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Genetic analysis of the hypervariable region of the human astrovirus nsp1a coding region: Design of a new RFLP typing method
Author(s) -
Guix Susana,
Caballero Santiago,
Fuentes Cristina,
Bosch Albert,
Pintó Rosa M.
Publication year - 2008
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.21058
Subject(s) - biology , hypervariable region , restriction fragment length polymorphism , genotype , subtyping , genetics , phylogenetic tree , typing , virology , genetic variability , astrovirus , coding region , viral quasispecies , virus , gene , hepatitis c virus , rotavirus , computer science , programming language
Human astroviruses (HAstV) are causative agents of viral gastroenteritis worldwide. A hypervariable region (HVR) is located close to the C‐terminus of the nsP1a, and recent data support the involvement of the HVR‐containing nonstructural protein in viral RNA replication processes, suggesting a correlation between variability in this region and pathogenic properties. The HVR of the C‐terminal nsP1a coding region of 104 wild‐type and reference isolates of HAstV was sequenced. A phylogenetic analysis was performed to identify different genotypes, and a restriction fragment length polymorphism (RFLP) method was designed. An extensive nucleotide and deduced amino acid sequence variability was observed, as well as many insertions and deletions that retained the reading frame. The resultant phylogenetic tree supported the subdivision of HAstV into the two previously described major genetic groups, genogroup A and B, and the identification of 12 genotypes (9 within genogroup A, and 3 within genogroup B), which could be identified by RFLP. A correlation analysis was performed between genotype information and viral load using information from 35 clinical samples. Significant differences were observed between the viral load in clinical samples and certain HAstV genotypes that belonged to the same serotype, confirming the influence of C‐terminal nsP1a variability on the viral replication phenotype. The use of the new RFLP typing method based on the HVR of the C‐terminal nsP1a coding region by diagnosticians would help to understand the relationship between different genotypes and the severity of the gastroenteritis. J. Med. Virol. 80:306–315, 2008. © 2007 Wiley‐Liss, Inc.