Evidence map›Paper›PMID 42487718›Full record

ArticleFrontiers in microbiology2026

Whole-genome characterization of neonatal group B Streptococcus infection isolates and contemporaneous maternal colonizing isolates in Southwest China.

Ziyi Yan, Liyuan Mu, Chenglin Miao, Yunhan Fu, Li Liu, Xingxin Liu, Jingjing Luo, Wenjing Wu, Jiaji Ling, Liting Liang and 3 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Ziyi YanDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Liyuan MuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Chenglin MiaoDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Yunhan FuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Li LiuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Xingxin LiuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Jingjing LuoDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Wenjing WuDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Jiaji LingDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Liting LiangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Yali CuiDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Yongmei JiangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.
Linghan KuangDepartment of Laboratory Medicine, West China Second University Hospital, Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Regional genomic data on neonatal GBS infection in Southwest China remain limited, particularly for studies integrating neonatal infection isolates with contemporaneous maternal colonizing isolates. This study defined the antimicrobial susceptibility, molecular composition, resistance and virulence gene profiles, and phylogenetic context of neonatal GBS infection in this region. Methods: We retrospectively analyzed 52 neonatal GBS infection isolates collected from March 2020 to March 2025 and compared them with 52 maternal vaginal colonizing isolates selected from the same period. Antimicrobial susceptibility testing, whole-genome sequencing, capsular serotyping, multilocus sequence typing, clonal complex assignment, gene screening, and core-genome phylogenetic analysis were performed. The 52 neonatal infection isolates were further contextualized with 1,060 publicly available blood- or cerebrospinal fluid-derived genomes from PubMLST. Results: All neonatal infection isolates were susceptible to penicillin and ampicillin, whereas resistance to erythromycin, clindamycin, tetracycline, and moxifloxacin was common. Serotype III was the most frequent serotype, followed by Ib. Compared with maternal colonizing isolates, neonatal infection isolates showed significant enrichment of ST17/CC17 and the III-2/CC17 lineage. The predominant neonatal infection-associated lineages were Ib/CC12, III-2/CC17, and III-1/CC19. Resistance and virulence gene carriage was strongly structured by clonal background, with several aminoglycoside resistance genes and Conclusion: Neonatal GBS infection in Southwest China was associated with selected phylogenetic backgrounds rather than directly mirroring the maternal colonizing population. These findings support integrated surveillance of antimicrobial susceptibility, molecular lineages, virulence markers, and vaccine-relevant serotypes.

Indexed as

antimicrobial resistanceclonal complexgroup B Streptococcusmaternal colonizationneonatal infectionStreptococcus agalactiaevirulence geneswhole-genome sequencing

Identifiers

PMID42487718
PMCPMC13388304

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