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Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo
Ocular chlamydial infections with the ocular serovars A, B, Ba, and C of Chlamydia trachomatis represent the world’s leading cause of infectious blindness. Carrageenans are naturally occurring, sulfated polysaccharides generally considered safe for food and topical applications. Carrageenans can inh...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096786/ https://www.ncbi.nlm.nih.gov/pubmed/30147240 http://dx.doi.org/10.1007/s10811-018-1435-0 |
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author | Inic-Kanada, Aleksandra Stein, Elisabeth Stojanovic, Marijana Schuerer, Nadine Ghasemian, Ehsan Filipovic, Ana Marinkovic, Emilija Kosanovic, Dejana Barisani-Asenbauer, Talin |
author_facet | Inic-Kanada, Aleksandra Stein, Elisabeth Stojanovic, Marijana Schuerer, Nadine Ghasemian, Ehsan Filipovic, Ana Marinkovic, Emilija Kosanovic, Dejana Barisani-Asenbauer, Talin |
author_sort | Inic-Kanada, Aleksandra |
collection | PubMed |
description | Ocular chlamydial infections with the ocular serovars A, B, Ba, and C of Chlamydia trachomatis represent the world’s leading cause of infectious blindness. Carrageenans are naturally occurring, sulfated polysaccharides generally considered safe for food and topical applications. Carrageenans can inhibit infection caused by a variety of viruses and bacteria. To investigate whether iota-carrageenan (I-C) isolated from the red alga Chondrus crispus could prevent ocular chlamydial infection, we assessed if targeted treatment of the conjunctival mucosa with I-C affects chlamydial attachment, entry, and replication in the host cell. Immortalized human conjunctival epithelial cells were treated with I-C prior to C. trachomatis infection and analyzed by flow cytometry and immunofluorescence microscopy. In vivo effects were evaluated in an ocular guinea pig inclusion conjunctivitis model. Ocular pathology was graded daily, and chlamydial clearance was investigated. Our study showed that I-C reduces the infectivity of C. trachomatis in vitro. In vivo results showed a slight reduced ocular pathology and significantly less shedding of infectious elementary bodies by infected animals. Our results indicate that I-C could be a promising agent to reduce the transmission of ocular chlamydial infection and opens perspectives to develop prophylactic approaches to block C. trachomatis entry into the host cell. |
format | Online Article Text |
id | pubmed-6096786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-60967862018-08-24 Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo Inic-Kanada, Aleksandra Stein, Elisabeth Stojanovic, Marijana Schuerer, Nadine Ghasemian, Ehsan Filipovic, Ana Marinkovic, Emilija Kosanovic, Dejana Barisani-Asenbauer, Talin J Appl Phycol Article Ocular chlamydial infections with the ocular serovars A, B, Ba, and C of Chlamydia trachomatis represent the world’s leading cause of infectious blindness. Carrageenans are naturally occurring, sulfated polysaccharides generally considered safe for food and topical applications. Carrageenans can inhibit infection caused by a variety of viruses and bacteria. To investigate whether iota-carrageenan (I-C) isolated from the red alga Chondrus crispus could prevent ocular chlamydial infection, we assessed if targeted treatment of the conjunctival mucosa with I-C affects chlamydial attachment, entry, and replication in the host cell. Immortalized human conjunctival epithelial cells were treated with I-C prior to C. trachomatis infection and analyzed by flow cytometry and immunofluorescence microscopy. In vivo effects were evaluated in an ocular guinea pig inclusion conjunctivitis model. Ocular pathology was graded daily, and chlamydial clearance was investigated. Our study showed that I-C reduces the infectivity of C. trachomatis in vitro. In vivo results showed a slight reduced ocular pathology and significantly less shedding of infectious elementary bodies by infected animals. Our results indicate that I-C could be a promising agent to reduce the transmission of ocular chlamydial infection and opens perspectives to develop prophylactic approaches to block C. trachomatis entry into the host cell. Springer Netherlands 2018-03-13 2018 /pmc/articles/PMC6096786/ /pubmed/30147240 http://dx.doi.org/10.1007/s10811-018-1435-0 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Inic-Kanada, Aleksandra Stein, Elisabeth Stojanovic, Marijana Schuerer, Nadine Ghasemian, Ehsan Filipovic, Ana Marinkovic, Emilija Kosanovic, Dejana Barisani-Asenbauer, Talin Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo |
title | Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo |
title_full | Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo |
title_fullStr | Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo |
title_full_unstemmed | Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo |
title_short | Effects of iota-carrageenan on ocular Chlamydia trachomatis infection in vitro and in vivo |
title_sort | effects of iota-carrageenan on ocular chlamydia trachomatis infection in vitro and in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096786/ https://www.ncbi.nlm.nih.gov/pubmed/30147240 http://dx.doi.org/10.1007/s10811-018-1435-0 |
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