TY - JOUR
T1 - PRRS virus receptors and their role for pathogenesis
AU - Zhang, Qingzhan
AU - Yoo, Dongwan
N1 - Funding Information:
This project was supported by the US National Pork Board (Grant # 13-245 ) and Agriculture and Food Research Initiative (AFRI) Competitive Grant No. 2013-67015-21243 of the USDA National Institute of Food and Agriculture (NIFA).
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/6/12
Y1 - 2015/6/12
N2 - Porcine reproductive and respiratory syndrome virus (PRRSV) is endemic in most pig producing countries worldwide and causes enormous economic losses to the swine industry. Specifically differentiated porcine alveolar macrophages are the primary target for PRRSV infection in pigs. At least six cellular molecules have been described so far as putative receptors for PRRSV, and they include heparan sulfate, vimentin, CD151, sialoadhesin (CD169; siglec-1), dendritic cell-specific intercellular adhesion melecule-3-grabbing non-integrin (DC-SIGN; CD209), and CD163 (SRCR, cysteine-rich scavenger receptor). Progress has been made to shed light on the interactions between cells and PRRSV, and this review describes the advances and current understanding of the entry of PRRSV to cells with a particular focus on the role of CD163 and sialoadhesin for infection and PRRSV pathogenesis. CD163 is most likely the primary and core receptor for PRRSV and determines the susceptibility of cells to the virus. Sialoadhesin is either unnecessary for infection or may function as an accessory protein. Sialoadhesin has been mostly studied for genotype I PRRSV whereas the utilization of CD163 has been mostly studied using genotype II PRRSV, and whether each genotype indeed utilizes a different receptor is unclear.
AB - Porcine reproductive and respiratory syndrome virus (PRRSV) is endemic in most pig producing countries worldwide and causes enormous economic losses to the swine industry. Specifically differentiated porcine alveolar macrophages are the primary target for PRRSV infection in pigs. At least six cellular molecules have been described so far as putative receptors for PRRSV, and they include heparan sulfate, vimentin, CD151, sialoadhesin (CD169; siglec-1), dendritic cell-specific intercellular adhesion melecule-3-grabbing non-integrin (DC-SIGN; CD209), and CD163 (SRCR, cysteine-rich scavenger receptor). Progress has been made to shed light on the interactions between cells and PRRSV, and this review describes the advances and current understanding of the entry of PRRSV to cells with a particular focus on the role of CD163 and sialoadhesin for infection and PRRSV pathogenesis. CD163 is most likely the primary and core receptor for PRRSV and determines the susceptibility of cells to the virus. Sialoadhesin is either unnecessary for infection or may function as an accessory protein. Sialoadhesin has been mostly studied for genotype I PRRSV whereas the utilization of CD163 has been mostly studied using genotype II PRRSV, and whether each genotype indeed utilizes a different receptor is unclear.
KW - Arterivirus
KW - CD163
KW - PRRSV
KW - Pathogenesis
KW - Receptor
KW - Sialoadhesin
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U2 - 10.1016/j.vetmic.2015.04.002
DO - 10.1016/j.vetmic.2015.04.002
M3 - Review article
C2 - 25912022
AN - SCOPUS:84928823475
SN - 0378-1135
VL - 177
SP - 229
EP - 241
JO - Veterinary Microbiology
JF - Veterinary Microbiology
IS - 3-4
ER -