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短小 blaTEM 编码质粒序列在流感嗜血杆菌中的存在及 blaTEM 基因 PCR 假阴性变异体的描述。

Sequences of small blaTEM-encoding plasmids in Haemophilus influenzae and description of variants falsely negative for blaTEM by PCR.

机构信息

School of Human Life Sciences, University of Tasmania, Launceston, Tasmania, Australia.

出版信息

J Antimicrob Chemother. 2012 Nov;67(11):2621-5. doi: 10.1093/jac/dks264. Epub 2012 Jul 10.

Abstract

OBJECTIVES

To characterize an unidentified β-lactamase and associated genetic background in a bla(TEM) and bla(ROB) PCR-negative Haemophilus influenzae isolate, and characterize small bla(TEM)-encoding plasmids in a collection of H. influenzae.

METHODS

The unidentified β-lactamase gene was identified by cloning and sequencing the encoding plasmid. Strains with small bla(TEM) plasmids were identified using negative PCR for integrative conjugative elements, but positive bla(TEM) PCR; plasmids from selected isolates were sequenced. PCR for rep and divergent bla(TEM) were evaluated for detecting small plasmids on selected H. influenzae isolates.

RESULTS

Small plasmids (4.8-5.5 kb) encoding bla(TEM) appear to be associated with remnants of Tn2 on a conserved plasmid core. The unidentified β-lactamase was actually a TEM-1, with negative bla(TEM) PCR associated with a previously unrecognized deletion of bp 1-27 of bla(TEM) (Sutcliffe numbering) associated with a larger deletion within Tn2. This deletion was found in other isolates and may be more common than previously thought. PCR for the conserved rep gene appears useful for screening for small bla(TEM)-encoding plasmids or associated cryptic plasmids in H. influenzae.

CONCLUSIONS

Small bla(TEM)-encoding plasmids in H. influenzae appear relatively conserved, but require further study to confirm this. PCR associated with the rep gene may be useful for studying these small plasmids. A deletion in part of bla(TEM) in some strains may interfere with some PCRs; therefore, care should be taken with primer selection or design and, preferably, regions within the open reading frame should be targeted.

摘要

目的

对一株 bla(TEM)和 bla(ROB)PCR 阴性流感嗜血杆菌分离株中未鉴定的β-内酰胺酶及其相关遗传背景进行分析,并对一组流感嗜血杆菌中携带的小型 bla(TEM)编码质粒进行鉴定。

方法

通过克隆和测序编码质粒来鉴定未鉴定的β-内酰胺酶基因。采用整合性接合元件阴性 PCR 但 bla(TEM)PCR 阳性的方法鉴定携带小型 bla(TEM)质粒的菌株;对选定分离株的质粒进行测序。针对 rep 和不同 bla(TEM)的 PCR 用于检测选定流感嗜血杆菌分离株上的小型质粒。

结果

携带 bla(TEM)的小型质粒(4.8-5.5kb)似乎与 Tn2 上的残留部分有关。未鉴定的β-内酰胺酶实际上是 TEM-1,bla(TEM)的阴性 PCR 与 bla(TEM)的 1-27bp 的缺失(Sutcliffe 编号)有关,该缺失与 Tn2 内的更大缺失有关。该缺失在其他分离株中也存在,可能比以前认为的更为常见。针对保守 rep 基因的 PCR 似乎可用于筛选流感嗜血杆菌中的小型 bla(TEM)编码质粒或相关隐匿质粒。

结论

流感嗜血杆菌中携带的小型 bla(TEM)编码质粒相对保守,但需要进一步研究证实。与 rep 基因相关的 PCR 可能对研究这些小型质粒有用。某些菌株中 bla(TEM)部分缺失可能会干扰某些 PCR;因此,应注意引物选择或设计,最好靶向开放阅读框内的区域。

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