Investigation of the effect of Mycobacterium bovis infection on bovine neutrophils functions

Tuberculosis

Volumn 93, Issue 6, 2013, Pages 675-687

  Wang, Jin ^a,b   Zhou, Xiangmei ^a,b   Pan, Bo ^a,b   Yang, Lifeng ^a,b   Yin, Xiaomin ^a,b   Xu, Binrui ^a   Zhao, Deming ^a,b  

^a CHINA AGRICULTURAL UNIVERSITY   (China)

^b AGRO ENVIRONMENTAL PROTECTION INSTITUTE   (China)

Author keywords

Autophagy; Bovine neutrophil; Microbicidal mechanism; Mycobacterium bovis; Phagocytosis

Indexed keywords

ANTIMYCOBACTERIAL AGENT; MESSENGER RNA;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; AUTOPHAGY; BOVINE TUBERCULOSIS; CATTLE; CELL FUNCTION; CONTROLLED STUDY; COW; CYTOKINE PRODUCTION; DEFENSE MECHANISM; GENE EXPRESSION; HAZARD; IN VITRO STUDY; LEUKOCYTE; MACROPHAGE; MYCOBACTERIUM; MYCOBACTERIUM BOVIS; MYCOBACTERIUM SMEGMATIS; NEUTROPHIL; NONHUMAN; PHAGOCYTOSIS; PHENOTYPE; PRIORITY JOURNAL; PUBLIC HEALTH; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA EXTRACTION; STARVATION; TIME;

AUTOPHAGY; BOVINE NEUTROPHIL; MICROBICIDAL MECHANISM; MYCOBACTERIUM BOVIS; PHAGOCYTOSIS;

ANIMALS; APOPTOSIS; AUTOPHAGY; BLOOD PROTEINS; CATTLE; CELL COMMUNICATION; CELLS, CULTURED; CYTOKINES; INFLAMMATION MEDIATORS; MACROPHAGES; MICROSCOPY, ELECTRON; MYCOBACTERIUM BOVIS; NEUTROPHILS; PHAGOCYTOSIS; REACTIVE OXYGEN SPECIES; RECEPTORS, IMMUNOLOGIC; TUBERCULOSIS, BOVINE;

EID: 84887410657     PISSN: 14729792     EISSN: 1873281X     Source Type: Journal    
DOI: 10.1016/j.tube.2013.07.002     Document Type: Article

References (38)

