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Toxoplasmosis in the Caribbean islands: literature review, seroprevalence in pregnant women in ten countries, isolation of viable Toxoplasma gondii from dogs from St. Kitts, West Indies with report of new T. gondii genetic types

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Abstract

Little is currently known of clinical toxoplasmosis in humans and animals in the Caribbean. We investigated the prevalence of IgG and IgM antibodies in 437 pregnant women from 10 English speaking Caribbean countries. Overall, antibodies (IgG) to Toxoplasma gondii (modified agglutination test, MAT, cut-off 1:6) were found in 174 (39.8 %) of 437 human sera; specifically 12 of 38 from Antigua-Barbuda, 26 of 52 from Belize, 9 of 50 from Bermuda, 29 of 49 from Dominica, 18 of 49 from Grenada, 16 of 47 from Jamaica, 5 of 15 from Montserrat, 8 of 44 from St. Kitts/Nevis, 24 of 45 from St. Lucia, and 27 of 50 from St. Vincent/Grenadines were seropositive. All IgG-positive sera were tested for IgM antibodies using the immunocapture method; all sera were negative for IgM antibodies. Additionally, tissues and sera of 45 dogs from St. Kitts were examined for T. gondii infection. Antibodies (IgG, MAT, 1:≥25) were found in 19 (42.2 %) of 45 dogs. Muscle samples (tongue, leg) of 19 seropositive dogs were digested in pepsin, and homogenates were bioassayed in mice. Viable T. gondii were isolated from 6 dogs. T. gondii isolates were further propagated in cell culture. PCR-RFLP genotyping of cell culture derived tachyzoites using 10 genetic markers, SAG1, SAG2 (5′ and 3′ SAG2, and alt.SAG2) SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, and Apico revealed that 4 isolates were ToxoDB PCR-RFLP genotype #2, and 2 were new genotypes #264 and #265. Review of 22 viable T. gondii isolates from chickens, dogs, and cats from Grenada and St. Kitts revealed that 1 isolate was type II, 13 were type III, and 8 were atypical. Thus, type III strains were predominant. Overall, the study revealed high prevalence of T. gondii in the Caribbean islands.

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References

  • Adesiyun AA, Gooding R, Ganta K, Seepersadsingh N, Ramsewak S (2007) Congenital toxoplasmosis in two health institutions in Trinidad. West Indian Med J 56:166–170

    Article  CAS  PubMed  Google Scholar 

  • Adesiyun A, Rahaman S, Bissessar S, Dookeran S, Stewart-Johnson A, Hilaire MG (2010) Seroprevalence of toxoplasmosis, leptospirosis and brucellosis in sugarcane field-workers in Trinidad and Tobago. West Indian Med J 59:14–19

    CAS  PubMed  Google Scholar 

  • Asthana SP, Macpherson CNL, Weiss SH, Stephens R, Sharma RN, Dubey JP (2006) Seroprevalence of Toxoplasma gondii in pregnant women and cats in Grenada, West Indies. J Parasitol 92:644–645

    Article  PubMed  Google Scholar 

  • Barbier D, Ancelle T, Martin-bouyer G (1983) Seroepidemiological survey of toxoplasmosis in La Guadeloupe, French West Indies. Am J Trop Med Hyg 32:935–942

    CAS  PubMed  Google Scholar 

  • Barrow G, Clarke TR, Carrington D, Harvey K, Barton EN (2010) An analysis of three opportunistic infections in an outpatient HIV clinic in Jamaica. West Indian Med J 59:393–399

    CAS  PubMed  Google Scholar 

  • Chikweto A, Kumthekar S, Tiwari K, Nyack B, Deokar MS, Stratton G, Macpherson CNL, Sharma RN, Dubey JP (2011) Seroprevalence of Toxoplasma gondii in pigs, sheep, goats, and cattle from Grenada and Carriacou, West Indies. J Parasitol 97:950–951

    Article  CAS  PubMed  Google Scholar 

  • De Roever-Bonnet H, Lelyveld J, Marinkelle CJ (1969) Toxoplasmosis in Latin-American countries. Trop Geogr Med 21:451–455

    PubMed  Google Scholar 

  • Desmonts G, Remington JS (1980) Direct agglutination test for diagnosis of Toxoplasma infection: method for increasing sensitivity and specificity. J Clin Microbiol 11:562–568

    CAS  PubMed  PubMed Central  Google Scholar 

  • Dubey JP (2010) Toxoplasmosis of animals and humans, 2nd edn. CRC Press, Boca Raton, FL, pp 1–313

