Virus Details


VHFID6792

Pathogen Information

Virus Name Porcine reproductive and respiratory syndrome virus
Virus Short Name PRRSV
Order Nidovirales
Virus Family Arteriviridae
Virus Subfamily N.A.
Genus Porartevirus
Species Porcine reproductive and respiratory syndrome virus
Host Vertebrates
Cell Tropism Primarily it's found in alveolar lung macrophages and macrophages of other tissues, later, is also found in testicular germ cells.
Associated Disease Abortions and respiratory disease
Mode of Transmission Transplacental, saliva, urine, semen and respiratory tract secretions
VIPR DB link N.A.
ICTV DB link https://talk.ictvonline.org/ictv-reports/ictv_9th_report/positive-sense-rna-viruses-2011/w/posrna_viruses/220/arteriviridae
Virus Host DB link N.A.

Publication Information

Paper Title MYH9 is an Essential Factor for Porcine Reproductive and Respiratory Syndrome Virus Infection
Author's Name Jiming Gao, Shuqi Xiao, Yihong Xiao, Xiangpeng Wang, Chong Zhang, Qin Zhao, Yuchen Nan, Baicheng Huang, Hongliang Liu, Ningning Liu, Junhua Lv, Taofeng Du, Yani Sun, Yang Mu, Gang Wang, Shahid Faraz Syed, Gaiping Zhang, Julian A. Hiscox, Ian Goodfellow & En-Min Zhou
Journal Name scintific report
Pubmed ID 27112594
Abstract Porcine reproductive and respiratory syndrome (PRRS) caused by the PRRS virus (PRRSV) is an important swine disease worldwide. PRRSV has a limited tropism for certain cells, which may at least in part be attributed to the expression of the necessary cellular molecules serving as the virus receptors or factors on host cells for virus binding or entry. However, these molecules conferring PRRSV infection have not been fully characterized. Here we show the identification of non-muscle myosin heavy chain 9 (MYH9) as an essential factor for PRRSV infection using the anti-idiotypic antibody specific to the PRRSV glycoprotein GP5. MYH9 physically interacts with the PRRSV GP5 protein via its C-terminal domain and confers susceptibility of cells to PRRSV infection. These findings indicate that MYH9 is an essential factor for PRRSV infection and provide new insights into PRRSV-host interactions and viral entry, potentially facilitating development of control strategies for this important swine disease.
Used Model PK-15, MARC-145, 293T, and COS-7 cells
DOI 10.1038/srep25120