Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis

Autores:: Ramírez G, René
Maldonado E, Juan

Tipo de recurso:: Article of journal

Fecha de publicación:: 2013

Institución:: Universidad de Córdoba

Repositorio:: Repositorio Institucional Unicórdoba

Idioma:: spa

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dc.title.spa.fl_str_mv	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
dc.title.translated.eng.fl_str_mv	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
title	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
spellingShingle	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis Bacteria cell mediated immunity infections immune evasion paratuberculosis
title_short	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
title_full	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
title_fullStr	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
title_full_unstemmed	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
title_sort	Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis
dc.creator.fl_str_mv	Ramírez G, René Maldonado E, Juan
dc.contributor.author.spa.fl_str_mv	Ramírez G, René Maldonado E, Juan
dc.subject.spa.fl_str_mv	Bacteria cell mediated immunity infections immune evasion paratuberculosis
topic	Bacteria cell mediated immunity infections immune evasion paratuberculosis
publishDate	2013
dc.date.accessioned.none.fl_str_mv	2013-09-05 00:00:00 2022-07-01T20:58:03Z
dc.date.available.none.fl_str_mv	2013-09-05 00:00:00 2022-07-01T20:58:03Z
dc.date.issued.none.fl_str_mv	2013-09-05
dc.type.spa.fl_str_mv	Artículo de revista
dc.type.eng.fl_str_mv	Journal article
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dc.language.iso.spa.fl_str_mv	spa
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dc.relation.references.spa.fl_str_mv	Clarke C J. The pathology and pathogenesis of paratuberculosis in ruminants and other species. J Comp Pathol 1997; 116:217–261. http://dx.doi.org/10.1016/S0021-9975(97)80001-1 Stevenson K, Alvarez J, Bakker D, Biet F, de Juan L, Denham S, et al. Occurrence of Mycobacterium avium subspecies paratuberculosis across host species and European countries with evidence for transmission between wildlife and domestic ruminants. BMC Microbiol 2009; 9:212. doi:10.1186/1471-2180-9-212. http://dx.doi.org/10.1186/1471-2180-9-212 Francis J, Macturk HM, Madinaveitia J, Snow GA. Mycobactin, a growth factor for Mycobacterium johnei. I. Isolation from Mycobacterium phlei. Biochem J 1953; 55:596-607. http://dx.doi.org/10.1042/bj0550596 Matthews PR, McDiarmid A, Collins P, Brown A. The dependence of some strains of Mycobacterium avium on mycobactin for initial and subsequent growth. J Med Microbiol 1978; 11:53-57. http://dx.doi.org/10.1099/00222615-11-1-53 Zapata MM, Rodas JD, Maldonado JG. "paratuberculosis bovina: ¿conocemos la situación real de la enfermedad en la ganadería colombiana?" Rev Colomb Cienc Pecu 2008; 21:420-435. Burrells C, Clarke CJ, Colston A, Kay JM, Porter J, Little D, et al. Interferon-gamma and interleukin-2 release by lymphocytes derived from the blood, mesenteric lymph nodes and intestines of normal sheep and those affected with paratuberculosis (Johne's disease). Vet Immunol Immunopathol 1999; 68:139-148. http://dx.doi.org/10.1016/S0165-2427(99)00022-7 Coussens PM, Verman N, Coussens MA, Elftman MD, McNulty AM. Cytokine gene expression in peripheral blood