The frequency and associated factors of typhoid carriage in patients undergoing cholecystectomy for gallbladder disease in Pakistan: A cross-sectional study.


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:
Jun 2024
Historique:
received: 16 11 2023
accepted: 22 04 2024
medline: 12 6 2024
pubmed: 12 6 2024
entrez: 12 6 2024
Statut: epublish

Résumé

Enteric fever is caused by Salmonella enterica serovars Typhi (S. Typhi) and Paratyphi A, B, and C. It continues to be a significant cause of morbidity and mortality worldwide. In highly endemic areas, children are disproportionately affected, and antimicrobial resistance reduces therapeutic options. It is estimated that 2-5% of enteric fever patients develop chronic asymptomatic infection. These carriers may act as reservoirs of infection; therefore, the prospective identification and treatment of carriers are critical for long-term disease control. We aimed to find the frequency of Salmonella Typhi carriers in patients undergoing cholecystectomy. We also compared the detection limit of culturing versus qPCR in detecting S. Typhi, performed a geospatial analysis of the carriers identified using this study, and evaluated the accuracy of anti-Vi and anti-YncE in identifying chronic typhoid carriage. We performed a cross-sectional study in two centers in Pakistan. Gallbladder specimens were subjected to quantitative PCR (qPCR) and serum samples were analyzed for IgG against YncE and Vi by ELISA. We also mapped the residential location of those with a positive qPCR result. Out of 988 participants, 3.4% had qPCR-positive gallbladder samples (23 S. Typhi and 11 S. Paratyphi). Gallstones were more likely to be qPCR positive than bile and gallbladder tissue. Anti-Vi and YncE were significantly correlated (r = 0.78 p<0.0001) and elevated among carriers as compared to qPCR negative controls, except for anti-Vi response in Paratyphi A. But the discriminatory values of these antigens in identifying carriers from qPCR negative controls were low. The high prevalence of typhoid carriers observed in this study suggests that further studies are required to gain information that will help in controlling future typhoid outbreaks in a superior manner than they are currently being managed.

Sections du résumé

BACKGROUND BACKGROUND
Enteric fever is caused by Salmonella enterica serovars Typhi (S. Typhi) and Paratyphi A, B, and C. It continues to be a significant cause of morbidity and mortality worldwide. In highly endemic areas, children are disproportionately affected, and antimicrobial resistance reduces therapeutic options. It is estimated that 2-5% of enteric fever patients develop chronic asymptomatic infection. These carriers may act as reservoirs of infection; therefore, the prospective identification and treatment of carriers are critical for long-term disease control. We aimed to find the frequency of Salmonella Typhi carriers in patients undergoing cholecystectomy. We also compared the detection limit of culturing versus qPCR in detecting S. Typhi, performed a geospatial analysis of the carriers identified using this study, and evaluated the accuracy of anti-Vi and anti-YncE in identifying chronic typhoid carriage.
METHODS METHODS
We performed a cross-sectional study in two centers in Pakistan. Gallbladder specimens were subjected to quantitative PCR (qPCR) and serum samples were analyzed for IgG against YncE and Vi by ELISA. We also mapped the residential location of those with a positive qPCR result.
FINDINGS RESULTS
Out of 988 participants, 3.4% had qPCR-positive gallbladder samples (23 S. Typhi and 11 S. Paratyphi). Gallstones were more likely to be qPCR positive than bile and gallbladder tissue. Anti-Vi and YncE were significantly correlated (r = 0.78 p<0.0001) and elevated among carriers as compared to qPCR negative controls, except for anti-Vi response in Paratyphi A. But the discriminatory values of these antigens in identifying carriers from qPCR negative controls were low.
CONCLUSION CONCLUSIONS
The high prevalence of typhoid carriers observed in this study suggests that further studies are required to gain information that will help in controlling future typhoid outbreaks in a superior manner than they are currently being managed.

Identifiants

pubmed: 38865361
doi: 10.1371/journal.pntd.0011775
pii: PNTD-D-23-01394
doi:

Substances chimiques

Antibodies, Bacterial 0
Immunoglobulin G 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0011775

Informations de copyright

Copyright: © 2024 Qureshi 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

Sonia Qureshi (S)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Noshi Maria (N)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Tabish Chawla (T)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Junaid Iqbal (J)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Abdul Momin Kazi (AM)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Mehreen Adnan (M)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Aneeta Hotwani (A)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Najeeb Rahman (N)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Muhammed Wahhaab Sadiq (MW)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

Richelle Charles (R)

Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Departments of Medicine and Pediatrics, Harvard Medical School, Boston, Massachusetts, United States of America.
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, United States of America.

Stephen Baker (S)

University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, United Kingdom.
Department of Medicine, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, United Kingdom.

Farah Naz Qamar (FN)

Department of Pediatrics and Child Health, Aga Khan University, Karachi, Sindh, Pakistan.

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Classifications MeSH