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鼻咽样本中非荚膜肺炎链球菌的快速鉴定,可检测共定植并重新评估其流行率。

Rapid identification of noncapsulated Streptococcus pneumoniae in nasopharyngeal samples allowing detection of co-colonization and reevaluation of prevalence.

机构信息

Laboratory of Molecular Genetics, Instituto de Tecnologia Química e Biológica (ITQB), Universidade Nova de Lisboa (UNL), Oeiras, Portugal.

出版信息

Diagn Microbiol Infect Dis. 2011 Nov;71(3):208-16. doi: 10.1016/j.diagmicrobio.2011.07.009. Epub 2011 Sep 9.

Abstract

Noncapsulated pneumococci are atypical Streptococcus pneumoniae that lack a capsule and therefore do not react with any available antisera. These isolates, which are often referred as nontypeable pneumococci (NTPn), are difficult to identify as their differentiation from closely related species such as Streptococcus pseudopneumoniae and other streptococcus of the mitis group is not always straightforward. We developed a low-cost and easy assay to detect and quantify NTPn in primary samples (which may contain multiple species) obtained from nasopharyngeal swabs. The strategy is based on a multiplex polymerase chain reaction targeting lytA, cpsA, aliB-like ORF2, and 16S rDNA genes, plus a restriction fragment length polymorphism assay to differentiate typical from atypical lytA. The application of the proposed methodology to over 500 nasopharyngeal samples found that the prevalence of NTPn in colonization was 3-fold higher than that estimated by routine methods (from 2.9% to 8.6% in the study collection). The international clone Norway(NT)ST344 was the major clone identified.

摘要

无荚膜肺炎球菌是非典型肺炎链球菌,缺乏荚膜,因此与任何现有抗血清均不反应。这些分离株通常被称为非分型肺炎球菌(NTPn),由于其与密切相关的物种(如肺炎链球菌假种和其他米氏链球菌)的区分并不总是直接的,因此难以识别。我们开发了一种低成本且易于操作的检测方法,可检测和定量从鼻咽拭子中获得的原始样本(可能包含多种物种)中的 NTPn。该策略基于针对 lytA、cpsA、aliB-like ORF2 和 16S rDNA 基因的多重聚合酶链反应,以及区分典型和非典型 lytA 的限制性片段长度多态性分析。该方法应用于 500 多个鼻咽样本,发现 NTPn 在定植中的流行率比常规方法估计的高 3 倍(研究样本中从 2.9%到 8.6%)。鉴定出的主要克隆是国际克隆挪威(NT)ST344。

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