Genetic characterization and transmission cycles of Cryptosporidium species isolated from humans in New Zealand

被引:82
作者
Learmonth, JJ
Ionas, G
Ebbett, MA
Kwan, ES
机构
[1] Massey Univ, Inst Mol Biosci, Protozoa Res Unit, Palmerston North, New Zealand
[2] Massey Univ, Inst Mol Biosci, MicroAqua Tech, Palmerston North, New Zealand
关键词
D O I
10.1128/AEM.70.7.3973-3978.2004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Little is known about the genetic characteristics, distribution, and transmission cycles of Cryptosporidium species that cause human disease in New Zealand. To address these questions, 423 fecal specimens containing Cryptosporidium oocysts and obtained from different regions were examined by the PCR-restriction fragment length polymorphism technique. Indeterminant results were resolved by DNA sequence analysis. Two regions supplied the majority of isolates: one rural and one urban. Overall, Cryptosporidium hominis accounted for 47% of the isolates, with the remaining 53% being the C. parvum bovine genotype. A difference, however, was observed between the Cryptosporidium species from rural and urban isolates, with C. hominis dominant in the urban region, whereas the C. parvum bovine genotype was prevalent in rural New Zealand. A shift in transmission cycles was detected between seasons, with an anthroponotic cycle in autumn and a zoonotic cycle in spring. A novel Cryptosporidium sp., which on DNA sequence analysis showed a close relationship with C. canis, was detected in two unrelated children from different regions, illustrating the genetic diversity within this genus.
引用
收藏
页码:3973 / 3978
页数:6
相关论文
共 46 条
[11]   Epidemiology of Cryptosporidium:: transmission, detection and identification [J].
Fayer, R ;
Morgan, U ;
Upton, SJ .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2000, 30 (12-13) :1305-1322
[12]   Foot and mouth disease and cryptosporidiosis: Possible interaction between two emerging infectious diseases [J].
Hunter, PR ;
Chalmers, RM ;
Syed, Q ;
Hughes, LS ;
Woodhouse, S ;
Swift, L .
EMERGING INFECTIOUS DISEASES, 2003, 9 (01) :109-112
[13]  
Khramtsov NV, 2000, J PARASITOL, V86, P275, DOI 10.1645/0022-3395(2000)086[0275:PODSRI]2.0.CO
[14]  
2
[15]   Virus-like, double-stranded RNAs in the parasitic protozoan Cryptosporidium parvum [J].
Khramtsov, NV ;
Woods, KM ;
Nesterenko, MV ;
Dykstra, CC ;
Upton, SJ .
MOLECULAR MICROBIOLOGY, 1997, 26 (02) :289-300
[16]  
Learmonth J, 2001, J EUKARYOT MICROBIOL, p34S
[17]   A rapid method for identifying diversity within PCR amplicons using a heteroduplex mobility assay and synthetic polynucleotides:: application to characterisation of dsRNA elements associated with Cryptosporidium [J].
Leoni, F ;
Gallimore, CI ;
Green, J ;
McLauchlin, J .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 54 (01) :95-103
[18]   Molecular epidemiological analysis of Cryptosporidium isolates from humans and animals by using a Heteroduplex mobility assay and nucleic acid sequencing based on a small double-stranded RNA element [J].
Leoni, F ;
Gallimore, CI ;
Green, J ;
McLauchlin, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (03) :981-992
[19]   Population structures and the role of genetic exchange in the zoonotic pathogen Cryptosporidium parvum [J].
Mallon, M ;
MacLeod, A ;
Wastling, J ;
Smith, H ;
Reilly, B ;
Tait, A .
JOURNAL OF MOLECULAR EVOLUTION, 2003, 56 (04) :407-417
[20]   Genetic characterization of Cryptosporidium strains from 218 patients with diarrhea diagnosed as having sporadic cryptosporidiosis [J].
McLauchlin, J ;
Pedraza-Díaz, S ;
Amar-Hoetzeneder, C ;
Nichols, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (10) :3153-3158