Distributional ecology of Andes hantavirus: a macroecological approach

Abstract Background Hantavirus pulmonary syndrome (HPS) is an infection endemic in Chile and Argentina, caused by Andes hantavirus (ANDV). The rodent Oligoryzomys longicaudatus is suggested as the main reservoir, although several other species of Sigmodontinae are known hosts of ANDV. Here, we explo...

Full description

Bibliographic Details
Main Authors: Francisca Astorga, Luis E. Escobar, Daniela Poo-Muñoz, Joaquin Escobar-Dodero, Sylvia Rojas-Hucks, Mario Alvarado-Rybak, Melanie Duclos, Daniel Romero-Alvarez, Blanca E. Molina-Burgos, Alexandra Peñafiel-Ricaurte, Frederick Toro, Francisco T. Peña-Gómez, A. Townsend Peterson
Format: Article
Language:English
Published: BMC 2018-06-01
Series:International Journal of Health Geographics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12942-018-0142-z
_version_ 1823960612823105536
author Francisca Astorga
Luis E. Escobar
Daniela Poo-Muñoz
Joaquin Escobar-Dodero
Sylvia Rojas-Hucks
Mario Alvarado-Rybak
Melanie Duclos
Daniel Romero-Alvarez
Blanca E. Molina-Burgos
Alexandra Peñafiel-Ricaurte
Frederick Toro
Francisco T. Peña-Gómez
A. Townsend Peterson
author_facet Francisca Astorga
Luis E. Escobar
Daniela Poo-Muñoz
Joaquin Escobar-Dodero
Sylvia Rojas-Hucks
Mario Alvarado-Rybak
Melanie Duclos
Daniel Romero-Alvarez
Blanca E. Molina-Burgos
Alexandra Peñafiel-Ricaurte
Frederick Toro
Francisco T. Peña-Gómez
A. Townsend Peterson
author_sort Francisca Astorga
collection DOAJ
description Abstract Background Hantavirus pulmonary syndrome (HPS) is an infection endemic in Chile and Argentina, caused by Andes hantavirus (ANDV). The rodent Oligoryzomys longicaudatus is suggested as the main reservoir, although several other species of Sigmodontinae are known hosts of ANDV. Here, we explore potential ANDV transmission risk to humans in southern South America, based on eco-epidemiological associations among: six rodent host species, seropositive rodents, and human HPS cases. Methods We used ecological niche modeling and macroecological approaches to determine potential geographic distributions and assess environmental similarity among rodents and human HPS cases. Results Highest numbers of rodent species (five) were in Chile between 35° and 41°S latitude. Background similarity tests showed niche similarity in 14 of the 56 possible comparisons: similarity between human HPS cases and the background of all species and seropositive rodents was supported (except for Abrothrix sanborni). Of interest among the results is the likely role of O. longicaudatus, Loxodontomys micropus, Abrothrix olivaceus, and Abrothrix longipilis in HPS transmission to humans. Conclusions Our results support a role of rodent species’ distributions as a risk factor for human HPS at coarse scales, and suggest that the role of the main reservoir (O. longicaudatus) may be supported by the broader rodent host community in some areas.
first_indexed 2024-12-17T16:52:06Z
format Article
id doaj.art-9d5ea8b92d4945a4b183588f69b084a6
institution Directory Open Access Journal
issn 1476-072X
language English
last_indexed 2024-12-17T16:52:06Z
publishDate 2018-06-01
publisher BMC
record_format Article
series International Journal of Health Geographics
spelling doaj.art-9d5ea8b92d4945a4b183588f69b084a62022-12-21T21:40:34ZengBMCInternational Journal of Health Geographics1476-072X2018-06-0117111210.1186/s12942-018-0142-zDistributional ecology of Andes hantavirus: a macroecological approachFrancisca Astorga0Luis E. Escobar1Daniela Poo-Muñoz2Joaquin Escobar-Dodero3Sylvia Rojas-Hucks4Mario Alvarado-Rybak5Melanie Duclos6Daniel Romero-Alvarez7Blanca E. Molina-Burgos8Alexandra Peñafiel-Ricaurte9Frederick Toro10Francisco T. Peña-Gómez11A. Townsend Peterson12Campus Huechuraba, Facultad de Ciencias, Universidad MayorDepartment of Fish and Wildlife Conservation, Virginia TechCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloDepartment of Ecology and Evolutionary Biology, Biodiversity Institute, University of KansasCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloCentro de Investigación para