全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Multilocus Genotyping of Human Giardia Isolates Suggests Limited Zoonotic Transmission and Association between Assemblage B and Flatulence in Children

DOI: 10.1371/journal.pntd.0001262

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background Giardia intestinalis is one of the most common diarrhea-related parasites in humans, where infection ranges from asymptomatic to acute or chronic disease. G. intestinalis consists of eight genetically distinct genotypes or assemblages, designated A–H, and assemblages A and B can infect humans. Giardiasis has been classified as a possible zoonotic disease but the role of animals in human disease transmission still needs to be proven. We tried to link different assemblages and sub-assemblages of G. intestinalis isolates from Swedish human patients to clinical symptoms and zoonotic transmission. Methodology/Principal Findings Multilocus sequence-based genotyping of 207 human Giardia isolates using three gene loci: ?-giardin, glutamate dehydrogenase (gdh), and triose phosphate isomerase (tpi) was combined with assemblage-specific tpi PCRs. This analysis identified 73 patients infected with assemblage A, 128 with assemblage B, and six with mixed assemblages A+B. Multilocus genotypes (MLGs) were easily determined for the assemblage A isolates, and most patients with this genotype had apparently been infected through anthroponotic transmission. However, we also found evidence of limited zoonotic transmission of Giardia in Sweden, since a few domestic human infections involved the same assemblage A MLGs previously reported in Swedish cats and ruminants. Assemblage B was detected more frequently than assemblage A and it was also more common in patients with suspected treatment failure. However, a large genetic variability made determination of assemblage B MLGs problematic. Correlation between symptoms and assemblages was found only for flatulence, which was significantly more common in children less than six years of age infected with assemblage B. Conclusions/Significance This study shows that certain assemblage A subtypes are potentially zoonotic and that flatulence is connected to assemblage B infections in young children. Determination of MLGs from assemblages A and B can be a valuable tool in outbreak situations and to help identify possible zoonotic transmission.

References

[1]  Lasek-Nesselquist E, Welch DM, Sogin ML (2010) The identification of a new Giardia duodenalis assemblage in marine vertebrates and a preliminary analysis of G. duodenalis population biology in marine systems. Int J Parasitol 40: 1063–1074. doi: 10.1016/j.ijpara.2010.02.015
[2]  Thompson RC (2000) Giardiasis as a re-emerging infectious disease and its zoonotic potential. Int J Parasitol 30: 1259–1267. doi: 10.1016/S0020-7519(00)00127-2
[3]  WHO (1996) The World Health Report 1996. Available from: http://www.who.int/whr/1996/en/index.htm?l.
[4]  Savioli L, Smith H, Thompson A (2006) Giardia and Cryptosporidium join the ‘Neglected Diseases Initiative’. Trends Parasitol 22: 203–208. doi: 10.1016/j.pt.2006.02.015
[5]  Monis PT, Andrews RH, Mayrhofer G, Ey PL (2003) Genetic diversity within the morphological species Giardia intestinalis and its relationship to host origin. Infect Genet Evol 3: 29–38. doi: 10.1016/S1567-1348(02)00149-1
[6]  WHO (1979) Parasitic zoonoses. Report of a WHO expert committee with the participation of FAO. Available from: http://whqlibdoc.who.int/trs/WHO_TRS_637?.pdf.
[7]  Inpankaew T, Traub R, Thompson RC, Sukthana Y (2007) Canine parasitic zoonoses in Bangkok temples. Southeast Asian J Trop Med Public Health 38: 247–255.
