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SAMJ: South African Medical Journal

versão On-line ISSN 2078-5135
versão impressa ISSN 0256-9574

SAMJ, S. Afr. med. j. vol.108 no.6 Pretoria Jun. 2018

http://dx.doi.org/10.7196/samj.2018.v108i6.13274 

EDITORIAL

 

How climate change can fuel listeriosis outbreaks in South Africa

 

 

The listeriosis outbreak that began in early 2017 in South Africa (SA) is the largest recorded globally.[1] The source of the outbreak was located in early March 2018, when traces of the Listeria monocytogenes bacterium were found in a food production facility in Polokwane, Limpopo Province, SA, which produces ready-to-eat processed meat products.[2] By the time the source was identified, about 950 cases of invasive disease had been confirmed and 180 deaths reported, almost certainly underestimates of the actual extent of the disease.[2] Actions to halt the outbreak, such as product recalls and closing implicated processing plants, are clearly an immediate priority, as are steps to enforce environmental health standards. It is also important, however, to pay attention to factors relating to the longer-term, structural environment in which such outbreaks unfold and which may contribute to an increased frequency of cases in the near future. One such factor is climate change, which has garnered little attention thus far in the discourse surrounding the outbreak.

The wide-ranging environmental effects associated with global climate change markedly alter the epidemiology of food-borne diseases, including L. monocytogenes.3Even though Listeria species are ubiquitous within the natural environment, several features of the epidemiology and characteristics of the microbe make it especially climate sensitive. Spikes in ambient temperature and high summer temperature peaks, for example, have been linked to the occurrence of listeriosis, as with most diarrhoeal pathogens.[4-6] Hot weather extremes that become more common with climate change, augment the replication cycles of L. monocytogenes and could cause breakdowns in food cooling chains, with rapid rises in numbers of the bacteria on food products.[7] But, aside from temperature increases, altered rainfall patterns and lengthened dry seasons - as we have seen in the western regions of SA - may influence Listeria transmission.

L. monocytogenes is classically associated with the food chain, during pre-harvesting and processing and at retail level.[8,9] Water scarcity can compromise hand hygiene, as well as cleaning and sanitising operations in the food products industry. Cleaning hands with sanitisers, increasingly the norm in drought-affected areas, is less effective than washing with soap and water.[10] More importantly, however, in food processing plants, water scarcity may hamper efforts to clean machines used for slicing, chopping or related processes. Intensive, deep cleaning is required to prevent persistence of L. mono-cytogenes on such machines, given that the bacterium can tolerate high salt and nitrate concentrations, desiccation, moderate heat, and both acidic and alkaline conditions.[9] With incomplete cleaning, especially of machines that have 'unhygienic' designs or are damaged, L. monocytogenes can persist in harbourage sites (i.e. cracks, niches or other hard-to-reach places).[9] The organisms can adhere to all food contact surfaces, forming biofilms, which are hard to eliminate. In a study in Gauteng, for example, the microbe was isolated from stainless steel surfaces in food plants after they had been cleaned and disinfected using a range of cleaning methods.[11] As could be expected, several studies have detected L. monocytogenes in food samples of street vendors, who have limited access to water and cleaning equipment[12,13] The bacterium has even been found in delicatessens in Johannesburg -in 10% of cleaning cloths.[14] These levels of contamination will possibly rise as water scarcity, which threatens much of the country, further reduces personal and industrial cleaning.

Another way that climate change influences the spread of L. mono-cytogenes is through inducing a switch in the types and sources of water used for agriculture and domestic purposes. When supplies of potable municipal water become limited, both subsistence and commercial farmers resort to using surface water for irrigation, which often naturally harbours Listeria species.[15,16] In both rural and urban areas, roof-harvested rainwater is increasingly being used for irrigation and domestic purposes. A study of rainwater tanks in villages in three provinces of SA found that 22% of samples were contaminated with L. monocytogenes, possibly from bird faeces and debris on rooftops.[17] The organism also proliferates in water within drainage ditches, which may then contaminate fruits and vegetables when used for irrigation.[3,18]

