Enterovirus 71 infection causes severe pulmonary lesions in gerbils, meriones unguiculatus, which can be prevented by passive immunization with specific antisera
Neurogenic pulmonary edema caused by severe brainstem encephalitis is the leading cause of death in young children infected by Enterovirus 71 (EV71). However, no pulmonary lesions have been found in EV71-infected transgenic or non-transgenic mouse models. Development of a suitable animal model is im...
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Veröffentlicht in: | PloS one 2015-03, Vol.10 (3), p.e0119173-e0119173 |
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creator | Xu, Fang Yao, Ping-Ping Xia, Yong Qian, Lei Yang, Zhang-Nv Xie, Rong-Hui Sun, Yi-Sheng Lu, Hang-Jing Miao, Zi-Ping Li, Chan Li, Xiao Liang, Wei-Feng Huang, Xiao-Xiao Xia, Shi-Chang Chen, Zhi-Ping Jiang, Jian-Min Zhang, Yan-Jun Mei, Ling-Ling Liu, She-Lan Gu, Hua Xu, Zhi-Yao Fu, Xiao-Fei Zhu, Zhi-Yong Zhu, Han-Ping |
description | Neurogenic pulmonary edema caused by severe brainstem encephalitis is the leading cause of death in young children infected by Enterovirus 71 (EV71). However, no pulmonary lesions have been found in EV71-infected transgenic or non-transgenic mouse models. Development of a suitable animal model is important for studying EV71 pathogenesis and assessing effect of therapeutic approaches. We had found neurological disorders in EV71-induced young gerbils previously. Here, we report severe pulmonary lesions characterized with pulmonary congestion and hemorrhage in a gerbil model for EV71 infection. In the EV71-infected gerbils, six 21-day-old or younger gerbils presented with a sudden onset of symptoms and rapid illness progression after inoculation with 1×105.5 TCID50 of EV71 via intraperitoneal (IP) or intramuscular (IM) route. Respiratory symptoms were observed along with interstitial pneumonia, pulmonary congestion and extensive lung hemorrhage could be detected in the lung tissues by histopathological examination. EV71 viral titer was found to be peak at late stages of infection. EV71-induced pulmonary lesions, together with severe neurological disorders were also observed in gerbils, accurately mimicking the disease process in EV71-infected patients. Passive transfer with immune sera from EV71 infected adult gerbils with a neutralizing antibody (GMT=89) prevented severe pulmonary lesion formation after lethal EV71 challenge. These results establish this gerbil model as a useful platform for studying the pathogenesis of EV71-induced pulmonary lesions, immunotherapy and antiviral drugs. |
doi_str_mv | 10.1371/journal.pone.0119173 |
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However, no pulmonary lesions have been found in EV71-infected transgenic or non-transgenic mouse models. Development of a suitable animal model is important for studying EV71 pathogenesis and assessing effect of therapeutic approaches. We had found neurological disorders in EV71-induced young gerbils previously. Here, we report severe pulmonary lesions characterized with pulmonary congestion and hemorrhage in a gerbil model for EV71 infection. In the EV71-infected gerbils, six 21-day-old or younger gerbils presented with a sudden onset of symptoms and rapid illness progression after inoculation with 1×105.5 TCID50 of EV71 via intraperitoneal (IP) or intramuscular (IM) route. Respiratory symptoms were observed along with interstitial pneumonia, pulmonary congestion and extensive lung hemorrhage could be detected in the lung tissues by histopathological examination. EV71 viral titer was found to be peak at late stages of infection. EV71-induced pulmonary lesions, together with severe neurological disorders were also observed in gerbils, accurately mimicking the disease process in EV71-infected patients. Passive transfer with immune sera from EV71 infected adult gerbils with a neutralizing antibody (GMT=89) prevented severe pulmonary lesion formation after lethal EV71 challenge. These results establish this gerbil model as a useful platform for studying the pathogenesis of EV71-induced pulmonary lesions, immunotherapy and antiviral drugs.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0119173</identifier><identifier>PMID: 25767882</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animal models ; Animals ; Antisera ; Antiviral agents ; Brain stem ; Child ; Children ; Congestion ; Development and progression ; Disease control ; Disease Models, Animal ; Disease prevention ; Disorders ; Drugs ; Edema ; Encephalitis ; Enterovirus ; Enterovirus A, Human - immunology ; Enterovirus Infections - immunology ; Enterovirus Infections - virology ; Epidemics ; Fever ; Genetic engineering ; Gerbillinae - immunology ; Gerbillinae - virology ; Hemorrhage ; Hospitals ; Humans ; Immune Sera - immunology ; Immune serum ; Immunization ; Immunization (passive) ; Immunization, Passive - methods ; Immunosuppressive agents ; Immunotherapy ; Infections ; Inoculation ; Lung - immunology ; Lung - virology ; Lung diseases ; Lung Diseases - immunology ; Lung Diseases - virology ; Lungs ; Meriones unguiculatus ; Mimicry ; Nervous system ; Nervous system diseases ; Nervous System Diseases - immunology ; Nervous System Diseases - virology ; Neurological diseases ; Pathogenesis ; Pediatrics ; Pulmonary lesions ; Tissues ; Transgenic mice</subject><ispartof>PloS one, 2015-03, Vol.10 (3), p.e0119173-e0119173</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Xu et al 2015 Xu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-8e1edc3ed4d1e841d2f8e94dd756c79f687cc4d6b6ce71a0b47bc446a98953553</citedby><cites>FETCH-LOGICAL-c692t-8e1edc3ed4d1e841d2f8e94dd756c79f687cc4d6b6ce71a0b47bc446a98953553</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/PMC4359154/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359154/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25767882$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Sun, Jie</contributor><creatorcontrib>Xu, Fang</creatorcontrib><creatorcontrib>Yao, Ping-Ping</creatorcontrib><creatorcontrib>Xia, Yong</creatorcontrib><creatorcontrib>Qian, Lei</creatorcontrib><creatorcontrib>Yang, Zhang-Nv</creatorcontrib><creatorcontrib>Xie, Rong-Hui</creatorcontrib><creatorcontrib>Sun, Yi-Sheng</creatorcontrib><creatorcontrib>Lu, Hang-Jing</creatorcontrib><creatorcontrib>Miao, Zi-Ping</creatorcontrib><creatorcontrib>Li, Chan</creatorcontrib><creatorcontrib>Li, Xiao</creatorcontrib><creatorcontrib>Liang, Wei-Feng</creatorcontrib><creatorcontrib>Huang, Xiao-Xiao</creatorcontrib><creatorcontrib>Xia, Shi-Chang</creatorcontrib><creatorcontrib>Chen, Zhi-Ping</creatorcontrib><creatorcontrib>Jiang, Jian-Min</creatorcontrib><creatorcontrib>Zhang, Yan-Jun</creatorcontrib><creatorcontrib>Mei, Ling-Ling</creatorcontrib><creatorcontrib>Liu, She-Lan</creatorcontrib><creatorcontrib>Gu, Hua</creatorcontrib><creatorcontrib>Xu, Zhi-Yao</creatorcontrib><creatorcontrib>Fu, Xiao-Fei</creatorcontrib><creatorcontrib>Zhu, Zhi-Yong</creatorcontrib><creatorcontrib>Zhu, Han-Ping</creatorcontrib><title>Enterovirus 71 infection causes severe pulmonary lesions in gerbils, meriones unguiculatus, which can be prevented by passive immunization with specific antisera</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Neurogenic pulmonary edema caused by severe brainstem encephalitis is the leading cause of death in young children infected by Enterovirus 71 (EV71). However, no pulmonary lesions have been found in EV71-infected transgenic or non-transgenic mouse models. Development of a suitable animal model is important for studying EV71 pathogenesis and assessing effect of therapeutic approaches. We had found neurological disorders in EV71-induced young gerbils previously. Here, we report severe pulmonary lesions characterized with pulmonary congestion and hemorrhage in a gerbil model for EV71 infection. In the EV71-infected gerbils, six 21-day-old or younger gerbils presented with a sudden onset of symptoms and rapid illness progression after inoculation with 1×105.5 TCID50 of EV71 via intraperitoneal (IP) or intramuscular (IM) route. Respiratory symptoms were observed along with interstitial pneumonia, pulmonary congestion and extensive lung hemorrhage could be detected in the lung tissues by histopathological examination. EV71 viral titer was found to be peak at late stages of infection. EV71-induced pulmonary lesions, together with severe neurological disorders were also observed in gerbils, accurately mimicking the disease process in EV71-infected patients. Passive transfer with immune sera from EV71 infected adult gerbils with a neutralizing antibody (GMT=89) prevented severe pulmonary lesion formation after lethal EV71 challenge. These results establish this gerbil model as a useful platform for studying the pathogenesis of EV71-induced pulmonary lesions, immunotherapy and antiviral drugs.</description><subject>Analysis</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antisera</subject><subject>Antiviral agents</subject><subject>Brain stem</subject><subject>Child</subject><subject>Children</subject><subject>Congestion</subject><subject>Development and progression</subject><subject>Disease control</subject><subject>Disease Models, Animal</subject><subject>Disease prevention</subject><subject>Disorders</subject><subject>Drugs</subject><subject>Edema</subject><subject>Encephalitis</subject><subject>Enterovirus</subject><subject>Enterovirus A, Human - immunology</subject><subject>Enterovirus Infections - immunology</subject><subject>Enterovirus Infections - virology</subject><subject>Epidemics</subject><subject>Fever</subject><subject>Genetic engineering</subject><subject>Gerbillinae - immunology</subject><subject>Gerbillinae - virology</subject><subject>Hemorrhage</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Immune Sera - immunology</subject><subject>Immune serum</subject><subject>Immunization</subject><subject>Immunization (passive)</subject><subject>Immunization, Passive - methods</subject><subject>Immunosuppressive agents</subject><subject>Immunotherapy</subject><subject>Infections</subject><subject>Inoculation</subject><subject>Lung - immunology</subject><subject>Lung - virology</subject><subject>Lung diseases</subject><subject>Lung Diseases - immunology</subject><subject>Lung Diseases - virology</subject><subject>Lungs</subject><subject>Meriones unguiculatus</subject><subject>Mimicry</subject><subject>Nervous system</subject><subject>Nervous system diseases</subject><subject>Nervous System Diseases - immunology</subject><subject>Nervous System Diseases - virology</subject><subject>Neurological diseases</subject><subject>Pathogenesis</subject><subject>Pediatrics</subject><subject>Pulmonary lesions</subject><subject>Tissues</subject><subject>Transgenic 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Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</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>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals (DOAJ)</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Fang</au><au>Yao, Ping-Ping</au><au>Xia, Yong</au><au>Qian, Lei</au><au>Yang, Zhang-Nv</au><au>Xie, Rong-Hui</au><au>Sun, Yi-Sheng</au><au>Lu, Hang-Jing</au><au>Miao, Zi-Ping</au><au>Li, Chan</au><au>Li, Xiao</au><au>Liang, Wei-Feng</au><au>Huang, Xiao-Xiao</au><au>Xia, Shi-Chang</au><au>Chen, Zhi-Ping</au><au>Jiang, Jian-Min</au><au>Zhang, Yan-Jun</au><au>Mei, Ling-Ling</au><au>Liu, She-Lan</au><au>Gu, Hua</au><au>Xu, Zhi-Yao</au><au>Fu, Xiao-Fei</au><au>Zhu, Zhi-Yong</au><au>Zhu, Han-Ping</au><au>Sun, Jie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enterovirus 71 infection causes severe pulmonary lesions in gerbils, meriones unguiculatus, which can be prevented by passive immunization with specific antisera</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-03-13</date><risdate>2015</risdate><volume>10</volume><issue>3</issue><spage>e0119173</spage><epage>e0119173</epage><pages>e0119173-e0119173</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Neurogenic pulmonary edema caused by severe brainstem encephalitis is the leading cause of death in young children infected by Enterovirus 71 (EV71). However, no pulmonary lesions have been found in EV71-infected transgenic or non-transgenic mouse models. Development of a suitable animal model is important for studying EV71 pathogenesis and assessing effect of therapeutic approaches. We had found neurological disorders in EV71-induced young gerbils previously. Here, we report severe pulmonary lesions characterized with pulmonary congestion and hemorrhage in a gerbil model for EV71 infection. In the EV71-infected gerbils, six 21-day-old or younger gerbils presented with a sudden onset of symptoms and rapid illness progression after inoculation with 1×105.5 TCID50 of EV71 via intraperitoneal (IP) or intramuscular (IM) route. Respiratory symptoms were observed along with interstitial pneumonia, pulmonary congestion and extensive lung hemorrhage could be detected in the lung tissues by histopathological examination. EV71 viral titer was found to be peak at late stages of infection. EV71-induced pulmonary lesions, together with severe neurological disorders were also observed in gerbils, accurately mimicking the disease process in EV71-infected patients. Passive transfer with immune sera from EV71 infected adult gerbils with a neutralizing antibody (GMT=89) prevented severe pulmonary lesion formation after lethal EV71 challenge. These results establish this gerbil model as a useful platform for studying the pathogenesis of EV71-induced pulmonary lesions, immunotherapy and antiviral drugs.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25767882</pmid><doi>10.1371/journal.pone.0119173</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2015-03, Vol.10 (3), p.e0119173-e0119173 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1663347049 |
source | Directory of Open Access Journals (DOAJ); MEDLINE; Free E-Journal (出版社公開部分のみ); PLoS_OA刊; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Analysis Animal models Animals Antisera Antiviral agents Brain stem Child Children Congestion Development and progression Disease control Disease Models, Animal Disease prevention Disorders Drugs Edema Encephalitis Enterovirus Enterovirus A, Human - immunology Enterovirus Infections - immunology Enterovirus Infections - virology Epidemics Fever Genetic engineering Gerbillinae - immunology Gerbillinae - virology Hemorrhage Hospitals Humans Immune Sera - immunology Immune serum Immunization Immunization (passive) Immunization, Passive - methods Immunosuppressive agents Immunotherapy Infections Inoculation Lung - immunology Lung - virology Lung diseases Lung Diseases - immunology Lung Diseases - virology Lungs Meriones unguiculatus Mimicry Nervous system Nervous system diseases Nervous System Diseases - immunology Nervous System Diseases - virology Neurological diseases Pathogenesis Pediatrics Pulmonary lesions Tissues Transgenic mice |
title | Enterovirus 71 infection causes severe pulmonary lesions in gerbils, meriones unguiculatus, which can be prevented by passive immunization with specific antisera |
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