[8]  Traub RJ, Monis PT, Robertson I, Irwin P, Mencke N, et al. (2004) Epidemiological and molecular evidence supports the zoonotic transmission of Giardia among humans and dogs living in the same community. Parasitology 128: 253–62. doi: 10.1017/S0031182003004505
[9]  Caccio SM, Ryan U (2008) Molecular epidemiology of giardiasis. Mol Biochem Parasitol 160: 75–80. doi: 10.1016/j.molbiopara.2008.04.006
[10]  Monis PT, Thompson RC (2003) Cryptosporidium and Giardia-zoonoses: fact or fiction? Infect Genet Evol 3: 233–244. doi: 10.1016/j.meegid.2003.08.003
[11]  Sprong H, Caccio SM, van der Giessen JW (2009) Identification of zoonotic genotypes of Giardia duodenalis. PLoS Negl Trop Dis 3: e558. doi: 10.1371/journal.pntd.0000558
[12]  Aydin AF, Besirbellioglu BA, Avci IY, Tanyuksel M, Araz E, et al. (2004) Classification of Giardia duodenalis parasites in Turkey into groups A and B using restriction fragment length polymorphism. Diagn Microbiol Infect Dis 50: 147–151. doi: 10.1016/j.diagmicrobio.2004.06.001
[13]  Haque R, Roy S, Kabir M, Stroup SE, Mondal D, et al. (2005) Giardia assemblage A infection and diarrhea in Bangladesh. J Infect Dis 192: 2171–2173. doi: 10.1086/498169
[14]  Homan WL, Mank TG (2001) Human giardiasis: genotype linked differences in clinical symptomatology. Int J Parasitol 31: 822–826. doi: 10.1016/S0020-7519(01)00183-7
[15]  Read C, Walters J, Robertson ID, Thompson RC (2002) Correlation between genotype of Giardia duodenalis and diarrhoea. Int J Parasitol 32: 229–231. doi: 10.1016/S0020-7519(01)00340-X
[16]  Sahagun J, Clavel A, Goni P, Seral C, Llorente MT, et al. (2008) Correlation between the presence of symptoms and the Giardia duodenalis genotype. Eur J Clin Microbiol Infect Dis 27: 81–83. doi: 10.1007/s10096-007-0404-3
[17]  Caccio SM, Beck R, Lalle M, Marinculic A, Pozio E (2008) Multilocus genotyping of Giardia duodenalis reveals striking differences between assemblages A and B. Int J Parasitol 32: 1023–1531. doi: 10.1016/S0020-7519(02)00068-1
[18]  Geurden T, Levecke B, Caccio SM, Visser A, De Groote G, et al. (2009) Multilocus genotyping of Cryptosporidium and Giardia in non-outbreak related cases of diarrhoea in human patients in Belgium. Parasitology 136: 1161–1168. doi: 10.1017/S0031182009990436
[19]  Levecke B, Geldhof P, Claerebout E, Dorny P, Vercammen F, et al. (2009) Molecular characterisation of Giardia duodenalis in captive non-human primates reveals mixed assemblage A and B infections and novel polymorphisms. Int J Parasitol 39: 1595–1601. doi: 10.1016/j.ijpara.2009.05.013
[20]  Lebbad M, Mattsson JG, Christensson B, Ljungstrom B, Backhans A, et al. (2010) From mouse to moose: multilocus genotyping of Giardia isolates from various animal species. Vet Parasitol 168: 231–239. doi: 10.1016/j.vetpar.2009.11.003
[21]  Svenungsson B, Velicko I, Petersson I, De Jong B, Andersson Y, et al. (2007) [Giardiasis as differential diagnosis in diarrhea outbreaks in child day centers. Written hygienic guidelines and adequate testing can reduce the transmission]. Lakartidningen 104: 500–503.
