High genetic similarity between non-typhoidal Salmonella isolated from paired blood and stool samples of children in the Democratic Republic of the Congo.


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:
07 2020
Historique:
received: 27 01 2020
accepted: 08 05 2020
entrez: 3 7 2020
pubmed: 3 7 2020
medline: 21 8 2020
Statut: epublish

Résumé

Non-typhoidal Salmonella (NTS) serotypes Typhimurium and Enteritidis are a major cause of bloodstream infections in children in sub-Saharan Africa but their reservoir is unknown. We compared pairs of NTS blood and stool isolates (with the same NTS serotype recovered in the same patient) for genetic similarity. Between November 2013 and April 2017, hospital-admitted children (29 days to 14 years) with culture-confirmed NTS bloodstream infections were enrolled in a cross-sectional study at Kisantu Hospital, DR Congo. Stool cultures for Salmonella were performed on a subset of enrolled children, as well as on a control group of non-febrile hospital-admitted children. Pairs of blood and stool NTS isolates were assessed for genetic similarity by multiple-locus variable-number of tandem repeats (MLVA) and genomics analysis. A total of 299 children with NTS grown from blood cultures (Typhimurium 68.6%, Enteritidis 30.4%, other NTS 1.0%) had a stool sample processed; in 105 (35.1%) of them NTS was detected (Typhimurium 70.5%, Enteritidis 25.7%, other NTS 3.8%). A total of 87/105 (82.9%) pairs of blood and stool NTS isolates were observed (representing 29.1% of the 299 children). Among 1598 controls, the proportion of NTS stool excretion was 2.1% (p < 0.0001). MLVA types among paired isolates were identical in 82/87 (94.3%) pairs (27.4% of the 299 children; 61/66 (92.4%) in Typhimurium and 21/21 (100%) in Enteritidis pairs). Genomics analysis confirmed high genetic similarity within 41/43 (95.3%) pairs, showing a median SNP difference of 1 (range 0-77) and 1 (range 0-4) for Typhimurium and Enteritidis pairs respectively. Typhimurium and Enteritidis isolates belonged to sequence types ST313 lineage II and ST11 respectively. Nearly 30% of children with NTS bloodstream infection showed stool excretion of an NTS isolate with high genetic similarity, adding to the evidence of humans as a potential reservoir for NTS.

Sections du résumé

BACKGROUND
Non-typhoidal Salmonella (NTS) serotypes Typhimurium and Enteritidis are a major cause of bloodstream infections in children in sub-Saharan Africa but their reservoir is unknown. We compared pairs of NTS blood and stool isolates (with the same NTS serotype recovered in the same patient) for genetic similarity.
METHODS
Between November 2013 and April 2017, hospital-admitted children (29 days to 14 years) with culture-confirmed NTS bloodstream infections were enrolled in a cross-sectional study at Kisantu Hospital, DR Congo. Stool cultures for Salmonella were performed on a subset of enrolled children, as well as on a control group of non-febrile hospital-admitted children. Pairs of blood and stool NTS isolates were assessed for genetic similarity by multiple-locus variable-number of tandem repeats (MLVA) and genomics analysis.
RESULTS
A total of 299 children with NTS grown from blood cultures (Typhimurium 68.6%, Enteritidis 30.4%, other NTS 1.0%) had a stool sample processed; in 105 (35.1%) of them NTS was detected (Typhimurium 70.5%, Enteritidis 25.7%, other NTS 3.8%). A total of 87/105 (82.9%) pairs of blood and stool NTS isolates were observed (representing 29.1% of the 299 children). Among 1598 controls, the proportion of NTS stool excretion was 2.1% (p < 0.0001). MLVA types among paired isolates were identical in 82/87 (94.3%) pairs (27.4% of the 299 children; 61/66 (92.4%) in Typhimurium and 21/21 (100%) in Enteritidis pairs). Genomics analysis confirmed high genetic similarity within 41/43 (95.3%) pairs, showing a median SNP difference of 1 (range 0-77) and 1 (range 0-4) for Typhimurium and Enteritidis pairs respectively. Typhimurium and Enteritidis isolates belonged to sequence types ST313 lineage II and ST11 respectively.
CONCLUSION
Nearly 30% of children with NTS bloodstream infection showed stool excretion of an NTS isolate with high genetic similarity, adding to the evidence of humans as a potential reservoir for NTS.