mononuclear cells and tissues of cattle infected with Mycobacterium avium subsp. paratuberculosis: evidence for an inherent proinflammatory gene expression pattern. Infect Immun 2004; 72:1409-1422. http://dx.doi.org/10.1128/IAI.72.3.1409-1422.2004 Verschoor CP, Pant SD, You Q, Kelton DF, Karrow NA. Gene expression profiling of PBMCs from Holstein and Jersey cows sub-clinically infected with Mycobacterium avium ssp. paratuberculosis. Vet Immunol Immunopathol 2010; 137:1-11. http://dx.doi.org/10.1016/j.vetimm.2010.03.026 Woo SR, Sotos J, Hart AP, Barletta R, Gand Czuprynski CJ. Bovine monocytes and a macrophage cell line differ in their ability to phagocytose and support the intracellular survival of Mycobacterium avium subsp. paratuberculosis. Vet Immunol Immunopathol 2006; 110:109–120. http://dx.doi.org/10.1016/j.vetimm.2005.09.010 Clarke CJ. The pathology and pathogenesis of paratuberculosis in ruminants and other species. J Comp Pathol 1997; 116:217–261. http://dx.doi.org/10.1016/S0021-9975(97)80001-1 Souza CD, Evanson OA, Weiss DJ. Mitogen activated protein kinasep38 pathway is an important component of the anti-inflammatory response in Mycobacterium avium subsp. paratuberculosis-infected bovine monocytes. Microb Pathogen 2006; 41:59–66. http://dx.doi.org/10.1016/j.micpath.2006.04.002 Armstrong J, Hart D. Response of cultured macrophages to Mycobacterium tuberculosis, with observations on fusion of lysosomes with phagosomes. J Exp Med 1971; 134:713–740. http://dx.doi.org/10.1084/jem.134.3.713 Souza CD, Weiss DJ, Evanson OA. Role of theMAPK-ERK pathway in regulating cytokine expression by Mycobacterium avium subsp. paratuberculosis- infected bovine monocytes. Am J Vet Res 2007; 68:625–630. http://dx.doi.org/10.2460/ajvr.68.6.625 Adams JL, Czuprynski CJ. Mycobacterial cell wall components induce the production of TNF-alpha, IL-1, and IL-6 by bovine monocytes and the murine macrophage cell line RAW 264.7. Microb Pathog 1994; 16:401-411. http://dx.doi.org/10.1006/mpat.1994.1040 Souza CD, Evanson OA, Sreevatsan S, Weiss DJ. Cell membrane receptors on bovine mononuclear phagocytes involved in phagocytosis of Mycobacterium avium subsp paratuberculosis. Am J Vet Res 2007; 68:975-980. http://dx.doi.org/10.2460/ajvr.68.9.975 Whittington RJ, Windsor PA. In utero infection of cattle with Mycobacterium avium subsp. paratuberculosis: a critical review and meta-analysis. Vet J 2009; 179:60-69. http://dx.doi.org/10.1016/j.tvjl.2007.08.023 Aly SS, Thurmond MC. Evaluation of Mycobacterium avium subsp paratuberculosis infection of dairy cows attributable to infection status of the dam. J Am Vet Med Assoc 2005; 227:450-454. http://dx.doi.org/10.2460/javma.2005.227.450 Wu CW, Livesey M, Schmoller SK, Manning EJ, Steinberg H, Davis WC, et al. Invasion and persistence of Mycobacterium paratuberculosis during early stages of Johne's disease in calves. Infect Immun 2007; 75:2110-2119. http://dx.doi.org/10.1128/IAI.01739-06 Secott TE, Lin TL, Wu CC. Mycobacterium avium subsp. paratuberculosis fibronectin attachment protein facilitates M-cell targeting and invasion through a fibronectin bridge with host integrins. Infect Immun 2004; 72:3724-3732. http://dx.doi.org/10.1128/IAI.72.7.3724-3732.2004 Momotani E, Whipple DL, Thiermann AB, Cheville NF. Role of M cells and macrophages in the entrance of Mycobacterium paratuberculosis into domes of ileal Peyer's patches