Epidemiology of Emergent Madariaga Encephalitis in a Region with Endemic Venezuelan Equine Encephalitis: Initial Host Studies and Human Cross-Sectional Study in Darien, Panama
Neurotropic arboviral infections are an important cause of encephalitis. A zoonotic, vector-borne alphavirus, Madariaga virus (MADV; formerly known as South American eastern equine encephalitis virus), caused its first documented human outbreak in 2010 in Darien, Panama, where the genetically simila...
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creator | Vittor, Amy Y Armien, Blas Gonzalez, Publio Carrera, Jean-Paul Dominguez, Claudia Valderrama, Anayansi Glass, Greg E Beltran, Davis Cisneros, Julio Wang, Eryu Castillo, Alex Moreno, Brechla Weaver, Scott C |
description | Neurotropic arboviral infections are an important cause of encephalitis. A zoonotic, vector-borne alphavirus, Madariaga virus (MADV; formerly known as South American eastern equine encephalitis virus), caused its first documented human outbreak in 2010 in Darien, Panama, where the genetically similar Venezuelan equine encephalitis virus (VEEV) is endemic. We report the results of a seroprevalence survey of animals and humans, illustrating contrasting features of MADV and VEEV ecology and epidemiology.
Small mammals were trapped in 42 sites in Darien, Panama, using Sherman traps, Tomahawk traps, and mist nets for bats. Blood was tested for the presence of neutralizing antibodies to MADV and VEEV. In addition, bird sera collected in 2007 in Chagres, Panama, were tested for MADV and VEEV neutralizing antibodies. Viremia was ascertained by RT-PCR. Human exposure to these two viruses was determined by IgG ELISA, followed by plaque reduction neutralization tests. To identify relevant risk factors for MADV or VEEV exposure, logistic regression analysis was performed, and the most parsimonious model was selected based on the Akaike information criterion.
The animal survey yielded 32 bats (16 species), 556 rodents (12 species), and 20 opossums (4 species). The short-tailed cane mouse (Zygodontomys brevicauda) found abundantly in pasture and farms, had the highest MADV seroprevalence (8.3%). For VEEV, the shrub and forest-dwelling long-whiskered rice rat (Transandinomys bolivaris) had the highest seroprevalence (19.0%). Viremia was detected in one animal (Z. brevicauda). Of the 159 bird sera (50 species) tested, none were positive for either virus. In humans (n = 770), neutralizing antibodies to MADV and VEEV were present in 4.8% and 31.5%, respectively. MADV seropositivity was positively associated with cattle ranching, farming, and fishing. Having VEEV antibodies and shrubs near the house diminished risk. Age, forest work, farming and fishing were risk factors for VEEV, while having MADV antibodies, glazed windows, waste pick-up and piped water were protective.
Our findings suggest that the short-tailed cane mouse and the long-whiskered rice rat serve as hosts for MADV and VEEV, respectively. The preferred habitat of these rodent species coincides with areas associated with human infection risk. Our findings also indicate that MADV emerged recently in humans, and that the transmission cycles of these two sympatric alphaviruses differ spatially and in host utilizat |
doi_str_mv | 10.1371/journal.pntd.0004554 |
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Small mammals were trapped in 42 sites in Darien, Panama, using Sherman traps, Tomahawk traps, and mist nets for bats. Blood was tested for the presence of neutralizing antibodies to MADV and VEEV. In addition, bird sera collected in 2007 in Chagres, Panama, were tested for MADV and VEEV neutralizing antibodies. Viremia was ascertained by RT-PCR. Human exposure to these two viruses was determined by IgG ELISA, followed by plaque reduction neutralization tests. To identify relevant risk factors for MADV or VEEV exposure, logistic regression analysis was performed, and the most parsimonious model was selected based on the Akaike information criterion.
