Hostname: page-component-76fb5796d-vfjqv Total loading time: 0 Render date: 2024-04-25T23:43:35.323Z Has data issue: false hasContentIssue false

An apple a day: an outbreak of cryptosporidiosis in Norway associated with self-pressed apple juice

Published online by Cambridge University Press:  11 March 2019

L. J. Robertson*
Affiliation:
Parasitology Lab., Department of Food Safety and Infection Biology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, PO Box 369 sentrum, 0102 Oslo, Norway
T. T. Temesgen
Affiliation:
Parasitology Lab., Department of Food Safety and Infection Biology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, PO Box 369 sentrum, 0102 Oslo, Norway
K. R. Tysnes
Affiliation:
Parasitology Lab., Department of Food Safety and Infection Biology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, PO Box 369 sentrum, 0102 Oslo, Norway
J. E. Eikås
Affiliation:
Smittevernlege, Postboks 184, Fjell kommune, 5342 Straume, Norway
*
Author for correspondence: L. J. Robertson, E-mail: lucy.robertson@nmbu.no
Rights & Permissions [Opens in a new window]

Abstract

In the autumn of 2018, an outbreak of cryptosporidiosis affected adult employees from the same company in Western Norway. The organism was Cryptosporidium parvum, GP60 subtype IIaA14G1R1. All those infected had drunk from the same container of self-pressed apple juice. Incubation period (1 week) and clinical signs were similar among those infected, although some experienced a more prolonged duration of symptoms (up to 2–3 weeks) than others. The infections resulted after consumption from only one of 40 containers of juice and not from any of the other containers. It seems that although Cryptosporidium oocysts were detected in a sample from another container, the contamination did not affect the whole batch. This is perhaps indicative of a restricted contamination event, either from contaminated ground in the orchard, or during collection of the fruit, or during processing. Although outbreaks of food-borne cryptosporidiosis have previously been associated with consumption of contaminated apple juice, most of the more recent outbreaks of food-borne cryptosporidiosis have been associated with salad vegetables or herbs. This outbreak, the first outside USA reported to be associated with apple juice, is a timely reminder that such juice is a suitable transmission vehicle for Cryptosporidium oocysts, and that appropriate hygienic measures are essential in the production of such juice, including artisanal (non-commercial) production.

Type
From the Field
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s) 2019

On Monday 15 October 2018, six employees at the same work unit in Western Norway reported absence due to illness. All had similar symptoms, as follows: violent diarrhoea, abdominal pain with severe colic, cough, pain in the thighs, pelvis and back and exhaustion and fatigue. Cryptosporidiosis was diagnosed in a number of individuals via samples provided to their general practitioners. It was rapidly apparent that all those who were sick had partaken of some freshly pressed apple juice that had been brought into the workplace the previous Monday (8 October) by one of those who were sick. The apple juice had been made by the employee herself during the previous weekend, with apples picked in the orchard of her family's farm, and had been pressed at a neighbouring farm. The 5-L container of apple juice brought into the workplace had been left in a communal area for everyone who wished to help themselves. Retrospective questioning of the employees identified seven who had enjoyed cups of juice from the container. All six cases were among those who had drunk the apple juice. In all of those infected, the diarrhoea and other symptoms continued for at least 1 week, before gradually subsiding; for some individuals, the symptoms persisted for up to 2–3 weeks.

Cryptosporidium has been identified as a potentially food-borne parasite of importance in Europe [Reference Bouwknegt1], although a recent report from the European Food Safety Authority (EFSA) concluded that the relative importance of food as a transmission route, as compared with other vehicles of infection, is unknown [2]. Symptomatic infection (cryptosporidiosis) is characterised by those symptoms experienced in this outbreak, with the predominant sign being voluminous watery diarrhoea; abdominal pain, nausea, mild fever, anorexia, malaise, fatigue and weight loss are also common in cryptosporidiosis [2]. Although symptoms generally last for 2 to 3 weeks, sometimes longer, they resolve spontaneously in otherwise healthy people, but relapses are not uncommon. However, individuals with impaired immune systems are at risk of symptoms being more severe and protracted. This is important, as very few drugs are available for treatment of cryptosporidiosis, and nitazoxanide, a broad-spectrum antiparasitic and antiviral drug with proven success against cryptosporidiosis in otherwise healthy adults, is not licensed for use in Europe. Various global studies have shown that Cryptosporidium is a major cause of moderate-to-severe diarrhoeal disease in children younger than 5 years in some regions (sub-Saharan Africa and South East Asia). Although there are several species of Cryptosporidium that are infectious to humans, most infections are due to either Cryptosporidium hominis or C. parvum. The latter is zoonotic, and is a common cause of diarrhoeal disease in young ruminants, particularly calves. Based on data compiled in the EFSA Opinion [2], the first reported food-borne outbreaks of cryptosporidiosis (from 1983 to 2008) were often associated with unpasteurised dairy products or pressed apples (apple cider), such that of 14 outbreaks in this period, six were associated with dairy products and three with apple cider. However, in the last decade (from 2008 onwards) of the 10 reported outbreaks, none was associated with apple cider and only one with dairy products. Although, reports of food-borne cryptosporidiosis seem to be skewed towards Nordic countries [Reference Robertson and Chalmers3], to date there have been no reports of cryptosporidiosis associated with either apple juice or dairy products from this region; all apple juice associated outbreaks have been reported from the USA, with the last reported outbreak in 2003 [Reference Blackburn4].

