Burden of Chikungunya Virus Infection during an Outbreak in Myanmar.
Myanmar
chikungunya burden
molecular detection
seropositivity
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
14 08 2023
14 08 2023
Historique:
received:
08
06
2023
revised:
31
07
2023
accepted:
11
08
2023
medline:
28
8
2023
pubmed:
26
8
2023
entrez:
26
8
2023
Statut:
epublish
Résumé
Chikungunya virus (CHIKV) infection is a re-emerging arboviral disease with no approved vaccine, although numerous options are in development. Before vaccine implementation, disease burden, affected age group, and hospitalization rate information should be documented. In 2019, a sizeable outbreak of the East Central South African genotype of CHIKV occurred in Myanmar, and during this period, a cross-sectional study was conducted in two regions, Mandalay and Yangon, to examine the molecular and seropositivity rate of the CHIKV infection. The participants (1124) included dengue-suspected pediatric patients, blood donors, and healthy volunteers, who were assessed using molecular assays (quantitative real-time RT-PCR), serological tests (anti-CHIKV IgM capture and IgG indirect enzyme-linked immunosorbent assays), and neutralization tests. The tests confirmed the following positivity rates: 11.3% (127/1124) for the molecular assay, 12.4% (139/1124) for the anti-CHIKV IgM Ab, 44.5% (500/1124) for the anti-CHIKV IgG Ab, and 46.3% (520/1124) for the CHIKV neutralizing Ab. The highest rate for the molecular test occurred with the dengue-suspected pediatric patients. The seroprevalence rate through natural infection was higher in the healthy volunteers and blood donors than that in the pediatric patients. The results of this study will help stakeholders determine the criteria for choosing appropriate recipients when a CHIKV vaccine is introduced in Myanmar.
Identifiants
pubmed: 37632076
pii: v15081734
doi: 10.3390/v15081734
pmc: PMC10459206
pii:
doi:
Substances chimiques
Antibodies, Viral
0
Immunoglobulin M
0
Immunoglobulin G
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Références
Emerg Infect Dis. 2014 Aug;20(8):1378-81
pubmed: 25062511
PLoS One. 2018 Apr 30;13(4):e0196630
pubmed: 29709007
Arch Public Health. 2023 May 1;81(1):80
pubmed: 37127721
Emerg Microbes Infect. 2019;8(1):1490-1500
pubmed: 31631794
Emerg Infect Dis. 2020 Nov;26(11):2741-2745
pubmed: 33079056
J Infect Dis. 2016 Dec 15;214(suppl 5):S488-S496
pubmed: 27920179
Jpn J Infect Dis. 2012;65(3):215-21
pubmed: 22627302
Pathogens. 2022 Jun 27;11(7):
pubmed: 35889978
Vaccine. 2013 Apr 18;31 Suppl 2:B122-8
pubmed: 23598473
Emerg Infect Dis. 2018 Mar;24(3):558-561
pubmed: 29460745
Virol J. 2010 Jan 21;7:13
pubmed: 20092632
PLoS One. 2021 Mar 4;16(3):e0247255
pubmed: 33661951
Bull World Health Organ. 1970;42(2):297-303
pubmed: 5310141
PLoS One. 2017 Jun 29;12(6):e0180560
pubmed: 28662144
PLoS One. 2007 Nov 14;2(11):e1168
pubmed: 18000540
Curr Infect Dis Rep. 2022;24(12):217-228
pubmed: 36415286
Southeast Asian J Trop Med Public Health. 1975 Jun;6(2):276-83
pubmed: 126493
PLoS One. 2017 Feb 9;12(2):e0171989
pubmed: 28182795
PLoS One. 2017 Dec 28;12(12):e0189879
pubmed: 29284012
Epidemiol Infect. 2016 Aug;144(11):2268-75
pubmed: 27018566
Arch Virol. 2021 Jul;166(7):1913-1920
pubmed: 33907861
New Microbes New Infect. 2015 Apr 15;7:23-5
pubmed: 26106482
Trans R Soc Trop Med Hyg. 1973;67(5):702-9
pubmed: 4779116
J Clin Microbiol. 2020 Nov 18;58(12):
pubmed: 32938736
Emerg Infect Dis. 2019 Aug;25(8):1535-1538
pubmed: 31310218
PLoS Negl Trop Dis. 2021 Dec 1;15(12):e0009961
pubmed: 34851949
Am J Trop Med Hyg. 2015 Oct;93(4):697-700
pubmed: 26195462
Virusdisease. 2019 Sep;30(3):469-473
pubmed: 31803816
Rev Med Virol. 2018 May;28(3):e1978
pubmed: 29671914
J Clin Virol. 2016 May;78:57-61
pubmed: 26991052
Rev Soc Bras Med Trop. 2021 Apr 12;54:e0855
pubmed: 33886823
Microbes Infect. 2023 Jul-Aug;25(6):105129
pubmed: 37030472