Cargando…

Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness

Dengue virus (DENV) transmission from humans to mosquitoes is a poorly documented, but critical component of DENV epidemiology. Magnitude of viremia is the primary determinant of successful human-to-mosquito DENV transmission. People with the same level of viremia, however, can vary in their infecti...

Descripción completa

Detalles Bibliográficos
Autores principales: Lambrechts, Louis, Reiner, Robert C., Briesemeister, M. Veronica, Barrera, Patricia, Long, Kanya C., Elson, William H., Vizcarra, Alfonso, Astete, Helvio, Bazan, Isabel, Siles, Crystyan, Vilcarromero, Stalin, Leguia, Mariana, Kawiecki, Anna B., Perkins, T. Alex, Lloyd, Alun L., Waller, Lance A., Kitron, Uriel, Jenkins, Sarah A., Hontz, Robert D., Campbell, Wesley R., Carrington, Lauren B., Simmons, Cameron P., Ampuero, J. Sonia, Vasquez, Gisella, Elder, John P., Paz-Soldan, Valerie A., Vazquez-Prokopec, Gonzalo M., Rothman, Alan L., Barker, Christopher M., Scott, Thomas W., Morrison, Amy C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501553/
https://www.ncbi.nlm.nih.gov/pubmed/37656759
http://dx.doi.org/10.1371/journal.pntd.0011593
_version_ 1785106134472851456
author Lambrechts, Louis
Reiner, Robert C.
Briesemeister, M. Veronica
Barrera, Patricia
Long, Kanya C.
Elson, William H.
Vizcarra, Alfonso
Astete, Helvio
Bazan, Isabel
Siles, Crystyan
Vilcarromero, Stalin
Leguia, Mariana
Kawiecki, Anna B.
Perkins, T. Alex
Lloyd, Alun L.
Waller, Lance A.
Kitron, Uriel
Jenkins, Sarah A.
Hontz, Robert D.
Campbell, Wesley R.
Carrington, Lauren B.
Simmons, Cameron P.
Ampuero, J. Sonia
Vasquez, Gisella
Elder, John P.
Paz-Soldan, Valerie A.
Vazquez-Prokopec, Gonzalo M.
Rothman, Alan L.
Barker, Christopher M.
Scott, Thomas W.
Morrison, Amy C.
author_facet Lambrechts, Louis
Reiner, Robert C.
Briesemeister, M. Veronica
Barrera, Patricia
Long, Kanya C.
Elson, William H.
Vizcarra, Alfonso
Astete, Helvio
Bazan, Isabel
Siles, Crystyan
Vilcarromero, Stalin
Leguia, Mariana
Kawiecki, Anna B.
Perkins, T. Alex
Lloyd, Alun L.
Waller, Lance A.
Kitron, Uriel
Jenkins, Sarah A.
Hontz, Robert D.
Campbell, Wesley R.
Carrington, Lauren B.
Simmons, Cameron P.
Ampuero, J. Sonia
Vasquez, Gisella
Elder, John P.
Paz-Soldan, Valerie A.
Vazquez-Prokopec, Gonzalo M.
Rothman, Alan L.
Barker, Christopher M.
Scott, Thomas W.
Morrison, Amy C.
author_sort Lambrechts, Louis
collection PubMed
description Dengue virus (DENV) transmission from humans to mosquitoes is a poorly documented, but critical component of DENV epidemiology. Magnitude of viremia is the primary determinant of successful human-to-mosquito DENV transmission. People with the same level of viremia, however, can vary in their infectiousness to mosquitoes as a function of other factors that remain to be elucidated. Here, we report on a field-based study in the city of Iquitos, Peru, where we conducted direct mosquito feedings on people naturally infected with DENV and that experienced mild illness. We also enrolled people naturally infected with Zika virus (ZIKV) after the introduction of ZIKV in Iquitos during the study period. Of the 54 study participants involved in direct mosquito feedings, 43 were infected with DENV-2, two with DENV-3, and nine with ZIKV. Our analysis excluded participants whose viremia was detectable at enrollment but undetectable at the time of mosquito feeding, which was the case for all participants with DENV-3 and ZIKV infections. We analyzed the probability of onward transmission during 50 feeding events involving 27 participants infected with DENV-2 based on the presence of infectious virus in mosquito saliva 7–16 days post blood meal. Transmission probability was positively associated with the level of viremia and duration of extrinsic incubation in the mosquito. In addition, transmission probability was influenced by the day of illness in a non-monotonic fashion; i.e., transmission probability increased until 2 days after symptom onset and decreased thereafter. We conclude that mildly ill DENV-infected humans with similar levels of viremia during the first two days after symptom onset will be most infectious to mosquitoes on the second day of their illness. Quantifying variation within and between people in their contribution to DENV transmission is essential to better understand the biological determinants of human infectiousness, parametrize epidemiological models, and improve disease surveillance and prevention strategies.
format Online
Article
Text
id pubmed-10501553
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-105015532023-09-15 Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness Lambrechts, Louis Reiner, Robert C. Briesemeister, M. Veronica Barrera, Patricia Long, Kanya C. Elson, William H. Vizcarra, Alfonso Astete, Helvio Bazan, Isabel Siles, Crystyan Vilcarromero, Stalin Leguia, Mariana Kawiecki, Anna B. Perkins, T. Alex Lloyd, Alun L. Waller, Lance A. Kitron, Uriel Jenkins, Sarah A. Hontz, Robert D. Campbell, Wesley R. Carrington, Lauren B. Simmons, Cameron P. Ampuero, J. Sonia Vasquez, Gisella Elder, John P. Paz-Soldan, Valerie A. Vazquez-Prokopec, Gonzalo M. Rothman, Alan L. Barker, Christopher M. Scott, Thomas W. Morrison, Amy C. PLoS Negl Trop Dis Research Article Dengue virus (DENV) transmission from humans to mosquitoes is a poorly documented, but critical component of DENV epidemiology. Magnitude of viremia is the primary determinant of successful human-to-mosquito DENV transmission. People with the same level of viremia, however, can