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
Hauptverfasser: 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
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container_volume 10
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. 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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><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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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>
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1932-6203
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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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