Multiple introductions of NRCS-A Staphylococcus capitis to the neonatal intensive care unit drive neonatal bloodstream infections: a case-control and environmental genomic survey.

IF 4 2区 生物学 Q1 GENETICS & HEREDITY
Emily A Lees, Jessica Gentry, Hermione Webster, Nicholas Sanderson, David Eyre, Daniel Wilson, Sam Lipworth, Derrick Crook, T H Nicholas Wong, Anthony Mark, Katie Jeffery, Stéphane Paulus, Bernadette C Young
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Abstract

Background. The Staphylococcus capitis NRCS-A strain has emerged as a global cause of late-onset sepsis associated with outbreaks in neonatal intensive care units (NICUs) whose transmission is incompletely understood.Methods. Demographic and clinical data for 45 neonates with S. capitis and 90 with other coagulase-negative staphylococci (CoNS) isolated from sterile sites were reviewed, and clinical significance was determined. S. capitis isolated from 27 neonates at 2 hospitals between 2017 and 2022 underwent long-read (ONT) (n=27) and short-read (Illumina) sequencing (n=18). These sequences were compared with S. capitis sequenced from blood culture isolates from other adult and paediatric patients in the same hospitals (n=6), S. capitis isolated from surface swabs (found in 5/150 samples), rectal swabs (in 2/69 samples) in NICU patients and NICU environmental samples (in 5/114 samples). Reads from all samples were mapped to a hybrid assembly of a local sterile site strain, forming a complete UK NRCS-A reference genome, for outbreak analysis and comparison with 826 other S. capitis from the UK and Germany.Results. S. capitis bacteraemia was associated with increased length of NICU stay at sampling (median day 22 vs day 12 for other CoNS isolated; P=0.05). A phylogeny of sequenced S. capitis revealed a cluster comprised of 25/27 neonatal sterile site isolates and 3/5 superficial, 2/2 rectal and 1/5 environmental isolates. No isolates from other wards belonged to this cluster. Phylogenetic comparison with published sequences confirmed that the cluster was NRCS-A outbreak strain but found a relatively high genomic diversity (mean pairwise distance of 84.9 SNPs) and an estimated NRCS-A S. capitis molecular clock of 5.1 SNPs/genome/year (95% credibility interval 4.3-5.9). The presence of S. capitis in superficial cultures did not correlate with neonatal bacteraemia, but both neonates with rectal NRCS-A S. capitis carriage identified also experienced S. capitis bacteraemia.Conclusions. S. capitis bacteraemia occurred in patients with longer NICU admission than other CoNS. Genomic analysis confirms clinically significant infections with the NRCS-A S. capitis strain, distinct from non-NICU clinical samples. Multiple introductions of S. capitis, rather than prolonged environmental persistence, were seen over 5 years of infections.

新生儿重症监护室多次引入NRCS-A型头葡萄球菌驱动新生儿血流感染:病例对照和环境基因组调查。
背景。头型葡萄球菌NRCS-A菌株已成为新生儿重症监护病房(NICUs)暴发的迟发性败血症的全球原因,其传播尚不完全清楚。本文回顾了45例头链球菌新生儿和90例无菌部位分离的其他凝固酶阴性葡萄球菌(con)新生儿的人口学和临床资料,并确定了临床意义。从2017年至2022年在2家医院的27名新生儿中分离出的头链球菌进行了长读(ONT) (n=27)和短读(Illumina)测序(n=18)。将这些序列与同一医院其他成人和儿科患者血培养分离物(n=6)、NICU患者表面拭子(5/150份样本)、直肠拭子(2/69份样本)和NICU环境样本(5/114份样本)分离的头链球菌序列进行比较。所有样本的Reads被映射到一个当地无菌位点菌株的杂交组合中,形成一个完整的英国NRCS-A参考基因组,用于爆发分析并与来自英国和德国的826个其他猪头链球菌进行比较。头链球菌菌血症与取样时新生儿重症监护病房的住院时间增加有关(隔离的其他con患者平均22天vs 12天;P = 0.05)。经测序的头链球菌的系统发育显示,该群由25/27的新生儿无菌部位分离株和3/5的浅表分离株、2/2的直肠分离株和1/5的环境分离株组成。其他病房的隔离物不属于该群集。与已发表序列的系统发育比较证实该聚类为NRCS-A爆发菌株,但发现基因组多样性相对较高(平均配对距离为84.9个snp),估计NRCS-A猪链球菌分子钟为5.1个snp /基因组/年(95%可信区间为4.3-5.9)。浅表培养中头链球菌的存在与新生儿菌血症无关,但两名直肠nrc - a型头链球菌携带的新生儿也经历了头链球菌菌血症。新生儿重症监护病房住院时间较长的患者出现了头链球菌菌血症。基因组分析证实,与非新生儿重症监护病房的临床样本不同,nrc - a头链球菌菌株存在显著的临床感染。在5年以上的感染中,多次引入猪链球菌,而不是长时间的环境持久性。
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来源期刊
Microbial Genomics
Microbial Genomics Medicine-Epidemiology
CiteScore
6.60
自引率
2.60%
发文量
153
审稿时长
12 weeks
期刊介绍: Microbial Genomics (MGen) is a fully open access, mandatory open data and peer-reviewed journal publishing high-profile original research on archaea, bacteria, microbial eukaryotes and viruses.
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