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Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection

The frequency and duration of Chlamydia trachomatis (Ct) ocular infections decrease with age, suggesting development of partial immunity. However, there is a lack of clear correlates of immunity to Ct infection in humans. We screened sera from a cohort of Gambian children followed for six-months aga...

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Autores principales: Pickering, Harry, Teng, Andy, Faal, Nkoyo, Joof, Hassan, Makalo, Pateh, Cassama, Eunice, Nabicassa, Meno, Last, Anna R., Burr, Sarah E., Rowland-Jones, Sarah L., Thomson, Nicholas R., Roberts, Chrissy h., Mabey, David C. W., Bailey, Robin L., Hayward, Richard D., de la Maza, Luis M., Holland, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575166/
https://www.ncbi.nlm.nih.gov/pubmed/28851925
http://dx.doi.org/10.1038/s41598-017-09193-2
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author Pickering, Harry
Teng, Andy
Faal, Nkoyo
Joof, Hassan
Makalo, Pateh
Cassama, Eunice
Nabicassa, Meno
Last, Anna R.
Burr, Sarah E.
Rowland-Jones, Sarah L.
Thomson, Nicholas R.
Roberts, Chrissy h.
Mabey, David C. W.
Bailey, Robin L.
Hayward, Richard D.
de la Maza, Luis M.
Holland, Martin J.
author_facet Pickering, Harry
Teng, Andy
Faal, Nkoyo
Joof, Hassan
Makalo, Pateh
Cassama, Eunice
Nabicassa, Meno
Last, Anna R.
Burr, Sarah E.
Rowland-Jones, Sarah L.
Thomson, Nicholas R.
Roberts, Chrissy h.
Mabey, David C. W.
Bailey, Robin L.
Hayward, Richard D.
de la Maza, Luis M.
Holland, Martin J.
author_sort Pickering, Harry
collection PubMed
description The frequency and duration of Chlamydia trachomatis (Ct) ocular infections decrease with age, suggesting development of partial immunity. However, there is a lack of clear correlates of immunity to Ct infection in humans. We screened sera from a cohort of Gambian children followed for six-months against a Ct-proteome microarray. At genome sequence level, we detected signatures of selection from a population of ocular Ct isolates from Guinea-Bissau. Together these approaches allowed us to highlight the focus of humoral responses and hypothesise new modes of pathogen immune evasion. Children who were susceptible to frequent and/or prolonged Ct infection had a less focussed antibody response, including preferential recognition of forty-two antigens. There was evidence of positive and purifying selection across the genome, but little balancing selection. In contrast, most antigens that were associated with susceptibility were under neutral selection. These data suggest an evasion strategy in which Ct presents a large panel of irrelevant antigens to the immune system to block or misdirect protective responses. Development of a focused immune response, possibly induced through vaccination, may be an effective strategy to promote protection to Ct infection.
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spelling pubmed-55751662017-09-01 Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection Pickering, Harry Teng, Andy Faal, Nkoyo Joof, Hassan Makalo, Pateh Cassama, Eunice Nabicassa, Meno Last, Anna R. Burr, Sarah E. Rowland-Jones, Sarah L. Thomson, Nicholas R. Roberts, Chrissy h. Mabey, David C. W. Bailey, Robin L. Hayward, Richard D. de la Maza, Luis M. Holland, Martin J. Sci Rep Article The frequency and duration of Chlamydia trachomatis (Ct) ocular infections decrease with age, suggesting development of partial immunity. However, there is a lack of clear correlates of immunity to Ct infection in humans. We screened sera from a cohort of Gambian children followed for six-months against a Ct-proteome microarray. At genome sequence level, we detected signatures of selection from a population of ocular Ct isolates from Guinea-Bissau. Together these approaches allowed us to highlight the focus of humoral responses and hypothesise new modes of pathogen immune evasion. Children who were susceptible to frequent and/or prolonged Ct infection had a less focussed antibody response, including preferential recognition of forty-two antigens. There was evidence of positive and purifying selection across the genome, but little balancing selection. In contrast, most antigens that were associated with susceptibility were under neutral selection. These data suggest an evasion strategy in which Ct presents a large panel of irrelevant antigens to the immune system to block or misdirect protective responses. Development of a focused immune response, possibly induced through vaccination, may be an effective strategy to promote protection to Ct infection. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5575166/ /pubmed/28851925 http://dx.doi.org/10.1038/s41598-017-09193-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pickering, Harry
Teng, Andy
Faal, Nkoyo
Joof, Hassan
Makalo, Pateh
Cassama, Eunice
Nabicassa, Meno
Last, Anna R.
Burr, Sarah E.
Rowland-Jones, Sarah L.
Thomson, Nicholas R.
Roberts, Chrissy h.
Mabey, David C. W.
Bailey, Robin L.
Hayward, Richard D.
de la Maza, Luis M.
Holland, Martin J.
Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection
title Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection
title_full Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection
title_fullStr Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection
title_full_unstemmed Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection
title_short Genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of Chlamydia trachomatis during ocular infection
title_sort genome-wide profiling of humoral immunity and pathogen genes under selection identifies immune evasion tactics of chlamydia trachomatis during ocular infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575166/
https://www.ncbi.nlm.nih.gov/pubmed/28851925
http://dx.doi.org/10.1038/s41598-017-09193-2
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