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Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections

BACKGROUND: Inflammatory response during urinary tract infection (UTI) is mediated by innate immune defense. Nod like receptors (NLRs) have been proposed to work simultaneously beside TLR pathways to mediate pro-inflammatory response and maintain tissue homeostasis. Some in vitro reports have showed...

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Autores principales: Verma, Vivek, Gupta, Surbhi, Kumar, Parveen, Yadav, Sonal, Dhanda, Rakesh Singh, Gaind, Rajni, Arora, Renu, Frimodt-Møller, Niels, Yadav, Manisha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734172/
https://www.ncbi.nlm.nih.gov/pubmed/31551961
http://dx.doi.org/10.3389/fmicb.2019.02020
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author Verma, Vivek
Gupta, Surbhi
Kumar, Parveen
Yadav, Sonal
Dhanda, Rakesh Singh
Gaind, Rajni
Arora, Renu
Frimodt-Møller, Niels
Yadav, Manisha
author_facet Verma, Vivek
Gupta, Surbhi
Kumar, Parveen
Yadav, Sonal
Dhanda, Rakesh Singh
Gaind, Rajni
Arora, Renu
Frimodt-Møller, Niels
Yadav, Manisha
author_sort Verma, Vivek
collection PubMed
description BACKGROUND: Inflammatory response during urinary tract infection (UTI) is mediated by innate immune defense. Nod like receptors (NLRs) have been proposed to work simultaneously beside TLR pathways to mediate pro-inflammatory response and maintain tissue homeostasis. Some in vitro reports have showed the involvement of NLRP3 inflammasome during uropathogenic Escherichia coli (UPEC) mediated UTI. So we have sought to determine the status of various inflammasomes and their components in UPEC mediated UTI. METHODS: A total of 186 females experiencing the first episode of UTI were recruited for the study and forty were found to be positive for UPEC (≥10(5) CFU/ml) in their urine (N = 40). Further, we analyzed the expression of NLRP3, NLRC4, NAIP, AIM2, ASC, CASPASE-4, and CASPASE-1 gene at mRNA and protein level in the blood of UPEC confirmed study subjects through real time qPCR and immunoblotting. Healthy females (N = 40) visiting the OPD for health checkups, family planning advice and subjects undergoing routine medical examinations, were recruited as healthy control subjects. Pro-inflammatory cytokines (IL-6, IL-8, IFN-γ, TNF-α and MCP-1) were measured in the plasma of patients and controls through ELISA. For investigation of the involvement of NLRC4 and NLRP3 inflammasome, in vitro studies were performed using co-immunoprecipitation and confocal microscopy. RESULTS: Most of the inflammatory regulators studied (i.e., NLRP3, NAIP, NLRC4, ASC, and CASPASE-1) were found to be up-regulated at both mRNA and protein levels in the UPEC infected UTI patients. Also, pro-inflammatory cytokines (IL-6, IL-8, IFN-γ, TNF-α, and MCP-1) were found to be up-regulated in the patients group. However, no significant difference was observed in the expression of AIM2 and CASPASE-4 genes at both mRNA and protein levels. Further, in vitro studies have shown the involvement of NLRC4 inflammasome in UPEC infected THP1 derived macrophages. CONCLUSION: Involvement of NLRP3 and NLRC4 inflammasomes in UPEC infected UTI is evident from our findings. This is the first report showing levels of inflammasome and its components in UTI patients suggesting a possible role during UPEC mediated UTI. We have also reported the involvement of NLRC4 inflammasome for the first time during UTI infection.
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spelling pubmed-67341722019-09-24 Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections Verma, Vivek Gupta, Surbhi Kumar, Parveen Yadav, Sonal Dhanda, Rakesh Singh Gaind, Rajni Arora, Renu Frimodt-Møller, Niels Yadav, Manisha Front Microbiol Microbiology BACKGROUND: Inflammatory response during urinary tract infection (UTI) is mediated by innate immune defense. Nod like receptors (NLRs) have been proposed to work simultaneously beside TLR pathways to mediate pro-inflammatory response and maintain tissue homeostasis. Some in vitro reports have showed the involvement of NLRP3 inflammasome during uropathogenic Escherichia coli (UPEC) mediated UTI. So we have sought to determine the status of various inflammasomes and their components in UPEC mediated UTI. METHODS: A total of 186 females experiencing the first episode of UTI were recruited for the study and forty were found to be positive for UPEC (≥10(5) CFU/ml) in their urine (N = 40). Further, we analyzed the expression of NLRP3, NLRC4, NAIP, AIM2, ASC, CASPASE-4, and CASPASE-1 gene at mRNA and protein level in the blood of UPEC confirmed study subjects through real time qPCR and immunoblotting. Healthy females (N = 40) visiting the OPD for health checkups, family planning advice and subjects undergoing routine medical examinations, were recruited as healthy control subjects. Pro-inflammatory cytokines (IL-6, IL-8, IFN-γ, TNF-α and MCP-1) were measured in the plasma of patients and controls through ELISA. For investigation of the involvement of NLRC4 and NLRP3 inflammasome, in vitro studies were performed using co-immunoprecipitation and confocal microscopy. RESULTS: Most of the inflammatory regulators studied (i.e., NLRP3, NAIP, NLRC4, ASC, and CASPASE-1) were found to be up-regulated at both mRNA and protein levels in the UPEC infected UTI patients. Also, pro-inflammatory cytokines (IL-6, IL-8, IFN-γ, TNF-α, and MCP-1) were found to be up-regulated in the patients group. However, no significant difference was observed in the expression of AIM2 and CASPASE-4 genes at both mRNA and protein levels. Further, in vitro studies have shown the involvement of NLRC4 inflammasome in UPEC infected THP1 derived macrophages. CONCLUSION: Involvement of NLRP3 and NLRC4 inflammasomes in UPEC infected UTI is evident from our findings. This is the first report showing levels of inflammasome and its components in UTI patients suggesting a possible role during UPEC mediated UTI. We have also reported the involvement of NLRC4 inflammasome for the first time during UTI infection. Frontiers Media S.A. 2019-09-03 /pmc/articles/PMC6734172/ /pubmed/31551961 http://dx.doi.org/10.3389/fmicb.2019.02020 Text en Copyright © 2019 Verma, Gupta, Kumar, Yadav, Dhanda, Gaind, Arora, Frimodt-Møller and Yadav. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Verma, Vivek
Gupta, Surbhi
Kumar, Parveen
Yadav, Sonal
Dhanda, Rakesh Singh
Gaind, Rajni
Arora, Renu
Frimodt-Møller, Niels
Yadav, Manisha
Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections
title Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections
title_full Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections
title_fullStr Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections
title_full_unstemmed Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections
title_short Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic E. coli Mediated Urinary Tract Infections
title_sort involvement of nlrp3 and nlrc4 inflammasome in uropathogenic e. coli mediated urinary tract infections
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734172/
https://www.ncbi.nlm.nih.gov/pubmed/31551961
http://dx.doi.org/10.3389/fmicb.2019.02020
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