Although epidemiological inference strongly indicated that the apple juice was the source of this particular outbreak, further investigations were conducted to back up this supposition, and to try to shed light on how the apple juice had been contaminated.

On 2 November 2018, a faecal sample from one of the patients and a 1.5 L sample of apple juice (not from the same 5 L container that had been taken to the work place) were received at the Parasitology Laboratory, Norwegian University of Life Sciences, and analysed for Cryptosporidium oocysts. The apple juice was concentrated by centrifugation followed by immunomagnetic separation (IMS); the very small faecal sample was resuspended in 1.5 mL water and also concentrated by IMS (using a modified method based on that previously described for Giardia cysts [Reference Robertson5]). Detection of Cryptosporidium oocysts in the concentrated samples was by immunofluorescent antibody staining (IFAT; Aqua-Glo, Waterborne Inc., New Orleans, USA), with 4′,6-diamidino-2-phenylindole used as an adjunct stain. Both the faecal sample and the apple juice sample were positive for Cryptosporidium oocysts. Only few oocysts were found in the faecal sample (as might be expected at the very end of an infection, for which symptoms had commenced over 2-weeks earlier), but large numbers (estimate of hundreds) of oocysts were found in the apple juice concentrate (after centrifugation and IMS), although many of them seemed distorted or broken. DNA was extracted from both the sample concentrates using the DNeasy® PowerSoil® kit (Qiagen, Norway) following the automated protocol IRT©V1 (QIAcube, Qiagen, Norway) in 50-μL elution volume. Nested polymerase chain reaction targeting the GP60 [Reference Alves6] and SSU-rRNA loci [Reference Xiao7] was conducted, with sequencing of amplicons via a commercial company. Although DNA amplification from the apple juice sample was unsuccessful, the faecal sample was shown to contain C. parvum oocysts of subtype IIaA14G1R1. This is similar, but not identical, to a C. parvum subtype previously associated with two earlier cryptosporidiosis outbreaks in Norway; IIaA19G1R1 [Reference Rimšelienė8, Reference Lange9], which were due to contact between schoolchildren and infected lambs and kids at a holiday farm. The same subtype has, however, been reported from faecal samples from calves in Poland [Reference Kaupke and Rzeżutka10] and Estonia [Reference Santoro11], yaks in China [Reference Mi12], and humans in Slovenia [Reference Soba and Logar13] and Slovakia [Reference Hatalová14].

How the juice had become contaminated has not been clarified. The apples had been picked by hand from the trees (rather than collected from the ground), at a family farm by a group of family and friends, none of whom had any symptoms of illness, during the weekend. Animals had not been grazing around the trees, and the nearest livestock were sheep at a neighbouring farm. There were no young lambs in the flock at that time, and the sheep were retained behind an electric fence. The apples were collected into clean, dry containers and then driven to a farm in the neighbourhood for pressing. This farm presses apples for commercial production, as well as renting their equipment for individuals to press their own fruit; commercial production and pressing of apples by customers with their own fruit are not done in parallel. The pressing equipment is located in an enclosed area, not accessible by animals, and the equipment is washed between customers.

