Multifoci and multiserotypes circulation of dengue virus in Senegal between 2017 and 2018.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
24 Aug 2021
Historique:
received: 11 01 2021
accepted: 03 08 2021
entrez: 25 8 2021
pubmed: 26 8 2021
medline: 1 9 2021
Statut: epublish

Résumé

Dengue fever is a mosquito born disease associated with self-limited to life threatening illness. First detected in Senegal in the nineteenth century, and despite its growing incidence this last decade, significant knowledge gaps exist in our knowledge of genetic diversity of circulating strains. This study highlights the circulating serotypes and genotypes between January 2017 and December 2018 and their spatial and temporal distribution throughout all regions of Senegal. We used 56 dengue virus (DENV) strains for the analysis collected from 11 sampling areas: 39 from all regions of Senegal, and 17 isolates from Thiès, a particular area of the country. Two real time RT-qPCR systems were used to confirm dengue infection and corresponding serotypes. For molecular characterization, CprM gene was sequenced and submitted to phylogenetic analysis for serotypes and genotypes assignment. Three dengue virus serotypes (DENV-1-3) were detected by all used methods. DENV-3 was detected in 50% (28/56) of the isolates, followed by DENV-1 and DENV-2, each representing 25% (14/56) of the isolates. DENV-3 belongs to genotype III, DENV-1 to genotype V and DENV-2 to Cosmopolitan genotype. Serotype 3 was detected in 7 sampling locations and a co-circulation of different serotypes was observed in Thiès, Fatick and Richard-toll. These results emphasize the need of continuous DENV surveillance in Senegal to detect DENV cases, to define circulating serotypes/genotypes and to prevent the spread and the occurrence of severe cases.

Sections du résumé

BACKGROUND BACKGROUND
Dengue fever is a mosquito born disease associated with self-limited to life threatening illness. First detected in Senegal in the nineteenth century, and despite its growing incidence this last decade, significant knowledge gaps exist in our knowledge of genetic diversity of circulating strains. This study highlights the circulating serotypes and genotypes between January 2017 and December 2018 and their spatial and temporal distribution throughout all regions of Senegal.
METHODS METHODS
We used 56 dengue virus (DENV) strains for the analysis collected from 11 sampling areas: 39 from all regions of Senegal, and 17 isolates from Thiès, a particular area of the country. Two real time RT-qPCR systems were used to confirm dengue infection and corresponding serotypes. For molecular characterization, CprM gene was sequenced and submitted to phylogenetic analysis for serotypes and genotypes assignment.
RESULTS RESULTS
Three dengue virus serotypes (DENV-1-3) were detected by all used methods. DENV-3 was detected in 50% (28/56) of the isolates, followed by DENV-1 and DENV-2, each representing 25% (14/56) of the isolates. DENV-3 belongs to genotype III, DENV-1 to genotype V and DENV-2 to Cosmopolitan genotype. Serotype 3 was detected in 7 sampling locations and a co-circulation of different serotypes was observed in Thiès, Fatick and Richard-toll.
CONCLUSIONS CONCLUSIONS
These results emphasize the need of continuous DENV surveillance in Senegal to detect DENV cases, to define circulating serotypes/genotypes and to prevent the spread and the occurrence of severe cases.

Identifiants

pubmed: 34429064
doi: 10.1186/s12879-021-06580-z
pii: 10.1186/s12879-021-06580-z
pmc: PMC8383925
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

867

Informations de copyright

© 2021. The Author(s).

