Case-control investigation of invasive Salmonella disease in Malawi reveals no evidence of environmental or animal transmission of invasive strains, and supports human to human transmission.


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:
12 2022
Historique:
received: 21 03 2022
accepted: 23 11 2022
revised: 22 12 2022
pubmed: 13 12 2022
medline: 27 12 2022
entrez: 12 12 2022
Statut: epublish

Résumé

Invasive Salmonella infections cause significant morbidity and mortality in Sub-Saharan Africa. However, the routes of transmission are uncertain. We conducted a case-control study of index-case and geographically-matched control households in Blantyre, Malawi, sampling Salmonella isolates from index cases, healthy people, animals, and the household environment. Sixty index cases of human invasive Salmonella infection were recruited (March 2015-Oct 2016). Twenty-eight invasive Non-Typhoidal Salmonella (iNTS) disease and 32 typhoid patients consented to household sampling. Each index-case household was geographically matched to a control household. Extensive microbiological sampling included stool sampling from healthy household members, stool or rectal swabs from household-associated animals and boot-sock sampling of the household environment. 1203 samples from 120 households, yielded 43 non-Typhoidal Salmonella (NTS) isolates from 25 households (overall sample positivity 3.6%). In the 28 iNTS patients, disease was caused by 3 STs of Salmonella Typhimurium, mainly ST313. In contrast, the isolates from households spanned 15 sequence types (STs). Two S. Typhimurium isolates from index cases closely matched isolates from their respective asymptomatic household members (2 and 3 SNP differences respectively). Despite the recovery of a diverse range of NTS, there was no overlap between the STs causing iNTS disease with any environmental or animal isolates. The finding of NTS strains from index cases that matched household members, coupled with lack of related animal or environmental isolates, supports a hypothesis of human to human transmission of iNTS infections in the household. The breadth of NTS strains found in animals and the household environment demonstrated the robustness of NTS sampling and culture methodology, and suggests a diverse ecology of Salmonella in this setting. Healthy typhoid (S. Typhi) carrier state was not detected. The lack of S. Typhi isolates from the household environment suggests that further methodological development is needed to culture S. Typhi from the environment.

Sections du résumé

BACKGROUND
Invasive Salmonella infections cause significant morbidity and mortality in Sub-Saharan Africa. However, the routes of transmission are uncertain. We conducted a case-control study of index-case and geographically-matched control households in Blantyre, Malawi, sampling Salmonella isolates from index cases, healthy people, animals, and the household environment.
METHODOLOGY
Sixty index cases of human invasive Salmonella infection were recruited (March 2015-Oct 2016). Twenty-eight invasive Non-Typhoidal Salmonella (iNTS) disease and 32 typhoid patients consented to household sampling. Each index-case household was geographically matched to a control household. Extensive microbiological sampling included stool sampling from healthy household members, stool or rectal swabs from household-associated animals and boot-sock sampling of the household environment.
FINDINGS
1203 samples from 120 households, yielded 43 non-Typhoidal Salmonella (NTS) isolates from 25 households (overall sample positivity 3.6%). In the 28 iNTS patients, disease was caused by 3 STs of Salmonella Typhimurium, mainly ST313. In contrast, the isolates from households spanned 15 sequence types (STs). Two S. Typhimurium isolates from index cases closely matched isolates from their respective asymptomatic household members (2 and 3 SNP differences respectively). Despite the recovery of a diverse range of NTS, there was no overlap between the STs causing iNTS disease with any environmental or animal isolates.
CONCLUSIONS
The finding of NTS strains from index cases that matched household members, coupled with lack of related animal or environmental isolates, supports a hypothesis of human to human transmission of iNTS infections in the household. The breadth of NTS strains found in animals and the household environment demonstrated the robustness of NTS sampling and culture methodology, and suggests a diverse ecology of Salmonella in this setting. Healthy typhoid (S. Typhi) carrier state was not detected. The lack of S. Typhi isolates from the household environment suggests that further methodological development is needed to culture S. Typhi from the environment.

Identifiants

pubmed: 36508466
doi: 10.1371/journal.pntd.0010982
pii: PNTD-D-22-00359
pmc: PMC9779717
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0010982

Subventions

Organisme : Wellcome Trust
ID : 206545/Z/17/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 106914/Z/15/Z
Pays : United Kingdom
Organisme : Department of Health
ID : NIHR300039
Pays : United Kingdom

Informations de copyright

Copyright: © 2022 Koolman 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.