    Google Scholar 

  • Dubey JP, Desmonts G (1987) Serological responses of equids fed Toxoplasma gondii oocysts. Equine Vet J 19:337–339

    Article  CAS  PubMed  Google Scholar 

  • Dubey JP, Stone D, Kwok OCH, Sharma RN (2008) Toxoplasma gondii and Neospora caninum antibodies in dogs from Grenada, West Indies. J Parasitol 94:750–751

    Article  CAS  PubMed  Google Scholar 

  • Dubey JP, Lappin MR, Kwok OCH, Mofya S, Chikweto A, Baffa A, Doherty D, Shakeri J, Macpherson CNL, Sharma RN (2009a) Seroprevalence of Toxoplasma gondii and concurrent Bartonella spp., feline immunodeficiency virus, and feline leukemia infections in cats from Grenada, West Indies. J Parasitol 95:1129–1133

    Article  CAS  PubMed  Google Scholar 

  • Dubey JP, Moura L, Sundar N, Velmurugan GV, Kwok OCH, Kelly P, Krecek RC, Su C (2009b) Isolation and characterization of viable Toxoplasma gondii isolates revealed possible high frequency of mixed infection in feral cats (Felis domesticus) from St Kitts, West Indies. Parasitology 136:589–594

    Article  CAS  PubMed  Google Scholar 

  • Dubey JP, Laurin E, Kwok OCH (2016) Validation of the modified agglutination test for detection of Toxoplasma gondii in free-range chickens by using cat and mouse bioassay. Parasitology. doi:10.1017/S0031182015001316

    Google Scholar 

  • Frenkel JK, Parker BB (1996) An apparent role of dogs in the transmission of Toxoplasma gondii. The probable importance of xenosmophilia. Ann N Y Acad Sci 791:402–407

    Article  CAS  PubMed  Google Scholar 

  • Hamilton CM, Kelly PJ, Bartley PM, Burrells A, Porco A, Metzler D, Crouch K, Ketzis JK, Innes EA, Katzer F (2015) Toxoplasma gondii in livestock in St. Kitts and Nevis, West Indies. Parasit Vectors 8:e166

    Article  Google Scholar 

  • Howe DK, Sibley LD (1995) Toxoplasma gondii comprises three clonal lineages: correlation of parasite genotype with human disease. J Infect Dis 172:1561–1566

    Article  CAS  PubMed  Google Scholar 

  • Lehmann T, Marcet PL, Graham DH, Dahl ER, Dubey JP (2006) Globalization and the population structure of Toxoplasma gondii. Proc Natl Acad Sci U S A 103:11423–11428

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lindsay DS, Dubey JP, Butler JM, Blagburn BL (1997) Mechanical transmission of Toxoplasma gondii oocysts by dogs. Vet Parasitol 73:27–33

    Article  CAS  PubMed  Google Scholar 

  • Moura L, Kelly P, Krecek RC, Dubey JP (2007) Seroprevalence of Toxoplasma gondii in cats from St. Kitts, West Indies. J Parasitol 93:952–953

    Article  CAS  PubMed  Google Scholar 

  • Orrett FA (1993) Sero-prevalence of Toxoplasma antibodies among pregnant women in Trinidad. Med Sci Res 21:399–400

    Google Scholar 

  • Pinon JM, Chemla C, Villena I, Foudrinier F, Aubert D, Puygauthier-Toubas D, Leroux B, Dupouy D, Quereux C, Talmud M, Trenque T, Potron G, Pluot M, Remy G, Bonhomme A (1996) Early neonatal diagnosis of congenital toxoplasmosis: value of comparative enzyme-linked immunofiltration assay immunological profiles and anti-Toxoplasma gondii immunoglobulin M (IgM) or IgA immunocapture and implications for postnatal therapeutic strategies. J Clin Microbiol 34:579–583

    CAS  PubMed  PubMed Central  Google Scholar 

  • Prabhakar P, Bailey A, Smikle MF, McCaw-Binns A, Ashley D (1991) Seroprevalence of Toxoplasma gondii, rubella virus, cytomegalovirus, herpes simplex virus (TORCH) and syphilis in Jamaican pregnant women. West Indian Med J 40:166–169

    CAS  PubMed  Google Scholar 

  • Rajendran C, Su C, Dubey JP (2012) Molecular genotyping of Toxoplasma gondii from Central and South America revealed high diversity within and between populations. Infect Genet Evol 12:356–368