[22]  Lebbad M, Ankarklev J, Tellez A, Leiva B, Andersson JO, et al. (2008) Dominance of Giardia assemblage B in Leon, Nicaragua. Acta Trop 106: 44–53. doi: 10.1016/j.actatropica.2008.01.004
[23]  Lalle M, Pozio E, Capelli G, Bruschi F, Crotti D, et al. (2005) Genetic heterogeneity at the beta-giardin locus among human and animal isolates of Giardia duodenalis and identification of potentially zoonotic subgenotypes. Int J Parasitol 35: 207–213. doi: 10.1016/j.ijpara.2004.10.022
[24]  Read CM, Monis PT, Thompson RC (2004) Discrimination of all genotypes of Giardia duodenalis at the glutamate dehydrogenase locus using PCR-RFLP. Infect Genet Evol 4: 125–130. doi: 10.1016/j.meegid.2004.02.001
[25]  Sulaiman IM, Fayer R, Bern C, Gilman RH, Trout JM, et al. (2003) Triosephosphate isomerase gene characterization and potential zoonotic transmission of Giardia duodenalis. Emerg Infect Dis 9: 1444–1452. doi: 10.3201/eid0911.030084
[26]  Lalle M, Bruschi F, Castagna B, Campa M, Pozio E, et al. (2009) High genetic polymorphism among Giardia duodenalis isolates from Sahrawi children. Trans R Soc Trop Med Hyg 103: 834–838. doi: 10.1016/j.trstmh.2009.04.017
[27]  Geurden T, Geldhof P, Levecke B, Martens C, Berkvens D, et al. (2008) Mixed Giardia duodenalis assemblage A and E infections in calves. Int J Parasitol 38: 259–264. doi: 10.1016/j.ijpara.2007.07.016
[28]  Caccio SM, De Giacomo M, Pozio E (2002) Sequence analysis of the beta-giardin gene and development of a polymerase chain reaction-restriction fragment length polymorphism assay to genotype Giardia duodenalis cysts from human faecal samples. Int J Parasitol 32: 1023–1030. doi: 10.1016/S0020-7519(02)00068-1
[29]  Stamatakis A, Ludwig T, Meier H (2005) RAxML-III: a fast program for maximum likelihood-based inference of large phylogenetic trees. Bioinformatics 21: 456–463. doi: 10.1093/bioinformatics/bti191
[30]  Abe N, Tanoue T, Noguchi E, Ohta G, Sakai H (2010) Molecular characterization of Giardia duodenalis isolates from domestic ferrets. Parasitol Res 106: 733–736. doi: 10.1007/s00436-009-1703-7
[31]  Robertson LJ, Forberg T, Hermansen L, Hamnes IS, Gjerde B (2007) Giardia duodenalis cysts isolated from wild moose and reindeer in Norway: genetic characterization by PCR-rflp and sequence analysis at two genes. J Wildl Dis 43: 576–585. doi: 10.7589/0090-3558-43.4.576
[32]  Trout JM, Santin M, Greiner E, Fayer R (2004) Prevalence of Giardia duodenalis genotypes in pre-weaned dairy calves. Vet Parasitol 124: 179–186. doi: 10.1016/j.vetpar.2004.07.010
[33]  Wielinga CM, Thompson RC (2007) Comparative evaluation of Giardia duodenalis sequence data. Parasitology 134: 1795–1821. doi: 10.1017/S0031182007003071
[34]  Breathnach AS, McHugh TD, Butcher PD (2010) Prevalence and clinical correlations of genetic subtypes of Giardia lamblia in an urban setting. Epidemiol Infect 1–9. doi: 10.1017/s0950268810000208
[35]  van der Giessen JW, de Vries A, Roos M, Wielinga P, Kortbeek LM, et al. (2006) Genotyping of Giardia in Dutch patients and animals: a phylogenetic analysis of human and animal isolates. Int J Parasitol 36: 849–858. doi: 10.1016/j.ijpara.2006.03.001
[36]  Yang R, Lee J, Ng J, Ryan U (2010) High prevalence Giardia duodenalis assemblage B and potentially zoonotic subtypes in sporadic human cases in Western Australia. Int J Parasitol 40: 293–297. doi: 10.1016/j.ijpara.2009.08.003
[37]  Abdel-Moneim SM, Sultan DM (2008) Genetic characterization of Giardia lamblia isolates from Egyptian patients with relation to clinical giardiasis. J Egypt Soc Parasitol 38: 547–560.
