Isolation of group B Streptococcus with reduced β-lactam susceptibility from pregnant women.


Journal

Emerging microbes & infections
ISSN: 2222-1751
Titre abrégé: Emerg Microbes Infect
Pays: United States
ID NLM: 101594885

Informations de publication

Date de publication:
2019
Historique:
entrez: 15 3 2019
pubmed: 15 3 2019
medline: 2 7 2019
Statut: ppublish

Résumé

β-Lactam antibiotics are first-line agents for the treatment and prevention of group B Streptococcus (GBS) infections. We previously reported clinical GBS isolates with reduced β-lactam susceptibility (GBS-RBS) and characterized them as harbouring amino acid substitutions in penicillin-binding proteins (PBPs). However, to our knowledge, GBS-RBS clinical isolates have never previously been isolated from pregnant women worldwide. We obtained 477 clinical GBS isolates from vaginal/rectal swabs of 4530 pregnant women in Japan. We determined the MICs of seven β-lactams for all 477 clinical isolates. Five clinical isolates showed reduced ceftibuten susceptibility. For these isolates, we performed sequencing analysis of pbp genes. None of the 477 isolates were non-susceptible to penicillin G, ampicillin, and meropenem. For five isolates, the MICs of ceftibuten were relatively high (64-128 μg/ml). Each of these isolates possessed a single amino acid substitution in PBP2X, and some of the substitutions had been previously found in GBS with reduced penicillin susceptibility. This is the first report of the isolation of clinical GBS-RBS isolates harbouring amino acid substitutions in PBP2X that confer reduced ceftibuten susceptibility from pregnant women.

Identifiants

pubmed: 30866792
doi: 10.1080/22221751.2018.1557987
pmc: PMC6455180
doi:

Substances chimiques

Bacterial Proteins 0
Penicillin-Binding Proteins 0
Ceftibuten IW71N46B4Y

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2-7

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Auteurs

Hiroaki Moroi (H)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.
b Department of Obstetrics and Gynecology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Kouji Kimura (K)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Tomomi Kotani (T)

b Department of Obstetrics and Gynecology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Hiroyuki Tsuda (H)

b Department of Obstetrics and Gynecology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Hirotsugu Banno (H)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Wanchun Jin (W)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Jun-Ichi Wachino (JI)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Keiko Yamada (K)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Takashi Mitsui (T)

c Kishokai Medical Corporation , Inazawa , Japan.

Mamoru Yamashita (M)

c Kishokai Medical Corporation , Inazawa , Japan.

Fumitaka Kikkawa (F)

b Department of Obstetrics and Gynecology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

Yoshichika Arakawa (Y)

a Department of Bacteriology , Nagoya University Graduate School of Medicine , Nagoya , Japan.

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Classifications MeSH