Table of Contents

    Topic review

    Cyclospora Cayetanensis

    Subjects: Microbiology | Others | Others
    View times: 50
    Submitted by: Dimitrios Tsaltas

    Definition

    Cyclospora cayetanensis is a coccidian protozoan that causes cyclosporiasis, a severe gastroenteric disease, especially for immunocompromised patients, children, and the elderly. The parasite is considered as an emerging organism and a major contributor of gastroenteritis worldwide. Although the global prevalence of cyclosporiasis morbidity and mortality has not been assessed, global concern has arisen since diarrheal illness and gastroenteritis significantly affect both developing and industrialized countries. In the last two decades, an increasing number of foodborne outbreaks have been associated with the consumption of fresh produce that is difficult to clean thoroughly and is consumed without processing. Investigations of these outbreaks have revealed the necessity to increase the awareness in clinicians of this infection, since this protozoan is often ignored by surveillance systems, and to establish control measures to reduce contamination of fresh produce.

    1. Introduction

    Diarrhea is one of the leading causes of mortality worldwide. In 2016, it was responsible for the death of more than 1.6 million people, with 90% of the deaths being reported in South Asia and sub-Saharan Africa [1]. It is also estimated that diarrhea is the second cause of death in children under five, killing nearly 525,000 every year [2]. Enteric protozoan parasites are among the leading causes of human diarrhea disease [3]C. cayetanensis is one of these protozoan parasites that is considered as an emerging organism able to cause cyclosporiasis, a severe gastro-enteric disease especially for immunocompromised patients, children, and elderly.

    Cyclospora is an apicomplexan, cyst-forming coccidian protozoan that belongs to subphylum Apicomplexa, subclass Coccidiasina, and family Eimeriidae [4]. Currently, nineteen Cyclospora species have been reported to be causative agents of disease in various animal species [5] and only one species, C. cayetanensis, is known to be associated with syndromes of acute and chronic diarrhea in humans. It is endemic in tropical and subtropical areas, but it has been identified as the causative agent of several outbreaks worldwide in the last two decades and it is also considered as a significant contributor to global gastroenteritis spread [6]. Most of the cyclosporiasis cases reported in non-endemic areas have been linked either with travelers returning from endemic areas or with imported foods from developing countries. It is however noteworthy that there is a significant number of reported cases in non-endemic areas, as the risk of exposure to uncommon diseases has been increased. This increase has mainly occurred because of the augmentation of international travel, the globalization of food supply and change in consumers’ dietary habits [4]Cyclospora is highly resistant to disinfectants used in the food industry [4], while globalization of food supply disseminates pathogenic organisms over wide geographical areas introducing important hazards. Besides, thanks to the increasing popularity of fresh fruits and vegetables—due to consumers’ tendency to eat healthier—produce have become important vehicles in food-borne illness statistics [7].

    2. Historic Taxonomy and Molecular Characteristics

    The genus Cyclospora was first described in Old World moles (Talpinae) and subsequently in reptiles, birds, and myriapods [8][9]. The first documented human cases were diagnosed in 1977 and 1978 and reported by Ashford in 1979 [10], who isolated the organism from the stools of three patients in Papua New Guinea and correctly concluded that the organism was a coccidian parasite. However, because of its morphology and his uncertainty about the number of the sporozoites in the sporocysts, he wrongly presumed that the organism was a species of Isospora [10].

    In 1986 Soave et al. [11] reported a new enteric pathogen that was the causative agent of a flu-like illness in four travelers to Haiti and Mexico, while in 1989 Naranjo et al. [12] described a ‘Cryptosporidium muris-like object’ reporting that it was probably an unidentified flagellate. In following reports, the organism was described as a cyanobacterium-like body, coccidian-like body (CLB), blue-green algae, or large Cryptosporidium [13][14][15][16]. Eventually, in 1993 Ortega et al. [17] classified this new organism in the genus Cyclospora and in 1994 they proposed the name C. cayetanensis for the new human parasite (derived from their university —Universidad Peruana Cayetano Heredia) [18]. Since then, many studies have been performed to identify the biological and epidemiological characteristics of this organism.

