Volume 15, Issue 3 (2012)                   Pathobiol Res 2012, 15(3): 1-9 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ahmadi E, Soleimanjahi H, Sadegizadeh M, Teimoori A. Rearranged Bovine Rotavirus Production through Cultivation of Virus by High Multiplicity of Infection (MOI) in Cell Culture and Amplification of Non-structural Genes using RT-PCR. Pathobiol Res. 2012; 15 (3) :1-9
URL: http://mjms.modares.ac.ir/article-30-2837-en.html
1- M.Sc. Student ,Department of virology,Faculty of Medical Sciences,Tarbiat Modares University,Tehran,Iran ., Tehran
2- Head of virology department/ Tarbiat Modares University, Faculty of Medical Science
3- Professor, Department of Genetics, Faculty of Basic Sciences , Tarbiat Modares University, Tehran , Iran ., Tehran
4- Ph.D. Candidate ,Virology Department, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran ., Tehran
Abstract:   (4931 Views)
Objective: Group A rotaviruses (GARV) are responsible for the vast majority of severe diarrhea worldwide that kills an estimated 600,000-870,000 children annually. Since infantile gastroenteritis is a main health problem, therefore diagnosis and treatment of this disease is crucial. Gene rearrangements have been detected in vitro during serial passages of the virus at a high multiplicity of infection (MOI) in cell culture, as well as in chronically infected immunodeficient individuals. In this study, we developed an RT-PCR method to detect and diagnose the standard and gene rearranged bovine rotavirus. Methods: Rotavirus RNA was extracted from confluent monolayers of infected MA-104 cells, stained with silver nitrate, and then electrophoresed in a 10% polyacrylamide gel. The full-length gene products that encoded the NSP1, 2, and 3 genes of the standard and rearranged rotavirus were amplified by RT-PCR using specific primers. Results: We observed rearranged NSP1 and NSP3 genes that had different migration patterns seen with polyacrylamide gel electrophoresis. NSP1, 2, and 3 gene segments from standard and rearranged rotaviruses were amplified by RT-PCR, then the complete nucleotide sequence of each gene was subjected to sequencing. The results showed the generation of gene rearrangement through serial passages of the bovine rotavirus RF strain. Conclusion: Serial passage of rotavirus in cell culture at a high MOI and chronic infection in immunodeficient target groups might alter rotavirus evolution. The methods utilized for detection and characterization of rotaviruses are continually evolving and being refined. Data collection is necessary to understand the molecular and antigenic features of the rotavirus in order to have a successful implementation of rotavirus studies and the development of a rotavirus vaccine. This study shows the importance of genetic variation and can provide valuable information about the amplification, diversity, biology, and evolution of rotaviruses.
Full-Text [PDF 416 kb]   (4053 Downloads)    
Article Type: Original Manuscipt | Subject: Virology|Molecular Genetics|Infectious Disease|Medical Virology
Received: 2012/09/22 | Accepted: 2012/12/12 | Published: 2012/12/12
* Corresponding Author Address: Tehran

Add your comments about this article : Your username or Email:
CAPTCHA