Evidence map›Paper›PMID 35750070›Full record

ArticleThe Lancet. Microbe2022

The international and intercontinental spread and expansion of antimicrobial-resistant Salmonella Typhi: a genomic epidemiology study.

Kesia Esther da Silva, Arif Mohammad Tanmoy, Agila Kumari Pragasam, Junaid Iqbal, Mohammad Saiful Islam Sajib, Ankur Mutreja, Balaji Veeraraghavan, Dipesh Tamrakar, Farah Naz Qamar, Gordon Dougan and 18 more

Abstract read
In one paragraph

Article in The Lancet. Microbe, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Azithromycin-resistantJAC-antimicrobial resistance · 2026
    Article
  6. Article
  7. Article
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  9. Review
  10. Article
  11. ConfrontingInfection and drug resistance · 2026
    Review
  12. Review
  13. Laboratory epidemiology ofOne health (Amsterdam, Netherlands) · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Whole-Genome Sequencing Analysis of Drug-ResistantPathogens (Basel, Switzerland) · 2025
    Article
  18. Article
  19. Article
  20. Article

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Kesia Esther da SilvaDivision of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, USA.
Arif Mohammad TanmoyChild Health Research Foundation, Dhaka, Bangladesh; Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center, Rotterdam, Netherlands.
Agila Kumari PragasamDepartment of Clinical Microbiology, Christian Medical College, Vellore, India.
Junaid IqbalDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Mohammad Saiful Islam SajibChild Health Research Foundation, Dhaka, Bangladesh; Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, UK.
Ankur MutrejaCambridge Institute of Therapeutic Immunology & Infectious Disease, Department of Medicine, University of Cambridge, Cambridge, UK.
Balaji VeeraraghavanDepartment of Clinical Microbiology, Christian Medical College, Vellore, India.
Dipesh TamrakarDepartment of Community Medicine, Dhulikhel Hospital, Kathmandu University Hospital, Kathmandu, Nepal.
Farah Naz QamarDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Gordon DouganDepartment of Medicine, Cambridge Biomedical Campus, Cambridge, UK; University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Isaac BogochDepartment of Medicine, University of Toronto, Toronto, ON, Canada.
Jessica C SeidmanApplied Epidemiology, Sabin Vaccine Institute, Washington, DC, USA.
Jivan ShakyaResearch and Development Division, Dhulikhel Hospital, Kathmandu University Hospital, Kathmandu, Nepal; Central Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.
Krista VaidyaResearch and Development Division, Dhulikhel Hospital, Kathmandu University Hospital, Kathmandu, Nepal.
Megan E CareyDepartment of Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Rajeev ShresthaDepartment of Pharmacology, Dhulikhel Hospital, Kathmandu University Hospital, Kathmandu, Nepal.
Seema IrfanDepartment of Pathology and Microbiology, Aga Khan University, Karachi, Pakistan.
Stephen BakerDepartment of Medicine, Cambridge Biomedical Campus, Cambridge, UK; University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Steve P LubyDivision of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, USA.
Yanjia CaoDepartment of Geography, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Zoe Anne DysonDepartment of Medicine, Cambridge Biomedical Campus, Cambridge, UK; Department of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK; Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, Australia; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Denise O GarrettApplied Epidemiology, Sabin Vaccine Institute, Washington, DC, USA.
Jacob JohnDepartment of Community Health, Christian Medical College, Vellore, India.
Gagandeep KangThe Wellcome Trust Research Laboratory, Division of Gastrointestinal Sciences, Christian Medical College, Vellore, India.
Yogesh HoodaChild Health Research Foundation, Dhaka, Bangladesh; MRC Laboratory Molecular Biology, Cambridge, UK.
Samir K SahaChild Health Research Foundation, Dhaka, Bangladesh; Department of Microbiology, Dhaka Shishu Hospital, Dhaka, Bangladesh.
Senjuti SahaChild Health Research Foundation, Dhaka, Bangladesh.
Jason R AndrewsDivision of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, USA. Electronic address: jandr@stanford.edu.

Funding

Bill & Melinda Gates Foundation INV-008335
6 · The paper itself

Abstract

backgroundThe emergence of increasingly antimicrobial-resistant Salmonella enterica serovar Typhi (S Typhi) threatens to undermine effective treatment and control. Understanding where antimicrobial resistance in S Typhi is emerging and spreading is crucial towards formulating effective control strategies.

methodsIn this genomic epidemiology study, we sequenced the genomes of 3489 S Typhi strains isolated from prospective enteric fever surveillance studies in Nepal, Bangladesh, Pakistan, and India (between 2014 and 2019), and combined these with a global collection of 4169 S Typhi genome sequences isolated between 1905 and 2018 to investigate the temporal and geographical patterns of emergence and spread of antimicrobial-resistant S Typhi. We performed non-parametric phylodynamic analyses to characterise changes in the effective population size of fluoroquinolone-resistant, extensively drug-resistant (XDR), and azithromycin-resistant S Typhi over time. We inferred timed phylogenies for the major S Typhi sublineages and used ancestral state reconstruction methods to estimate the frequency and timing of international and intercontinental transfers.

findingsOur analysis revealed a declining trend of multidrug resistant typhoid in south Asia, except for Pakistan, where XDR S Typhi emerged in 2016 and rapidly replaced less-resistant strains. Mutations in the quinolone-resistance determining region (QRDR) of S Typhi have independently arisen and propagated on at least 94 occasions, nearly all occurring in south Asia. Strains with multiple QRDR mutations, including triple mutants with high-level fluoroquinolone resistance, have been increasing in frequency and displacing strains with fewer mutations. Strains containing acrB mutations, conferring azithromycin resistance, emerged in Bangladesh around 2013 and effective population size of these strains has been steadily increasing. We found evidence of frequent international (n=138) and intercontinental transfers (n=59) of antimicrobial-resistant S Typhi, followed by local expansion and replacement of drug-susceptible clades.

interpretationIndependent acquisition of plasmids and homoplastic mutations conferring antimicrobial resistance have occurred repeatedly in multiple lineages of S Typhi, predominantly arising in south Asia before spreading to other regions.

fundingBill & Melinda Gates Foundation.

Indexed as

Anti-Infective AgentsQuinolonesTyphoid FeverAnti-Bacterial AgentsAzithromycinDrug Resistance, BacterialFluoroquinolonesGenomicsHumansProspective StudiesSalmonella typhiAnti-Bacterial AgentsAnti-Infective AgentsAzithromycinFluoroquinolonesQuinolones

Identifiers

PMID35750070
PMCPMC9329132

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.