Changes in precipitation patterns wrought by large-scale climate disruption also impact on Listeria dispersal. Rainfall occurring in short bursts of 5 - 10 minutes favours the dispersal of Listeria and other pathogens from the soil onto plants, while lengthier downpours exert a washout effect.[3] As with fresh produce, run-off water may contaminate the water in fish farms, an effect especially noticeable during summer months.[19] As this water filters through the fishes' gills, they become contaminated with L. monocytogenes, and the organism is then introduced into food processing plants.[20]

In summary, long-term water scarcity can influence cleaning practices and alter water sources in ways that favour the persistence of Listeria in food-processing plants, but also in retail outlets and domestic settings. Much closer monitoring of food industry standards, changes in dietary habits of the public and heightened responses to listeriosis outbreaks are required, in conjunction with efforts to increase the volume of potable municipal water and to ensure that all citizens have access to this water.

Ultimately, infectious disease outbreaks, which may become more frequent with rising ambient temperatures and water scarcity, are the proverbial canary in a coal mine. They serve as but one reminder of the devastating effects of climate change presently unfolding in SA. As with all nations, the country needs to takes rigorous steps to prepare for these changes. The high levels of carbon emissions in SA, especially its reliance on coal for power, may well worsen the impact of climate change. In SA, 93% of electricity production is still obtained from coal, more than double the global average (42%), and renewable energy sources account for <2% of electricity compared with a world average of 22%.[21] Also, challenges in public transport in the country, especially with train services,[22] have heightened the use of taxis, cars and other forms of carbon-intensive transport. Without concerted action to prepare for the health effects of climate change, and in the absence of efforts to reduce further environmental degradation, South Africans may face many more large outbreaks of infectious diseases in years to come.

 

M F Chersich, F Scorgie, H Rees

Wits Reproductive Health and HIV Institute, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa mchersich@wrhi.ac.za

C Y Wright

Environment and Health Research Unit, South African Medical Research Council and Department of Geography, Geoinformatics and Meteorology, Faculty of Natural and Agricultural Sciences, University of Pretoria, South Africa

 

References

1. Spies D. WHO: South Africa's listeriosis outbreak 'largest ever'. News 24, 13 January 2018. https://www.news24.com/SouthAfrica/News/who-south-africas-listeriosis-outbreak-largest-ever-20180113 (accessed 10 May 2018).         [ Links ]

2. Motsoaledi A. Media statement by the Minister of Health Dr Aaron Motsoaledi regarding the update on the listeriosis outbreak in South Africa. 2017. http://www.kznhealth.gov.za/Listeriosis/Media-statement-NDOH-04032018.pdf (accessed 15 May 2018).         [ Links ]

3. Hellberg RS, Chu E. Effects of climate change on the persistence and dispersal of foodborne bacterial pathogens in the outdoor environment: A review. Crit Rev Microbiol 2016;42(4):548-572. https://doi.org/10.3109/1040841x.2014.972335        [ Links ]

4. Goulet V, Jacquet C, Martin P, et al Surveillance of human listeriosis in France, 2001 - 2003. Euro Surveill 2006;11(6):79-81.         [ Links ]

5. Musengimana G, Mukinda FK, Machekano R, Mahomed H. Temperature variability and occurrence of diarrhoea in children under five-years-old in Cape Town metropolitan sub-districts. Int J Environ Res Public Health 2016;13(9):859. https://doi.org/10.3390/ijerph13090859        [ Links ]

6. European Food Safety Authority, European Centre for Disease Prevention and Control. The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2016. 2017. https://ecdc.europa.eu/sites/portal/nles/documents/summary-report-zoonoses-foodborne-outbreaks-2016.pdf (accessed 10 May 2018).         [ Links ]

7. Miettinen MK, Siitonen A, Heiskanen P, et al. Molecular epidemiology of an outbreak of febrile gastroenteritis caused by Listeria monocytogenes in cold-smoked rainbow trout. J Clin Microbiol 1999;37(7):2358-2360.         [ Links ]

8. Henriques AR, Gama LT, Fraqueza MJ. Tracking Listeria monocytogenes contamination and virulence-associated characteristics in the ready-to-eat meat-based food products industry according to the hygiene level. Int J Food Microbiol 2017;242:101-106. https://doi.org/10.1016/j.ijfoodmicro.2016.11.020        [ Links ]

