首页> 外文期刊>Antimicrobial agents and chemotherapy. >Comparison of Three PCR Primer Sets for Identification of vanB Gene Carriage in Feces and Correlation with Carriage of Vancomycin-Resistant Enterococci: Interference by vanB-Containing Anaerobic Bacilli.
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Comparison of Three PCR Primer Sets for Identification of vanB Gene Carriage in Feces and Correlation with Carriage of Vancomycin-Resistant Enterococci: Interference by vanB-Containing Anaerobic Bacilli.

机译:三种PCR引物组用于鉴定粪便中的vanB基因运输以及与耐万古霉素的肠球菌运输相关的比较:含vanB的厌氧芽孢杆菌的干扰。

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摘要

We assessed the sensitivities and specificities of three previously described PCR primers on enrichment broth cultures of feces for the accurate detection of fecal carriage of vancomycin-resistant enterococci (VRE). In addition, we investigated specimens that were vanB PCR positive but VRE culture negative for the presence of other vanB-containing pathogens. Feces from 59 patients (12 patients carrying vanB Enterococcus faecium strains and 47 patients negative for VRE carriage) were cultured for 36 h in aerobic brain heart infusion (BHI) broth, anaerobic BHI (AnO(2)BHI) broth, or aerobic Enterococcosel (EC) broth. DNA was extracted from the cultures and tested for the presence of vanB by using the PCR primers of Dutka-Malen et al. (S. Dutka-Malen, S. Evers, and P. Courvalin, J. Clin. Microbiol. 33:24-27, 1995), Bell et al. (J. M. Bell, J. C. Paton, and J. Turnidge, J. Clin. Microbiol. 36:2187-2190, 1998), and Stinear et al. (T. P. Stinear, D. C. Olden, P. D. R. Johnson, J. K. Davies, and M. L. Grayson,Lancet 357:855-856, 2001). The sensitivity (specificity) of PCR compared with the results of culture on BHI, AnO(2)BHI, and EC broths were 67% (96%), 50% (94%), and 17% (100%), respectively, with the primers of Dutka-Malen et al.; 92% (60%), 92% (45%), and 92% (83%), respectively, with the primers of Bell et al.; and 92% (49%), 92% (43%), and 100% (51%) respectively, with the primers of Stinear et al. The primers of both Bell et al. and Stinear et al. were significantly more sensitive than those of Dutka-Malen et al. in EC broth (P = 0.001 and P < 0.001, respectively). The poor specificities for all primer pairs were due in part to the isolation and identification of six anaerobic gram-positive bacilli, Clostridium hathewayi (n = 3), a Clostridium innocuum-like organism (n = 1), Clostridium bolteae (n = 1), and Ruminococcus lactaris-like (n = 1), from five fecal specimens that were vanB positive but VRE culture negative. All six organisms were demonstrated to contain a vanB gene identical to that of VRE. VanB-containing bowel anaerobes may result in false-positive interpretation of PCR-positive fecal enrichment cultures as VRE, regardless of the primers and protocols used.
机译:我们评估了三种先前描述的PCR引物在粪便富集肉汤培养物中的敏感性和特异性,以准确检测对万古霉素耐药的肠球菌(VRE)的粪便运输。此外,我们调查了存在其他vanB病原体的vanB PCR阳性但VRE培养阴性的标本。在有氧脑心灌注(BHI)肉汤,无氧BHI(AnO(2)BHI)肉汤或有氧肠球菌( EC)肉汤。从培养物中提取DNA,并使用Dutka-Malen等人的PCR引物测试vanB的存在。 (S.Dutka-Malen,S.Evers和P.Courvalin,J.Clin.Microbiol.33:24-27,1995),Bell等。 (J.M.Bell,J.C.Paton,和J.Turnidge,J.Clin.Microbiol.36:2187-2190,1998),和Stinear等。 (T.P. Stinear,D.C。Olden,P.D.R。Johnson,J.K.Davies和M.L.Grayson,《柳叶刀》 357:855-856,2001)。与在BHI,AnO(2)BHI和EC肉汤中培养的结果相比,PCR的敏感性(特异性)分别为67%(96%),50%(94%)和17%(100%)。用Dutka-Malen等人的引物;使用Bell等人的引物分别达到92%(60%),92%(45%)和92%(83%);分别用Stinear等人的引物和92%(49%),92%(43%)和100%(51%)的引物。贝尔等人的引物。和Stinear等。比Dutka-Malen等人更敏感。 EC肉汤中的浓度(分别为P = 0.001和P <0.001)。所有引物对的特异性均较差,部分原因是分离和鉴定了六个厌氧革兰氏阳性杆菌,梭状芽胞杆菌(n = 3),无毒梭状芽孢杆菌(n = 1),青枯菌(n = 1)。 )和乳酸菌球菌(n = 1),来自五个粪便标本,它们均为vanB阳性,但VRE培养阴性。证实所有六个生物都含有与VRE相同的vanB基因。含VanB的肠厌氧菌可能导致PCR阳性粪便富集培养物作为VRE的假阳性解释,而与所使用的引物和方案无关。

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