The animal survey yielded 32 bats (16 species), 556 rodents (12 species), and 20 opossums (4 species). The short-tailed cane mouse (Zygodontomys brevicauda) found abundantly in pasture and farms, had the highest MADV seroprevalence (8.3%). For VEEV, the shrub and forest-dwelling long-whiskered rice rat (Transandinomys bolivaris) had the highest seroprevalence (19.0%). Viremia was detected in one animal (Z. brevicauda). Of the 159 bird sera (50 species) tested, none were positive for either virus. In humans (n = 770), neutralizing antibodies to MADV and VEEV were present in 4.8% and 31.5%, respectively. MADV seropositivity was positively associated with cattle ranching, farming, and fishing. Having VEEV antibodies and shrubs near the house diminished risk. Age, forest work, farming and fishing were risk factors for VEEV, while having MADV antibodies, glazed windows, waste pick-up and piped water were protective.
Our findings suggest that the short-tailed cane mouse and the long-whiskered rice rat serve as hosts for MADV and VEEV, respectively. The preferred habitat of these rodent species coincides with areas associated with human infection risk. Our findings also indicate that MADV emerged recently in humans, and that the transmission cycles of these two sympatric alphaviruses differ spatially and in host utilization.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0004554</identifier><identifier>PMID: 27101567</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alphavirus - immunology ; Alphavirus - isolation & purification ; Alphavirus Infections - epidemiology ; Alphavirus Infections - virology ; Animal carriers of disease ; Animals ; Antibodies, Neutralizing - blood ; Antibodies, Viral - blood ; Biology and Life Sciences ; Birds ; Cross-Sectional Studies ; Disease ; Disease Reservoirs ; Encephalitis ; Encephalitis, Viral - epidemiology ; Encephalitis, Viral - veterinary ; Encephalitis, Viral - virology ; Enzyme-Linked Immunosorbent Assay ; Epidemics ; Epidemiology ; Equine encephalomyelitis ; Farms ; Field study ; Fishing ; Health risks ; Humans ; Immunoglobulin G - blood ; Immunoglobulins ; Infections ; Mammals ; Medical research ; Medicine and Health Sciences ; Mice ; Mist ; Mosquitoes ; Natural history ; Neutralization ; Neutralization Tests ; Panama - epidemiology ; Pasture ; Regression analysis ; Research and Analysis Methods ; Reverse Transcriptase Polymerase Chain Reaction ; Risk factors ; RNA viruses ; RNA, Viral - blood ; Rodents ; Seroepidemiologic Studies ; Tropical diseases ; Venezuelan equine encephalitis virus ; Viral encephalitis ; Viral Plaque Assay ; Viremia - diagnosis ; Viruses ; Zoonoses ; Zoonoses - epidemiology ; Zoonoses - virology</subject><ispartof>PLoS neglected tropical diseases, 2016-04, Vol.10 (4), p.e0004554-e0004554</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Vittor AY, Armien B, Gonzalez P, Carrera J-P, Dominguez C, Valderrama A, et al. (2016) Epidemiology of Emergent Madariaga Encephalitis in a Region with Endemic Venezuelan Equine Encephalitis: Initial Host Studies and Human Cross-Sectional Study in Darien, Panama. PLoS Negl Trop Dis 10(4): e0004554. doi:10.1371/journal.pntd.0004554</rights><rights>2016 Vittor et al 2016 Vittor et al</rights><rights>2016 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Vittor AY, Armien B, Gonzalez P, Carrera J-P, Dominguez C, Valderrama A, et al. (2016) Epidemiology of Emergent Madariaga Encephalitis in a Region with Endemic Venezuelan Equine Encephalitis: Initial Host Studies and Human Cross-Sectional Study in Darien, Panama. PLoS Negl Trop Dis 10(4): e0004554. doi:10.1371/journal.pntd.0004554</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c657t-45e37d3b6d7c2f366e5e37ab4e12cb3114b76d5963ec555d08ba982ca8ff8fbb3</citedby><cites>FETCH-LOGICAL-c657t-45e37d3b6d7c2f366e5e37ab4e12cb3114b76d5963ec555d08ba982ca8ff8fbb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839771/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839771/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23847,27903,27904,53768,53770,79345,79346</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27101567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Armstrong, Philip M.</contributor><creatorcontrib>Vittor, Amy Y</creatorcontrib><creatorcontrib>Armien, Blas</creatorcontrib><creatorcontrib>Gonzalez, Publio</creatorcontrib><creatorcontrib>Carrera, Jean-Paul</creatorcontrib><creatorcontrib>Dominguez, Claudia</creatorcontrib><creatorcontrib>Valderrama, Anayansi</creatorcontrib><creatorcontrib>Glass, Greg E</creatorcontrib><creatorcontrib>Beltran, Davis</creatorcontrib><creatorcontrib>Cisneros, Julio</creatorcontrib><creatorcontrib>Wang, Eryu</creatorcontrib><creatorcontrib>Castillo, Alex</creatorcontrib><creatorcontrib>Moreno, Brechla</creatorcontrib><creatorcontrib>Weaver, Scott C</creatorcontrib><title>Epidemiology of Emergent Madariaga Encephalitis in a Region with Endemic Venezuelan Equine Encephalitis: Initial Host Studies and Human Cross-Sectional Study in Darien, Panama</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Neurotropic arboviral infections are an important cause of encephalitis. A zoonotic, vector-borne alphavirus, Madariaga virus (MADV; formerly known as South American eastern equine encephalitis virus), caused its first documented human outbreak in 2010 in Darien, Panama, where the genetically similar Venezuelan equine encephalitis virus (VEEV) is endemic. We report the results of a seroprevalence survey of animals and humans, illustrating contrasting features of MADV and VEEV ecology and epidemiology.
Small mammals were trapped in 42 sites in Darien, Panama, using Sherman traps, Tomahawk traps, and mist nets for bats. Blood was tested for the presence of neutralizing antibodies to MADV and VEEV. In addition, bird sera collected in 2007 in Chagres, Panama, were tested for MADV and VEEV neutralizing antibodies. Viremia was ascertained by RT-PCR. Human exposure to these two viruses was determined by IgG ELISA, followed by plaque reduction neutralization tests. To identify relevant risk factors for MADV or VEEV exposure, logistic regression analysis was performed, and the most parsimonious model was selected based on the Akaike information criterion.
The animal survey yielded 32 bats (16 species), 556 rodents (12 species), and 20 opossums (4 species). The short-tailed cane mouse (Zygodontomys brevicauda) found abundantly in pasture and farms, had the highest MADV seroprevalence (8.3%). For VEEV, the shrub and forest-dwelling long-whiskered rice rat (Transandinomys bolivaris) had the highest seroprevalence (19.0%). Viremia was detected in one animal (Z. brevicauda). Of the 159 bird sera (50 species) tested, none were positive for either virus. In humans (n = 770), neutralizing antibodies to MADV and VEEV were present in 4.8% and 31.5%, respectively. MADV seropositivity was positively associated with cattle ranching, farming, and fishing. Having VEEV antibodies and shrubs near the house diminished risk. Age, forest work, farming and fishing were risk factors for VEEV, while having MADV antibodies, glazed windows, waste pick-up and piped water were protective.
Our findings suggest that the short-tailed cane mouse and the long-whiskered rice rat serve as hosts for MADV and VEEV, respectively. The preferred habitat of these rodent species coincides with areas associated with human infection risk. Our findings also indicate that MADV emerged recently in humans, and that the transmission cycles of these two sympatric alphaviruses differ spatially and in host utilization.</description><subject>Alphavirus - immunology</subject><subject>Alphavirus - isolation & purification</subject><subject>Alphavirus Infections - epidemiology</subject><subject>Alphavirus Infections - virology</subject><subject>Animal carriers of disease</subject><subject>Animals</subject><subject>Antibodies, Neutralizing - blood</subject><subject>Antibodies, Viral - blood</subject><subject>Biology and Life Sciences</subject><subject>Birds</subject><subject>Cross-Sectional Studies</subject><subject>Disease</subject><subject>Disease Reservoirs</subject><subject>Encephalitis</subject><subject>Encephalitis, Viral - epidemiology</subject><subject>Encephalitis, Viral - veterinary</subject><subject>Encephalitis, Viral - virology</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Epidemics</subject><subject>Epidemiology</subject><subject>Equine encephalomyelitis</subject><subject>Farms</subject><subject>Field study</subject><subject>Fishing</subject><subject>Health risks</subject><subject>Humans</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulins</subject><subject>Infections</subject><subject>Mammals</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Mist</subject><subject>Mosquitoes</subject><subject>Natural history</subject><subject>Neutralization</subject><subject>Neutralization Tests</subject><subject>Panama - epidemiology</subject><subject>Pasture</subject><subject>Regression analysis</subject><subject>Research and Analysis Methods</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Risk factors</subject><subject>RNA viruses</subject><subject>RNA, Viral - blood</subject><subject>Rodents</subject><subject>Seroepidemiologic Studies</subject><subject>Tropical diseases</subject><subject>Venezuelan equine encephalitis virus</subject><subject>Viral encephalitis</subject><subject>Viral Plaque Assay</subject><subject>Viremia - diagnosis</subject><subject>Viruses</subject><subject>Zoonoses</subject><subject>Zoonoses - 