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Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo
BACKGROUND AND THE PURPOSE OF THE STUDY: The cervico-vaginal mucosa which is populated with microflora (mostly includes lactobacilli) is the portal of entry for sexually transmitted pathogens. METHODS: The in vitro anti-viral effect of vaginal and non-vaginal lactobacillus was evaluated using single...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555973/ https://www.ncbi.nlm.nih.gov/pubmed/23351891 http://dx.doi.org/10.1186/2008-2231-20-53 |
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author | Zabihollahi, Rezvan Motevaseli, Elahe Sadat, Seyed Mehdi Azizi-Saraji, Ali Reza Asaadi-Dalaie, Sogol Modarressi, Mohammad Hossein |
author_facet | Zabihollahi, Rezvan Motevaseli, Elahe Sadat, Seyed Mehdi Azizi-Saraji, Ali Reza Asaadi-Dalaie, Sogol Modarressi, Mohammad Hossein |
author_sort | Zabihollahi, Rezvan |
collection | PubMed |
description | BACKGROUND AND THE PURPOSE OF THE STUDY: The cervico-vaginal mucosa which is populated with microflora (mostly includes lactobacilli) is the portal of entry for sexually transmitted pathogens. METHODS: The in vitro anti-viral effect of vaginal and non-vaginal lactobacillus was evaluated using single cycle HIV-1 replication and HSV-2 plaque reduction assays. The XTT proliferation assay was used to monitor the cellular toxicity. The in vivo anti-HSV-1 activity was evaluated in BALB/c mouse model by monitoring skin lesion and immune response development. RESULTS AND MAJOR CONCLUSION: DMEM culture supernatant of L. Gasseri and L. fermentum (PH 7.3) did not show toxic effect but inhibited 50% of HIV replication at 12 and 31% concentrations, respectively. Co-culture of L. gasseri (1000 CFU/ target cell) showed mild cytotoxicity but inhibited 68% of HIV replication. The supernatant of L. crispatus inhibited 50% of HSV replication at 4% and also co-culture of L. gasseri, L. rhamnosus and L. crispatus revokes almost all of the HSV multiplication. Culture supernatants of L. gasseri and L. crispatus had significant virucidal effect against the HIV and HSV and inhibited HSV infection in a stage before viral entry to the target cells. Alive L. gasseri cells showed high potential for inhibiting HSV-1 infection in vivo condition. Current data indicates that lactobacilli supernatant encompasses components with neutralizing activity against HIV and HSV and it would be a determinant factor for viral diseases transmission and promising lead for anti-viral probiotic design. |
format | Online Article Text |
id | pubmed-3555973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35559732013-01-31 Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo Zabihollahi, Rezvan Motevaseli, Elahe Sadat, Seyed Mehdi Azizi-Saraji, Ali Reza Asaadi-Dalaie, Sogol Modarressi, Mohammad Hossein Daru Research Article BACKGROUND AND THE PURPOSE OF THE STUDY: The cervico-vaginal mucosa which is populated with microflora (mostly includes lactobacilli) is the portal of entry for sexually transmitted pathogens. METHODS: The in vitro anti-viral effect of vaginal and non-vaginal lactobacillus was evaluated using single cycle HIV-1 replication and HSV-2 plaque reduction assays. The XTT proliferation assay was used to monitor the cellular toxicity. The in vivo anti-HSV-1 activity was evaluated in BALB/c mouse model by monitoring skin lesion and immune response development. RESULTS AND MAJOR CONCLUSION: DMEM culture supernatant of L. Gasseri and L. fermentum (PH 7.3) did not show toxic effect but inhibited 50% of HIV replication at 12 and 31% concentrations, respectively. Co-culture of L. gasseri (1000 CFU/ target cell) showed mild cytotoxicity but inhibited 68% of HIV replication. The supernatant of L. crispatus inhibited 50% of HSV replication at 4% and also co-culture of L. gasseri, L. rhamnosus and L. crispatus revokes almost all of the HSV multiplication. Culture supernatants of L. gasseri and L. crispatus had significant virucidal effect against the HIV and HSV and inhibited HSV infection in a stage before viral entry to the target cells. Alive L. gasseri cells showed high potential for inhibiting HSV-1 infection in vivo condition. Current data indicates that lactobacilli supernatant encompasses components with neutralizing activity against HIV and HSV and it would be a determinant factor for viral diseases transmission and promising lead for anti-viral probiotic design. BioMed Central 2012-10-15 /pmc/articles/PMC3555973/ /pubmed/23351891 http://dx.doi.org/10.1186/2008-2231-20-53 Text en Copyright ©2012 Zabihollahi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zabihollahi, Rezvan Motevaseli, Elahe Sadat, Seyed Mehdi Azizi-Saraji, Ali Reza Asaadi-Dalaie, Sogol Modarressi, Mohammad Hossein Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo |
title | Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo |
title_full | Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo |
title_fullStr | Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo |
title_full_unstemmed | Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo |
title_short | Inhibition of HIV and HSV infection by vaginal lactobacilli in vitro and in vivo |
title_sort | inhibition of hiv and hsv infection by vaginal lactobacilli in vitro and in vivo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555973/ https://www.ncbi.nlm.nih.gov/pubmed/23351891 http://dx.doi.org/10.1186/2008-2231-20-53 |
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