Identifiants

pubmed: 32614856
doi: 10.1371/journal.pntd.0008377
pii: PNTD-D-20-00088
pmc: PMC7331982
doi:

Banques de données

figshare
['10.6084/m9.figshare.11611680']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0008377

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Rev Infect Dis. 1984 May-Jun;6(3):345-56
pubmed: 6377442
Genome Res. 2009 Dec;19(12):2279-87
pubmed: 19901036
Lancet. 2012 Jun 30;379(9835):2489-2499
pubmed: 22587967
Front Microbiol. 2014 Aug 04;5:391
pubmed: 25136336
PLoS One. 2013 Dec 31;8(12):e84055
pubmed: 24391880
PLoS Negl Trop Dis. 2012;6(11):e1921
pubmed: 23166855
Nat Genet. 2016 Oct;48(10):1211-1217
pubmed: 27548315
Clin Microbiol Rev. 2018 Nov 28;32(1):
pubmed: 30487167
Nucleic Acids Res. 2015 Feb 18;43(3):e15
pubmed: 25414349
Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S259-65
pubmed: 26449940
Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S346-53
pubmed: 26449951
Nucleic Acids Res. 2016 Jul 8;44(W1):W242-5
pubmed: 27095192
PLoS Negl Trop Dis. 2020 Feb 21;14(2):e0007875
pubmed: 32084128
PLoS Negl Trop Dis. 2013 Oct 10;7(10):e2487
pubmed: 24130915
J Transl Med. 2018 Aug 30;16(1):239
pubmed: 30165857
Nucleic Acids Res. 2011 Jul;39(Web Server issue):W347-52
pubmed: 21672955
PLoS Negl Trop Dis. 2015 Mar 24;9(3):e0003611
pubmed: 25803844
PLoS Negl Trop Dis. 2019 Oct 14;13(10):e0007782
pubmed: 31609964
PLoS One. 2015 Feb 18;10(2):e0117950
pubmed: 25693200
Bioinformatics. 2014 May 1;30(9):1312-3
pubmed: 24451623
Microb Genom. 2016 Apr 29;2(4):e000056
pubmed: 28348851
Clin Infect Dis. 2016 Mar 15;62 Suppl 1:S50-5
pubmed: 26933022
Nat Genet. 2012 Nov;44(11):1215-21
pubmed: 23023330
PLoS Negl Trop Dis. 2017 Jan 5;11(1):e0005118
pubmed: 28056035
Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S235-40
pubmed: 26449937
PLoS Negl Trop Dis. 2020 Apr 2;14(4):e0008121
pubmed: 32240161
Malar J. 2014 Oct 13;13:400
pubmed: 25311375
PLoS Negl Trop Dis. 2013;7(3):e2103
pubmed: 23516651
Nucleic Acids Res. 2016 Jul 8;44(W1):W16-21
pubmed: 27141966
Adv Exp Med Biol. 2013;764:13-26
pubmed: 23654054
Clin Infect Dis. 2017 Oct 1;65(7):1229-1231
pubmed: 29136410
J Med Microbiol. 2006 May;55(Pt 5):585-591
pubmed: 16585646
J Clin Microbiol. 2015 Nov;53(11):3507-14
pubmed: 26311853
Lancet Infect Dis. 2019 Dec;19(12):1312-1324
pubmed: 31562022
J Bacteriol. 2014 Aug 15;196(16):3036-44
pubmed: 24957617
Trans R Soc Trop Med Hyg. 2015 May;109(5):334-9
pubmed: 25758855
Clin Infect Dis. 2019 Mar 7;68(Suppl 2):S130-S137
pubmed: 30845337
Nat Commun. 2019 Sep 19;10(1):4280
pubmed: 31537784
Euro Surveill. 2011 Aug 11;16(32):
pubmed: 21871223
Bioinformatics. 2009 Aug 15;25(16):2078-9
pubmed: 19505943
Clin Infect Dis. 2015 Nov 1;61 Suppl 4:S266-71
pubmed: 26449941
Clin Microbiol Rev. 2015 Oct;28(4):901-37
pubmed: 26180063
Clin Infect Dis. 2016 Apr 1;62(7):879-886
pubmed: 26740515

Auteurs

Marie-France Phoba (MF)

Department of Microbiology, Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Department of Microbiology, University Hospital of Kinshasa, Democratic Republic of the Congo.

Barbara Barbé (B)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Benedikt Ley (B)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Sandra Van Puyvelde (S)

Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, United Kingdom.

Annelies Post (A)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Wesley Mattheus (W)

Department of Human Bacterial Diseases, Sciensano, Brussels, Belgium.

Stijn Deborggraeve (S)

Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Octavie Lunguya (O)

Department of Microbiology, Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Department of Microbiology, University Hospital of Kinshasa, Democratic Republic of the Congo.

Jan Jacobs (J)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH