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Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models

OBJECTIVE: Saffold virus (SAFV), a picornavirus, is occasionally detected in children with acute flaccid paralysis, meningitis, and cerebellitis; however, the neuropathogenicity of SAFV remains undetermined. METHODS: The virulence of two clinical isolates of SAFV type 3 (SAFV-3) obtained from a pati...

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Autores principales: Kotani, Osamu, Naeem, Asif, Suzuki, Tadaki, Iwata-Yoshikawa, Naoko, Sato, Yuko, Nakajima, Noriko, Hosomi, Takushi, Tsukagoshi, Hiroyuki, Kozawa, Kunihisa, Hasegawa, Hideki, Taguchi, Fumihiro, Shimizu, Hiroyuki, Nagata, Noriyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734772/
https://www.ncbi.nlm.nih.gov/pubmed/26828718
http://dx.doi.org/10.1371/journal.pone.0148184
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author Kotani, Osamu
Naeem, Asif
Suzuki, Tadaki
Iwata-Yoshikawa, Naoko
Sato, Yuko
Nakajima, Noriko
Hosomi, Takushi
Tsukagoshi, Hiroyuki
Kozawa, Kunihisa
Hasegawa, Hideki
Taguchi, Fumihiro
Shimizu, Hiroyuki
Nagata, Noriyo
author_facet Kotani, Osamu
Naeem, Asif
Suzuki, Tadaki
Iwata-Yoshikawa, Naoko
Sato, Yuko
Nakajima, Noriko
Hosomi, Takushi
Tsukagoshi, Hiroyuki
Kozawa, Kunihisa
Hasegawa, Hideki
Taguchi, Fumihiro
Shimizu, Hiroyuki
Nagata, Noriyo
author_sort Kotani, Osamu
collection PubMed
description OBJECTIVE: Saffold virus (SAFV), a picornavirus, is occasionally detected in children with acute flaccid paralysis, meningitis, and cerebellitis; however, the neuropathogenicity of SAFV remains undetermined. METHODS: The virulence of two clinical isolates of SAFV type 3 (SAFV-3) obtained from a patient with aseptic meningitis (AM strain) and acute upper respiratory inflammation (UR strain) was analyzed in neonatal and young mice utilizing virological, pathological, and immunological methods. RESULTS: The polyproteins of the strains differed in eight amino acids. Both clinical isolates were infective, exhibited neurotropism, and were mildly neurovirulent in neonatal ddY mice. Both strains pathologically infected neural progenitor cells and glial cells, but not large neurons, with the UR strain also infecting epithelial cells. UR infection resulted in longer inflammation in the brain and spinal cord because of demyelination, while the AM strain showed more infectivity in the cerebellum in neonatal ddY mice. Additionally, young BALB/c mice seroconverted following mucosal inoculation with the UR, but not the AM, strain. CONCLUSIONS: Both SAFV-3 isolates had neurotropism and mild neurovirulence but showed different cell tropisms in both neonatal and young mouse models. This animal model has the potential to recapitulate the potential neuropathogenicity of SAFV-3.
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spelling pubmed-47347722016-02-04 Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models Kotani, Osamu Naeem, Asif Suzuki, Tadaki Iwata-Yoshikawa, Naoko Sato, Yuko Nakajima, Noriko Hosomi, Takushi Tsukagoshi, Hiroyuki Kozawa, Kunihisa Hasegawa, Hideki Taguchi, Fumihiro Shimizu, Hiroyuki Nagata, Noriyo PLoS One Research Article OBJECTIVE: Saffold virus (SAFV), a picornavirus, is occasionally detected in children with acute flaccid paralysis, meningitis, and cerebellitis; however, the neuropathogenicity of SAFV remains undetermined. METHODS: The virulence of two clinical isolates of SAFV type 3 (SAFV-3) obtained from a patient with aseptic meningitis (AM strain) and acute upper respiratory inflammation (UR strain) was analyzed in neonatal and young mice utilizing virological, pathological, and immunological methods. RESULTS: The polyproteins of the strains differed in eight amino acids. Both clinical isolates were infective, exhibited neurotropism, and were mildly neurovirulent in neonatal ddY mice. Both strains pathologically infected neural progenitor cells and glial cells, but not large neurons, with the UR strain also infecting epithelial cells. UR infection resulted in longer inflammation in the brain and spinal cord because of demyelination, while the AM strain showed more infectivity in the cerebellum in neonatal ddY mice. Additionally, young BALB/c mice seroconverted following mucosal inoculation with the UR, but not the AM, strain. CONCLUSIONS: Both SAFV-3 isolates had neurotropism and mild neurovirulence but showed different cell tropisms in both neonatal and young mouse models. This animal model has the potential to recapitulate the potential neuropathogenicity of SAFV-3. Public Library of Science 2016-02-01 /pmc/articles/PMC4734772/ /pubmed/26828718 http://dx.doi.org/10.1371/journal.pone.0148184 Text en © 2016 Kotani et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kotani, Osamu
Naeem, Asif
Suzuki, Tadaki
Iwata-Yoshikawa, Naoko
Sato, Yuko
Nakajima, Noriko
Hosomi, Takushi
Tsukagoshi, Hiroyuki
Kozawa, Kunihisa
Hasegawa, Hideki
Taguchi, Fumihiro
Shimizu, Hiroyuki
Nagata, Noriyo
Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
title Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
title_full Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
title_fullStr Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
title_full_unstemmed Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
title_short Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
title_sort neuropathogenicity of two saffold virus type 3 isolates in mouse models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734772/
https://www.ncbi.nlm.nih.gov/pubmed/26828718
http://dx.doi.org/10.1371/journal.pone.0148184
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