in calves. Vet Pathol 1988; 25:131-137. http://dx.doi.org/10.1177/030098588802500205 Khalifeh MS, Stabel JR. Effects of gamma interferon, interleukin-10, and transforming growth factor beta on the survival of Mycobacterium avium subsp. paratuberculosis in monocyte-derived macrophages from naturally infected cattle. Infect Immun 2004; 72:1974-1982. http://dx.doi.org/10.1128/IAI.72.4.1974-1982.2004 Buza JJ, Hikono H, Mori Y. Neutralization of interleukin-10 significantly enhances gamma interferon expression in peripheral blood by stimulation with Johnin purified protein derivative and by infection with Mycobacterium avium subsp. paratuberculosis in experimentally infected cattle with paratuberculosis. Infect Immun 2004; 72:2425-2428. http://dx.doi.org/10.1128/IAI.72.4.2425-2428.2004 Jorgensen JB. Survival of Mycobacterium paratuberculosis in slurry. Nord Vet Med 1977; 29:267-270. Nigou J, Zelle-Rieser C, Gilleron M, Thurnjer M, Puzo G. Mannosylated lipoarabinomannans inhibit IL-12 production by human dendritic cells: evidence for a negative signal delivered through the mannose receptor. J Immunol 2001; 166:7477-7485. http://dx.doi.org/10.4049/jimmunol.166.12.7477 Biet F, Bay S, Thibault VC, Euphrasie D, Grayon M, Ganneau C, et al. Lipopentapeptide induces a strong host humoral response and distinguishes Mycobacterium avium subsp. paratuberculosis from M. avium subsp. avium. Vaccine 2008; 26:257-268. http://dx.doi.org/10.1016/j.vaccine.2007.10.059 Dheenadhayalan V, Shin KS, Chang CF, Chang CD, Wang SJ, McDonough S, et al. Cloning and characterization of the genes coding for antigen 85A, 85B and 85C of Mycobacterium avium subsp. paratuberculosis. DNA Seq 2002; 13:287-294. http://dx.doi.org/10.1080/1042517021000019269 Gatfield J, Pieters J. Molecular mechanisms of host-pathogen interaction: entry and survival of mycobacteria in macrophages. Adv Immunol 2003; 81:45-96. http://dx.doi.org/10.1016/S0065-2776(03)81002-7 Ferwerda G, Kullberg BJ, de Jong DJ, Girardin SE, Langenberg DM, van Crevel R, et al. Mycobacterium paratuberculosis is recognized by Toll-like receptors and NOD2. J Leukoc Biol 2007; 82:1011-1018. http://dx.doi.org/10.1189/jlb.0307147 Weiss DJ, Souza CD. Review paper: modulation of mononuclear phagocyte function by Mycobacterium avium subsp. paratuberculosis. Vet Pathol 2008; 45:829-841. http://dx.doi.org/10.1354/vp.45-6-829 Weiss DJ, Evanson OA, McClenahan DJ, Abrahamsen MS, Walcheck BK. Regulation of expression of major histocompatibility antigens by bovine macrophages infected with Mycobacterium avium subsp. paratuberculosis or Mycobacterium avium subsp. avium. Infect Immun 2001; 69:1002-1008. http://dx.doi.org/10.1128/IAI.69.2.1002-1008.2001 Chiodini RJ, Davis WC. The cellular immunology of bovine paratuberculosis: the predominant response is mediated by cytotoxic gamma/delta T lymphocytes which prevent CD4+ activity. Microb Pathog 1992; 13:447-463. http://dx.doi.org/10.1016/0882-4010(92)90012-D Bassey EO, Collins MT. Study of T-lymphocyte subsets of healthy and Mycobacterium avium subsp. paratuberculosis-infected cattle. Infect Immun 1997; 65:4869-4872. Koo HC, Park YH, Hamilton MJ, Barrington GM, Davies CJ, Kim JB, et al. Analysis of the immune response to Mycobacterium avium subsp. paratuberculosis in experimentally infected calves. Infect Immun 2004; 72:6870-6883. http://dx.doi.org/10.1128/IAI.72.12.6870-6883.2004 Sommer