Clinical characteristics and molecular epidemiology of invasive Streptococcus agalactiae infections between 2007 and 2016 in Nara, Japan.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 20 03 2020
accepted: 30 09 2020
entrez: 19 10 2020
pubmed: 20 10 2020
medline: 15 12 2020
Statut: epublish

Résumé

Invasive Streptococcus agalactiae (GBS) infections are increasingly common among neonates and the elderly. Therefore, GBS surveillance for better antibiotic treatment and prophylaxis strategies are needed. We retrospectively evaluated the clinical aspects of invasive infections and the phenotypic and genetic diversity of infectious isolates from Nara, Japan, collected between 2007 and 2016, by using information from hospital records. GBS strains collected from the blood and cerebrospinal fluid cultures were evaluated for capsular types, multi-locus sequence typing (MLST), antibiotic susceptibility, antibiotics resistance gene, and pulsed-field gel electrophoresis. Forty GBS isolates (10 from children and 30 from adults) were analyzed, and the distribution of molecular serotype and allelic profiles varied between children and adults. We found the rates of early-onset disease in neonates with birth complications to be higher than that of previous reports, indicating that there could be relevance between complications at birth and early-onset disease. Standard antibiotic prophylaxis strategies may need to be reconsidered in patients with birth complications. In adults, the mean age of the patients was 68 years (male: 63%). Primary bacteremia was the most common source of infection. In the neonates, six had early-onset diseases and four had late-onset diseases. The most frequently identified strains were molecular serotype Ia ST23 (40%) and molecular serotype Ib ST10 (20%) in children and molecular serotype Ib ST10 (17%), molecular serotype VI ST1 (13%), and molecular serotype V ST1 (13%) in adults. Levofloxacin-resistant molecular serotype Ib strains and molecular serotypes V and VI ST1 were common causes of GBS infection in adults but were rarely found in children. Furthermore, pulsed-field gel electrophoresis in our study showed that specific clone isolates, that tend to have antibiotics resistance were widespread horizontally for a decade. Continuous surveillance and molecular investigation are warranted to identify the transmission route and improve antibiotic treatment strategies.

Identifiants

pubmed: 33075112
doi: 10.1371/journal.pone.0240590
pii: PONE-D-20-08051
pmc: PMC7571711
doi:

Substances chimiques

Levofloxacin 6GNT3Y5LMF

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0240590

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist. BML Biomedical Laboratories R&D Center, Inc., provided support in the form of salaries for the author MO and SI, but did not have any additional role in the study design, data collection and analysis, decision to poublish, or preparation of the manuscript. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Nobuyasu Hirai (N)

Department of Pathogen, Infection and Immunity, Nara Medical University, Kashihara, Nara, Japan.
Center for Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.
Department of Microbiology and Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Kei Kasahara (K)

Center for Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Ryuichi Nakano (R)

Department of Microbiology and Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Yoshihiko Ogawa (Y)

Center for Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Yuki Suzuki (Y)

Department of Microbiology and Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Miho Ogawa (M)

BML Biomedical Laboratories R&D Center, Inc., Kawagoe, Saitama, Japan.

Naokuni Hishiya (N)

Department of Microbiology and Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Akiyo Nakano (A)

Department of Microbiology and Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Sadahiro Ichimura (S)

BML Biomedical Laboratories R&D Center, Inc., Kawagoe, Saitama, Japan.

Hisakazu Yano (H)

Department of Microbiology and Infectious Diseases, Nara Medical University, Kashihara, Nara, Japan.

Masahide Yoshikawa (M)

Department of Pathogen, Infection and Immunity, Nara Medical University, Kashihara, Nara, Japan.

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