Molecular characterization of a 13-amino acid deletion in VP1 (1D) protein and novel amino acid substitutions in 3D polymerase protein of foot and mouth disease virus subtype A/Iran87.
10.4142/jvs.2011.12.4.363
- Author:
Majid ESMAELIZAD
1
;
Saber JELOKHANI-NIARAKI
;
Khadije HASHEMNEJAD
;
Morteza KAMALZADEH
;
Mohsen LOTFI
Author Information
1. Department of Biotechnology, Razi Vaccine and Serum Research Institute, Karaj 3197619751, Iran. m.esmaelizad@rvsri.ir
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
3Dpol protein;
deletion;
RGD;
VP1 protein
- MeSH:
Amino Acid Sequence;
Amino Acid Substitution;
Antigens, Viral/chemistry/*genetics/metabolism;
Capsid Proteins/chemistry/*genetics/metabolism;
Cloning, Molecular;
Foot-and-Mouth Disease Virus/classification/*genetics/*metabolism;
Gene Expression Regulation, Viral;
Molecular Sequence Data;
Phylogeny;
Viral Nonstructural Proteins/chemistry/*genetics/metabolism
- From:Journal of Veterinary Science
2011;12(4):363-371
- CountryRepublic of Korea
- Language:English
-
Abstract:
The nucleotide sequence of the VP1 (1D) and partial 3D polymerase (3Dpol) coding regions of the foot and mouth disease virus (FMDV) vaccine strain A/Iran87, a highly passaged isolate (~150 passages), was determined and aligned with previously published FMDV serotype A sequences. Overall analysis of the amino acid substitutions revealed that the partial 3Dpol coding region contained four amino acid alterations. Amino acid sequence comparison of the VP1 coding region of the field isolates revealed deletions in the highly passaged Iranian isolate (A/Iran87). The prominent G-H loop of the FMDV VP1 protein contains the conserved arginine-glycine-aspartic acid (RGD) tripeptide, which is a well-known ligand for a specific cell surface integrin. Despite losing the RGD sequence of the VP1 protein and an Asp26-->Glu substitution in a beta sheet located within a small groove of the 3Dpol protein, the virus grew in BHK 21 suspension cell cultures. Since this strain has been used as a vaccine strain, it may be inferred that the RGD deletion has no critical role in virus attachment to the cell during the initiation of infection. It is probable that this FMDV subtype can utilize other pathways for cell attachment.