S, Pudrith CB, Colvin CJ, Coussens PM. Mycobacterium avium subspecie paratuberculosis suppresses expression of IL-12p40 and iNOS genes induced by signalling through CD40 in bovine monocyte-derived macrophages. Vet Immunol Immunopathol 2009; 128:44-52. http://dx.doi.org/10.1016/j.vetimm.2008.10.036 http://dx.doi.org/10.1016/j.vetimm.2008.10.294 de Almeida DE, Colvin CJ, Coussens PM. Antigen–specific regulatory T cells in bovine paratuberculosis. Vet Immunol Immunopathol 2008; 125:234–245. http://dx.doi.org/10.1016/j.vetimm.2008.05.019 Haddad JJ, Saade NE, Safieh-Garanedian B. Interleukin-10 and the regulation of mitogen-activated protein kinases: are these signaling modules targets for the anti-inflammatory action of this cytokine? Cell Signal 2003; 15:255–267. http://dx.doi.org/10.1016/S0898-6568(02)00075-X Koul A, Herget T, Klebl B, Ullrich A. Interplay between mycobacteria and host signaling pathways. Nature Rev 2004; 2:189–202. Schorey JS, Cooper AM. Macrophage signaling upon mycobacterial infection: the MAP kinases lead the way. Cell Micro 2003; 5:133-142. http://dx.doi.org/10.1046/j.1462-5822.2003.00263.x Blumenthal A, Ehlers S, Ernst M, Flad HD, Reiling N. Control of mycobacterial replication in human macrophages: roles of extracellular signal-regulated kinases 1 and 2 and p38 mitogen-activated protein kinase pathways. Infect Immun 2002; 70:4961–4967. http://dx.doi.org/10.1128/IAI.70.9.4961-4967.2002 Khalifeh MS, Stabel JR. Upregulation of transforming growth factor-beta and interleukin-10 in cows with clinical Johne's disease. Vet Immunol Immunopathol 2004: 99:39-46. http://dx.doi.org/10.1016/j.vetimm.2004.01.009 Hao XR, Cao DL, Hu YW, Li XX, Liu XH, Xiao J, et al. IFN-gamma down-regulates ABCA1 expression by inhibiting LXRalpha in a JAK/STAT signaling pathway-dependent manner. Atherosclerosis 2009; 203:417-428. http://dx.doi.org/10.1016/j.atherosclerosis.2008.07.029 Zhao B, Collins MT, Czuprynski CJ. Effects of gamma interferon and nitric oxide on the interaction of Mycobacterium avium subsp. paratuberculosis with bovine monocytes. Infect Immun 1997; 65:1761–1766. McBribe JM, Jung T, de Vries JE, Aversa G. IL-10 alters DC function via modulation of cell surface molecules resulting in impaired T-cell responses. Cell Immunol 2002; 217:162–172. http://dx.doi.org/10.1016/S0008-8749(02)00007-2 Lei L, Hostetter JM. Limited phenotypic and functional maturation of bovine monocyte-derived dendritic cells following Mycobacterium avium subspecies paratuberculosis infection In vitro. Vet Immunol Immunopathol 2007; 120:177-186. http://dx.doi.org/10.1016/j.vetimm.2007.06.031 Olsen I, Boysen P, Kulberg S, Hope JC, Jungersen G, Storset AK. Bovine NK cells can produce gamma interferon in response to the secreted mycobacterial proteins ESAT-6 and MPP14 but not in response to MPB70. Infect Immun 2005; 73:5628-5635. http://dx.doi.org/10.1128/IAI.73.9.5628-5635.2005 Conti P, Kempuraj D, Kandere K, Di Gioacchino M, Barbacane RC, Castellani ML, et al. IL-10, an inflammatory/inhibitory cytokine, but not always. Immunol Lett 2003; 86:123–1299. http://dx.doi.org/10.1016/S0165-2478(03)00002-6 Motiwala AS, Janagama HK, Paustian ML, Zhu X, Bannantine JP, Kapur V, et al. Comparative transcriptional analysis of human macrophages exposed to animal and human isolates of Mycobacterium avium subspecies paratuberculosis with diverse genotypes. Infect Immun 2006; 