首页> 美国卫生研究院文献>Emerging Microbes Infections >Phenotypic and molecular analysis of nontypeable Group B streptococci: identification of cps2a and hybrid cps2a/cps5 Group B streptococcal capsule gene clusters
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Phenotypic and molecular analysis of nontypeable Group B streptococci: identification of cps2a and hybrid cps2a/cps5 Group B streptococcal capsule gene clusters

机译:无法分型的B组链球菌的表型和分子分析:cps2a和杂种cps2a / cps5 B组链球菌胶囊基因簇的鉴定

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摘要

The Group B streptococcus (GBS) can express a capsular polysaccharide (CPS). There are ten recognized CPSs (Ia, Ib, and II–IX). A GBS isolate is considered nontypeable (NT) when CPS cannot be identified as one of ten types. Two groups of GBS NT isolates were studied, isolates without surface sialic acid (sia(−)) and isolates with surface sialic acid (sia(+)). The first objective was to characterize NT sia(−) isolates that failed CPS identification by an immunodiffusion antisera typing assay and a RT-PCR capsule typing assay. NT sia(−) isolates were characterized by assaying phenotypic changes and identifying covR/S mutations that may potentially have a role in the altered phenotypes. The second objective was to characterize NT sia(+) isolates that failed to identify as one of the ten CPS types by an immundiffusion antisera-based typing assay and a RT-PCR capsule typing assay yet expressed capsule. Fifteen NT sia(−) isolates displayed increased β hemolysis/orange pigmentation, decreased CAMP activity, inability to form biofilm, and susceptibility to phagocytosis by human blood. DNA sequence analysis of the covR/S genes in the sia(−) isolates found mutations in 14 of 15 isolates assayed. These mutations in the covR/S genes may potentially contribute to lack of expression of phenotypic traits assayed in vitro. For the three NT sia(+) isolates, whole-genome sequence analyses identified two isolates with cps gene clusters identical to the recently described and uncommon CPSIIa type. The third isolate possessed a hybrid cluster containing cps genes for both CPSIIa and CPSV suggesting recombination between these two gene clusters.
机译:B组链球菌(GBS)可以表达荚膜多糖(CPS)。有十个公认的CPS(Ia,Ib和II–IX)。如果不能将CPS识别为十种类型之一,则将GBS隔离株视为不可分型(NT)。研究了两组GBS NT分离株,无表面唾液酸的分离株(sia(-))和有表面唾液酸的分离株(sia(+))。第一个目标是鉴定通过免疫扩散抗血清分型测定和RT-PCR胶囊分型测定未能通过CPS鉴定的NT sia(-)分离株。通过分析表型变化和鉴定可能在改变表型中起作用的covR / S突变来表征NT sia(-)分离株。第二个目标是鉴定通过免疫扩散基于抗血清的分型测定和RT-PCR胶囊分型测定尚未表达的胶囊,无法鉴定为十种CPS类型之一的NT sia(+)分离株。 15个NT sia(-)分离株显示出增加的β溶血/橙色色素沉着,CAMP活性降低,无法形成生物膜以及易被人血吞噬。 sia(-)分离物中covR / S基因的DNA序列分析发现了15个分离株中的14个突变。 covR / S基因中的这些突变可能潜在地导致缺乏在体外测定的表型性状的表达。对于三个NT sia(+)分离株,全基因组序列分析确定了两个分离株,它们具有与最近描述的罕见CPSIIa类型相同的cps基因簇。第三分离株具有包含CPSIIa和CPSV的cps基因的杂合簇,表明这两个基因簇之间重组。

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