3 research outputs found

    Extended-spectrum ÎČ-lactamases, transferable quinolone resistance, and virulotyping in extra-intestinal E. coli in Uruguay

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    Introduction: To characterize extended-spectrum ÎČ-lactamases (ESBLs) and plasmid-mediated quinolone resistance (PMQR) genes in Escherichia coli isolates obtained from extra-intestinal samples in three Uruguayan hospitals. Methodology: Fifty-five ESBL-producing E. coli isolates were studied. Virulence genes, ESBLs, and PMQR genes were detected by polymerase chain reaction. ESBL-producing isolates were compared by pulsed-field gel electrophoresis. Multi-locus sequence typing was also performed on 13 selected isolates. Results: Thirty-seven isolates harbored blaCTX-M-15 (67.3%), eight blaCTX-M-2 (14.6%), five blaCTX-M-14 (9.1%), three carried both blaCTX-M-2 and blaCTX-M-14, one blaCTX-M-9, and one blaCTX-M-8. Among the CTX-M-15 producers, 92% belonged to sequence types ST131 and ST405, and carried aac(6’)Ib-cr as well. Isolates harboring blaCTX-M-2, blaCTX-M-14, blaCTX-M-9, or blaCTX-M-8 were found to be genetically unrelated. Conclusions: The successful dissemination of CTX-M-15-producing E.coli isolates seems to be linked to the spreading of high-risk clones and horizontal gene transfer. A trade-off between carrying more antibiotic resistance and less virulence-related genes could partially account for the evolutionary advantages featured by successful clones.Fil: Vignoli, Rafael. Universidad de la RepĂșblica; UruguayFil: GarcĂ­a Fulgueiras, Virginia. Universidad de la RepĂșblica; UruguayFil: Cordeiro, NicolĂĄs F.. Universidad de la RepĂșblica; UruguayFil: Bado, InĂ©s. Universidad de la RepĂșblica; UruguayFil: Seija, VerĂłnica. Universidad de la RepĂșblica; Uruguay. Hospital Pasteur de Montevideo; UruguayFil: Aguerrebere, Paula. Universidad de la RepĂșblica; UruguayFil: Laguna, Gabriel. Universidad de la RepĂșblica; UruguayFil: AraĂșjo, LucĂ­a. Universidad de la RepĂșblica; UruguayFil: Bazet, Cristina. Universidad de la RepĂșblica; UruguayFil: Gutkind, Gabriel Osvaldo. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; Argentina. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Houssay; ArgentinaFil: Chabalgoity RodrĂ­guez, JosĂ© Alejandro. Universidad de la RepĂșblica; Urugua

    Innate immune responses to Proteus mirabilis flagellin in the urinary tract

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    Flagella are bacterial virulence factors allowing microorganisms to move over surfaces. Flagellin, the structural component of flagella, is sensed by the host via Toll and NOD-like receptors and triggers pro-inflammatory responses. The use of Toll-like receptors agonists to modulate innate immune responses has aroused great interest as an alternative to improve the treatment of diverse infectious diseases. Proteus mirabilis is a Gram negative bacterium that causes urinary tract infections in humans. In the present work we used different approaches to study the ability of P. mirabilis flagellin to induce an innate immune response. We demonstrated that P. mirabilis flagellin has the ability to induce pro-inflammatory chemokines expression in T24 bladder cultures cells and in the mouse bladder after instillation. It was evidenced also that flagellin from different P. mirabilis strains differed in their capacity to induce an innate immune response in the CacoCCL20-Luc system. Also, flagellin elicited inflammation, with recruitment of leukocytes to the bladder epithelium. Flagellin instillation before an experimental P. mirabilis infection showed that the inflammatory response due to flagellin did not help to clear the infection but favored bacterial colonization. Thus, induction of inflammatory response in the bladder did not contribute to P. mirabilis infection neutralizationFil: UmpiĂ©rrez, AnalĂ­a Alejandra SofĂ­a. Instituto de Investigaciones BiolĂłgicas "Clemente Estable"; UruguayFil: Scavone, Paola. Instituto de Investigaciones BiolĂłgicas "Clemente Estable"; UruguayFil: Romanin, David Emmanuel. Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Departamento de Ciencias BiolĂłgicas. Laboratorio de Investigaciones del Sistema Inmune; Argentina. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; ArgentinaFil: MarquĂ©s, Juan MartĂ­n. Universidad de la RepĂșblica; UruguayFil: Chabalgoity RodrĂ­guez, JosĂ© Alejandro. Universidad de la RepĂșblica; UruguayFil: Rumbo, MartĂ­n. Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Departamento de Ciencias BiolĂłgicas. Laboratorio de Investigaciones del Sistema Inmune; Argentina. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; ArgentinaFil: Zunino, Pablo. Instituto de Investigaciones BiolĂłgicas "Clemente Estable"; Urugua

    Draft genome sequence of Salmonella enterica subsp. enterica serovar Infantis strain SPE101, isolated from a chronic human infection

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    We report a 4.99-Mb draft genome sequence of Salmonella enterica subsp. enterica serovar Infantis strain SPE101, isolated from feces of a 5-month-old breast-fed female showing diarrhea associated with severe dehydration and malnutrition. The infection prolonged for 6 months despite antibiotic treatment.Fil: Iriarte, AndrĂ©s. Universidad de la RepĂșblica; UruguayFil: Giner Lamia, JoaquĂ­n. Consejo Superior de Investigaciones CientĂ­ficas; EspañaFil: Silva, Claudia. Universidad Nacional AutĂłnoma de MĂ©xico. Instituto de BiotecnologĂ­a; MĂ©xicoFil: Betancor, Laura. Universidad de la RepĂșblica; UruguayFil: Astocondor, Lizeth. Universidad Peruana Cayetano Heredia; PerĂșFil: Cestero, Juan J.. Consejo Superior de Investigaciones CientĂ­ficas; EspañaFil: Ochoa, Theresa. Universidad Peruana Cayetano Heredia; PerĂșFil: GarcĂ­a, Coralith. Universidad Peruana Cayetano Heredia; PerĂșFil: Puente, JosĂ© L.. Universidad de la RepĂșblica; Uruguay. Universidad Nacional AutĂłnoma de MĂ©xico. Instituto de BiotecnologĂ­a; MĂ©xicoFil: Chabalgoity RodrĂ­guez, JosĂ© Alejandro. Universidad de la RepĂșblica; UruguayFil: GarcĂ­a del Portillo, Francisco. Consejo Superior de Investigaciones CientĂ­ficas; EspañaFil: Soncini, Fernando Carlos. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Centro CientĂ­fico TecnolĂłgico Conicet - Rosario. Instituto de BiologĂ­a Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias BioquĂ­micas y FarmacĂ©uticas. Instituto de BiologĂ­a Molecular y Celular de Rosario; ArgentinaFil: Garcia Vescovi, Eleonora. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Centro CientĂ­fico TecnolĂłgico Conicet - Rosario. Instituto de BiologĂ­a Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias BioquĂ­micas y FarmacĂ©uticas. Instituto de BiologĂ­a Molecular y Celular de Rosario; ArgentinaFil: Soleto, Lorena. Cenetrop; BoliviaFil: Flores, Griselda. Cenetrop; BoliviaFil: Pedraza, JosĂ©. Cenetrop; BoliviaFil: Yim, Lucia. Universidad de la RepĂșblica; UruguayFil: Hinostroza, NoemĂ­. Universidad Peruana Cayetano Heredia; PerĂșFil: Pucciarelli, M. Graciela. Universidad AutĂłnoma de Madrid; Españ
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