74:6046-6056. http://dx.doi.org/10.1128/IAI.00326-06 Sut A, Sirugue S, Sixou S, Lakhdar-Ghazal F, Tocanne JF, Laneele G. Mycobacteria glycolipids as potential pathogenity effectors: alterations of model and natural membranes. Biochemisty 1990; 29:8498–8502. http://dx.doi.org/10.1021/bi00488a042 Fratazzi C, Arbeit RD, Carini C, Balcewicz-Sablinska MK, Keane J, Kornfeld H, Remold HG. Macrophage apoptosis in mycobacterial infections. J Leukocyte Biol 1999; 66:763-764. Coussens PM, Pudrith CB, Skovgaard K, Ren X, Suchyta SP, Stabel JR, et al. Johne's disease in cattle is associated with enhanced expression of genes encoding IL-5, GATA-3, tissue inhibitors of matrix metalloproteinases 1 and 2, and factors promoting apoptosis in peripheral blood mononuclear cells. Vet Immunol Immunopathol 2005; 105:221-234. http://dx.doi.org/10.1016/j.vetimm.2005.02.009 Jahraus A, Tjelle TE, Beerg T, Habermann A, Storrie B, Ulrich O, Griffiths G. In vitro fusion of phagosomes with different endocytic organelles from J774 macrophages. J Biol Chem 1998; 46:30379–30390. http://dx.doi.org/10.1074/jbc.273.46.30379 Knutson KL, Hmama Z, Herrera-Velit P, Rochford R, Reimer NE. Lipoarabinomannan of Mycobacterium tuberculosis promotes tyrosine dephosphorylation and inhibition of mitogen-activated protein kinase in human mononuclear phagocytes. J Biol Chem 1998; 273:645–652. http://dx.doi.org/10.1074/jbc.273.1.645 Hackam DJ, Rotstein OD, Zhang WJ, Demaurex N, Woodside M, Tsai O, et al. Regulation of phagosomal acidification. J Biol Chem 1997; 272:29810—29820. http://dx.doi.org/10.1074/jbc.272.47.29810 Coussens PM, Colvin CJ, Wiersma K, Abouzied A, Sipkovsky S. Gene expression profiling of peripheral blood mononuclear cells from cattle infected with Mycobacterium paratuberculosis. Infect Immun 2002; 70:5494-5502. http://dx.doi.org/10.1128/IAI.70.10.5494-5502.2002 Coussens PM, Colvin CJ, Rosa GJ, Perez Laspiur J, Elftman MD. Evidence for a novel gene expression program in peripheral blood mononuclear cells from Mycobacterium avium subsp. paratuberculosis-infected cattle. Infect Immun 2003; 71:6487-6498. http://dx.doi.org/10.1128/IAI.71.11.6487-6498.2003 Weiss DJ, Evanson OA, Deng M, Abrahamsen MS. Gene expression and antimicrobial activity of bovine macrophages in responses to Mycobacterium avium subsp. paratuberculosis. Vet Pathol 2004; 41:326-337. http://dx.doi.org/10.1354/vp.41-4-326 Janagama HK, Lamont EA, George S, Bannantine JP, Xu WW, Tu ZJ, et al. Primary transcriptomes of Mycobacterium avium subsp. paratuberculosis reveal proprietary pathways in tissue and macrophages. BMC Genomics 2010; 11:561. http://dx.doi.org/10.1186/1471-2164-11-561 Sechi LA, Felis GE, Ahmed N, Paccagnini D, Usai D, Ortu S, et al. Genome and transcriptome scale portrait of sigma factors in Mycobacterium avium subsp. paratuberculosis. Infect Genet Evol 2007; 7:424-432. http://dx.doi.org/10.1016/j.meegid.2007.01.001 Gumber S, Taylor DL, Marsh IB, Whittington RJ. Growth pattern and partial proteome of Mycobacterium avium subsp. paratuberculosis during the stress response to hypoxia and nutrient starvation. Vet Microbiol 2009; 133:344-357. http://dx.doi.org/10.1016/j.vetmic.2008.07.021 Gomes MS, Paul S, Moreira AL, Appelbereg R, Rabinovitch M, Kaplan G: Survival of Mycobacterium avium and Mycobacterium tuberculosis in acidified phagosomes of murine macrophages. Infect Immun 1999; 67:3199–3206.