vary in their infectiousness to mosquitoes as a function of other factors that remain to be elucidated. Here, we report on a field-based study in the city of Iquitos, Peru, where we conducted direct mosquito feedings on people naturally infected with DENV and that experienced mild illness. We also enrolled people naturally infected with Zika virus (ZIKV) after the introduction of ZIKV in Iquitos during the study period. Of the 54 study participants involved in direct mosquito feedings, 43 were infected with DENV-2, two with DENV-3, and nine with ZIKV. Our analysis excluded participants whose viremia was detectable at enrollment but undetectable at the time of mosquito feeding, which was the case for all participants with DENV-3 and ZIKV infections. We analyzed the probability of onward transmission during 50 feeding events involving 27 participants infected with DENV-2 based on the presence of infectious virus in mosquito saliva 7–16 days post blood meal. Transmission probability was positively associated with the level of viremia and duration of extrinsic incubation in the mosquito. In addition, transmission probability was influenced by the day of illness in a non-monotonic fashion; i.e., transmission probability increased until 2 days after symptom onset and decreased thereafter. We conclude that mildly ill DENV-infected humans with similar levels of viremia during the first two days after symptom onset will be most infectious to mosquitoes on the second day of their illness. Quantifying variation within and between people in their contribution to DENV transmission is essential to better understand the biological determinants of human infectiousness, parametrize epidemiological models, and improve disease surveillance and prevention strategies. Public Library of Science 2023-09-01 /pmc/articles/PMC10501553/ /pubmed/37656759 http://dx.doi.org/10.1371/journal.pntd.0011593 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Lambrechts, Louis
Reiner, Robert C.
Briesemeister, M. Veronica
Barrera, Patricia
Long, Kanya C.
Elson, William H.
Vizcarra, Alfonso
Astete, Helvio
Bazan, Isabel
Siles, Crystyan
Vilcarromero, Stalin
Leguia, Mariana
Kawiecki, Anna B.
Perkins, T. Alex
Lloyd, Alun L.
Waller, Lance A.
Kitron, Uriel
Jenkins, Sarah A.
Hontz, Robert D.
Campbell, Wesley R.
Carrington, Lauren B.
Simmons, Cameron P.
Ampuero, J. Sonia
Vasquez, Gisella
Elder, John P.
Paz-Soldan, Valerie A.
Vazquez-Prokopec, Gonzalo M.
Rothman, Alan L.
Barker, Christopher M.
Scott, Thomas W.
Morrison, Amy C.
Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
title Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
title_full Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
title_fullStr Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
title_full_unstemmed Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
title_short Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
title_sort direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousness
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501553/
https://www.ncbi.nlm.nih.gov/pubmed/37656759
http://dx.doi.org/10.1371/journal.pntd.0011593
work_keys_str_mv AT lambrechtslouis directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT reinerrobertc directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT briesemeistermveronica directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT barrerapatricia directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT longkanyac directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT elsonwilliamh directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT vizcarraalfonso directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT astetehelvio directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT bazanisabel directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT silescrystyan directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT vilcarromerostalin directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT leguiamariana directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT kawieckiannab directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT perkinstalex directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT lloydalunl directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT wallerlancea directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT kitronuriel directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT jenkinssaraha directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT hontzrobertd directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT campbellwesleyr directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT carringtonlaurenb directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT simmonscameronp directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT ampuerojsonia directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT vasquezgisella directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT elderjohnp directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT pazsoldanvaleriea directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT vazquezprokopecgonzalom directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT rothmanalanl directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT barkerchristopherm directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT scottthomasw directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness
AT morrisonamyc directmosquitofeedingsondengue2virusinfectedpeoplerevealdynamicsofhumaninfectiousness