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immunology</topic><topic>Alphavirus - isolation & purification</topic><topic>Alphavirus Infections - epidemiology</topic><topic>Alphavirus Infections - virology</topic><topic>Animal carriers of disease</topic><topic>Animals</topic><topic>Antibodies, Neutralizing - blood</topic><topic>Antibodies, Viral - blood</topic><topic>Biology and Life Sciences</topic><topic>Birds</topic><topic>Cross-Sectional Studies</topic><topic>Disease</topic><topic>Disease Reservoirs</topic><topic>Encephalitis</topic><topic>Encephalitis, Viral - epidemiology</topic><topic>Encephalitis, Viral - veterinary</topic><topic>Encephalitis, Viral - virology</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Epidemics</topic><topic>Epidemiology</topic><topic>Equine encephalomyelitis</topic><topic>Farms</topic><topic>Field study</topic><topic>Fishing</topic><topic>Health risks</topic><topic>Humans</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulins</topic><topic>Infections</topic><topic>Mammals</topic><topic>Medical research</topic><topic>Medicine and Health Sciences</topic><topic>Mice</topic><topic>Mist</topic><topic>Mosquitoes</topic><topic>Natural history</topic><topic>Neutralization</topic><topic>Neutralization Tests</topic><topic>Panama - epidemiology</topic><topic>Pasture</topic><topic>Regression analysis</topic><topic>Research and Analysis Methods</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Risk factors</topic><topic>RNA viruses</topic><topic>RNA, Viral - blood</topic><topic>Rodents</topic><topic>Seroepidemiologic Studies</topic><topic>Tropical diseases</topic><topic>Venezuelan equine encephalitis virus</topic><topic>Viral encephalitis</topic><topic>Viral Plaque Assay</topic><topic>Viremia - diagnosis</topic><topic>Viruses</topic><topic>Zoonoses</topic><topic>Zoonoses - epidemiology</topic><topic>Zoonoses - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vittor, Amy Y</creatorcontrib><creatorcontrib>Armien, Blas</creatorcontrib><creatorcontrib>Gonzalez, Publio</creatorcontrib><creatorcontrib>Carrera, Jean-Paul</creatorcontrib><creatorcontrib>Dominguez, Claudia</creatorcontrib><creatorcontrib>Valderrama, Anayansi</creatorcontrib><creatorcontrib>Glass, Greg E</creatorcontrib><creatorcontrib>Beltran, Davis</creatorcontrib><creatorcontrib>Cisneros, Julio</creatorcontrib><creatorcontrib>Wang, Eryu</creatorcontrib><creatorcontrib>Castillo, Alex</creatorcontrib><creatorcontrib>Moreno, Brechla</creatorcontrib><creatorcontrib>Weaver, Scott C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>Oceanic Abstracts</collection><collection>Safety Science and Risk</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vittor, Amy Y</au><au>Armien, Blas</au><au>Gonzalez, Publio</au><au>Carrera, Jean-Paul</au><au>Dominguez, Claudia</au><au>Valderrama, Anayansi</au><au>Glass, Greg E</au><au>Beltran, Davis</au><au>Cisneros, Julio</au><au>Wang, Eryu</au><au>Castillo, Alex</au><au>Moreno, Brechla</au><au>Weaver, Scott C</au><au>Armstrong, Philip M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidemiology of Emergent Madariaga Encephalitis in a Region with Endemic Venezuelan Equine Encephalitis: Initial Host Studies and Human Cross-Sectional Study in Darien, Panama</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2016-04-21</date><risdate>2016</risdate><volume>10</volume><issue>4</issue><spage>e0004554</spage><epage>e0004554</epage><pages>e0004554-e0004554</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Neurotropic arboviral infections are an important cause of encephalitis. A zoonotic, vector-borne alphavirus, Madariaga virus (MADV; formerly known as South American eastern equine encephalitis virus), caused its first documented human outbreak in 2010 in Darien, Panama, where the genetically similar Venezuelan equine encephalitis virus (VEEV) is endemic. We report the results of a seroprevalence survey of animals and humans, illustrating contrasting features of MADV and VEEV ecology and epidemiology.
