Literature DB >> 31104302

Analysis of inflammatory cytokine expression in the urinary tract of BALB/c mice infected with Proteus (P.) mirabilis and enteroaggregative Escherichia (E.) coli (EAEC) strains.

Araceli Melendez-Avalos1, Teresita Sainz-Espuñes2, Laura Estela Castrillón-Rivera2, Felipe Mendoza-Pérez2, Alejandro Palma-Ramos2, Jorge Ismael Castañeda-Sánchez2, Elisa Maria Drago-Serrano3.   

Abstract

This study aimed to analyze the proinflammatory cytokine mRNA expression in the urinary tract of BALB/c mice infected with bacterial strains with uropathogenic potential. Groups of four 6-week-old female BALB/c mice were intraurethrally inoculated with 5 × 107 colony-forming units (CFU) of P. mirabilis ATCC29906, EAEC O42, P. mirabilis RTX339, or sterile saline (control group) and then sacrificed at 0, 2, 4, 7, or 10 days post-infection (p.i.). Samples were cultured to determine the CFU/mL in urine or CFU/g in the bladders and kidneys. Cytokine expression (tumor necrosis factor (TNF)-α and interleukin (IL)-1β, -6, and -8) was evaluated in the target organs using real-time PCR and immunohistochemistry; histology was examined with hematoxylin and eosin staining. The results are presented as the means and standard deviations and were compared using one-way ANOVA, with p < 0.05 indicating significant differences. Bacteriuria was not detected in the infected groups; bacterial colonization occurred in the target organs at all time points, but was higher in mice infected with EAEC O42 or P. mirabilis RTX339 at 7 days p.i. The expression of all cytokine mRNAs was seen, but only the levels of the IL-8 protein increased in situ at 7 days p.i. in the P. mirabilis RTX339 and EAEC O42 groups in both organs. Morphological alterations, observed in all of the infected groups, were more prominent in the EAEC O42 and P. mirabilis RTX339 groups. The findings provide insights into the uropathogenicity and inflammatory cytokine expression in the urinary tract of mice infected with three previously untested bacterial strains.

Entities:  

Keywords:  Ascending urinary tract infection; Enteroaggregative Escherichia coli; Proteus mirabilis; Urinary tract inflammation

Year:  2019        PMID: 31104302     DOI: 10.1007/s12223-019-00714-2

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.099


  32 in total

1.  The fimbriae of enteroaggregative Escherichia coli induce epithelial inflammation in vitro and in a human intestinal xenograft model.

Authors:  Erik J Boll; Carsten Struve; Anja Sander; Zachary Demma; James P Nataro; Beth A McCormick; Karen A Krogfelt
Journal:  J Infect Dis       Date:  2012-06-21       Impact factor: 5.226

Review 2.  Global epidemiology of urinary tract infections.

Authors:  Zafer Tandogdu; Florian M E Wagenlehner
Journal:  Curr Opin Infect Dis       Date:  2016-02       Impact factor: 4.915

3.  The Pathogenic Potential of Proteus mirabilis Is Enhanced by Other Uropathogens during Polymicrobial Urinary Tract Infection.

Authors:  Chelsie E Armbruster; Sara N Smith; Alexandra O Johnson; Valerie DeOrnellas; Kathryn A Eaton; Alejandra Yep; Lona Mody; Weisheng Wu; Harry L T Mobley
Journal:  Infect Immun       Date:  2017-01-26       Impact factor: 3.441

4.  Enteroaggregative Escherichia coli expresses a novel flagellin that causes IL-8 release from intestinal epithelial cells.

Authors:  T S Steiner; J P Nataro; C E Poteet-Smith; J A Smith; R L Guerrant
Journal:  J Clin Invest       Date:  2000-06       Impact factor: 14.808

5.  Role of enteroaggregative Escherichia coli virulence factors in uropathogenesis.

Authors:  Erik J Boll; Carsten Struve; Nadia Boisen; Bente Olesen; Steen G Stahlhut; Karen A Krogfelt
Journal:  Infect Immun       Date:  2013-01-28       Impact factor: 3.441

6.  Proteus mirabilis fimbriae: construction of an isogenic pmfA mutant and analysis of virulence in a CBA mouse model of ascending urinary tract infection.

Authors:  G Massad; C V Lockatell; D E Johnson; H L Mobley
Journal:  Infect Immun       Date:  1994-02       Impact factor: 3.441

7.  Pet serine protease from enteroaggregative Escherichia coli stimulates the inflammatory response activating human macrophages.

Authors:  L M Rocha-Ramírez; U Hernández-Chiñas; D Baños-Rojas; J Xicohtencatl-Cortés; M E Chávez-Berrocal; G Rico-Rosillo; R Kretschmer; C A Eslava
Journal:  BMC Microbiol       Date:  2016-07-20       Impact factor: 3.605

8.  Pathogenic Lifestyles of E. coli Pathotypes in a Standardized Epithelial Cell Model Influence Inflammatory Signaling Pathways and Cytokines Secretion.

Authors:  Javier Sanchez-Villamil; Gabriela Tapia-Pastrana; Fernando Navarro-Garcia
Journal:  Front Cell Infect Microbiol       Date:  2016-10-07       Impact factor: 5.293

9.  The Role of Fibronectin in the Adherence and Inflammatory Response Induced by Enteroaggregative Escherichia coli on Epithelial Cells.

Authors:  Dominique Yáñez; Mariana Izquierdo; Fernando Ruiz-Perez; James P Nataro; Jorge A Girón; Roberto M Vidal; Mauricio J Farfan
Journal:  Front Cell Infect Microbiol       Date:  2016-12-08       Impact factor: 5.293

10.  Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1.

Authors:  Erik J Boll; Jorge Ayala-Lujan; Rose L Szabady; Christopher Louissaint; Rachel Z Smith; Karen A Krogfelt; James P Nataro; Fernando Ruiz-Perez; Beth A McCormick
Journal:  mBio       Date:  2017-06-06       Impact factor: 7.867

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