The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.

Both human parvovirus B19 (B19V) and human bocavirus (HBoV) are known to be important human pathogens of the Parvoviridae family. Our earlier investigation demonstrated that both B19V-VP1u and HBoV-VP1u have a significantly disruptive effect on tight junctions (TJs) in A549 cells, implying the essen...

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Main Authors: Chun-Yu Lin, Yu-Han Chung, Ya-Fang Shi, Bor-Show Tzang, Tsai-Ching Hsu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6095614?pdf=render
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author Chun-Yu Lin
Yu-Han Chung
Ya-Fang Shi
Bor-Show Tzang
Tsai-Ching Hsu
author_facet Chun-Yu Lin
Yu-Han Chung
Ya-Fang Shi
Bor-Show Tzang
Tsai-Ching Hsu
author_sort Chun-Yu Lin
collection DOAJ
description Both human parvovirus B19 (B19V) and human bocavirus (HBoV) are known to be important human pathogens of the Parvoviridae family. Our earlier investigation demonstrated that both B19V-VP1u and HBoV-VP1u have a significantly disruptive effect on tight junctions (TJs) in A549 cells, implying the essential role of parvovirus in airway infection and lung injury. However, no direct evidence that B19V-VP1u and HBoV-VP1u induce lung injury exists. The present study further investigates the induction of lung injury by B19V-VP1u and HBoV-VP1u in naïve Balb/c mice following subcutaneous injection of PBS, recombinant B19V-VP1u or HBoV-VP1u. The experimental results reveal significantly increased activity, protein expression and ratio of matrix metalloproteinase-9 (MMP-9) to MMP-2 in Balb/c mice that received B19V-VP1u or HBoV-VP1u compared to those that received PBS. Significantly higher levels of inflammatory cytokines, including IL-6 and IL-1β, and greater lymphocyte infiltration in lung tissue sections were detected in mice that received B19V-VP1u or HBoV-VP1u. Additionally, significantly increased levels of phosphorylated p65 (NF-κB) and MAPK signaling proteins were observed in lung tissue of mice that received B19V-VP1u or HBoV-VP1u compared to those of mice that received PBS. These findings demonstrate for the first time that B19V-VP1u and HBoV-VP1u proteins induce lung inflammatory reactions through p65 (NF-κB) and MAPK signaling.
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spelling doaj.art-2511c0de9f0d46d28d38a050537044bb2022-12-22T01:38:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01138e020266710.1371/journal.pone.0202667The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.Chun-Yu LinYu-Han ChungYa-Fang ShiBor-Show TzangTsai-Ching HsuBoth human parvovirus B19 (B19V) and human bocavirus (HBoV) are known to be important human pathogens of the Parvoviridae family. Our earlier investigation demonstrated that both B19V-VP1u and HBoV-VP1u have a significantly disruptive effect on tight junctions (TJs) in A549 cells, implying the essential role of parvovirus in airway infection and lung injury. However, no direct evidence that B19V-VP1u and HBoV-VP1u induce lung injury exists. The present study further investigates the induction of lung injury by B19V-VP1u and HBoV-VP1u in naïve Balb/c mice following subcutaneous injection of PBS, recombinant B19V-VP1u or HBoV-VP1u. The experimental results reveal significantly increased activity, protein expression and ratio of matrix metalloproteinase-9 (MMP-9) to MMP-2 in Balb/c mice that received B19V-VP1u or HBoV-VP1u compared to those that received PBS. Significantly higher levels of inflammatory cytokines, including IL-6 and IL-1β, and greater lymphocyte infiltration in lung tissue sections were detected in mice that received B19V-VP1u or HBoV-VP1u. Additionally, significantly increased levels of phosphorylated p65 (NF-κB) and MAPK signaling proteins were observed in lung tissue of mice that received B19V-VP1u or HBoV-VP1u compared to those of mice that received PBS. These findings demonstrate for the first time that B19V-VP1u and HBoV-VP1u proteins induce lung inflammatory reactions through p65 (NF-κB) and MAPK signaling.http://europepmc.org/articles/PMC6095614?pdf=render
spellingShingle Chun-Yu Lin
Yu-Han Chung
Ya-Fang Shi
Bor-Show Tzang
Tsai-Ching Hsu
The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.
PLoS ONE
title The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.
title_full The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.
title_fullStr The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.
title_full_unstemmed The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.
title_short The VP1 unique region of human parvovirus B19 and human bocavirus induce lung injury in naïve Balb/c mice.
title_sort vp1 unique region of human parvovirus b19 and human bocavirus induce lung injury in naive balb c mice
url http://europepmc.org/articles/PMC6095614?pdf=render
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