Browse > Article
http://dx.doi.org/10.4014/jmb.1408.08059

Whole-Blood Gene-Expression Profiles of Cows Infected with Mycobacterium avium subsp. paratuberculosis Reveal Changes in Immune Response and Lipid Metabolism  

Shin, Min-Kyoung (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Park, Hong-Tae (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Shin, Seung Won (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Jung, Myunghwan (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Im, Young Bin (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Park, Hyun-Eui (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Cho, Yong-Il (Department of Animal Resources Development, National Institute of Animal Science, Rural Development Administration)
Yoo, Han Sang (Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University)
Publication Information
Journal of Microbiology and Biotechnology / v.25, no.2, 2015 , pp. 255-267 More about this Journal
Abstract
Mycobacterium avium subsp. paratuberculosis (MAP) is the causative agent of Johne's disease, a chronic debilitating disease affecting ruminants worldwide. In the present study, we aimed to determine the major gene networks and pathways underlying the immune response to MAP infection using whole-blood cells, as well as provide the potential transcriptional markers for identifying the status of MAP infection. We analyzed the transcriptional profiles of whole-blood cells of cattle identified and grouped according to the presence of MAP-specific antibodies and the MAP shed by them. The grouping was based on the results obtained by ELISA and PCR analyses as follows: i) Test1 group: MAP-negative results obtained by ELISA and positive results obtained by PCR; ii) Test2 group: MAP-positive results obtained by ELISA and negative results obtained by PCR; iii) Test3 group: MAP-positive results obtained by ELISA and positive results obtained by PCR; iv) uninfected control: MAP-negative results obtained both by ELISA and PCR analysis. The results showed down-regulated production and metabolism of reactive oxygen species in the Test1 group, activation of pathways related to the host-defense response against MAP (LXR/RXR activation and complement system) in the Test2 and Test3 groups, and anti-inflammatory response (activation of IL-10 signaling pathway) only in the Test3 group. Our data indicate a balanced response that serves the immune-limiting mechanism while the host-defense responses are progressing.
Keywords
Mycobacterium avium subsp. paratuberculosis; Johne's disease; bovine; whole blood; transcriptome;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
연도 인용수 순위
1 Chiodini RJ, Vankruiningen HJ, Thayer WR, Merkal RS, Coutu JA. 1984. Possible role of mycobacteria in inflammatory boweldisease. 1. An unclassified Mycobacterium species isolated from patients with Crohns-disease. Digest. Dis. Sci. 29: 1073-1079.   DOI
2 Borelli V, Banfi E, Perrotta MG, Zabucchi G. 1999. Myeloperoxidase exerts microbicidal activity against Mycobacterium tuberculosis. Infect. Immun. 67: 4149-4152.
3 Rivas-Santiago B, Sada E, Tsutsumi V, Aguilar-Leon D, Contreras JL, Hernandez-Pando R. 2006. Beta-defensin gene expression during the course of experimental tuberculosis infection. J. Infect. Dis. 194: 697-701.   DOI   ScienceOn
4 Seth M, Lamont EA, Janagama HK, Widdel A, Vulchanova L, Stabel JR, et al. 2009. Biomarker discovery in subclinical mycobacterial infections of cattle. PLoS One 4: e5478.   DOI   ScienceOn
5 Yoo HS, Shin SJ. 2012. Recent research on bovine paratuberculosis in South Korea. Vet. Immunol. Immunopathol. 148: 23-28.   DOI   ScienceOn
6 Silbiger VN, Luchessi AD, Hirata RD, Lima-Neto LG, Cavichioli D, Carracedo A, et al. 2013. Novel genes detected by transcriptional profiling from whole-blood cells in patients with early onset of acute coronary syndrome. Clin. Chim. Acta 421: 184-190.   DOI   ScienceOn
7 Stabel JR, Whitlock RH. 2001. An evaluation of a modified interferon-gamma assay for the detection of paratuberculosis in dairy herds. Vet. Immunol. Immunopathol. 79: 69-81.   DOI   ScienceOn
8 Yakes BJ, Lipert RJ, Bannantine JP, Porter MD. 2008. Detection of Mycobacterium avium subsp. paratuberculosis by a sonicate immunoassay based on surface-enhanced Raman scattering. Clin. Vaccine Immunol. 15: 227-234.   DOI   ScienceOn
9 Zhong L, Taylor D, Begg DJ, Whittington RJ. 2011. Biomarker discovery for ovine paratuberculosis (Johne’s disease) by proteomic serum profiling. Comp. Immunol. Microbiol. Infect. Dis. 34: 315-326.   DOI   ScienceOn
10 Cha SB, Yoo A, Park HT, Sung KY, Shin MK, Yoo HS. 2013. Analysis of transcriptional profiles to discover biomarker candidates in Mycobacterium avium subsp. paratuberculosis-infected macrophages, RAW 264.7. J. Microbiol. Biotechnol. 23: 1167-1175.   DOI   ScienceOn
11 Coffman F. 2008. Chitinase 3-Like-1 (CHI3L1): a putative disease marker at the interface of proteomics and glycomics. Crit. Rev. Clin. Lab. Sci. 45: 531-562.   DOI
12 Dorshorst NC, Collins MT, Lombard JE. 2006. Decision analysis model for paratuberculosis control in commercial dairy herds. Prev. Vet. Med. 75: 92-122.   DOI   ScienceOn
13 Collins MT, Sockett DC, Goodger WJ, Conrad TA, Thomas CB, Carr DJ. 1994. Herd prevalence and geographic distribution of, and risk factors for, bovine paratuberculosis in Wisconsin. J. Am. Vet. Med. Assoc. 204: 636-641.
