Evidence map›Paper›PMID 41372809›Full record

ArticleBMC infectious diseases2025

High prevalence of multi-drug resistant H58 Salmonella Typhi and emerging fluoroquinolone resistance among febrile children in Nairobi County, Kenya.

Susan Mutile Kavai, Cecilia Mbae, Michael Mugo, Peter Njoroge, Jessica Chepchirchir, Naomi Wambui, Steve Anyona, Diana Imoli, Ronald Ng'etich, Evans Kibet and 21 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

31 authors.

Susan Mutile KavaiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya. ssnkavai8@gmail.com.
Cecilia MbaeCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Michael MugoCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Peter NjorogeCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Jessica ChepchirchirCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Naomi WambuiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Steve AnyonaCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Diana ImoliCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Ronald Ng'etichCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Evans KibetCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Georgina OdityoCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Sheillah MundaloCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Celestine WairimuCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Mary KariukiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Amos NjugunaCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Evelyn WamuciiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Winfred MbithiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Darius OwegiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Peter MuturiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Collins KebeneiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Humphrey MiritiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Naomi KomenCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Christine KiokoCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Maureen KawiraCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
June KavaiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Rahma OsmanCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Zillah WakioCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Beatrice OngadiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Robert OnsareCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Kelvin KeringCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Samuel KariukiCentre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.

Funding

Integrating geographical and genetic mapping of salmonella disease in an endemicR01AI099525 · NIAID · KENYA MEDICAL RESEARCH INSTITUTE (KEMRI) · PI GUNN, JOHN S, KARIUKI, SAMUEL M · 2013 to 2024
$1.3M
National Institute of Allergy and Infectious Diseases of the National Institutes of Health R01AI099525NIAID NIH HHS R01 AI099525
6 · The paper itself

Abstract

backgroundTyphoid fever is a serious infection that primarily affects humans, with approximately 20 million cases reported each year, mostly in low- and middle-income countries (LMICs). Continuous monitoring of Salmonella enterica serovar Typhi (S. Typhi) in these endemic areas is crucial for tracking trends in antimicrobial resistance (AMR) and developing effective control measures. This study focused on S. Typhi isolates from children aged ≤ 16 years who showed symptoms of fever in Mukuru and Kibera informal settlements in Nairobi County, Kenya.

methodsBlood samples for culture were collected from participants at four health facilities within Nairobi County. Antimicrobial susceptibility profiles were assessed using the Kirby–Bauer disc diffusion technique, and whole-genome sequencing (WGS) was performed on selected multidrug-resistant (MDR) isolates. The genomes were assembled and analysed using https://pathogen.watch/ to identify genotypes, resistance genes, and phylogenetic relationships.

resultsOut of 120 S. Typhi isolates tested, 50% were found to be MDR. Resistance to first-line antibiotics was common, with 65.6% resistant to ampicillin, 62.3% to sulfamethoxazole-trimethoprim, and 59% to chloramphenicol. Thirty-seven selected MDR isolates underwent WGS, all belonging to the genotype 4.3.1 (H58), which is the most prevalent MDR clade globally. These were further categorised into sublineage 4.3.1.1 EA (East Africa 1), accounting for 40.5% of the sequenced isolates. Genomic analysis identified several AMR genes, including blaTEM−1D, catA1, dfrA7, sul1, and sul2. Additionally, point mutations in the quinolone resistance-determining region (QRDR) of gyrA were found in 67.6% of the isolates, with the most common mutation being S83Y. These mutations are linked to decreased susceptibility to ciprofloxacin, a key treatment for typhoid in Kenya.

conclusionThe high rate of MDR S. Typhi, especially in children who are most affected by the disease, raises significant public health concerns. The presence of QRDR mutations further complicates treatment options for typhoid fever, highlighting the urgent need for alternative approaches. These may include broader use of typhoid conjugate vaccines (TCVs), strengthening antimicrobial stewardship programs, and investing in improvements in water, sanitation, and hygiene (WASH) infrastructure in these endemic settings in Kenya.

Indexed as

Anti-Bacterial AgentsDrug Resistance, Multiple, BacterialFluoroquinolonesSalmonella typhiTyphoid FeverAdolescentChildChild, PreschoolFemaleGenotypeHumansInfantKenyaMaleMicrobial Sensitivity TestsPhylogenyAnti-Bacterial AgentsFluoroquinolonesChildrenKenyaKiberaMukuruMulti-drug resistanceNairobiS. TyphiSystemic

Identifiers

PMID41372809
PMCPMC12801635

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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.