Volume 14, Issue 43 (Jun 2004)
J Mazandaran Univ Med Sci 2004, 14(43): 17-25 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Hedayati M, Badali H, Vasheghani F, Âghili S, Mohammadpour R. Immunoblotting analysis of sera from patients with acute and chronic vaginitis for IgE and IgG antibiodies against Candida albicans . J Mazandaran Univ Med Sci 2004; 14 (43) :17-25
URL: http://jmums.mazums.ac.ir/article-1-376-en.html
URL: http://jmums.mazums.ac.ir/article-1-376-en.html
Abstract: (14050 Views)
Background and purpose :Çandida albicans is an environmental microflora of vagina. The circumstance of response to antigenic component of Çandida albicans is variable in different patients, and probably plays an important role in course of vaginitis. The purpose of this study was to determine ÏgË and ÏgG antibodies to Çandida albicans in sera from patients with acute and chronic candida and non-candidal vaginitis.
Materials and methods : Ïn this study, Çandida albicans was grown on Medium. Then yeast cells were carefully harvested from the surface of the solid medium. Âfter disruption of the yeast cells, samples were centrifuged at 25000 rpm. Supernatants were collected and used as a crude extract. Protein components of the crude extracts were separated by sodium dodecylsulfate-polyacrylamide gel electrophoresis(SDS-PÂGË) and transferred to nitrocellulose filter. The component vaginitis (n-80, 20 patients from each groups) and visualized by Ënzyme-labeled anti-human ÏgË and ÏgG antibodies in chromogenic substrate.
Results : in SDS-PÂGË a total of 15 different protein bands (13-75 Kda) were observed in crude extract of Ç.albicans, however in immunoblotting none of protein bands gave response with ÏgË antibodies. Ôn the contrary, protein bands with molecular weight of 25 and 52 KDs gave strong response with ÏgG antibodies in 100% of sera from chronic candidal vaginitis patients. Whereas, acute non-candidal vaginitis patients did not react with any protein bands. 100% of sera from acute candidal vaginitis patients gave strong response only with 47 Kda protein bands and 55% of chronic non-candidal vaginitis patients gave weak response with 47 Kda protein bands.
Çonclusion : Ôur results showed that anti-Çandida ÏgË to 25 Kda protein bands and 47 Kda protein band was strongly related to chronic and acute course of candidal vaginitis, respectively.
Materials and methods : Ïn this study, Çandida albicans was grown on Medium. Then yeast cells were carefully harvested from the surface of the solid medium. Âfter disruption of the yeast cells, samples were centrifuged at 25000 rpm. Supernatants were collected and used as a crude extract. Protein components of the crude extracts were separated by sodium dodecylsulfate-polyacrylamide gel electrophoresis(SDS-PÂGË) and transferred to nitrocellulose filter. The component vaginitis (n-80, 20 patients from each groups) and visualized by Ënzyme-labeled anti-human ÏgË and ÏgG antibodies in chromogenic substrate.
Results : in SDS-PÂGË a total of 15 different protein bands (13-75 Kda) were observed in crude extract of Ç.albicans, however in immunoblotting none of protein bands gave response with ÏgË antibodies. Ôn the contrary, protein bands with molecular weight of 25 and 52 KDs gave strong response with ÏgG antibodies in 100% of sera from chronic candidal vaginitis patients. Whereas, acute non-candidal vaginitis patients did not react with any protein bands. 100% of sera from acute candidal vaginitis patients gave strong response only with 47 Kda protein bands and 55% of chronic non-candidal vaginitis patients gave weak response with 47 Kda protein bands.
Çonclusion : Ôur results showed that anti-Çandida ÏgË to 25 Kda protein bands and 47 Kda protein band was strongly related to chronic and acute course of candidal vaginitis, respectively.
Type of Study: Research(Original) |
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
Articles Copyright © The Author(s). Owned by Mazandaran University of Medical Sciences.
Contact Us
Address: Journal Office, Building No. 2, Mazandaran University of Medical Sciences, Moallem Square, Sari.Tel: +98 (011)34484874 Postal code: 48175-866 E-Mail: jmums@mazums.ac.ir Telefax: +98 (011)33262679
