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通过对溶血素A(hlyA)和内化素A(iap)这两个基因进行聚合酶链反应-限制性内切酶分析对单核细胞增生李斯特菌进行分型

Classification of Listeria monocytogenes by PCR-restriction enzyme analysis in the two genes of hlyA and iap.

作者信息

Saito A, Sawada T, Ueda F, Hondo R

机构信息

Food Microbiology Section, Saitama Institute of Public Health, Japan.

出版信息

New Microbiol. 1998 Jan;21(1):87-92.

PMID:9497934
Abstract

PCR-restriction enzyme analysis in the two virulence-associated genes was performed. The hlyA gene cording for listeriolysin O and the iap gene cording for an invasion associated factor were amplified with primers SH2 or SI3. The PCR products obtained were cleaved with 32 restriction enzymes, and restriction profiles from 12 strains, 6 each of serotypes 1/2a and 4b, were compared. We obtained two profiles for the hlyA using 4 restriction enzymes and eight profiles for the iap by using AluI, and the results of the profiles did not correlate with the serotypes. The polymorphism in the iap region was of a higher degree than that in the hlyA region, and the PCR-restriction enzyme analysis of the iap gene with primers SI3 and AluI was confirmed as one of the useful epidemiological analysis methods for listerosis outbreaks.

摘要

对两个与毒力相关的基因进行了聚合酶链反应-限制性酶切分析。用引物SH2或SI3扩增编码李斯特菌溶血素O的hlyA基因和编码侵袭相关因子的iap基因。将获得的聚合酶链反应产物用32种限制性酶进行酶切,并比较了12株菌株(血清型1/2a和4b各6株)的限制性图谱。使用4种限制性酶对hlyA获得了两种图谱,使用AluI对iap获得了8种图谱,且这些图谱的结果与血清型不相关。iap区域的多态性程度高于hlyA区域,并且用引物SI3和AluI对iap基因进行的聚合酶链反应-限制性酶切分析被确认为是用于李斯特菌病暴发的有用的流行病学分析方法之一。

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