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从布加勒斯特地区女性携带者中分离出的无乳链球菌菌株的遗传多样性和抗菌药物耐药性。

Genetic diversity and antimicrobial resistance in Streptococcus agalactiae strains recovered from female carriers in the Bucharest area.

作者信息

Usein Codruţa-Romaniţa, Militaru Mădălina, Cristea Violeta, Străuţ Monica

机构信息

Molecular Epidemiology Laboratory, Cantacuzino National Institute of Research/Development for Microbiology and Immunology, Bucharest, Romania.

Synevo Laboratories, Judetul Ilfov, Romania.

出版信息

Mem Inst Oswaldo Cruz. 2014 Apr;109(2):189-96. doi: 10.1590/0074-0276140431. Epub 2014 Mar 5.

Abstract

For the first time, we used multilocus sequence typing (MLST) to understand how Romanian group B streptococcus (GBS) strains fit into the global GBS population structure. Colonising isolates recovered from adult human females were tested for antibiotic resistance, were molecularly serotyped based on the capsular polysaccharide synthesis (cps) gene cluster and further characterised using a set of molecular markers (surface protein genes, pilus-encoded islands and mobile genetic elements inserted in the scpB-lmb intergenic region). Pulsed-field gel electrophoresis was used to complement the MLST clonal distribution pattern of selected strains. Among the 55 strains assigned to six cps types (Ia, Ib, II-V), 18 sequence types (STs) were identified by MLST. Five STs represented new entries to the MLST database. The prevalent STs were ST-1, ST-17, ST-19 and ST-28. Twenty molecular marker profiles were identified. The most common profiles (rib+GBSi1+PI-1, rib+GBSi1+PI-1, PI-2b and alp2/3+PI-1, PI-2a) were associated with the cps III/ST-17 and cps V/ST-1 strains. A cluster of fluoroquinolone-resistant strains was detected among the cps V/ST-19 members; these strains shared alp1 and IS1548 and carried PI-1, PI-2a or both. Our results support the usefulness of implementing an integrated genotyping system at the reference laboratory level to obtain the reliable data required to make comparisons between countries.

摘要

我们首次使用多位点序列分型(MLST)来了解罗马尼亚B族链球菌(GBS)菌株如何融入全球GBS种群结构。对从成年女性中分离出的定殖菌株进行抗生素耐药性测试,基于荚膜多糖合成(cps)基因簇进行分子血清分型,并使用一组分子标记(表面蛋白基因、菌毛编码岛以及插入scpB-lmb基因间区域的移动遗传元件)进行进一步表征。脉冲场凝胶电泳用于补充所选菌株的MLST克隆分布模式。在55株分为六种cps类型(Ia、Ib、II-V)的菌株中,通过MLST鉴定出18种序列类型(STs)。五种STs是MLST数据库中的新条目。流行的STs是ST-1、ST-17、ST-19和ST-28。鉴定出20种分子标记谱。最常见的谱(rib+GBSi1+PI-1、rib+GBSi1+PI-1、PI-2b和alp2/3+PI-1、PI-2a)与cps III/ST-17和cps V/ST-1菌株相关。在cps V/ST-19成员中检测到一组耐氟喹诺酮菌株;这些菌株共享alp1和IS1548,并携带PI-1、PI-2a或两者。我们的结果支持在参考实验室层面实施综合基因分型系统以获取进行国家间比较所需可靠数据的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2c9/4015262/eb6f8c35416d/0074-0276-mioc-109-02-00189-gf01.jpg

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