Small mammals were trapped in 42 sites in Darien, Panama, using Sherman traps, Tomahawk traps, and mist nets for bats. Blood was tested for the presence of neutralizing antibodies to MADV and VEEV. In addition, bird sera collected in 2007 in Chagres, Panama, were tested for MADV and VEEV neutralizing antibodies. Viremia was ascertained by RT-PCR. Human exposure to these two viruses was determined by IgG ELISA, followed by plaque reduction neutralization tests. To identify relevant risk factors for MADV or VEEV exposure, logistic regression analysis was performed, and the most parsimonious model was selected based on the Akaike information criterion.
The animal survey yielded 32 bats (16 species), 556 rodents (12 species), and 20 opossums (4 species). The short-tailed cane mouse (Zygodontomys brevicauda) found abundantly in pasture and farms, had the highest MADV seroprevalence (8.3%). For VEEV, the shrub and forest-dwelling long-whiskered rice rat (Transandinomys bolivaris) had the highest seroprevalence (19.0%). Viremia was detected in one animal (Z. brevicauda). Of the 159 bird sera (50 species) tested, none were positive for either virus. In humans (n = 770), neutralizing antibodies to MADV and VEEV were present in 4.8% and 31.5%, respectively. MADV seropositivity was positively associated with cattle ranching, farming, and fishing. Having VEEV antibodies and shrubs near the house diminished risk. Age, forest work, farming and fishing were risk factors for VEEV, while having MADV antibodies, glazed windows, waste pick-up and piped water were protective.
Our findings suggest that the short-tailed cane mouse and the long-whiskered rice rat serve as hosts for MADV and VEEV, respectively. The preferred habitat of these rodent species coincides with areas associated with human infection risk. Our findings also indicate that MADV emerged recently in humans, and that the transmission cycles of these two sympatric alphaviruses differ spatially and in host utilization.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27101567</pmid><doi>10.1371/journal.pntd.0004554</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1935-2735 |
ispartof | PLoS neglected tropical diseases, 2016-04, Vol.10 (4), p.e0004554-e0004554 |
issn | 1935-2735 1935-2727 1935-2735 |
language | eng |
recordid | cdi_plos_journals_1789545812 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access; Public Library of Science (PLoS) |
subjects | Alphavirus - immunology Alphavirus - isolation & purification Alphavirus Infections - epidemiology Alphavirus Infections - virology Animal carriers of disease Animals Antibodies, Neutralizing - blood Antibodies, Viral - blood Biology and Life Sciences Birds Cross-Sectional Studies Disease Disease Reservoirs Encephalitis Encephalitis, Viral - epidemiology Encephalitis, Viral - veterinary Encephalitis, Viral - virology Enzyme-Linked Immunosorbent Assay Epidemics Epidemiology Equine encephalomyelitis Farms Field study Fishing Health risks Humans Immunoglobulin G - blood Immunoglobulins Infections Mammals Medical research Medicine and Health Sciences Mice Mist Mosquitoes Natural history Neutralization Neutralization Tests Panama - epidemiology Pasture Regression analysis Research and Analysis Methods Reverse Transcriptase Polymerase Chain Reaction Risk factors RNA viruses RNA, Viral - blood Rodents Seroepidemiologic Studies Tropical diseases Venezuelan equine encephalitis virus Viral encephalitis Viral Plaque Assay Viremia - diagnosis Viruses Zoonoses Zoonoses - epidemiology Zoonoses - virology |
title | Epidemiology of Emergent Madariaga Encephalitis in a Region with Endemic Venezuelan Equine Encephalitis: Initial Host Studies and Human Cross-Sectional Study in Darien, Panama |
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