    Phylogenetic analysis of the C. cayetanensis small subunit rRNA (SSU rRNA) gene sequences and mitochondrial genome have demonstrated that this organism is closely related to the Eimeria genus [19][20], while phylogenetic analysis based on the 18S rDNA sequences has indicated that this relation can even be compared to that existing within Eimeria species [21]. At the same time, cluster analysis of apicoplast (non-photosynthetic plastids) genomes originating from different Apicomplexan parasites have revealed a strong relation among C. cayetanensisEimeria, and Toxoplasma, and a common evolutionary history [22]

    Lack of geographic segregation and existence of genetically homogeneous C. cayetanensis parasites has also been demonstrated [23][24]. In 2013, Sulaiman et al. reported a lack of genetic polymorphism at the regions of 70kDa heat shock protein (HSP70) locus, while a year later a study revealed minimal genetic diversity among 17 human C. cayetanensis isolates based on their 18S ribosomal RNA gene [24]. In 2016, Cinar et al. [22] performed comparative analysis of 11 C. cayetanensis apicoplast genomes originating from different geographical areas and reported high conservation with only a few polymorphisms. Nevertheless, it has not been indicated yet whether all human Cyclospora isolates belong to the same species, or that species that are disease agents in low primates cannot also infect humans [6].Studies have reported that C. cayetanensis was not detected in primates, suggesting that some primates are unlikely to be reservoirs for the human pathogen [21][25][26]. Moreover, the strong relationship that characterizes Cyclospora and Eimeria suggests that Cyclospora is probably a host-specific pathogen [27]. However, the pathogen genome’s further characterization is necessary to improve knowledge of this organism regarding its taxonomic position, as well as to understand its transmission dynamics and pathogenic potential.

    3. Control and Prevention

    Cyclosporiasis is an infection that occurs after the consumption of contaminated foods or water, while person-to person transmission is unlikely. Therefore, avoiding food and water from contaminated sources is the optimum way to prevent Cyclospora infection, especially when water sanitation programs are less attentive (e.g., in developing countries). Good agricultural practices, such as rigorously sanitized irrigation water, can be conducive to decreased parasite contamination in the field and in the produce packing plants. Furthermore, good personal hygiene, appropriate food washing, and sanitary conditions can reduce the pathogen transmission, especially in endemic areas. However, it has been indicated that, even if these practices are strictly followed, the risk of exposure in this parasite may be reduced but not eliminated [4][28].

    Hence, several studies have been performed to validate the efficiency of different hurdle methods in the reduction and inactivation of the parasite oocysts (viability indicator). According to Sathyanarayanan and Ortega [29], parasite’s oocyst exposure in extremely low or high temperatures (−70 °C, 70 °C and 100 °C) resulted in sporulation inactivation in basil samples, whereas room and refrigeration temperatures, did not affect the sporulation in various food samples. Treatment with chemical disinfectants has also been examined, with significant reductions in sporulation and protozoan population being reported. Magnesium oxide (MgO) nanoparticles showed antimicrobial activity against C. cayetanensis sporulated and unsporulated oocysts [30], while the population levels of the parasite decreased when fruits and vegetables were dipped in sodium dichloro-isocyanurate (NaDCC) solution (1 g/L) [31]. Despite this, chemical disinfection cannot guarantee product safety, since its efficacy depends on various factors, such as the initial population level of the microbe, the food matrix, and the environmental conditions [32]. In addition, irradiation (gamma and ultraviolet) and high-pressure technologies have also been evaluated utilizing surrogate parasites (e.g., Eimeria acervulina), revealing effective anti-parasite activities [33][34]. Nevertheless, the data are limited, and further research is necessary for the development of reliable control methods for this pathogenic parasite.

    4. Conclusions

    C. cayetanensis was indicated as a foodborne pathogen in the mid-1990s. Since then, efforts have been made to identify the variability of the parasite and develop methods for its detection. However, the increase of foodborne outbreaks, especially related to produce consumption, continuously underlines the necessity for a better global understanding of the pathogen and the establishment of drastic control measures.

    The low infectious dose and the long sporulation period complicate the performance of active surveillance. However, the outbreaks that occur highlight the necessity to overcome these difficulties and control the presence of the pathogen in water and fresh produce, especially in endemic countries. This will be achieved by cooperation between developed and developing countries. Developed countries ought to conduct further research on epidemiological aspects of this infection and coordinate with endemic countries to set up measures that will decrease the risk of producing and distributing unsafe food items.

    At the same time, cyclosporiasis outbreaks that have occurred in developed countries have revealed the necessity to raise physicians’ awareness of this infection. Clinicians should be well informed about the infection’s typical symptoms and should request specific diagnostic tests for Cyclospora detection, especially in patients with prolonged diarrhea and travel history. Patients’ travel history should be recorded to provide important information for doctors and investigators and to assist investigators in determining the source of contamination. Moreover, clinical laboratories should be aware of the existing testing methods, and new techniques such as genome sequencing should be developed to investigate and detect the source of outbreaks.

    Finally, it is noteworthy that the control procedures that currently exist in the fresh produce chain mainly examine the presence and levels of pathogenic and spoilage bacteria, without addressing the impact of these procedures on parasites’ survival. Hence, investigations on current methods and their effect on parasites, including C. cayetanensis, should be performed and addressed. In addition, novel methods that will ensure parasites’ control should be determined and included in the existing procedures that concern fresh produce safety.