Références

Viruses. 2021 Jan 04;13(1):
pubmed: 33406660
J Clin Microbiol. 1992 Mar;30(3):545-51
pubmed: 1372617
BMC Infect Dis. 2020 Jul 2;20(1):466
pubmed: 32615988
Nucleic Acids Res. 2002 Jul 15;30(14):3059-66
pubmed: 12136088
Int J Infect Dis. 2020 Feb;91:129-136
pubmed: 31821892
Infect Genet Evol. 2003 May;3(1):19-28
pubmed: 12797969
Emerg Infect Dis. 2008 Aug;14(8):1326-7
pubmed: 18680674
PLoS Negl Trop Dis. 2010 Mar 02;4(3):e617
pubmed: 20209155
Lancet Infect Dis. 2016 Jun;16(6):712-723
pubmed: 26874619
Euro Surveill. 2010 Feb 18;15(7):
pubmed: 20184854
Paediatr Int Child Health. 2012 May;32 Suppl 1:18-21
pubmed: 22668445
J Trop Med. 2021 Mar 31;2021:8817987
pubmed: 33868410
J Mol Biol. 1990 Oct 5;215(3):403-10
pubmed: 2231712
J Clin Virol. 2010 Jul;48(3):187-92
pubmed: 20556888
Infect Genet Evol. 2019 Nov;75:103947
pubmed: 31276800
PeerJ. 2016 Aug 24;4:e2326
pubmed: 27635316
Emerg Infect Dis. 2011 Aug;17(8):1349-54
pubmed: 21801609
Epidemiol Infect. 2018 Dec;146(16):2049-2055
pubmed: 30196797
Emerg Infect Dis. 2014 Mar;20(3):456-9
pubmed: 24572297
Res Virol. 1992 Nov-Dec;143(6):417-22
pubmed: 1297177
Arch Virol. 2008;153(6):1175-9
pubmed: 18446424
PLoS One. 2013 Oct 21;8(10):e78030
pubmed: 24205075
Travel Med Infect Dis. 2019 Mar - Apr;28:107-108
pubmed: 30408524
Trans R Soc Trop Med Hyg. 2004 Sep;98(9):553-62
pubmed: 15251405
Nature. 2013 Apr 25;496(7446):504-7
pubmed: 23563266
PLoS One. 2019 Mar 25;14(3):e0214328
pubmed: 30908535
PLoS One. 2018 Feb 22;13(2):e0192672
pubmed: 29470509
PLoS Negl Trop Dis. 2019 Nov 15;13(11):e0007889
pubmed: 31730672
Emerg Infect Dis. 2004 Oct;10(10):1872-3
pubmed: 15504282
BMC Infect Dis. 2018 Aug 7;18(1):375
pubmed: 30086716
Lancet. 2015 Jan 31;385(9966):453-65
pubmed: 25230594
Infect Dis Poverty. 2016 Apr 05;5:23
pubmed: 27044528
Virol J. 2013 Oct 22;10:311
pubmed: 24148652
Annu Rev Microbiol. 1990;44:649-88
pubmed: 2174669
J Infect Public Health. 2013 Aug;6(4):302-6
pubmed: 23806706
J Travel Med. 2019 Oct 14;26(7):
pubmed: 30407572
Diagnostics (Basel). 2020 Jun 16;10(6):
pubmed: 32560073
Emerg Infect Dis. 2018 Aug;24(8):1544-1547
pubmed: 30015610
Viruses. 2020 Jul 30;12(8):
pubmed: 32751561
Front Microbiol. 2016 Jun 07;7:875
pubmed: 27375595
Emerg Infect Dis. 2018 Jan;24(1):170-172
pubmed: 29260685
J Clin Microbiol. 2006 Apr;44(4):1295-304
pubmed: 16597854
BMC Evol Biol. 2018 Apr 24;18(1):58
pubmed: 29699483
J Clin Virol. 2008 Feb;41(2):138-42
pubmed: 18006376
Sci Transl Med. 2011 Dec 21;3(114):114ra128
pubmed: 22190239
PLoS One. 2018 Oct 3;13(10):e0204143
pubmed: 30281633
Nat Microbiol. 2019 Sep;4(9):1508-1515
pubmed: 31182801
PLoS One. 2014 Mar 27;9(3):e93227
pubmed: 24675982
Science. 2015 Sep 18;349(6254):1338-43
pubmed: 26383952

Auteurs

Idrissa Dieng (I)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal. idrissa.DIENG@pasteur.sn.

Marie Henriette Dior Ndione (MHD)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Cheikh Fall (C)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Moussa Moïse Diagne (MM)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Mamadou Diop (M)

Epidemiology, Clinical Research and Data Science Unit, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Aboubacry Gaye (A)

Epidemiology, Clinical Research and Data Science Unit, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Mamadou Aliou Barry (MA)

Epidemiology, Clinical Research and Data Science Unit, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Boly Diop (B)

Prevention Department, Ministry of Health, Dakar, Senegal.

Mamadou Ndiaye (M)

Prevention Department, Ministry of Health, Dakar, Senegal.

Abdoulaye Bousso (A)

Prevention Department, Ministry of Health, Dakar, Senegal.

Gamou Fall (G)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Cheikh Loucoubar (C)

Epidemiology, Clinical Research and Data Science Unit, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Oumar Faye (O)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Amadou Alpha Sall (AA)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Ousmane Faye (O)

Arboviruses and Haemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, 220, Dakar, Senegal.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

[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

Classifications MeSH