9. Carpentier B, Cerf O. Review. Persistence of Listeria monocytogenes in food industry equipment and premises. Int J Food Microbiol 2011;145(1):1-8. https://doi.org/10.1016/j.ijfoodmicro.2011.01.005        [ Links ]

10. Farber T. Day Zero may fan deadly listeriosis outbreak. Sunday Times, 28 January 2018. https://www.timeslive.co.za/sunday-times/news/2018-01-27-day-zero-may-fan--deadly-listeriosis-outbreak/ (accessed 10 May 2018).         [ Links ]

11. Lambrechts AA, Human IS, Doughari JH, Lues JF. Efficacy of low-pressure foam cleaning compared to conventional cleaning methods in the removal of bacteria from surfaces associated with convenience food. Afr Health Sci 2014;14(3):585-592. https://doi.org/10.4314/ahs.v14i3.13        [ Links ]

12. Nyenje ME, Odjadjare CE, Tanih NF, Green E, Ndip RN. Foodborne pathogens recovered from ready-to-eat foods from roadside cafeterias and retail outlets in Alice, Eastern Cape Province, South Africa: Public health implications. Int J Environ Res Public Health 2012;9(8):2608-2619. https://doi.org/10.3390/ijerph9082608        [ Links ]

13. Plessis EMD, Govender S, Pillay B, Korsten L. Exploratory study into the microbiological quality of spinach and cabbage purchased from street vendors and retailers in Johannesburg, South Africa. J Food Prot 2017;80(10):1726-1733. https://doi.org/10.4315/0362-028x.jfp-16-540        [ Links ]

14. Christison CA, Lindsay D, von Holy A. Cleaning and handling implements as potential reservoirs for bacterial contamination of some ready-to-eat foods in retail delicatessen environments. J Food Prot 2007;70(12):2878-2883.         [ Links ]

15. Olaniran AO, Nzimande SB, Mkize NG. Antimicrobial resistance and virulence signatures of Listeria and Aeromonas species recovered from treated wastewater effluent and receiving surface water in Durban, South Africa. BMC Microbiol 2015;15:234. https://doi.org/10.1186/s12866-015-0570-x        [ Links ]

16. Odjadjare EE, Obi LC, Okoh AI. Municipal wastewater effluents as a source of listerial pathogens in the aquatic milieu of the Eastern Cape Province of South Africa: A concern of public health importance. Int J Environ Res Public Health 2010;7(5):2376-2394. https://doi.org/10.3390/ijerph7052376        [ Links ]

17. Jongman M, Korsten L. Microbial quality and suitability of roof-harvested rainwater in rural villages for crop irrigation and domestic use. J Water Health 2016;14(6):961-971. https://doi.org/10.2166/wh.2016.058        [ Links ]

18. Markland SM, Ingram D, Kniel KE, Sharma M. Water for agriculture: The convergence of sustainability and safety. Microbiol Spectr 2017;5(3). https://doi.org/10.1128/microbiolspec.PFS-0014-2016        [ Links ]

19. Miettinen H, Wirtanen G. Ecology of Listeria spp. in a fish farm and molecular typing of Listeria monocytogenes from fish farming and processing companies. Int J Food Microbiol 2006;112(2):138-146. https://doi.org/10.1016/j.ijfoodmicro.2006.06.016        [ Links ]

20. Miettinen H, Wirtanen G. Prevalence and location of Listeria monocytogenes in farmed rainbow trout. Int J Food Microbiol 2005;104(2):135-143. https://doi.org/10.1016/j.ijfoodmicro.2005.01.013        [ Links ]

21. International Energy Agency. Statistics. 2014. http://www.iea.org/statistics/statisticssearch/ (accessed 10 May 2018).         [ Links ]

22. Public Protector. 'Derailed'. A report on an investigation into allegations of maladminstration relating to financial mismanagement, tender irregularities and appointment irregularities against the Passenger Rail Agency of South Africa (PRASA). Report No: 3 of 2015/2016. 2015. http://allafrica.com/download/resource/main/main/idatcs/00091794:b2efdd85e08 e1e087813a4b7a417f4e4.pdf (accessed 15 May 2018).         [ Links ]

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