    The entry is from 10.3390/foods9111703

    References

    1. Global Burden of Diseases (GBD). Estimates of the global, regional, and national morbidity, mortality, and aetiologies of diarrhoea in 195 countries: A systematic analysis for the Global Burden of Disease Study 2016. Lancet Infect. Dis. 2018, 18, 1211–1228.
    2. World Health Organization (WHO). Diarrhoeal Disease. Available online: https://www.who.int/en/news-room/fact-sheets/detail/diarrhoeal-disease (accessed on 2 February 2020).
    3. Di Genova, B.M.; Tonelli, R.R. Infection strategies of intestinal parasite pathogens and host cell responses. Front. Microbiol 2016, 7, 256.
    4. Ortega, Y.R.; Sanchez, R. Update on Cyclospora cayetanensis, a food-borne and waterborne parasite. Clin. Microbiol. Rev. 2010, 23, 218–234.
    5. Lainson, R. The genus Cyclospora: (Apicomplexa: Eimeriidae), with a description of Cyclospora schneideri n.sp. in the snake Anilius scytale (Anilüdae) from Amazonian Brazil—A review. Mem. Inst. Oswaldo Cruz. 2005, 100, 103–115.
    6. Chacín-Bonilla, L. Cyclospora cayetanensis. In Global Water Pathogens Project; Rose, J.B., Jimenez-Cisneros, B., Eds.; Michigan State University: East Lansing, MI, USA, 2017; pp. 1–43.
    7. Beuchat, L.R.; World Health Organization (WHO). Surface Decontamination of Fruits and Vegetables Eaten Raw: A Review; World Health Organization: Geneva, Switzerland, 2002.
    8. Levine, N.D. Taxonomy and life cycles of coccidia. In The Biology of the Coccidia; Long, P.L., Ed.; Edward Arnold: London, UK, 1982; pp. 1–33.
    9. Mohamed, H.A.; Molyneux, D.H. Developmental stages of Cyclospora talpae in the liver and bile duct of the mole (Talpa europa). Parasitology 1990, 101, 345–420.
    10. Ashford, R.W. Occurrence of an undescribed coccidian in man in Papua New Guinea. Ann. Trop. Med. Parasitol. 1979, 73, 497–500.
    11. Soave, R.; Dubey, J.P.; Ramos, L.J.; Tummings, M. A new intestinal pathogen? Clin. Res. 1986, 34, 533.
    12. Naranjo, J.; Sterling, C.R.; Gilman, R. Cryptosporidium muris-like objects from fecal samples of Peruvians. In Proceedings of the 38th Annual Meeting of the American Society of Tropical Medicine and Hygiene, Honolulu, HI, USA, 10–14 December 1989.
    13. Long, E.G.; Ebrahimzadeh, A.; White, E.H.; Swisher, B.; Callaway, C.S. Alga associated with diarrhea in patients with acquired immunodeficiency syndrome and in travelers. J. Clin. Microbiol. 1990, 28, 1101–1104.
    14. Long, E.G.; White, E.H.; Carmichael, W.W.; Quinlisk, P.M.; Raja, R.; Swisher, B.L.; Daugharty, H.; Cohen, M.T. Morphologic and staining characteristics of a cyanobacterium-like organism associated with diarrhea. J. Infect. Dis. 1991, 164, 199–202.
    15. Bendall, R.P.; Lucas, S.; Moody, A.; Tovey, G.; Chiodini, P.L. Diarrhea associated with cyanobacterium-like bodies: A new coccidian enteritis of man. Lancet 1993, 341, 590–592.
    16. Connor, B.A.; Shlim, D.R.; Scholes, J.V.; Rayburn, J.L.; Reidy, J.; Rajah, R. Pathologic changes in the small bowel in nine patients with diarrhea associated with a coccidia-like body. Ann. Intern. Med. 1993, 119, 377–382.
    17. Ortega, Y.R.; Sterling, C.R.; Gilman, R.H.; Cama, V.A.; Diaz, F. Cyclospora species—A new protozoan pathogen of humans. N. Engl. J. Med. 1993, 328, 1308–1312.
    18. Ortega, Y.R.; Gilman, R.H.; Sterling, C.R. A new coccidian parasite (Apicomplexa: Eimeriidae) from humans. J. Parasitol. 1994, 80, 625–629.
    19. Li, J.; Chang, Y.; Shi, K.E.; Wang, R.; Fu, K.; Li, S.; Xu, J.; Jia, L.; Guo, Z.; Zhang, L. Multilocus sequence typing and clonal population genetic structure of Cyclospota cayetanensis in humans. Parasitology 2017, 144, 1890–1897.