la Sustentabilidad y Programa de Doctorado en Medicina de la Conservación, Facultad de Ciencias de la Vida, Universidad Andres BelloDepartamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de ChileDepartment of Ecology and Evolutionary Biology, Biodiversity Institute, University of KansasAbstract Background Hantavirus pulmonary syndrome (HPS) is an infection endemic in Chile and Argentina, caused by Andes hantavirus (ANDV). The rodent Oligoryzomys longicaudatus is suggested as the main reservoir, although several other species of Sigmodontinae are known hosts of ANDV. Here, we explore potential ANDV transmission risk to humans in southern South America, based on eco-epidemiological associations among: six rodent host species, seropositive rodents, and human HPS cases. Methods We used ecological niche modeling and macroecological approaches to determine potential geographic distributions and assess environmental similarity among rodents and human HPS cases. Results Highest numbers of rodent species (five) were in Chile between 35° and 41°S latitude. Background similarity tests showed niche similarity in 14 of the 56 possible comparisons: similarity between human HPS cases and the background of all species and seropositive rodents was supported (except for Abrothrix sanborni). Of interest among the results is the likely role of O. longicaudatus, Loxodontomys micropus, Abrothrix olivaceus, and Abrothrix longipilis in HPS transmission to humans. Conclusions Our results support a role of rodent species’ distributions as a risk factor for human HPS at coarse scales, and suggest that the role of the main reservoir (O. longicaudatus) may be supported by the broader rodent host community in some areas.http://link.springer.com/article/10.1186/s12942-018-0142-zAndes hantavirusBunyaviridaeEcological niche modelingMaxentRodent reservoirsZoonoses
spellingShingle Francisca Astorga
Luis E. Escobar
Daniela Poo-Muñoz
Joaquin Escobar-Dodero
Sylvia Rojas-Hucks
Mario Alvarado-Rybak
Melanie Duclos
Daniel Romero-Alvarez
Blanca E. Molina-Burgos
Alexandra Peñafiel-Ricaurte
Frederick Toro
Francisco T. Peña-Gómez
A. Townsend Peterson
Distributional ecology of Andes hantavirus: a macroecological approach
International Journal of Health Geographics
Andes hantavirus
Bunyaviridae
Ecological niche modeling
Maxent
Rodent reservoirs
Zoonoses
title Distributional ecology of Andes hantavirus: a macroecological approach
title_full Distributional ecology of Andes hantavirus: a macroecological approach
title_fullStr Distributional ecology of Andes hantavirus: a macroecological approach
title_full_unstemmed Distributional ecology of Andes hantavirus: a macroecological approach
title_short Distributional ecology of Andes hantavirus: a macroecological approach
title_sort distributional ecology of andes hantavirus a macroecological approach
topic Andes hantavirus
Bunyaviridae
Ecological niche modeling
Maxent
Rodent reservoirs
Zoonoses
url http://link.springer.com/article/10.1186/s12942-018-0142-z
work_keys_str_mv AT franciscaastorga distributionalecologyofandeshantavirusamacroecologicalapproach
AT luiseescobar distributionalecologyofandeshantavirusamacroecologicalapproach
AT danielapoomunoz distributionalecologyofandeshantavirusamacroecologicalapproach
AT joaquinescobardodero distributionalecologyofandeshantavirusamacroecologicalapproach
AT sylviarojashucks distributionalecologyofandeshantavirusamacroecologicalapproach
AT marioalvaradorybak distributionalecologyofandeshantavirusamacroecologicalapproach
AT melanieduclos distributionalecologyofandeshantavirusamacroecologicalapproach
AT danielromeroalvarez distributionalecologyofandeshantavirusamacroecologicalapproach
AT blancaemolinaburgos distributionalecologyofandeshantavirusamacroecologicalapproach
AT alexandrapenafielricaurte distributionalecologyofandeshantavirusamacroecologicalapproach
AT fredericktoro distributionalecologyofandeshantavirusamacroecologicalapproach
AT franciscotpenagomez distributionalecologyofandeshantavirusamacroecologicalapproach
AT atownsendpeterson distributionalecologyofandeshantavirusamacroecologicalapproach