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Real-Time PCR for Molecular Detection of Zoonotic and Non-Zoonotic Giardia spp. in Wild Rodents
被引:8
作者:
Klotz, Christian
[1
]
Radam, Elke
[1
]
Rausch, Sebastian
[2
]
Gosten-Heinrich, Petra
[1
]
Aebischer, Toni
[1
]
机构:
[1] Robert Koch Inst, Dept Infect Dis, Unit 16 Mycot & Parasit Agents & Mycobacteria, D-13353 Berlin, Germany
[2] Free Univ Berlin, Inst Immunol, Ctr Infect Med, D-14163 Berlin, Germany
关键词:
Giardia spp;
wild rodents;
molecular detection;
qPCR;
CRYPTOSPORIDIUM SPP;
DUODENALIS;
PREVALENCE;
LAMBLIA;
IDENTIFICATION;
EPIDEMIOLOGY;
ASSEMBLAGES;
PATHOGENS;
ALBERTA;
D O I:
10.3390/microorganisms9081610
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Giardiasis in humans is a gastrointestinal disease transmitted by the potentially zoonotic Giardia duodenalis genotypes (assemblages) A and B. Small wild rodents such as mice and voles are discussed as potential reservoirs for G. duodenalis but are predominantly populated by the two rodent species Giardia microti and Giardia muris. Currently, the detection of zoonotic and non-zoonotic Giardia species and genotypes in these animals relies on cumbersome PCR and sequencing approaches of genetic marker genes. This hampers the risk assessment of potential zoonotic Giardia transmissions by these animals. Here, we provide a workflow based on newly developed real-time PCR schemes targeting the small ribosomal RNA multi-copy gene locus to distinguish G. muris, G. microti and G. duodenalis infections. For the identification of potentially zoonotic G. duodenalis assemblage types A and B, an established protocol targeting the single-copy gene 4E1-HP was used. The assays were specific for the distinct Giardia species or genotypes and revealed an analytical sensitivity of approximately one or below genome equivalent for the multi-copy gene and of about 10 genome equivalents for the single-copy gene. Retesting a biobank of small rodent samples confirmed the specificity. It further identified the underlying Giardia species in four out of 11 samples that could not be typed before by PCR and sequencing. The newly developed workflow has the potential to facilitate the detection of potentially zoonotic and non-zoonotic Giardia species in wild rodents.
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页数:11
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