    Article  Google Scholar 

  • Ramsewak S, Gooding R, Ganta K, Seepersadsingh N, Adesiyun AA (2008) Seroprevalence and risk factors of Toxoplasma gondii infection among pregnant women in Trinidad and Tobago. Rev Panam Salud Publica 23:164–170

    Article  PubMed  Google Scholar 

  • Rawlins SC, Prabhakar P (1989) Toxoplasmosis in young Jamaicans. J Trop Pediatr 35:234–236

    Article  CAS  PubMed  Google Scholar 

  • Richomme C, Aubert D, Gilot-Fromont E, Ajzenberg D, Mercier A, Ducrot C, Ferté H, Delorme D, Villena I (2009) Genetic characterization of Toxoplasma gondii from wild boar (Sus scrofa) in France. Vet Parasitol 164:296–300

    Article  CAS  PubMed  Google Scholar 

  • Schares G, Pantchev N, Barutzki D, Heydorn AO, Bauer C, Conraths FJ (2005) Oocysts of Neospora caninum, Hammondia heydorni, Toxoplasma gondii and Hammondia hammondi in faeces collected from dogs in Germany. Int J Parasitol 35:1525–1537

    Article  CAS  PubMed  Google Scholar 

  • Sepulveda-Arias JC, Gomez-Marin JE, Bobic B, Naranjo-Galvis CA, Djurkovic-Djakovic O (2014) Toxoplasmosis as a travel risk. Travel Med Infect Dis 12:592–601

    Article  PubMed  Google Scholar 

  • Sharma RN, Tiwari K, Chikweto A, Deallie C, Bhaiyat MI (2014) Prevalence of antibodies to Toxoplasma gondii and Neospora caninum in pigs in Grenada, West Indies. Scientific Research Publishing Inc 5:138–141

    Google Scholar 

  • Shwab EK, Zhu XQ, Majumdar D, Pena HFJ, Gennari SM, Dubey JP, Su C (2014) Geographical patterns of Toxoplasma gondii genetic diversity revealed by multilocus PCR-RFLP genotyping. Parasitology 141:453–461

    Article  PubMed  Google Scholar 

  • Sterlin GA, Dixon HG (1959) Congenital toxoplasmosis in a Jamaican child. West Indian Med J 8:124–127

    Google Scholar 

  • Su C, Shwab EK, Zhou P, Zhu XQ, Dubey JP (2010) Moving towards an integrated approach to molecular detection and identification of Toxoplasma gondii. Parasitology 137:1–11

    Article  CAS  PubMed  Google Scholar 

  • Tribouley J, Tribouley-Duret J, Appriou M, Baltz D, Pautrizel R (1978) Étude séroépidémiologique de la toxoplasmose à la Guadeloupe et à la Martinique. Ann Parasitol 53:21–31

    CAS  Google Scholar 

  • Van Oostdam JC, Dewailly E, Gilman A, Hansen JC, Odland JO, Chashchin V, Berner J, Butler-Walker J, Lagerkvist BJ, Olafsdottir K, Soininen L, Bjerregard P, Klopov V, Weber JP (2004) Circumpolar maternal blood contaminant survey, 1994–1997 organochlorine compounds. Sci Total Environ 330:55–70

    Article  PubMed  Google Scholar 

  • Villena I, Durand B, Aubert D, Blaga R, Geers R, Thomas M, Perret C, Alliot A, Escotte-Binet S, Thébault A, Boireau P, Halos L (2012) New strategy for the survey of Toxoplasma gondii in meat for human consumption. Vet Parasitol 183:203–208

    Article  PubMed  Google Scholar 

  • Wood H, Drebot MA, Dewailly E, Dillon L, Dimitrova K, Forde M, Grolla A, Lee E, Loftis A, Makowski K, Morrison K, Robertson L, Krecek RC (2014) Seroprevalence of seven zoonotic pathogens in pregnant women from the Caribbean. Am J Trop Med Hyg 91:642–644

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

We would like to thank Matt McMillan, Binh Ho-Thanh, and Oliver Kwok for technical assistance with the dog study.

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Correspondence to Jitender P. Dubey.

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Dubey, J.P., Verma, S.K., Villena, I. et al. Toxoplasmosis in the Caribbean islands: literature review, seroprevalence in pregnant women in ten countries, isolation of viable Toxoplasma gondii from dogs from St. Kitts, West Indies with report of new T. gondii genetic types. Parasitol Res 115, 1627–1634 (2016). https://doi.org/10.1007/s00436-015-4900-6

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