14 Coussens PM. 2001. Mycobacterium paratuberculosis and the bovine immune system. Anim. Health Res. Rev. 2: 141-161.   DOI
15 Cyktor JC, Carruthers B, Stromberg P, Flano E, Pircher H, Turner J. 2013. Killer cell lectin-like receptor G1 deficiency significantly enhances survival after Mycobacterium tuberculosis infection. Infect. Immun. 81: 1090-1099.   DOI   ScienceOn
16 Gumber S, Taylor DL, Whittington RJ. 2009. Evaluation of the immunogenicity of recombinant stress-associated proteins during Mycobacterium avium subsp. paratuberculosis infection: implications for pathogenesis and diagnosis. Vet. Microbiol. 137: 290-296.   DOI   ScienceOn
17 Hasonova L, Pavlik I. 2006. Economic impact of paratuberculosis in dairy cattle herds: a review. Vet. Med. Czech. 51: 193-211.
18 Hill BB, West M, Brock KV. 2003. An estimated prevalence of Johne’s disease in a subpopulation of Alabama beef cattle. J. Vet. Diagn. Invest. 15: 21-25.   DOI   ScienceOn
19 Jungersen G, Huda A, Hansen JJ, Lind P. 2002. Interpretation of the gamma interferon test for diagnosis of subclinical paratuberculosis in cattle. Clin. Diagn. Lab. Immunol. 9: 453-460.
20 Hoang LT, Lynn DJ, Henn M, Birren BW, Lennon NJ, Le PT, et al. 2010. The early whole-blood transcriptional signature of dengue virus and features associated with progression to dengue shock syndrome in Vietnamese children and young adults. J. Virol. 84: 12982-12994.   DOI   ScienceOn
21 Lamont EA, Xu WW, Sreevatsan S. 2013. Host-Mycobacterium avium subsp. paratuberculosis interactome reveals a novel iron assimilation mechanism linked to nitric oxide stress during early infection. BMC Genomics 14: 694.   DOI   ScienceOn
22 Kang DD, Lin Y, Moreno JR, Randall TD, Khader SA. 2011. Profiling early lung immune responses in the mouse model of tuberculosis. PLoS One 6: e16161.   DOI   ScienceOn
23 Killick KE, Browne JA, Park SD, Magee DA, Martin I, Meade KG, et al. 2011. Genome-wide transcriptional profiling of peripheral blood leukocytes from cattle infected with Mycobacterium bovis reveals suppression of host immune genes. BMC Genomics 12: 611.   DOI
24 Kim BH, Shenoy AR, Kumar P, Das R, Tiwari S, MacMicking JD. 2011. A family of IFN-gamma-inducible 65-kD GTPases protects against bacterial infection. Science 332: 717-721.   DOI   ScienceOn
25 Lande R, Giacomini E, Grassi T, Remoli ME, Iona E, Miettinen M, et al. 2003. IFN-alpha beta released by Mycobacterium tuberculosis-infected human dendritic cells induces the expression of CXCL10: selective recruitment of NK and activated T cells. J. Immunol. 170: 1174-1182.   DOI
26 Lang R. 2005. Tuning of macrophage responses by Stat3-inducing cytokines: molecular mechanisms and consequences in infection. Immunobiology 210: 63-76.   DOI   ScienceOn
27 Marcuzzi A, Bianco AM, Girardelli M, Tommasini A, Martelossi S, Monasta L, et al. 2013. Genetic and functional profiling of Crohn’s disease: autophagy mechanism and susceptibility to infectious diseases. Biomed. Res. Int. 2013: 297501.
28 Machugh DE, Taraktsoglou M, Killick KE, Nalpas NC, Browne JA, Park S, et al. 2012. Pan-genomic analysis of bovine monocyte-derived macrophage gene expression in response to in vitro infection with Mycobacterium avium subspecies paratuberculosis. Vet. Res. 43: 25.   DOI
29 Manning EJ, Collins MT. 2001. Mycobacterium avium subsp. paratuberculosis: pathogen, pathogenesis and diagnosis. Rev. Sci. Tech. 20: 133-150.   DOI
30 Nielsen SS, Toft N. 2009. A review of prevalences of paratuberculosis in farmed animals in Europe. Prev. Vet. Med. 88: 1-14.   DOI   ScienceOn
31 Mejias A, Dimo B, Suarez NM, Garcia C, Suarez-Arrabal MC, Jartti T, et al. 2013. Whole blood gene expression profiles to assess pathogenesis and disease severity in infants with respiratory syncytial virus infection. PLoS Med. 10: e1001549.   DOI
32 Nielsen SS, Toft N. 2008. Ante mortem diagnosis of paratuberculosis: a review of accuracies of ELISA, interferon-gamma assay and faecal culture techniques. Vet. Microbiol. 129: 217-235.   DOI   ScienceOn
33 O’Leary S, O’Sullivan MP, Keane J. 2011. IL-10 blocks phagosome maturation in Mycobacterium tuberculosis-infected human macrophages. Am. J. Respir. Cell. Mol. Biol. 45: 172-180.   DOI
34 Poccia F, Cipriani E, Vendetti S, Colizzi V, Poquet Y, Battistini L, et al. 1997. CD94/NKG2 inhibitory receptor complex modulates both anti-viral and anti-tumoral responses of polyclonal phosphoantigen-reactive V gamma 9V delta 2 T lymphocytes. J. Immunol. 159: 6009-6017.
35 Aly S, Laskay T, Mages J, Malzan A, Lang R, Ehlers S. 2007. Interferon-gamma-dependent mechanisms of mycobacteriainduced pulmonary immunopathology: the role of angiostasis and CXCR3-targeted chemokines for granuloma necrosis. J. Pathol. 212: 295-305.   DOI   ScienceOn