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2
The hypervirulent Group B Streptococcus HvgA adhesin promotes central nervous system invasion through transcellular crossing of the choroid plexus.高毒力 B 组链球菌 HvgA 黏附素通过脉络丛的细胞间穿越促进中枢神经系统侵袭。
Fluids Barriers CNS. 2024 Aug 16;21(1):66. doi: 10.1186/s12987-024-00564-2.
3
A multi-organ, feto-maternal interface organ-on-chip, models pregnancy pathology and is a useful preclinical extracellular vesicle drug trial platform.一种多器官、胎儿-母体界面的芯片器官,可模拟妊娠病理学,是一个有用的临床前细胞外囊泡药物试验平台。
Extracell Vesicle. 2024 Jun;3. doi: 10.1016/j.vesic.2024.100035. Epub 2024 Feb 22.
4
Erratum for Cinar et al., "Serine-rich repeat proteins: well-known yet little-understood bacterial adhesins".希纳尔等人所著《富含丝氨酸重复序列蛋白:广为人知却又知之甚少的细菌黏附素》的勘误
J Bacteriol. 2024 Jun 20;206(6):e0015324. doi: 10.1128/jb.00153-24. Epub 2024 May 10.
5
Characterization of invasive Group B isolates from Western Australian infants, 2004-2020.2004-2020 年西澳大利亚婴儿侵袭性 B 群分离株的特征。
J Med Microbiol. 2024 Apr;73(4). doi: 10.1099/jmm.0.001822.
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Feto-Maternal Interface Organ-on-Chip: A New Technology to Study Ascending Infection.胎儿-母体界面类器官芯片:研究上行感染的新技术。
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7
Antimicrobial Resistance Profile of Group B Colonization in a Sample Population of Pregnant Women from Romania.罗马尼亚孕妇样本群体中B族定植的抗菌药物耐药情况
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孕期及生命早期的B族链球菌感染

Group B streptococcal infections in pregnancy and early life.

作者信息

Manuel Gygeria, Twentyman Joy, Noble Kristen, Eastman Alison J, Aronoff David M, Seepersaud Ravin, Rajagopal Lakshmi, Adams Waldorf Kristina M

机构信息

Department of Obstetrics & Gynecology, University of Washington, Seattle, Washington, USA.

Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, Washington, USA.

出版信息

Clin Microbiol Rev. 2025 Mar 13;38(1):e0015422. doi: 10.1128/cmr.00154-22. Epub 2024 Nov 25.

DOI:10.1128/cmr.00154-22
PMID:39584819
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11905376/
Abstract

SUMMARYBacterial infections with Group B (GBS) are an important cause of adverse outcomes in pregnant individuals, neonates, and infants. GBS is a common commensal in the genitourinary and gastrointestinal tracts and can be detected in the vagina of approximately 20% of women globally. GBS can infect the fetus either during pregnancy or vaginal delivery resulting in preterm birth, stillbirth, or early-onset neonatal disease (EOD) in the first week of life. The mother can also become infected with GBS leading to postpartum endometritis, and rarely, maternal sepsis. An invasive GBS infection of the neonate may present after the first week of life (late-onset disease, LOD) through transmission from caregivers, breast milk, and other sources. Invasive GBS infections in neonates can result in sepsis, pneumonia, meningitis, neurodevelopmental impairment, death, and lifelong disability. A policy of routine screening for GBS rectovaginal colonization in well-resourced countries can trigger the administration of intrapartum antibiotic prophylaxis (IAP) when prenatal testing is positive, which drastically reduces rates of EOD. However, many countries do not routinely screen pregnant women for GBS colonization but may administer IAP in cases with a high risk of EOD. IAP does not reduce rates of LOD. A global vaccination campaign is needed to reduce the significant burden of invasive GBS disease that remains among infants and pregnant individuals. In this narrative review, we provide a comprehensive overview of the global impact of GBS colonization and infection, virulence factors and pathogenesis, and current and future prophylactics and therapeutics.

摘要

摘要

B族链球菌(GBS)感染是导致孕妇、新生儿和婴儿出现不良结局的重要原因。GBS是泌尿生殖道和胃肠道常见的共生菌,全球约20%的女性阴道中可检测到该菌。GBS可在孕期或经阴道分娩时感染胎儿,导致早产、死产或出生后第一周内的早发型新生儿疾病(EOD)。母亲也可能感染GBS,引发产后子宫内膜炎,极少数情况下会导致产妇败血症。新生儿的侵袭性GBS感染可能在出生第一周后(晚发型疾病,LOD)通过护理人员、母乳和其他来源传播而出现。新生儿侵袭性GBS感染可导致败血症、肺炎、脑膜炎、神经发育障碍、死亡和终身残疾。在资源丰富的国家,对GBS直肠阴道定植进行常规筛查的政策,可在产前检测呈阳性时启动产时抗生素预防(IAP),这可大幅降低EOD的发生率。然而,许多国家并未对孕妇进行GBS定植的常规筛查,但可能在EOD风险较高的情况下实施IAP。IAP并不能降低LOD的发生率。需要开展全球疫苗接种运动,以减轻婴儿和孕妇中仍然存在的侵袭性GBS疾病的重大负担。在这篇叙述性综述中,我们全面概述了GBS定植和感染的全球影响、毒力因子和发病机制,以及当前和未来的预防和治疗方法。