, Tucker, GR, Bi, P. Morbidity and mortality during heatwaves in metropolitan Adelaide. Medical Journal of Australia 2007; 187: 662665.Google ScholarPubMed
24. Hansen, A, et al. The effect of heat waves on mental health in a temperate Australian city. Environmental Health Perspectives 2008; 116: 13691375.CrossRefGoogle Scholar
25. Xiang, J, et al. The impact of heatwaves on workers’ health and safety in Adelaide, South Australia. Environmental Research 2014; 133: 9095.CrossRefGoogle ScholarPubMed
26. Tryhorn, L, Risbey, J. On the distribution of heat waves over the Australian region. Australian Meteorological Magazine 2006; 55: 169182.Google Scholar
27. Bhaskaran, K, et al. Time series regression studies in environmental epidemiology. International Journal of Epidemiology 2013; 42: 11871195.CrossRefGoogle ScholarPubMed
28. Muggeo, VM. Estimating regression models with unknown break-points. Statistics in Medicine 2003; 22: 30553071.CrossRefGoogle Scholar
29. Basu, R. High ambient temperature and mortality: a review of epidemiologic studies from 2001 to 2008. Environmental Health 2009; 8: 40.CrossRefGoogle ScholarPubMed
30. Bronowski, C, James, CE, Winstanley, C. Role of environmental survival in transmission of Campylobacter jejuni . FEMS Microbiology Letters 2014; 356: 819.CrossRefGoogle ScholarPubMed
31. Hall, GV, et al. Frequency of infectious gastrointestinal illness in Australia, 2002: regional, seasonal and demographic variation. Epidemiology and Infection 2006; 134: 111118.CrossRefGoogle ScholarPubMed
32. Kovats, RS, et al. The effect of temperature on food poisoning: a time-series analysis of salmonellosis in ten European countries. Epidemiology and Infection 2004; 132: 443453.CrossRefGoogle Scholar
33. Domingues, AR, et al. Source attribution of human campylobacteriosis using a meta-analysis of case-control studies of sporadic infections. Epidemiology and Infection 2012; 140: 970981.CrossRefGoogle Scholar
34. Whiley, H, et al. The role of environmental reservoirs in human campylobacteriosis. International Journal of Environmental Research and Public Health 2013; 10: 58865907.CrossRefGoogle ScholarPubMed
35. Craig, D, Batholomaeus, A. Agents of Foodborne Illness. a Technical Series Summarising Key Information on Microorganisms Associated With Foodborne Illness. Canberra: Food Standards Australia New Zealand, 2011.Google Scholar
36. Ekdahl, K, Normann, B, Andersson, Y. Could flies explain the elusive epidemiology of campylobacteriosis? BMC Infectious Diseases 2005; 5: 11.CrossRefGoogle ScholarPubMed
37. Newell, DG, et al. Food-borne diseases – the challenges of 20 years ago still persist while new ones continue to emerge. International Journal of Food Microbiology 2010; 139(Suppl. 1): S3S15.CrossRefGoogle ScholarPubMed
38. Stafford, RJ, et al. Population-attributable risk estimates for risk factors associated with Campylobacter infection, Australia. Emerging Infectious Diseases 2008; 14: 895901.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. Annual distribution of monthly notifications of Campylobacter infection, 1990–2012, Adelaide, South Australia.

Figure 1

Table 1. Daily maximum temperature (Tmax) by season, 1990 to 2012, Adelaide, South Australia

Figure 2

Fig. 2. Exposure–response relationship between maximum temperature and daily Campylobacter notifications, reported in the warm season (October to March), 1990–2012, Adelaide, South Australia.

Figure 3

Table 2. Effect estimates of heatwave characteristics on daily Campylobacter cases

You have Access
5
Cited by

Send article to Kindle

To send this article to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about sending to your Kindle. Find out more about sending to your Kindle.

Note you can select to send to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be sent to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

The effects of ambient temperature and heatwaves on daily Campylobacter cases in Adelaide, Australia, 1990–2012
Available formats
×

Send article to Dropbox

To send this article to your Dropbox account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Dropbox.

The effects of ambient temperature and heatwaves on daily Campylobacter cases in Adelaide, Australia, 1990–2012
Available formats
×

Send article to Google Drive

To send this article to your Google Drive account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Google Drive.

The effects of ambient temperature and heatwaves on daily Campylobacter cases in Adelaide, Australia, 1990–2012
Available formats
×
×

Reply to: Submit a response

Please enter your response.

Your details

Please enter a valid email address.

Conflicting interests

Do you have any conflicting interests? *