dc.contributorPedroza-Roldán, C., Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Col. Colinas de la NormalGuadalajara, Jalisco, Mexico, Dpto. de Medicina Veterinaria. Hospital Veterinario-CUCBA, Universidad de Guadalajara, Av. Prolongación Parres Arias No. 735. Col. Bosques Del Centinela II. C.P. 45187. ZapopanJalisco, Mexico; Aceves-Sánchez, M.J., Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Col. Colinas de la NormalGuadalajara, Jalisco, Mexico; Zaveri, A., Department of Molecular Reproduction, Development and Genetics, Indian Institute of ScienceBangalore, India; Charles-Niño, C., Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Sierra Mojada 950, Edificio PGuadalajara, Jalisco, Mexico; Elizondo-Quiroga, D.E., Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Col. Colinas de la NormalGuadalajara, Jalisco, Mexico; Hernández-Gutiérrez, R., Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Col. Colinas de la NormalGuadalajara, Jalisco, Mexico; Allen, K., Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Col. Colinas de la NormalGuadalajara, Jalisco, Mexico; Visweswariah, S.S., Department of Molecular Reproduction, Development and Genetics, Indian Institute of ScienceBangalore, India; Flores-Valdez, M.A., Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Col. Colinas de la NormalGuadalajara, Jalisco, Mexico
dc.creatorPedroza-Roldan, C.
dc.creatorAceves-Sanchez, M.J.
dc.creatorZaveri, A.
dc.creatorCharles-Nino, C.
dc.creatorElizondo-Quiroga, D.E.
dc.creatorHernandez-Gutierrez, R.
dc.creatorAllen, K.
dc.creatorVisweswariah, S.S.
dc.creatorFlores-Valdez, M.A.
dc.date.accessioned2015-11-19T18:57:48Z
dc.date.accessioned2022-11-02T15:24:02Z
dc.date.available2015-11-19T18:57:48Z
dc.date.available2022-11-02T15:24:02Z
dc.date.created2015-11-19T18:57:48Z
dc.date.issued2014
dc.identifierhttp://hdl.handle.net/20.500.12104/71233
dc.identifier10.1007/s12223-014-0335-1
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84919335827&partnerID=40&md5=92c4ab10320534a42ef4122f6231e511
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5013410
dc.description.abstractAll organisms have the capacity to sense and respond to environmental changes. These signals often involve the use of second messengers such as cyclic adenosine monophosphate (cAMP). This second messenger is widely distributed among organisms and coordinates gene expression related with pathogenesis, virulence, and environmental adaptation. Genomic analysis in Mycobacterium tuberculosis has identified 16 adenylyl cyclases (AC) and one phosphodiesterase, which produce and degrade cAMP, respectively. To date, ten AC have been biochemically characterized and only one (Rv0386) has been found to be important during murine infection with M. tuberculosis. Here, we investigated the impact of hsp60-driven Rv2212 gene expression in Mycobacterium bovis Bacillus Calmette-Guerin (BCG) during growth in vitro, and during macrophage and mice infection. We found that hsp60-driven expression of Rv2212 resulted in an increased capacity of replication in murine macrophages but an attenuated phenotype in lungs and spleen when administered intravenously in mice. Furthermore, this strain displayed an altered proteome mainly affecting proteins associated with stress conditions (bfrB, groEL-2, DnaK) that could contribute to the attenuated phenotype observed in mice. © 2014, Institute of Microbiology, Academy of Sciences of the Czech Republic, v.v.i.
dc.relationFolia Microbiologica
dc.relation60
dc.relation1
dc.relation21
dc.relation31
dc.relationScopus
dc.relationWOS
dc.titleThe adenylyl cyclase Rv2212 modifies the proteome and infectivity of Mycobacterium bovis BCG
dc.typeArticle


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