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Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs

Bacterial infections represent an unsolved problem today since bacteria can evade antibiotics and suppress the host’s immune response. A family of TRIM proteins is known to play a role in antiviral defense. However, the data on the involvement of the corresponding genes in the antibacterial response...

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Autores principales: Stepanenko, Ekaterina, Bondareva, Natalia, Sheremet, Anna, Fedina, Elena, Tikhomirov, Alexei, Gerasimova, Tatiana, Poberezhniy, Daniil, Makarova, Irina, Tarantul, Vyacheslav, Zigangirova, Nailya, Nenasheva, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487655/
https://www.ncbi.nlm.nih.gov/pubmed/37686095
http://dx.doi.org/10.3390/ijms241713290
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author Stepanenko, Ekaterina
Bondareva, Natalia
Sheremet, Anna
Fedina, Elena
Tikhomirov, Alexei
Gerasimova, Tatiana
Poberezhniy, Daniil
Makarova, Irina
Tarantul, Vyacheslav
Zigangirova, Nailya
Nenasheva, Valentina
author_facet Stepanenko, Ekaterina
Bondareva, Natalia
Sheremet, Anna
Fedina, Elena
Tikhomirov, Alexei
Gerasimova, Tatiana
Poberezhniy, Daniil
Makarova, Irina
Tarantul, Vyacheslav
Zigangirova, Nailya
Nenasheva, Valentina
author_sort Stepanenko, Ekaterina
collection PubMed
description Bacterial infections represent an unsolved problem today since bacteria can evade antibiotics and suppress the host’s immune response. A family of TRIM proteins is known to play a role in antiviral defense. However, the data on the involvement of the corresponding genes in the antibacterial response are limited. Here, we used RT-qPCR to profile the transcript levels of TRIM genes, as well as interferons and inflammatory genes, in human cell lines (in vitro) and in mice (in vivo) after bacterial infections caused by Pseudomonas aeruginosa and Chlamydia spp. As a result, the genes were identified that are involved in the overall immune response and associated primarily with inflammation in human cells and in mouse organs when infected with both pathogens (TRIM7, 8, 14, 16, 17, 18, 19, 20, 21, 47, 68). TRIMs specific to the infection (TRIM59 for P. aeruginosa, TRIM67 for Chlamydia spp.) were revealed. Our findings can serve as a basis for further, more detailed studies on the mechanisms of the immune response to P. aeruginosa and Chlamydia spp. Studying the interaction between bacterial pathogens and the immune system contributes to the search for new ways to successfully fight bacterial infections.
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spelling pubmed-104876552023-09-09 Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs Stepanenko, Ekaterina Bondareva, Natalia Sheremet, Anna Fedina, Elena Tikhomirov, Alexei Gerasimova, Tatiana Poberezhniy, Daniil Makarova, Irina Tarantul, Vyacheslav Zigangirova, Nailya Nenasheva, Valentina Int J Mol Sci Article Bacterial infections represent an unsolved problem today since bacteria can evade antibiotics and suppress the host’s immune response. A family of TRIM proteins is known to play a role in antiviral defense. However, the data on the involvement of the corresponding genes in the antibacterial response are limited. Here, we used RT-qPCR to profile the transcript levels of TRIM genes, as well as interferons and inflammatory genes, in human cell lines (in vitro) and in mice (in vivo) after bacterial infections caused by Pseudomonas aeruginosa and Chlamydia spp. As a result, the genes were identified that are involved in the overall immune response and associated primarily with inflammation in human cells and in mouse organs when infected with both pathogens (TRIM7, 8, 14, 16, 17, 18, 19, 20, 21, 47, 68). TRIMs specific to the infection (TRIM59 for P. aeruginosa, TRIM67 for Chlamydia spp.) were revealed. Our findings can serve as a basis for further, more detailed studies on the mechanisms of the immune response to P. aeruginosa and Chlamydia spp. Studying the interaction between bacterial pathogens and the immune system contributes to the search for new ways to successfully fight bacterial infections. MDPI 2023-08-27 /pmc/articles/PMC10487655/ /pubmed/37686095 http://dx.doi.org/10.3390/ijms241713290 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stepanenko, Ekaterina
Bondareva, Natalia
Sheremet, Anna
Fedina, Elena
Tikhomirov, Alexei
Gerasimova, Tatiana
Poberezhniy, Daniil
Makarova, Irina
Tarantul, Vyacheslav
Zigangirova, Nailya
Nenasheva, Valentina
Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs
title Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs
title_full Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs
title_fullStr Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs
title_full_unstemmed Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs
title_short Identification of Key TRIM Genes Involved in Response to Pseudomonas aeruginosa or Chlamydia spp. Infections in Human Cell Lines and in Mouse Organs
title_sort identification of key trim genes involved in response to pseudomonas aeruginosa or chlamydia spp. infections in human cell lines and in mouse organs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487655/
https://www.ncbi.nlm.nih.gov/pubmed/37686095
http://dx.doi.org/10.3390/ijms241713290
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