Références

Clin Infect Dis. 2008 Apr 1;46(7):963-9
pubmed: 18444810
MMWR Morb Mortal Wkly Rep. 2019 Jan 18;68(2):44-45
pubmed: 30653487
Clin Infect Dis. 2021 Oct 5;73(7):e1570-e1578
pubmed: 32777036
PLoS Negl Trop Dis. 2020 Aug 3;14(8):e0008440
pubmed: 32745137
Lancet. 2012 Jun 30;379(9835):2489-2499
pubmed: 22587967
Bioinformatics. 2019 Nov 1;35(21):4453-4455
pubmed: 31070718
Hum Vaccin Immunother. 2020 Sep 1;16(9):2056-2071
pubmed: 32692622
PLoS Negl Trop Dis. 2020 Nov 24;14(11):e0008796
pubmed: 33232324
Trop Med Int Health. 2009 Dec;14(12):1467-74
pubmed: 19793081
Lancet Infect Dis. 2019 Dec;19(12):1312-1324
pubmed: 31562022
Clin Infect Dis. 2012 Apr;54(8):1091-9
pubmed: 22357703
Clin Microbiol Rev. 2015 Oct;28(4):901-37
pubmed: 26180063
Lancet Glob Health. 2021 Dec;9(12):e1688-e1696
pubmed: 34798028
PLoS Negl Trop Dis. 2017 Nov 27;11(11):e0006103
pubmed: 29176791
PLoS Negl Trop Dis. 2018 Jan 12;12(1):e0006156
pubmed: 29329299
Lancet Infect Dis. 2022 May;22(5):692-705
pubmed: 35114140
Int J Food Microbiol. 2020 Feb 16;315:108382
pubmed: 31710971
Sci Rep. 2021 Nov 3;11(1):21617
pubmed: 34732799
Genome Res. 2009 Dec;19(12):2279-87
pubmed: 19901036
J S Afr Vet Assoc. 2018 Nov 07;89(0):e1-e10
pubmed: 30456978
PLoS Negl Trop Dis. 2019 Oct 14;13(10):e0007782
pubmed: 31609964
Nat Genet. 2012 Nov;44(11):1215-21
pubmed: 23023330
PLoS Negl Trop Dis. 2017 Jan 5;11(1):e0005118
pubmed: 28056035
Lancet. 1990 Sep 1;336(8714):545-9
pubmed: 1975046
Lancet Glob Health. 2017 Mar;5(3):e310-e323
pubmed: 28193398
Nat Microbiol. 2021 Mar;6(3):327-338
pubmed: 33349664
Appl Environ Microbiol. 2013 Jul;79(13):4106-14
pubmed: 23624481
BMC Infect Dis. 2020 Jun 17;20(1):422
pubmed: 32552753
Genome Res. 2020 Jan;30(1):138-152
pubmed: 31809257
Clin Infect Dis. 2009 Aug 15;49(4):606-11
pubmed: 19591599
N Engl J Med. 2005 Jan 6;352(1):39-47
pubmed: 15635111
Nat Genet. 2016 Oct;48(10):1211-1217
pubmed: 27548315
Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S332-8
pubmed: 26449949
Genome Med. 2017 Oct 31;9(1):92
pubmed: 29084588
J Infect. 2001 Jan;42(1):44-9
pubmed: 11243753
Lancet Infect Dis. 2010 Jun;10(6):417-32
pubmed: 20510282
Clin Infect Dis. 2021 Aug 16;73(4):631-641
pubmed: 33493332
PLoS Negl Trop Dis. 2011;5(5):e1148
pubmed: 21655353
J Med Microbiol. 2006 May;55(Pt 5):585-591
pubmed: 16585646
Lancet Infect Dis. 2019 Apr;19(4):369-381
pubmed: 30792131
Clin Infect Dis. 2020 Mar 17;70(7):1278-1284
pubmed: 31144715
PLoS Genet. 2018 Apr 5;14(4):e1007261
pubmed: 29621240
Antimicrob Agents Chemother. 2019 Oct 22;63(11):
pubmed: 31427293
PLoS Negl Trop Dis. 2015 Apr 24;9(4):e0003748
pubmed: 25909750
J Clin Microbiol. 2015 Jan;53(1):262-72
pubmed: 25392358
Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S363-71
pubmed: 26449953
Medicine (Baltimore). 2017 Mar;96(13):e6448
pubmed: 28353576

Auteurs

Leonard Koolman (L)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Reenesh Prakash (R)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Yohane Diness (Y)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.

Chisomo Msefula (C)

Kamuzu University of Health Sciences, Blantyre, Malawi.

Tonney S Nyirenda (TS)

Kamuzu University of Health Sciences, Blantyre, Malawi.

Franziska Olgemoeller (F)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Paul Wigley (P)

Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Blanca Perez-Sepulveda (B)

Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Jay C D Hinton (JCD)

Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Siân V Owen (SV)

Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Nicholas A Feasey (NA)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Philip M Ashton (PM)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Melita A Gordon (MA)

Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Kamuzu University of Health Sciences, Blantyre, Malawi.

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