The Pathogenesis of 3 Neurotropic Flaviviruses in a Mouse Model Depends on the Route of Neuroinvasion After Viremia
Neurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from viremia to central nervous system (CNS) invasion are uncertain. Here, we intravenously infected BALB/c mice with 3 neurotropic flaviviruses, t...
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Published in | Journal of neuropathology and experimental neurology Vol. 74; no. 3; pp. 250 - 260 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
American Association of Neuropathologists, Inc
01.03.2015
by American Association of Neuropathologists, Inc |
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Abstract | Neurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from viremia to central nervous system (CNS) invasion are uncertain. Here, we intravenously infected BALB/c mice with 3 neurotropic flaviviruses, then examined the clinical manifestations and histopathologic changes. The Sofjin strain of tick-borne encephalitis virus–infected mice exhibited dose-dependent survival. The animals showed distention of the small intestine caused by peripheral neuritis because of infection of the myenteric plexus. Histopathologically, the strongly neurotropic Sofjin strain invaded the CNS of viremic mice via the autonomic nerves running from the plexus. The JaTH-160 strain of Japanese encephalitis virus was isolated from the lymph nodes during the preclinical phase of viral encephalitis. Therefore, this strain might infect the CNS via a hematogenous pathway, including through lymphoid tissues. The NY99-6922 strain of the West Nile virus caused clinical signs suggestive of intestinal, lymphoid, and/or neurologic involvement; the infected mice had prolonged viremia, suggesting that NY99-6922 may mainly use the hematogenous pathway; however, there was also histopathologic evidence of involvement of the autonomic nervous system pathway. In conclusion, the three neurotropic flaviviruses showed different pathogenesis, which were dependent upon overlapping but distinct pathways to CNS invasion after viremia. |
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AbstractList | Neurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from viremia to central nervous system (CNS) invasion are uncertain. Here, we intravenously infected BALB/c mice with 3 neurotropic flaviviruses, then examined the clinical manifestations and histopathologic changes. The Sofjin strain of tick-borne encephalitis virus-infected mice exhibited dose-dependent survival. The animals showed distention of the small intestine caused by peripheral neuritis because of infection of the myenteric plexus. Histopathologically, the strongly neurotropic Sofjin strain invaded the CNS of viremic mice via the autonomic nerves running from the plexus. The JaTH-160 strain of Japanese encephalitis virus was isolated from the lymph nodes during the preclinical phase of viral encephalitis. Therefore, this strain might infect the CNS via a hematogenous pathway, including through lymphoid tissues. The NY99-6922 strain of the West Nile virus caused clinical signs suggestive of intestinal, lymphoid, and/or neurologic involvement; the infected mice had prolonged viremia, suggesting that NY99-6922 may mainly use the hematogenous pathway; however, there was also histopathologic evidence of involvement of the autonomic nervous system pathway. In conclusion, the three neurotropic flaviviruses showed different pathogenesis, which were dependent upon overlapping but distinct pathways to CNS invasion after viremia. Neurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from viremia to central nervous system (CNS) invasion are uncertain. Here, we intravenously infected BALB/c mice with 3 neurotropic flaviviruses, then examined the clinical manifestations and histopathologic changes. The Sofjin strain of tick-borne encephalitis virus-infected mice exhibited dose-dependent survival. The animals showed distention of the small intestine caused by peripheral neuritis because of infection of the myenteric plexus. Histopathologically, the strongly neurotropic Sofjin strain invaded the CNS of viremic mice via the autonomic nerves running from the plexus. The JaTH-160 strain of Japanese encephalitis virus was isolated from the lymph nodes during the preclinical phase of viral encephalitis. Therefore, this strain might infect the CNS via a hematogenous pathway, including through lymphoid tissues. The NY99-6922 strain of the West Nile virus caused clinical signs suggestive of intestinal, lymphoid, and/or neurologic involvement; the infected mice had prolonged viremia, suggesting that NY99-6922 may mainly use the hematogenous pathway; however, there was also histopathologic evidence of involvement of the autonomic nervous system pathway. In conclusion, the three neurotropic flaviviruses showed different pathogenesis, which were dependent upon overlapping but distinct pathways to CNS invasion after viremia.Neurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from viremia to central nervous system (CNS) invasion are uncertain. Here, we intravenously infected BALB/c mice with 3 neurotropic flaviviruses, then examined the clinical manifestations and histopathologic changes. The Sofjin strain of tick-borne encephalitis virus-infected mice exhibited dose-dependent survival. The animals showed distention of the small intestine caused by peripheral neuritis because of infection of the myenteric plexus. Histopathologically, the strongly neurotropic Sofjin strain invaded the CNS of viremic mice via the autonomic nerves running from the plexus. The