A total of around 200 L of apple juice was made, and as this was being produced it was collected into previously unused 5-L volume containers. These containers were divided amongst those who had been involved in picking and pressing the apples, and one of them ended in the work place where the infection occurred. However, there were no other reports of infections associated with the consumption of the apple juice in the other containers (another container was similarly shared with colleagues at another work place, without anyone becoming ill), indicating that the contamination did not extend to the entire 200 L, and was perhaps limited to only a couple of containers. This suggests that maybe only a very few apples used to make the juice had been contaminated. It was speculated that perhaps a couple may have been accidentally dropped during collection and then retrieved; if by misfortune they had landed in an area of high contamination, then there could have been localised high contamination in a very few apples. Although there was the possibility to wash the apples before pressing, spiking experiments have indicated that it is difficult to remove Cryptosporidium oocysts from the surfaces of apples; the most effective methods, such as rigorous manual washing in water with a detergent or by agitation in an orbital shaker with Tris-sodium dodecyl sulphate buffer, were found to remove less than 40% [Reference Macarisin15]. This experiment with spiked apples further indicated that Cryptosporidium oocysts on apple surfaces retain their infectivity for at least 4 weeks [Reference Macarisin15].

An alternative route of contamination of the apple juice could have been that the equipment was contaminated before use, and the oocysts were washed into the initial containers of apple juice. There is no evidence for the latter suggestion, and there were no reports of illness by others using the press. Nevertheless, the owner of the apple press reported the intention to implement use of a high-pressure hot water cleaner for use between apple lots and customers to assist in and improve the equipment cleaning process.

In conclusion, here we describe the first outbreak of apple juice-related cryptosporidiosis reported in Europe, and the first reported globally since 2003. Although the outbreak did not involve many people, it serves as a timely reminder that apple juice, and other beverages, may serve as efficient transmission vehicles for cryptosporidiosis.

Author ORCIDs

L. J. Robertson, 0000-0001-5186-4421.

References

1.Bouwknegt, M et al. (2016) The Euro-FBP workshop participants (2018). Prioritisation of food-borne parasites in Europe. Eurosurveillance 2018, 23. doi: 10.2807/1560-7917.ES.2018.23.9.17-00161.Google Scholar
2.EFSA BIOHAZ Panel (EFSA Panel on Biological Hazards) (2018) Scientific opinion on the public health risks associated with food-borne parasites. EFSA Journal 16, 5495, 113 pp.Google Scholar
3.Robertson, LJ and Chalmers, RM (2013) Foodborne cryptosporidiosis: is there really more in Nordic countries? Trends in Parasitology 29, 39.Google Scholar
4.Blackburn, BG et al. (2006) Cryptosporidiosis associated with ozonated apple cider. Emerging Infectious Diseases 12, 684686.Google Scholar
5.Robertson, LJ et al. (2006) Application of genotyping during an extensive outbreak of waterborne giardiasis in Bergen, Norway, during autumn and winter 2004. Applied and Environmental Microbiology 72, 22122217.Google Scholar
6.Alves, M et al. (2003) Subgenotype analysis of Cryptosporidium isolates from humans, cattle, and zoo ruminants in Portugal. Journal of Clinical Microbiology 41, 27442747.Google Scholar
7.Xiao, L et al. (1999) Genetic diversity within Cryptosporidium parvum and related Cryptosporidium species. Applied and Environmental Microbiology 65, 33863391.Google Scholar
8.Rimšelienė, G et al. (2011) An outbreak of gastroenteritis among schoolchildren staying in a wildlife reserve: thorough investigation reveals Norway's largest cryptosporidiosis outbreak. Scandinavian Journal of Public Health 39, 287295.Google Scholar
9.Lange, H et al. (2014) Second outbreak of infection with a rare Cryptosporidium parvum genotype among schoolchildren associated with contact with lambs/goat kids at a holiday farm in Norway. Epidemiology and Infection 142, 21052113.Google Scholar
10.Kaupke, A and Rzeżutka, A (2015) Emergence of novel subtypes of Cryptosporidium parvum in calves in Poland. Parasitology Research 114, 47094716.Google Scholar
11.Santoro, A et al. (2018) Molecular epidemiology of Cryptosporidium spp. in calves in Estonia: high prevalence of Cryptosporidium parvum shedding and 10 subtypes identified. Parasitology 8, 17.Google Scholar
12.Mi, R et al. (2013) Prevalence and genetic characterization of Cryptosporidium in yaks in Qinghai Province of China. PLoS One 8, e74985.Google Scholar
13.Soba, B and Logar, J (2008) Genetic classification of Cryptosporidium isolates from humans and calves in Slovenia. Parasitology 135, 12631270.Google Scholar
14.Hatalová, E et al. (2018). The first report of animal genotypes of Cryptosporidium parvum in immunosuppressed and immunocompetent humans in Slovakia. Transboundary and Emerging Diseases Published online: 4 September 2018. doi: 10.1111/tbed.13009.Google Scholar
15.Macarisin, D et al. (2010) Infectivity of Cryptosporidium parvum oocysts after storage of experimentally contaminated apples. Journal of Food Protection 73, 18241829.Google Scholar