Whole-genome sequencing of non-typeable Haemophilus influenzae isolated from a tertiary care hospital in Surabaya, Indonesia.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
03 Oct 2024
Historique:
received: 12 03 2024
accepted: 28 08 2024
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 2 10 2024
Statut: epublish

Résumé

Haemophilus influenzae causes life-threatening invasive diseases such as septicaemia and meningitis. Reports on circulating H. influenzae causing invasive disease in lower-middle income settings, including Indonesia, are lacking. This study describes the serotype distributions and whole-genome sequence (WGS) data of H. influenzae isolated from hospitalized patients at Soetomo Hospital, Surabaya, Indonesia. H. influenzae isolates were isolated from blood and pleural fluid specimens and identified using culture-based and molecular methods, followed by serotyping and WGS using RT‒PCR and Illumina MiSeq, respectively. Sequencing reads were assembled, and further analyses were undertaken to determine the genomic content and reconstruct the phylogeny. A second dataset consisting of publicly available H. influenzae genomes was curated to conduct phylogenetic analyses of isolates in this study in the context of globally circulating isolates. Ten H. influenzae isolates from hospitalized patients were collected, and septicaemia was the most common diagnosis (n=8). RT‒PCR and WGS were performed to determine whether all the isolates were nontypeable H. influenzae (NTHi). There were four newly identified STs distributed across the two main clusters. A total of 91 out of 126 virulence factor (VF)-related genes in Haemophilus sp. were detected in at least one isolate. Further evaluation incorporating a global collection of H. influenzae genomes confirmed the diverse population structure of NTHi in this study. This study showed that all H. influenzae recovered from invasive disease patients were nonvaccine-preventable NTHi isolates. The inclusion of WGS revealed four novel STs and the possession of key VF-associated genes.

Sections du résumé

BACKGROUND BACKGROUND
Haemophilus influenzae causes life-threatening invasive diseases such as septicaemia and meningitis. Reports on circulating H. influenzae causing invasive disease in lower-middle income settings, including Indonesia, are lacking. This study describes the serotype distributions and whole-genome sequence (WGS) data of H. influenzae isolated from hospitalized patients at Soetomo Hospital, Surabaya, Indonesia.
METHODS METHODS
H. influenzae isolates were isolated from blood and pleural fluid specimens and identified using culture-based and molecular methods, followed by serotyping and WGS using RT‒PCR and Illumina MiSeq, respectively. Sequencing reads were assembled, and further analyses were undertaken to determine the genomic content and reconstruct the phylogeny. A second dataset consisting of publicly available H. influenzae genomes was curated to conduct phylogenetic analyses of isolates in this study in the context of globally circulating isolates.
RESULTS RESULTS
Ten H. influenzae isolates from hospitalized patients were collected, and septicaemia was the most common diagnosis (n=8). RT‒PCR and WGS were performed to determine whether all the isolates were nontypeable H. influenzae (NTHi). There were four newly identified STs distributed across the two main clusters. A total of 91 out of 126 virulence factor (VF)-related genes in Haemophilus sp. were detected in at least one isolate. Further evaluation incorporating a global collection of H. influenzae genomes confirmed the diverse population structure of NTHi in this study.
CONCLUSION CONCLUSIONS
This study showed that all H. influenzae recovered from invasive disease patients were nonvaccine-preventable NTHi isolates. The inclusion of WGS revealed four novel STs and the possession of key VF-associated genes.

Identifiants

pubmed: 39358708
doi: 10.1186/s12879-024-09826-8
pii: 10.1186/s12879-024-09826-8
doi:

Substances chimiques

Virulence Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1097

Subventions

Organisme : CDC HHS
ID : NU2GGH001852-03
Pays : United States
Organisme : CDC HHS
ID : NU2GGH001852-03
Pays : United States
Organisme : CDC HHS
ID : NU2GGH001852-03
Pays : United States
Organisme : CDC HHS
ID : NU2GGH001852-03
Pays : United States

Informations de copyright

© 2024. The Author(s).

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Auteurs

Made Ananda Krisna (MA)

Eijkman Research Centre for Molecular Biology, National Research and Innovation Agency, Cibinong, West Java, Indonesia. made.krisna@biology.ox.ac.uk.
Department of Biology, University of Oxford, Oxford, UK. made.krisna@biology.ox.ac.uk.

Lindawati Alimsardjono (L)

Department of Clinical Microbiology, Dr. Soetomo Academic General Hospital, Surabaya, Indonesia.

Korrie Salsabila (K)

Eijkman Research Centre for Molecular Biology, National Research and Innovation Agency, Cibinong, West Java, Indonesia.
Graduate School of Medical and Pharmaceutical Sciences, Chiba University, Chiba, Japan.

Naritha Vermasari (N)

Department of Clinical Microbiology, Dr. Soetomo Academic General Hospital, Surabaya, Indonesia.

Wa Ode Dwi Daningrat (WOD)

Eijkman Research Centre for Molecular Biology, National Research and Innovation Agency, Cibinong, West Java, Indonesia.
Centre for Genomic Pathogen Surveillance, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

Kuntaman Kuntaman (K)

Department of Clinical Microbiology, Dr. Soetomo Academic General Hospital, Surabaya, Indonesia.

Odile Barbara Harrison (OB)

Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Martin Christopher James Maiden (MCJ)

Department of Biology, University of Oxford, Oxford, UK.

Dodi Safari (D)

Eijkman Research Centre for Molecular Biology, National Research and Innovation Agency, Cibinong, West Java, Indonesia. dodi004@brin.go.id.

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