    20. Cinar, H.N.; Gopinath, G.K.; Jarvis, K.; Murphy, H.R. The complete mitochondrial genome of the foodborne parasitic pathogen Cyclospora cayetanensis. PLoS ONE 2015, 10, e0128645.
    21. Zhao, G.H.; Cong, M.M.; Bian, Q.Q.; Cheng, W.Y.; Wang, R.J.; Qi, M.; Zhang, L.X.; Lin, Q.; Zhu, X.Q. Molecular characterization of Cyclospora-like organisms from golden snub-nosed monkeys in Qinling Mountain in Shaanxi province, northwestern China. PLoS ONE 2013, 8, e58216.
    22. Cinar, H.N.; Qvarnstrom, Y.; Wei-Pridgeon, Y.; Li, W.; Nascimento, F.S.; Arrowood, M.J.; Murphy, H.R.; Jang, A.Y.; Kim, E.; Kim, R.Y.; et al. Comparative sequence analysis of Cyclospora cayetanensis apicoplast genomes originating from diverse geographical regions. Parasit. Vectors 2016, 9, 1–14.
    23. Sulaiman, I.M.; Torres, P.; Simpson, S.; Kerdahi, K.; Ortega, Y. Sequence characterization of heat shock protein gene of Cyclospora cayetanensis isolates from Nepal, Mexico, and Peru. J. Parasitol. 2013, 99, 379–382.
    24. Sulaiman, I.M.; Ortega, Y.; Simpson, S.; Kerdahi, K. Genetic characterization of human-pathogenic Cyclospora cayetanensis parasites from three endemic regions at the 18S ribosomal RNA locus. Infect. Genet. Evol. 2014, 22, 229–234.
    25. Eberhard, M.L.; Da Silva, A.J.; Lilley, B.G.; Pieniazek, N.J. Morphologic and molecular characterization of new Cyclospora species from Ethiopian monkeys: C. cercopitheci sp.n., C. colobi sp.n., and C. papionis sp.n. Emerg. Infect. Dis. 1999, 5, 651–658.
    26. Eberhard, M.L.; Njenga, M.N.; DaSilva, A.J.; Owino, D.; Nace, E.K.; Won, K.Y.; Mwenda, J.M. A survey for Cyclospora spp. in Kenyan primates, with some notes on its biology. J. Parasitol. 2001, 87, 1394–1397.
    27. Reiman, D.A.; Schmidt, T.M.; Gajadhar, A.; Sogin, M.; Cross, J.; Yoder, K.; Sethabutr, O.; Echeverria, P. Molecular phylogenetic analysis of Cyclospora, the human intestinal pathogen, suggests that it is closely related to Eimeria species. J. Infect. Dis. 1996, 173, 440–445.
    28. Almeira, S.; Cinar, H.N.; Dubey, J.P. Cyclospora cayetanensis and Cyclosporiasis: An Update. Microorganisms 2019, 7, 317.
    29. Sathyanarayanan, L.; Ortega, Y. Effects of temperature and different food matrices on Cyclospora cayetanensis oocyst sporulation. J. Parasitol. 2006, 92, 218–222.
    30. Hussein, E.M.; Ahmed, S.A.; Mokhtar, A.B.; Elzagawy, S.M.; Yahi, S.H.; Hussein, A.M.; El-Tantawey, F. Antiprotozoal activity of magnesium oxide (MgO) nanoparticles against Cyclospora cayetanensis oocysts. Parasitol. Int. 2018, 67, 666–674.
    31. El Zawawy, L.A.; El-Said, D.; Ali, S.M.; Fathy, F.M. Disinfection efficacy of sodium dichloroisocyanurate(NADCC) against common food-borne intestinal protozoa. J. Egypt. Soc. Parasitol. 2010, 40, 165–185.
    32. Gérard, C.; Franssen, F.; La Carbona, S.; Monteiro, S.; Cozma-Petruţ, A.; Utaaker, K.S.; Jambrakg, A.R.; Rowanh, N.; Rodríguez-Lazaroi, D.; Nasserj, A.; et al. Inactivation of parasite transmission stages: Efficacy of treatments on foods of non-animal origin. Trends Food Sci. Technol. 2019, 91, 12–23.
    33. Lee, M.B.; Lee, E.H. Coccidial contamination of raspberries: Mock contamination with Eimeria acervulina as a model for decontamination treatment studies. J. Food Protect. 2001, 64, 1854–1857.
    34. Kniel, K.E.; Shearer, A.E.H.; Cascarino, J.L.; Wilkins, G.C.; Jenkins, M.C. High hydrostatic pressure and UV light treatment of produce contaminated with Eimeria acervulina as a Cyclospora cayetanensis surrogate. J. Food Protect. 2007, 70, 2837–2842.
    More