[38]  Volotao AC, Costa-Macedo LM, Haddad FS, Brandao A, Peralta JM, et al. (2007) Genotyping of Giardia duodenalis from human and animal samples from Brazil using beta-giardin gene: a phylogenetic analysis. Acta Trop 102: 10–19. doi: 10.1016/j.actatropica.2007.02.010
[39]  Kohli A, Bushen OY, Pinkerton RC, Houpt E, Newman RD, et al. (2008) Giardia duodenalis assemblage, clinical presentation and markers of intestinal inflammation in Brazilian children. Trans R Soc Trop Med Hyg 102: 718–725. doi: 10.1016/j.trstmh.2008.03.002
[40]  Gelanew T, Lalle M, Hailu A, Pozio E, Caccio SM (2007) Molecular characterization of human isolates of Giardia duodenalis from Ethiopia. Acta Trop 102: 92–99. doi: 10.1016/j.actatropica.2007.04.003
[41]  Almeida A, Pozio E, Caccio SM (2010) Genotyping of Giardia duodenalis cysts by new real-time PCR assays for detection of mixed infections in human samples. Appl Environ Microbiol 76: 1895–1901. doi: 10.1128/AEM.02305-09
[42]  Beck R, Sprong H, Bata I, Lucinger S, Pozio E, et al. (2011) Prevalence and molecular typing of Giardia spp. in captive mammals at the zoo of Zagreb, Croatia. Vet Parasitol 175: 40–46. doi: 10.1016/j.vetpar.2010.09.026
[43]  Solarczyk P (2009) [Occurrence of Giardia species and genotypes in humans and animals in Wielkopolska region, Poland]. Wiad Parazytol 55: 459–462.
[44]  Winkworth CL, Learmonth JJ, Matthaei CD, Townsend CR (2008) Molecular characterization of Giardia isolates from calves and humans in a region in which dairy farming has recently intensified. Appl Environ Microbiol 74: 5100–5105. doi: 10.1128/AEM.00232-08
[45]  Robertson LJ, Forberg T, Hermansen L, Gjerde BK, Langeland N (2007) Molecular characterisation of Giardia isolates from clinical infections following a waterborne outbreak. J Infect 55: 79–88. doi: 10.1016/j.jinf.2007.02.001
[46]  Hussein AI, Yamaguchi T, Nakamoto K, Iseki M, Tokoro M (2009) Multiple-subgenotype infections of Giardia intestinalis detected in Palestinian clinical cases using a subcloning approach. Parasitol Int 58: 258–262. doi: 10.1016/j.parint.2009.04.002
[47]  Kosuwin R, Putaporntip C, Pattanawong U, Jongwutiwes S (2010) Clonal diversity in Giardia duodenalis isolates from Thailand: evidences for intragenic recombination and purifying selection at the beta giardin locus. Gene 449: 1–8. doi: 10.1016/j.gene.2009.09.010
[48]  Lasek-Nesselquist E, Bogomolni AL, Gast RJ, Welch DM, Ellis JC, et al. (2008) Molecular characterization of Giardia intestinalis haplotypes in marine animals: variation and zoonotic potential. Dis Aquat Organ 81: 39–51. doi: 10.3354/dao01931
[49]  Franzen O, Jerlstrom-Hultqvist J, Castro E, Sherwood E, Ankarklev J, et al. (2009) Draft genome sequencing of giardia intestinalis assemblage B isolate GS: is human giardiasis caused by two different species? PLoS Pathog 5: e1000560. doi: 10.1371/journal.ppat.1000560
[50]  Morrison HG, McArthur AG, Gillin FD, Aley SB, Adam RD, et al. (2007) Genomic minimalism in the early diverging intestinal parasite Giardia lamblia. Science 317: 1921–1926. doi: 10.1126/science.1143837

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133