Evidence map›Paper›PMID 37312043›Full record

ArticleBMC microbiology2023

Whole genome sequencing of Salmonella enterica serovars isolated from humans, animals, and the environment in Lagos, Nigeria.

Kabiru Olusegun Akinyemi, Christopher Oladimeji Fakorede, Jörg Linde, Ulrich Methner, Gamal Wareth, Herbert Tomaso, Heinrich Neubauer

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.0field-weighted citation impact, top 3% of its field
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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  15. Drug resistance and genotyping studies ofFrontiers in veterinary science · 2025
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  18. Microbial genomics · 2025
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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

7 authors at 2 institutions in 3 countries.

Kabiru Olusegun AkinyemiDepartment of Microbiology, Faculty of Science, Lagos State University, Ojo, Lagos, Nigeria. kabiru.akinyemi@lasu.edu.ng.
Christopher Oladimeji FakoredeDepartment of Microbiology, Faculty of Science, Lagos State University, Ojo, Lagos, Nigeria.
Jörg LindeInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institute, Jena, Germany.
Ulrich MethnerInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institute, Jena, Germany.
Gamal WarethInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institute, Jena, Germany.
Herbert TomasoInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institute, Jena, Germany.
Heinrich NeubauerInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institute, Jena, Germany.
Friedrich-Loeffler-Institut · DELagos State University · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSalmonella infections remain an important public health issue worldwide. Some serovars of non-typhoidal Salmonella (NTS) have been associated with bloodstream infections and gastroenteritis, especially in children in Sub-Saharan Africa with circulating S. enterica serovars with drug resistance and virulence genes. This study identified and verified the clonal relationship of Nigerian NTS strains isolated from humans, animals, and the environment.

methodsIn total, 2,522 samples were collected from patients, animals (cattle and poultry), and environmental sources between December 2017 and May 2019. The samples were subjected to a standard microbiological investigation. All the isolates were identified using Microbact 24E, and MALDI-TOF MS. The isolates were serotyped using the Kauffmann-White scheme. Antibiotic susceptibility testing was conducted using the disc diffusion method and the Vitek 2 compact system. Virulence and antimicrobial resistance genes, sequence type, and cluster analysis were investigated using WGS data.

resultsForty-eight (48) NTS isolates (1.9%) were obtained. The prevalence of NTS from clinical sources was 0.9%, while 4% was recorded for animal sources. The serovars identified were S. Cotham (n = 17), S. Give (n = 16), S. Mokola (n = 6), S. Abony (n = 4), S. Typhimurium (n = 4), and S. Senftenberg (n = 1). All 48 Salmonella isolates carried intrinsic and acquired resistant genes such as aac.6…Iaa, mdf(A), qnrB, qnrB19 genes and golT, golS, pcoA, and silP, mediated by plasmid Col440I_1, incFIB.B and incFII. Between 100 and 118 virulence gene markers distributed across several Salmonella pathogenicity islands (SPIs), clusters, prophages, and plasmid operons were found in each isolate. WGS revealed that strains of each Salmonella serovar could be assigned to a single 7-gene MLST cluster, and strains within the clusters were identical strains and closely related as defined by the 0 and 10 cgSNPs and likely shared a common ancestor. The dominant sequence types were S. Give ST516 and S. Cotham ST617.

conclusionWe found identical Salmonella sequence types in human, animal, and environmental samples in the same locality, which demonstrates the great potential of the applied tools to trace back outbreak strains. Strategies to control and prevent the spread of NTS in the context of one's health are essential to prevent possible outbreaks.

Indexed as

Salmonella entericaTyphoid FeverAnimalsCattleChildHumansMultilocus Sequence TypingNigeriaOperonSerogroupMLSTNigeriaResistant geneSalmonellaSerotypingVirulence geneWGS

Identifiers

PMID37312043
PMCPMC10262361
OpenAlexW4380577695

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.