Cargando…
Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019
BACKGROUND: The transmission patterns and genetic diversity of dengue virus (DENV) circulating in Africa remain poorly understood. Circulation of the DENV serotype 1 (DENV1) in Angola was detected in 2013, while DENV serotype 2 (DENV2) was detected in 2018. Here, we report results from molecular and...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166355/ https://www.ncbi.nlm.nih.gov/pubmed/35584153 http://dx.doi.org/10.1371/journal.pntd.0010255 |
_version_ | 1784720583990181888 |
---|---|
author | Neto, Zoraima Martinez, Pedro A. Hill, Sarah C. Jandondo, Domingos Thézé, Julien Mirandela, Marinela Aguiar, Renato Santana Xavier, Joilson dos Santos Sebastião, Cruz Cândido, Ana Luísa Micolo Vaz, Filipa Castro, Gisel Reyes Paixão, Joana Paula Loman, Nicholas J. Lemey, Philippe Pybus, Oliver G. Vasconcelos, Jocelyne Faria, Nuno Rodrigues de Morais, Joana |
author_facet | Neto, Zoraima Martinez, Pedro A. Hill, Sarah C. Jandondo, Domingos Thézé, Julien Mirandela, Marinela Aguiar, Renato Santana Xavier, Joilson dos Santos Sebastião, Cruz Cândido, Ana Luísa Micolo Vaz, Filipa Castro, Gisel Reyes Paixão, Joana Paula Loman, Nicholas J. Lemey, Philippe Pybus, Oliver G. Vasconcelos, Jocelyne Faria, Nuno Rodrigues de Morais, Joana |
author_sort | Neto, Zoraima |
collection | PubMed |
description | BACKGROUND: The transmission patterns and genetic diversity of dengue virus (DENV) circulating in Africa remain poorly understood. Circulation of the DENV serotype 1 (DENV1) in Angola was detected in 2013, while DENV serotype 2 (DENV2) was detected in 2018. Here, we report results from molecular and genomic investigations conducted at the Ministry of Health national reference laboratory (INIS) in Angola on suspected dengue cases detected between January 2017 and February 2019. METHODS: A total of 401 serum samples from dengue suspected cases were collected in 13 of the 18 provinces in Angola. Of those, 351 samples had complete data for demographic and epidemiological analysis, including age, gender, province, type of residence, clinical symptoms, as well as dates of onset of symptoms and sample collection. RNA was extracted from residual samples and tested for DENV-RNA using two distinct real time RT-PCR protocols. On-site whole genome nanopore sequencing was performed on RT-PCR+ samples. Bayesian coalescent models were used to estimate date and origin of outbreak emergence, as well as population growth rates. RESULTS: Molecular screening showed that 66 out of 351 (19%) suspected cases were DENV-RNA positive across 5 provinces in Angola. DENV RT-PCR+ cases were detected more frequently in urban sites compared to rural sites. Of the DENV RT-PCR+ cases most were collected within 6 days of symptom onset. 93% of infections were confirmed by serotype-specific RT-PCR as DENV2 and 1 case (1.4%) was confirmed as DENV1. Six CHIKV RT-PCR+ cases were also detected during the study period, including 1 co-infection of CHIKV with DENV1. Most cases (87%) were detected in Luanda during the rainy season between April and October. Symptoms associated with severe dengue were observed in 11 patients, including 2 with a fatal outcome. On-site nanopore genome sequencing followed by genetic analysis revealed an introduction of DENV2 Cosmopolitan genotype (also known as DENV2-II genotype) possibly from India in or around October 2015, at least 1 year before its detection in the country. Coalescent models suggest relatively moderately rapid epidemic growth rates and doubling times, and a moderate expansion of DENV2 in Angola during the studied period. CONCLUSION: This study describes genomic, epidemiological and demographic characteristic of predominately urban transmission of DENV2 in Angola. We also find co-circulation of DENV2 with DENV1 and CHIKV and report several RT-PCR confirmed severe dengue cases in the country. Increasing dengue awareness in healthcare professional, expanding the monitorization of arboviral epidemics across the country, identifying most common mosquito breeding sites in urban settings, implementing innovative vector control interventions and dengue vaccination campaigns could help to reduce vector presence and DENV transmission in Angola. |
format | Online Article Text |
id | pubmed-9166355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91663552022-06-05 Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 Neto, Zoraima Martinez, Pedro A. Hill, Sarah C. Jandondo, Domingos Thézé, Julien Mirandela, Marinela Aguiar, Renato Santana Xavier, Joilson dos Santos Sebastião, Cruz Cândido, Ana Luísa Micolo Vaz, Filipa Castro, Gisel Reyes Paixão, Joana Paula Loman, Nicholas J. Lemey, Philippe Pybus, Oliver G. Vasconcelos, Jocelyne Faria, Nuno Rodrigues de Morais, Joana PLoS Negl Trop Dis Research Article BACKGROUND: The transmission patterns and genetic diversity of dengue virus (DENV) circulating in Africa remain poorly understood. Circulation of the DENV serotype 1 (DENV1) in Angola was detected in 2013, while DENV serotype 2 (DENV2) was detected in 2018. Here, we report results from molecular and genomic investigations conducted at the Ministry of Health national reference laboratory (INIS) in Angola on suspected dengue cases detected between January 2017 and February 2019. METHODS: A total of 401 serum samples from dengue suspected cases were collected in 13 of the 18 provinces in Angola. Of those, 351 samples had complete data for demographic and epidemiological analysis, including age, gender, province, type of residence, clinical symptoms, as well as dates of onset of symptoms and sample collection. RNA was extracted from residual samples and tested for DENV-RNA using two distinct real time RT-PCR protocols. On-site whole genome nanopore sequencing was performed on RT-PCR+ samples. Bayesian coalescent models were used to estimate date and origin of outbreak emergence, as well as population growth rates. RESULTS: Molecular screening showed that 66 out of 351 (19%) suspected cases were DENV-RNA positive across 5 provinces in Angola. DENV RT-PCR+ cases were detected more frequently in urban sites compared to rural sites. Of the DENV RT-PCR+ cases most were collected within 6 days of symptom onset. 93% of infections were confirmed by serotype-specific RT-PCR as DENV2 and 1 case (1.4%) was confirmed as DENV1. Six CHIKV RT-PCR+ cases were also detected during the study period, including 1 co-infection of CHIKV with DENV1. Most cases (87%) were detected in Luanda during the rainy season between April and October. Symptoms associated with severe dengue were observed in 11 patients, including 2 with a fatal outcome. On-site nanopore genome sequencing followed by genetic analysis revealed an introduction of DENV2 Cosmopolitan genotype (also known as DENV2-II genotype) possibly from India in or around October 2015, at least 1 year before its detection in the country. Coalescent models suggest relatively moderately rapid epidemic growth rates and doubling times, and a moderate expansion of DENV2 in Angola during the studied period. CONCLUSION: This study describes genomic, epidemiological and demographic characteristic of predominately urban transmission of DENV2 in Angola. We also find co-circulation of DENV2 with DENV1 and CHIKV and report several RT-PCR confirmed severe dengue cases in the country. Increasing dengue awareness in healthcare professional, expanding the monitorization of arboviral epidemics across the country, identifying most common mosquito breeding sites in urban settings, implementing innovative vector control interventions and dengue vaccination campaigns could help to reduce vector presence and DENV transmission in Angola. Public Library of Science 2022-05-18 /pmc/articles/PMC9166355/ /pubmed/35584153 http://dx.doi.org/10.1371/journal.pntd.0010255 Text en © 2022 Neto et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Neto, Zoraima Martinez, Pedro A. Hill, Sarah C. Jandondo, Domingos Thézé, Julien Mirandela, Marinela Aguiar, Renato Santana Xavier, Joilson dos Santos Sebastião, Cruz Cândido, Ana Luísa Micolo Vaz, Filipa Castro, Gisel Reyes Paixão, Joana Paula Loman, Nicholas J. Lemey, Philippe Pybus, Oliver G. Vasconcelos, Jocelyne Faria, Nuno Rodrigues de Morais, Joana Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 |
title | Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 |
title_full | Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 |
title_fullStr | Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 |
title_full_unstemmed | Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 |
title_short | Molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in Angola, 2017–2019 |
title_sort | molecular and genomic investigation of an urban outbreak of dengue virus serotype 2 in angola, 2017–2019 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166355/ https://www.ncbi.nlm.nih.gov/pubmed/35584153 http://dx.doi.org/10.1371/journal.pntd.0010255 |
work_keys_str_mv | AT netozoraima molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT martinezpedroa molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT hillsarahc molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT jandondodomingos molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT thezejulien molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT mirandelamarinela molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT aguiarrenatosantana molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT xavierjoilson molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT dossantossebastiaocruz molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT candidoanaluisamicolo molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT vazfilipa molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT castrogiselreyes molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT paixaojoanapaula molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT lomannicholasj molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT lemeyphilippe molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT pybusoliverg molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT vasconcelosjocelyne molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT farianunorodrigues molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 AT demoraisjoana molecularandgenomicinvestigationofanurbanoutbreakofdenguevirusserotype2inangola20172019 |