Predominance of multidrug-resistant Salmonella Typhi genotype 4.3.1 with low-level ciprofloxacin resistance in Zanzibar.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
17 Apr 2024
Historique:
received: 06 10 2023
accepted: 02 04 2024
medline: 17 4 2024
pubmed: 17 4 2024
entrez: 17 4 2024
Statut: aheadofprint

Résumé

Typhoid fever is a common cause of febrile illness in low- and middle-income countries. While multidrug-resistant (MDR) Salmonella Typhi (S. Typhi) has spread globally, fluoroquinolone resistance has mainly affected Asia. Consecutively, 1038 blood cultures were obtained from patients of all age groups with fever and/or suspicion of serious systemic infection admitted at Mnazi Mmoja Hospital, Zanzibar in 2015-2016. S. Typhi were analyzed with antimicrobial susceptibility testing and with short read (61 strains) and long read (9 strains) whole genome sequencing, including three S. Typhi strains isolated in a pilot study 2012-2013. Sixty-three S. Typhi isolates (98%) were MDR carrying blaTEM-1B, sul1 and sul2, dfrA7 and catA1 genes. Low-level ciprofloxacin resistance was detected in 69% (43/62), with a single gyrase mutation gyrA-D87G in 41 strains, and a single gyrA-S83F mutation in the non-MDR strain. All isolates were susceptible to ceftriaxone and azithromycin. All MDR isolates belonged to genotype 4.3.1 lineage I (4.3.1.1), with the antimicrobial resistance determinants located on a composite transposon integrated into the chromosome. Phylogenetically, the MDR subgroup with ciprofloxacin resistance clusters together with two external isolates. We report a high rate of MDR and low-level ciprofloxacin resistant S. Typhi circulating in Zanzibar, belonging to genotype 4.3.1.1, which is widespread in Southeast Asia and African countries and associated with low-level ciprofloxacin resistance. Few therapeutic options are available for treatment of typhoid fever in the study setting. Surveillance of the prevalence, spread and antimicrobial susceptibility of S. Typhi can guide treatment and control efforts.

Sections du résumé

BACKGROUND BACKGROUND
Typhoid fever is a common cause of febrile illness in low- and middle-income countries. While multidrug-resistant (MDR) Salmonella Typhi (S. Typhi) has spread globally, fluoroquinolone resistance has mainly affected Asia.
METHODS METHODS
Consecutively, 1038 blood cultures were obtained from patients of all age groups with fever and/or suspicion of serious systemic infection admitted at Mnazi Mmoja Hospital, Zanzibar in 2015-2016. S. Typhi were analyzed with antimicrobial susceptibility testing and with short read (61 strains) and long read (9 strains) whole genome sequencing, including three S. Typhi strains isolated in a pilot study 2012-2013.
RESULTS RESULTS
Sixty-three S. Typhi isolates (98%) were MDR carrying blaTEM-1B, sul1 and sul2, dfrA7 and catA1 genes. Low-level ciprofloxacin resistance was detected in 69% (43/62), with a single gyrase mutation gyrA-D87G in 41 strains, and a single gyrA-S83F mutation in the non-MDR strain. All isolates were susceptible to ceftriaxone and azithromycin. All MDR isolates belonged to genotype 4.3.1 lineage I (4.3.1.1), with the antimicrobial resistance determinants located on a composite transposon integrated into the chromosome. Phylogenetically, the MDR subgroup with ciprofloxacin resistance clusters together with two external isolates.
CONCLUSIONS CONCLUSIONS
We report a high rate of MDR and low-level ciprofloxacin resistant S. Typhi circulating in Zanzibar, belonging to genotype 4.3.1.1, which is widespread in Southeast Asia and African countries and associated with low-level ciprofloxacin resistance. Few therapeutic options are available for treatment of typhoid fever in the study setting. Surveillance of the prevalence, spread and antimicrobial susceptibility of S. Typhi can guide treatment and control efforts.

Identifiants

pubmed: 38630840
doi: 10.1371/journal.pntd.0012132
pii: PNTD-D-23-01255
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0012132

Informations de copyright

Copyright: © 2024 Onken et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Annette Onken (A)

Department of Clinical Science, University of Medicine, Bergen, Norway.
National Centre for Tropical Infectious Diseases, Haukeland University Hospital, Bergen, Norway.
Department of Microbiology, Vestre Viken Hospital Trust, Drammen, Norway.

Sabrina Moyo (S)

Department of Clinical Science, University of Medicine, Bergen, Norway.
Department of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Mohammed Khamis Miraji (MK)

Department of Internal Medicine, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Jon Bohlin (J)

Department of methods and analysis, Section of modelling and bioinformatics, Domain of Infection Control, Oslo, Norway.
Center for Fertility and Health analysis, Norwegian Institute of Public Health, Oslo, Norway.

Msafiri Marijani (M)

Pathology Laboratory Department, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Joel Manyahi (J)

Department of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Kibwana Omar Kibwana (KO)

Department of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Fredrik Müller (F)

Department of Microbiology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Pål A Jenum (PA)

Department of Microbiology, Vestre Viken Hospital Trust, Drammen, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Khamis Ali Abeid (KA)

Department of Pediatrics, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Marianne Reimers (M)

Emergency Care Clinic, Haukeland University Hospital, Bergen, Norway.

Nina Langeland (N)

Department of Clinical Science, University of Medicine, Bergen, Norway.
National Centre for Tropical Infectious Diseases, Haukeland University Hospital, Bergen, Norway.

Kristine Mørch (K)

Department of Clinical Science, University of Medicine, Bergen, Norway.
National Centre for Tropical Infectious Diseases, Haukeland University Hospital, Bergen, Norway.

Bjørn Blomberg (B)

Department of Clinical Science, University of Medicine, Bergen, Norway.
National Centre for Tropical Infectious Diseases, Haukeland University Hospital, Bergen, Norway.

Classifications MeSH