JaTH-160 strain of Japanese encephalitis virus was isolated from the lymph nodes during the preclinical phase of viral encephalitis. Therefore, this strain might infect the CNS via a hematogenous pathway, including through lymphoid tissues. The NY99-6922 strain of the West Nile virus caused clinical signs suggestive of intestinal, lymphoid, and/or neurologic involvement; the infected mice had prolonged viremia, suggesting that NY99-6922 may mainly use the hematogenous pathway; however, there was also histopathologic evidence of involvement of the autonomic nervous system pathway. In conclusion, the three neurotropic flaviviruses showed different pathogenesis, which were dependent upon overlapping but distinct pathways to CNS invasion after viremia. ABSTRACTNeurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from viremia to central nervous system (CNS) invasion are uncertain. Here, we intravenously infected BALB/c mice with 3 neurotropic flaviviruses, then examined the clinical manifestations and histopathologic changes. The Sofjin strain of tick-borne encephalitis virus–infected mice exhibited dose-dependent survival. The animals showed distention of the small intestine caused by peripheral neuritis because of infection of the myenteric plexus. Histopathologically, the strongly neurotropic Sofjin strain invaded the CNS of viremic mice via the autonomic nerves running from the plexus. The JaTH-160 strain of Japanese encephalitis virus was isolated from the lymph nodes during the preclinical phase of viral encephalitis. Therefore, this strain might infect the CNS via a hematogenous pathway, including through lymphoid tissues. The NY99-6922 strain of the West Nile virus caused clinical signs suggestive of intestinal, lymphoid, and/or neurologic involvement; the infected mice had prolonged viremia, suggesting that NY99-6922 may mainly use the hematogenous pathway; however, there was also histopathologic evidence of involvement of the autonomic nervous system pathway. In conclusion, the three neurotropic flaviviruses showed different pathogenesis, which were dependent upon overlapping but distinct pathways to CNS invasion after viremia. |
Author | Iwata-Yoshikawa, Naoko Sato, Yuko Kurane, Ichiro Takashima, Ikuo Kojima, Asato Nagata, Noriyo Sata, Tetsutaro Hayasaka, Daisuke Kariwa, Hiroaki Hasegawa, Hideki Takasaki, Tomohiko |
AuthorAffiliation | From the Departments of Pathology (NN, NI-Y, YS, AK, TS, HH) and Virology 1 (TT, IK), National Institute of Infectious Diseases, Tokyo; Department of Virology, Institute of Tropical Medicine, GCOE Program, Leading Graduate School Program, Nagasaki University, Nagasaki (DH); and Laboratory of Public Health, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido (HK, IT), Japan |
AuthorAffiliation_xml | – name: From the Departments of Pathology (NN, NI-Y, YS, AK, TS, HH) and Virology 1 (TT, IK), National Institute of Infectious Diseases, Tokyo; Department of Virology, Institute of Tropical Medicine, GCOE Program, Leading Graduate School Program, Nagasaki University, Nagasaki (DH); and Laboratory of Public Health, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido (HK, IT), Japan |
Author_xml | – sequence: 1 givenname: Noriyo surname: Nagata fullname: Nagata, Noriyo email: nnagata@niid.go.jp organization: National Institute of Infectious Diseases – sequence: 2 givenname: Naoko surname: Iwata-Yoshikawa fullname: Iwata-Yoshikawa, Naoko organization: National Institute of Infectious Diseases – sequence: 3 givenname: Daisuke surname: Hayasaka fullname: Hayasaka, Daisuke organization: Institute of Tropical Medicine, GCOE Program, Leading Graduate School Program, Nagasaki University – sequence: 4 givenname: Yuko surname: Sato fullname: Sato, Yuko organization: National Institute of Infectious Diseases – sequence: 5 givenname: Asato surname: Kojima fullname: Kojima, Asato organization: National Institute of Infectious Diseases – sequence: 6 givenname: Hiroaki surname: Kariwa fullname: Kariwa, Hiroaki organization: Graduate School of Veterinary Medicine, Hokkaido University – sequence: 7 givenname: Ikuo surname: Takashima fullname: Takashima, Ikuo organization: Graduate School of Veterinary Medicine, Hokkaido University – sequence: 8 givenname: Tomohiko surname: Takasaki fullname: Takasaki, Tomohiko organization: National Institute of Infectious Diseases – sequence: 9 givenname: Ichiro surname: Kurane fullname: Kurane, Ichiro organization: National Institute of Infectious Diseases – sequence: 10 givenname: Tetsutaro surname: Sata fullname: Sata, Tetsutaro organization: National Institute of Infectious Diseases – sequence: 11 givenname: Hideki surname: Hasegawa fullname: Hasegawa, Hideki organization: National Institute of Infectious Diseases |
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Snippet | Neurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the pathways from... ABSTRACTNeurotropic flavivirus infection of humans results in viremia subsequently; in some cases, it causes meningitis encephalomyelitis, although the... |
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SubjectTerms | Animals Central Nervous System - pathology Central Nervous System - virology Cercopithecus aethiops Cricetinae Disease Models, Animal Encephalitis Viruses, Tick-Borne - isolation & purification Female Flavivirus - isolation & purification Flavivirus Infections - pathology Mice Mice, Inbred BALB C Vero Cells Viremia - pathology |
Title | The Pathogenesis of 3 Neurotropic Flaviviruses in a Mouse Model Depends on the Route of Neuroinvasion After Viremia |
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