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Emergence of Multidrug-Resistant Pneumococcal Serotype 35B among Children in the United States.美国儿童中多重耐药肺炎球菌35B血清型的出现。
J Clin Microbiol. 2017 Mar;55(3):724-734. doi: 10.1128/JCM.01778-16. Epub 2016 Nov 9.
2
Whole genome sequencing of Streptococcus pneumoniae: development, evaluation and verification of targets for serogroup and serotype prediction using an automated pipeline.肺炎链球菌全基因组测序:使用自动化流程开发、评估和验证血清群及血清型预测靶点
PeerJ. 2016 Sep 14;4:e2477. doi: 10.7717/peerj.2477. eCollection 2016.
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Strain features and distributions in pneumococci from children with invasive disease before and after 13-valent conjugate vaccine implementation in the USA.美国13价结合疫苗实施前后侵袭性疾病患儿肺炎球菌的菌株特征及分布情况
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Roary: rapid large-scale prokaryote pan genome analysis.Roary:快速大规模原核生物泛基因组分析
Bioinformatics. 2015 Nov 15;31(22):3691-3. doi: 10.1093/bioinformatics/btv421. Epub 2015 Jul 20.
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Identification of pneumococcal colonization determinants in the stringent response pathway facilitated by genomic diversity.通过基因组多样性促进在严格反应途径中鉴定肺炎球菌定植决定因素。
BMC Genomics. 2015 May 9;16(1):369. doi: 10.1186/s12864-015-1573-6.
6
Recent functional insights into the role of (p)ppGpp in bacterial physiology.近期对(p)ppGpp在细菌生理学中作用的功能见解。
Nat Rev Microbiol. 2015 May;13(5):298-309. doi: 10.1038/nrmicro3448. Epub 2015 Apr 8.
7
Five winters of pneumococcal serotype replacement in UK carriage following PCV introduction.在英国引入肺炎球菌结合疫苗(PCV)后,连续五个冬季肺炎球菌血清型的更替情况。
Vaccine. 2015 Apr 21;33(17):2015-21. doi: 10.1016/j.vaccine.2015.03.012. Epub 2015 Mar 14.
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SRST2: Rapid genomic surveillance for public health and hospital microbiology labs.SRST2:用于公共卫生和医院微生物实验室的快速基因组监测。
Genome Med. 2014 Nov 20;6(11):90. doi: 10.1186/s13073-014-0090-6. eCollection 2014.
9
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins.使用Gubbins对重组细菌全基因组序列的大量样本进行快速系统发育分析。
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10
The emergence of bacterial "hopeful monsters".细菌“有希望的怪物”的出现。
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美国非疫苗血清型青霉素不敏感肺炎球菌引起侵袭性疾病的基因组流行病学

Genomic Epidemiology of Penicillin-Nonsusceptible Pneumococci with Nonvaccine Serotypes Causing Invasive Disease in the United States.

作者信息

Andam Cheryl P, Mitchell Patrick K, Callendrello Alanna, Chang Qiuzhi, Corander Jukka, Chaguza Chrispin, McGee Lesley, Beall Bernard W, Hanage William P

机构信息

Department of Epidemiology, Center for Communicable Disease Dynamics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA

Department of Epidemiology, Center for Communicable Disease Dynamics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

出版信息

J Clin Microbiol. 2017 Apr;55(4):1104-1115. doi: 10.1128/JCM.02453-16. Epub 2017 Jan 18.

DOI:10.1128/JCM.02453-16
PMID:28100596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5377837/
Abstract

Conjugate vaccination against seven pneumococcal serotypes (PCV7) reduced disease prevalence due to antibiotic-resistant strains throughout the 2000s. However, diseases caused by resistant nonvaccine type (NVT) strains increased. Some of these emerging strains were derived from vaccine types (VT) that had changed their capsule by recombination. The introduction of a vaccine targeting 13 serotypes (PCV13) in 2010 has led to concern that this scenario will repeat itself. We generated high-quality draft genomes from 265 isolates of NVT pneumococci not susceptible to penicillin (PNSP) in 2009 and compared them with the genomes of 581 isolates from 2012 to 2013 collected by the Active Bacterial Core surveillance (ABCs) of the Centers for Disease Control and Prevention (CDC). Of the seven sequence clusters (SCs) identified, three SCs fell into a single lineage associated with serogroup 23, which had an origin in 1908 as dated by coalescent analysis and included isolates with a divergent 23B capsule locus. Three other SCs represented relatively deep-branching lineages associated with serotypes 35B, 15A, and 15BC. In all cases, the resistant clones originated prior to 2010, indicating that PNSP are at present dominated by descendants of NVT clones present before vaccination. With one exception (15BC/ST3280), these SCs were related to clones identified by the Pneumococcal Molecular Epidemiology Network (PMEN). We conclude that postvaccine diversity in NVT PNSP between 2009 and 2013 was driven mainly by the persistence of preexisting strains rather than through adaptation, with few cases of serotype switching. Future surveillance is essential for documenting the long-term dynamics and resistance of NVT PNSP.

摘要

21世纪头十年,针对七种肺炎球菌血清型的联合疫苗接种(PCV7)降低了由抗生素耐药菌株引起的疾病流行率。然而,由耐药非疫苗型(NVT)菌株引起的疾病有所增加。其中一些新出现的菌株源自通过重组改变了荚膜的疫苗型(VT)。2010年引入的针对13种血清型的疫苗(PCV13)引发了人们对这种情况会再次出现的担忧。我们从2009年265株对青霉素不敏感的NVT肺炎球菌分离株中生成了高质量的基因组草图,并将它们与2012年至2013年由疾病控制与预防中心(CDC)的活性细菌核心监测(ABCs)收集的581株分离株的基因组进行了比较。在鉴定出的七个序列簇(SCs)中,三个SCs属于与血清群23相关的单一谱系,通过溯祖分析确定其起源于1908年,并且包括具有不同23B荚膜位点的分离株。其他三个SCs代表与血清型35B、15A和15BC相关的相对深分支谱系。在所有情况下,耐药克隆均起源于2010年之前,这表明目前青霉素不敏感肺炎球菌主要由疫苗接种前存在的NVT克隆的后代主导。除了一个例外(15BC/ST3280),这些SCs与肺炎球菌分子流行病学网络(PMEN)鉴定的克隆有关。我们得出结论,2009年至2013年期间NVT青霉素不敏感肺炎球菌的疫苗接种后多样性主要是由现有菌株的持续存在驱动的,而不是通过适应性变化,血清型转换的情况很少。未来的监测对于记录NVT青霉素不敏感肺炎球菌的长期动态和耐药性至关重要。