1. O. Cosivi, J.M. Grange, C. Daborn, M.C. Raviglione, T. Fujikura, D. Cousins, R. Robinson, H. Huchzermeyer, I. De Kantor, and F. Meslin Zoonotic tuberculosis due to Mycobacterium bovis in developing countries Emerg Infect Dis 4 1998 59
2. T. Garnier, K. Eiglmeier, J.-C. Camus, N. Medina, H. Mansoor, M. Pryor, S. Duthoy, S. Grondin, C. Lacroix, and C. Monsempe The complete genome sequence of Mycobacterium bovis Proc Natl Acad Sci U S A 100 2003 7877 7882
3. B.D. Perry Investing in animal health research to alleviate poverty 2002 ILRI (aka ILCA and ILRAD)
4. A. Renwick, P. White, and R. Bengis Bovine tuberculosis in southern African wildlife: a multi-species host-pathogen system Epidemiol Infect 135 2007 529 540
5. C. Nathan Neutrophils and immunity: challenges and opportunities Nat Rev Immunol 6 2006 173 182
6. N. Borregaard Neutrophils, from marrow to microbes Immunity 33 2010 657 670
7. P. González-Cano, R. Mondragón-Flores, L.E. Sánchez-Torres, S. González-Pozos, M. Silva-Miranda, A. Monroy-Ostria, S. Estrada-Parra, and I. Estrada-García Mycobacterium tuberculosis H37Rv induces ectosome release in human polymorphonuclear neutrophils Tuberculosis 90 2010 125 134
8. R. Appelberg Neutrophils and intracellular pathogens: beyond phagocytosis and killing Trends Microbiol 15 2007 87 92
9. A. Mantovani, M.A. Cassatella, C. Costantini, and S. Jaillon Neutrophils in the activation and regulation of innate and adaptive immunity Nat Rev Immunol 11 2011 519 531
10. G.P. Sandilands, Z. Ahmed, N. Perry, M. Davison, A. Lupton, and B. Young Cross-linking of neutrophil CD11b results in rapid cell surface expression of molecules required for antigen presentation and T-cell activation Immunology 114 2005 354 368
11. B. Abdel-Salam T-cell proliferation by surface molecules expression on polymorphonuclear neutrophils stimulated with IL-4 in superantigen presence Allergol Immunopathol (Madr) 40 2012 81 87
12. J. Pedrosa, B.M. Saunders, R. Appelberg, I.M. Orme, M.T. Silva, and A.M. Cooper Neutrophils play a protective nonphagocytic role in systemic Mycobacterium tuberculosis infection of mice Infect Immun 68 2000 577 583
13. J. Barrios-Payan, D. Aguilar-Leon, R. Lascurain-Ledezma, and R. Hernandez-Pando Neutrophil participation in early control and immune activation during experimental pulmonary tuberculosis Gac Med Mex 142 2006 273
14. P. Seiler, P. Aichele, S. Bandermann, A.E. Hauser, B. Lu, N.P. Gerard, C. Gerard, S. Ehlers, H.J. Mollenkopf, and S.H. Kaufmann Early granuloma formation after aerosol Mycobacterium tuberculosis infection is regulated by neutrophils via CXCR3-signaling chemokines Eur J Immunol 33 2003 2676 2686
15. M.P. Berry, C.M. Graham, F.W. McNab, Z. Xu, S.A. Bloch, T. Oni, K.A. Wilkinson, R. Banchereau, J. Skinner, and R.J. Wilkinson An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis Nature 466 2010 973 977
16. D.M. Lowe, P.S. Redford, R.J. Wilkinson, A. O'Garra, and A.R. Martineau Neutrophils in tuberculosis: friend or foe? Trends Immunol 33 2012 14 25
17. J. Nancy Hilda, A. Selvaraj, and S.D. Das Mycobacterium tuberculosis H37Rv is more effective compared to vaccine strains in modulating neutrophil functions: an in vitro study FEMS Immunol Med Microbiol 66 2012 372 381
18. Y. Huang, X. Zhou, Y. Bai, L. Yang, X. Yin, Z. Wang, and D. Zhao Phagolysosome maturation of macrophages was reduced by PE-PGRS 62 protein expressing in Mycobacterium smegmatis and induced in IFN-γ priming Vet Microbiol 160 2012 117 125
19. S. Rivas-Fuentes, E. García-García, G. Nieto- Castañeda, and C. Rosales Fcγ receptors exhibit different phagocytosis potential in human neutrophils Cell Immunol 263 2010 114 121
20. N. Reiling, C. Hölscher, A. Fehrenbach, S. Kröger, C.J. Kirschning, S. Goyert, and S. Ehlers Cutting edge: Toll-like receptor (TLR) 2-and TLR4-mediated pathogen recognition in resistance to airborne infection with Mycobacterium tuberculosis J Immunol 169 2002 3480 3484
21. M.A. Cassatella Neutrophil-derived proteins: selling cytokines by the pound Adv Immunol 73 1999 369-509
22. X. Zhang, Y. Kluger, Y. Nakayama, R. Poddar, C. Whitney, A. DeTora, S.M. Weissman, and P.E. Newburger Gene expression in mature neutrophils: early responses to inflammatory stimuli J Leukoc Biol 75 2004 358 372
23. B. Amulic, C. Cazalet, G.L. Hayes, K.D. Metzler, and A. Zychlinsky Neutrophil function: from mechanisms to disease Annu Rev Immunol 30 2012 459 489
24. M. Faurschou, and N. Borregaard Neutrophil granules and secretory vesicles in inflammation Microbes Infect 5 2003 1317 1327
25. K.A. Brogden Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria? Nat Rev Microbiol 3 2005 238 250
26. M. Aleman, A. Garcia, M.A. Saab, S.S. de la Barrera, M. Finiasz, E. Abbate, and M.C. Sasiain Mycobacterium tuberculosis-induced activation accelerates apoptosis in peripheral blood neutrophils from patients with active tuberculosis Am J Respir Cell Mol Biol 27 2002 583 592
27. O. Soehnlein, C. Weber, and L. Lindbom Neutrophil granule proteins tune monocytic cell function Trends Immunol 30 2009 538 546
28. J. Huang, V. Canadien, G.Y. Lam, B.E. Steinberg, M.C. Dinauer, M.A. Magalhaes, M. Glogauer, S. Grinstein, and J.H. Brumell Activation of antibacterial autophagy by NADPH oxidases Proc Natl Acad Sci U S A 106 2009 6226 6231
29. I. Mitroulis, I. Kourtzelis, K. Kambas, S. Rafail, A. Chrysanthopoulou, M. Speletas, and K. Ritis Regulation of the autophagic machinery in human neutrophils Eur J Immunol 40 2010 1461 1472
30. M.G. Gutierrez, S.S. Master, S.B. Singh, G.A. Taylor, M.I. Colombo, and V. Deretic Autophagy is a defense mechanism inhibiting BCG and Mycobacterium tuberculosis survival in infected macrophages Cell 119 2004 753 766
31. Q. Remijsen, T. Kuijpers, E. Wirawan, S. Lippens, P. Vandenabeele, and T.V. Berghe Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality Cell Death Differ 18 2011 581 588
32. M. Songane, J. Kleinnijenhuis, M.G. Netea, and R. van Crevel The role of autophagy in host defence against Mycobacterium tuberculosis infection Tuberculosis 92 2012 388 396
33. C. Braian, V. Hogea, and O. Stendahl Mycobacterium tuberculosis-induced neutrophil extracellular traps activate human macrophages J Innate Immun 6 2013 10.1159/000348676
34. S.-Y. Eum, J.-H. Kong, M.-S. Hong, Y.-J. Lee, J.-H. Kim, S.-H. Hwang, S.-N. Cho, L.E. Via, and C.E. Barry Neutrophils are the predominant infected phagocytic cells in the airways of patients with active pulmonary TB Chest J 137 2010 122 128
35. B. Corleis, D. Korbel, R. Wilson, J. Bylund, R. Chee, and U.E. Schaible Escape of Mycobacterium tuberculosis from oxidative killing by neutrophils Cell Microbiol 14 2012 1109 1121
36. P. Seiler, P. Aichele, B. Raupach, B. Odermatt, U. Steinhoff, and S.H. Kaufmann Rapid neutrophil response controls fast-replicating intracellular bacteria but not slow-replicating Mycobacterium tuberculosis J Infect Dis 181 2000 671 680
37. E.B. Eruslanov, I.V. Lyadova, T.K. Kondratieva, K.B. Majorov, I.V. Scheglov, M.O. Orlova, and A.S. Apt Neutrophil responses to Mycobacterium tuberculosis infection in genetically susceptible and resistant mice Infect Immun 73 2005 1744 1753
38. D. Kumar, L. Nath, M.A. Kamal, A. Varshney, A. Jain, S. Singh, and K.V. Rao Genome-wide analysis of the host intracellular network that regulates survival of Mycobacterium tuberculosis Cell 140 2010 731 743