New Molecular Quantitative PCR Assay for Detection of Host-Specific Bifidobacteriaceae Suitable for Microbial Source Tracking

被引:35
|
作者
Gomez-Donate, Marta [1 ]
Balleste, Elisenda [1 ]
Muniesa, Maite [1 ]
Blanch, Anicet R. [1 ]
机构
[1] Univ Barcelona, Dept Microbiol, Barcelona, Spain
关键词
SORBITOL-FERMENTING BIFIDOBACTERIA; HUMAN FECAL POLLUTION; RNA-TARGETED PROBES; COLONY HYBRIDIZATION; IDENTIFY SOURCES; MULTIPLEX-PCR; FRESH-WATER; INDICATORS; IDENTIFICATION; STRAINS;
D O I
10.1128/AEM.00895-12
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
Bifidobacterium spp. belong to the commensal intestinal microbiota of warm-blooded animals. Some strains of Bifidobacterium show host specificity and have thus been proposed as host-specific targets to determine the origin of fecal pollution. Most strains have been used in microbial-source-tracking (MST) studies based on culture-dependent methods. Although some of these approaches have proved very useful, the low prevalence of culturable Bifidobacterium strains in the environment means that molecular culture-independent procedures could provide practical applications for MST. Reported here is a set of common primers and four Bifidobacterium sp. host-associated (human, cattle, pig, and poultry) probes for quantitative-PCR (qPCR) assessment of fecal source tracking. This set was tested using 25 water samples of diverse origin: urban sewage samples, wastewater from four abattoirs (porcine, bovine, and poultry), and water from a river with a low pollution load. The selected sequences showed a high degree of host specificity. There were no cross-reactions between the qPCR assays specific for each origin and samples from different fecal origins. On the basis of the findings, it was concluded that the host-specific qPCRs are sufficiently robust to be applied in environmental MST studies.
引用
收藏
页码:5788 / 5795
页数:8
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