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Enhanced cell fusion activity in porcine epidemic diarrhea virus adapted to suckling mice

Identifieur interne : 002822 ( Main/Exploration ); précédent : 002821; suivant : 002823

Enhanced cell fusion activity in porcine epidemic diarrhea virus adapted to suckling mice

Auteurs : Kazuya Shirato [Japon] ; Madoka Maejima [Japon] ; Asuka Hirai [Japon] ; Yasushi Ami [Japon] ; Natsumi Takeyama [Japon] ; Kotaro Tsuchiya [Japon] ; Kouich Kusanagi [Japon] ; Tetsuo Nunoya [Japon] ; Fumihiro Taguchi [Japon]

Source :

RBID : ISTEX:D5E3BA48C010EC6D50FF1930007DDA90DAE6AAC0

Descripteurs français

English descriptors

Abstract

Abstract: Porcine epidemic diarrhea virus (PEDV) is the major causative agent of fatal diarrhea in piglets. To study the pathogenic features of PEDV using a mouse model, PEDV with virulence in mice is required. In pursuit of this, we adapted a tissue-culture-passed PEDV MK strain to suckling mouse brains. PEDV obtained after ten passages through the brains (MK-p10) had increased virulence for mice, and its fusion activity in cultured cells exceeded that of the original strain. However, the replication kinetics of MK and MK-p10 did not differ from each other in the brain and in cultured cells. The spike (S) protein of MK-p10 had four amino acid substitutions relative to the original strain. One of these (an H-to-R substitution at residue 1,381) was first detected in PEDV isolated after eight passages, and both this virus (MK-p8) and MK-p10 showed enhanced syncytium formation relative to the original MK strain and viruses isolated after two, four, and six passages, suggesting the possibility that the H-to-R mutation was responsible for this activity. This mutation could be also involved in the increased virulence of PEDV observed for MK-p10.

Url:
DOI: 10.1007/s00705-010-0790-1


Affiliations:


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<div type="abstract" xml:lang="en">Abstract: Porcine epidemic diarrhea virus (PEDV) is the major causative agent of fatal diarrhea in piglets. To study the pathogenic features of PEDV using a mouse model, PEDV with virulence in mice is required. In pursuit of this, we adapted a tissue-culture-passed PEDV MK strain to suckling mouse brains. PEDV obtained after ten passages through the brains (MK-p10) had increased virulence for mice, and its fusion activity in cultured cells exceeded that of the original strain. However, the replication kinetics of MK and MK-p10 did not differ from each other in the brain and in cultured cells. The spike (S) protein of MK-p10 had four amino acid substitutions relative to the original strain. One of these (an H-to-R substitution at residue 1,381) was first detected in PEDV isolated after eight passages, and both this virus (MK-p8) and MK-p10 showed enhanced syncytium formation relative to the original MK strain and viruses isolated after two, four, and six passages, suggesting the possibility that the H-to-R mutation was responsible for this activity. This mutation could be also involved in the increased virulence of PEDV observed for MK-p10.</div>
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