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spelling	Ramírez G, Renéad827c50-15f5-4e54-8cc5-a0d3f646ae8c-1Maldonado E, Juanffe9b0f4-f4da-4973-9e70-739e599acdaa-12013-09-05 00:00:002022-07-01T20:58:03Z2013-09-05 00:00:002022-07-01T20:58:03Z2013-09-050122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/538410.21897/rmvz.163https://doi.org/10.21897/rmvz.1631909-0544application/pdfspaUniversidad de Córdobahttps://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://revistamvz.unicordoba.edu.co/article/view/163Bacteriacell mediated immunityinfectionsimmune evasionparatuberculosisEvasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosisEvasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosisArtículo de revistaJournal articleinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREFhttp://purl.org/coar/version/c_970fb48d4fbd8a85Clarke C J. The pathology and pathogenesis of paratuberculosis in ruminants and other species. J Comp Pathol 1997; 116:217–261. http://dx.doi.org/10.1016/S0021-9975(97)80001-1Stevenson K, Alvarez J, Bakker D, Biet F, de Juan L, Denham S, et al. Occurrence of Mycobacterium avium subspecies paratuberculosis across host species and European countries with evidence for transmission between wildlife and domestic ruminants. BMC Microbiol 2009; 9:212. doi:10.1186/1471-2180-9-212. http://dx.doi.org/10.1186/1471-2180-9-212Francis J, Macturk HM, Madinaveitia J, Snow GA. Mycobactin, a growth factor for Mycobacterium johnei. I. Isolation from Mycobacterium phlei. Biochem J 1953; 55:596-607. http://dx.doi.org/10.1042/bj0550596Matthews PR, McDiarmid A, Collins P, Brown A. The dependence of some strains of Mycobacterium avium on mycobactin for initial and subsequent growth. J Med Microbiol 1978; 11:53-57. http://dx.doi.org/10.1099/00222615-11-1-53Zapata MM, Rodas JD, Maldonado JG. "paratuberculosis bovina: ¿conocemos la situación real de la enfermedad en la ganadería colombiana?" Rev Colomb Cienc Pecu 2008; 21:420-435.Burrells C, Clarke CJ, Colston A, Kay JM, Porter J, Little D, et al. Interferon-gamma and interleukin-2 release by lymphocytes derived from the blood, mesenteric lymph nodes and intestines of normal sheep and those affected with paratuberculosis (Johne's disease). Vet Immunol Immunopathol 1999; 68:139-148. http://dx.doi.org/10.1016/S0165-2427(99)00022-7Coussens PM, Verman N, Coussens MA, Elftman MD, McNulty AM. Cytokine gene expression in peripheral blood mononuclear cells and tissues of cattle infected with Mycobacterium avium subsp. paratuberculosis: evidence for an inherent proinflammatory gene expression pattern. Infect Immun 2004; 72:1409-1422. http://dx.doi.org/10.1128/IAI.72.3.1409-1422.2004Verschoor CP, Pant SD, You Q, Kelton DF, Karrow NA. Gene expression profiling of PBMCs from Holstein and Jersey cows sub-clinically infected with Mycobacterium avium ssp. paratuberculosis. Vet Immunol Immunopathol 2010; 137:1-11. http://dx.doi.org/10.1016/j.vetimm.2010.03.026Woo SR, Sotos J, Hart AP, Barletta R, Gand Czuprynski CJ. Bovine monocytes and a macrophage cell line differ in their ability to phagocytose and support the intracellular survival of Mycobacterium avium subsp. paratuberculosis. Vet Immunol Immunopathol 2006; 110:109–120. http://dx.doi.org/10.1016/j.vetimm.2005.09.010Clarke CJ. The pathology and pathogenesis of paratuberculosis in ruminants and other species. J Comp Pathol 1997; 116:217–261. http://dx.doi.org/10.1016/S0021-9975(97)80001-1Souza CD, Evanson OA, Weiss DJ. Mitogen activated protein kinasep38 pathway is an important component of the anti-inflammatory response in Mycobacterium avium subsp. paratuberculosis-infected bovine monocytes. 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Infect Immun 1999; 67:3199–3206.https://revistamvz.unicordoba.edu.co/article/download/163/232Núm. 3 , Año 2013 : Revista MVZ Córdoba Volumen 18(3) Septiembre-Diciembre 201339073389718Revista MVZ CórdobaPublicationOREORE.xmltext/xml2591http://172.16.14.198/bitstreams/9aa34887-b5fc-454c-9c92-f47029a18ba3/downloadbc14e2265684232ce4a651de9e4f3f75MD51ucordoba/5384oai:172.16.14.198:ucordoba/53842023-10-06 00:45:20.025https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttp://172.16.14.198Repositorio Universidad de Córdobabdigital@metabiblioteca.com

Evasión molecular de la activación del macrófago bovino por Mycobacterium avium subespecie paratuberculosis

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