Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line

In the present paper, we report that C. trachomatis can be efficiently propagated and affect mRNA expression for two major cytokines, relevant to tumor progression, in CWR-R1 cells, a malignant prostate cell line. CWR-R1 and McCoy cells, a classic cell line for chlamydial research, were grown and in...

Full description

Bibliographic Details
Main Authors: Ivan M. Petyaev, Naylia A. Zigangirova, Elena Y. Morgunova, Nigel H. Kyle, Elena D. Fedina, Yuriy K. Bashmakov
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Advances in Urology
Online Access:http://dx.doi.org/10.1155/2019/6287057
id doaj-151546c743954611b5d9fe4f094bcc8d
record_format Article
spelling doaj-151546c743954611b5d9fe4f094bcc8d2020-11-25T01:01:14ZengHindawi LimitedAdvances in Urology1687-63691687-63772019-01-01201910.1155/2019/62870576287057Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell LineIvan M. Petyaev0Naylia A. Zigangirova1Elena Y. Morgunova2Nigel H. Kyle3Elena D. Fedina4Yuriy K. Bashmakov5Lycotec Ltd., Granta Park, Cambridge CB21 6GP, UKDepartment of Medical Microbiology, Gamaleya National Research Center of Epidemiology and Microbiology, Ministry of Health, 18 Gamaleya Str, Moscow 123098, RussiaDepartment of Medical Microbiology, Gamaleya National Research Center of Epidemiology and Microbiology, Ministry of Health, 18 Gamaleya Str, Moscow 123098, RussiaLycotec Ltd., Granta Park, Cambridge CB21 6GP, UKDepartment of Medical Microbiology, Gamaleya National Research Center of Epidemiology and Microbiology, Ministry of Health, 18 Gamaleya Str, Moscow 123098, RussiaLycotec Ltd., Granta Park, Cambridge CB21 6GP, UKIn the present paper, we report that C. trachomatis can be efficiently propagated and affect mRNA expression for two major cytokines, relevant to tumor progression, in CWR-R1 cells, a malignant prostate cell line. CWR-R1 and McCoy cells, a classic cell line for chlamydial research, were grown and infected with C. trachomatis under similar conditions. Cell monolayers were harvested for RNA analysis and immunostaining with major outer membrane protein (MOMP) antibody at 24, 48, and 72 hours of the postinfection (hpi) period. It was shown that the infectious cycle of chlamydial pathogen in CWR-R1 cells resembles the progression of C. trachomatis infection in McCoy cells but with a few important differences. First of all, the initial stage of C. trachomatis propagation in CWR-R1 cells (24 hpi) was characterized by larger inclusion bodies and more intense, specific immunofluorescent staining of infected cells as compared with McCoy cells. Moreover, there was a corresponding increase in infective progeny formation in CWR-R1 cells along with mRNA for EUO, a crucial gene controlling the early phase of the chlamydial development cycle (24 hpi). These changes were more minimal and became statistically insignificant at a later time point in the infectious cycle (48 hpi). Altogether, these data suggest that the early phase of C. trachomatis infection in CWR-R1 cells is accompanied by more efficient propagation of the pathogen as compared with the growth of C. trachomatis in McCoy cells. Furthermore, propagation of C. trachomatis in CWR-R1 cells leads to enhanced transcription of interleukin-6 and fibroblast growth factor-2, genes encoding two important proinflammatory cytokines implicated in the molecular mechanisms of chemoresistance of prostate cancer and its ability to metastasize. The possible roles of reactive oxygen species and impaired mitochondrial oxidation in the prostate cancer cell line are discussed as factors promoting the early stages of C. trachomatis growth in CWR-R1 cells.http://dx.doi.org/10.1155/2019/6287057
collection DOAJ
language English
format Article
sources DOAJ
author Ivan M. Petyaev
Naylia A. Zigangirova
Elena Y. Morgunova
Nigel H. Kyle
Elena D. Fedina
Yuriy K. Bashmakov
spellingShingle Ivan M. Petyaev
Naylia A. Zigangirova
Elena Y. Morgunova
Nigel H. Kyle
Elena D. Fedina
Yuriy K. Bashmakov
Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line
Advances in Urology
author_facet Ivan M. Petyaev
Naylia A. Zigangirova
Elena Y. Morgunova
Nigel H. Kyle
Elena D. Fedina
Yuriy K. Bashmakov
author_sort Ivan M. Petyaev
title Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line
title_short Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line
title_full Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line
title_fullStr Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line
title_full_unstemmed Chlamydia trachomatis Growth and Cytokine mRNA Response in a Prostate Cancer Cell Line
title_sort chlamydia trachomatis growth and cytokine mrna response in a prostate cancer cell line
publisher Hindawi Limited
series Advances in Urology
issn 1687-6369
1687-6377
publishDate 2019-01-01
description In the present paper, we report that C. trachomatis can be efficiently propagated and affect mRNA expression for two major cytokines, relevant to tumor progression, in CWR-R1 cells, a malignant prostate cell line. CWR-R1 and McCoy cells, a classic cell line for chlamydial research, were grown and infected with C. trachomatis under similar conditions. Cell monolayers were harvested for RNA analysis and immunostaining with major outer membrane protein (MOMP) antibody at 24, 48, and 72 hours of the postinfection (hpi) period. It was shown that the infectious cycle of chlamydial pathogen in CWR-R1 cells resembles the progression of C. trachomatis infection in McCoy cells but with a few important differences. First of all, the initial stage of C. trachomatis propagation in CWR-R1 cells (24 hpi) was characterized by larger inclusion bodies and more intense, specific immunofluorescent staining of infected cells as compared with McCoy cells. Moreover, there was a corresponding increase in infective progeny formation in CWR-R1 cells along with mRNA for EUO, a crucial gene controlling the early phase of the chlamydial development cycle (24 hpi). These changes were more minimal and became statistically insignificant at a later time point in the infectious cycle (48 hpi). Altogether, these data suggest that the early phase of C. trachomatis infection in CWR-R1 cells is accompanied by more efficient propagation of the pathogen as compared with the growth of C. trachomatis in McCoy cells. Furthermore, propagation of C. trachomatis in CWR-R1 cells leads to enhanced transcription of interleukin-6 and fibroblast growth factor-2, genes encoding two important proinflammatory cytokines implicated in the molecular mechanisms of chemoresistance of prostate cancer and its ability to metastasize. The possible roles of reactive oxygen species and impaired mitochondrial oxidation in the prostate cancer cell line are discussed as factors promoting the early stages of C. trachomatis growth in CWR-R1 cells.
url http://dx.doi.org/10.1155/2019/6287057
work_keys_str_mv AT ivanmpetyaev chlamydiatrachomatisgrowthandcytokinemrnaresponseinaprostatecancercellline
AT nayliaazigangirova chlamydiatrachomatisgrowthandcytokinemrnaresponseinaprostatecancercellline
AT elenaymorgunova chlamydiatrachomatisgrowthandcytokinemrnaresponseinaprostatecancercellline
AT nigelhkyle chlamydiatrachomatisgrowthandcytokinemrnaresponseinaprostatecancercellline
AT elenadfedina chlamydiatrachomatisgrowthandcytokinemrnaresponseinaprostatecancercellline
AT yuriykbashmakov chlamydiatrachomatisgrowthandcytokinemrnaresponseinaprostatecancercellline
_version_ 1725209992483569664