[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Editorial Board::
Executive Members::
Instruction to Authors::
Peer Review::
Articles Archive::
Indexing Databases::
Contact Us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
:: Volume 17, Issue 3 (10-2015) ::
J Gorgan Univ Med Sci 2015, 17(3): 114-121 Back to browse issues page
Detection of heat-labile toxin in enterotoxigenic Escherichia coli using PCR-ELISA technique
Esfandiari P1 , Amani J * 2, Imani Fooladi AA3 , Forghanifard MM4 , Mirhossaini SA5
1- Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran and Department of Biology, Damghan Branch, Islamic Azad University, Damghan, Iran
2- Associate Professor, Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran , jafar.amani@gmail.com
3- Associate Professor, Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
4- Assistant Professor, Department of Biology, Damghan Branch, Islamic Azad University, Damghan, Iran
5- Ph.D Candidate in Bacterial Toxin, Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
Abstract:   (12575 Views)
Background and Objective: Enterotoxigenic Escherichia coli (ETEC) are the most common agent which causes diarrhea, worldwide. ETEC is colonized along the cells and then producing heat-labile (LT) and heat-stable enterotoxigenic which enter into intestinal epithelial cells and causes water and electrolyte loss from intestinal epithelial cells and eventually cause diarrhea.This study was done to detect the heat-labile toxin in Enterotoxigenic Escherichia coli using PCR-ELISA technique. Methods: In this descriptive study, DIG-labeled PCR products were bounded to streptoavidin-coated wells of a microtiter plate and detected by anti-DIG–peroxidase conjugate. The biotin-labeled internal probe was used for verification of PCR products. Results: Heat-labile toxin was detected by PCR-ELISA method. The sensitivity of heat-labile toxin was 1.9 ng. This method did not cross-react with bacteria from this variety. Conclusion: PCR-ELISA method is 100 times more sensitive than conventional PCR method and due to lack of agarose gel and electrophoresis device it can be a good alternative to traditional method.
Keywords: Enterotoxigenic Escherichia coli, PCR-ELISA, Heat-labile enterotoxin
Full-Text [PDF 308 kb] [English Abstract]   (16616 Downloads)    
Type of Study: Original Articles | Subject: Microbiology
Send email to the article author


XML   Persian Abstract   Print


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

Esfandiari P, Amani J, Imani Fooladi AA, Forghanifard MM, Mirhossaini SA. Detection of heat-labile toxin in enterotoxigenic Escherichia coli using PCR-ELISA technique. J Gorgan Univ Med Sci 2015; 17 (3) :114-121
URL: http://goums.ac.ir/journal/article-1-2511-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 17, Issue 3 (10-2015) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
Persian site map - English site map - Created in 0.05 seconds with 36 queries by YEKTAWEB 4660
Creative Commons License
This work is licensed under a Creative Commons — Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)