Effects of virulent and attenuated transmissible gastroenteritis virus on the ability of porcine dendritic cells to sample and present antigen

Veterinary Microbiology

Volumn 171, Issue 1-2, 2014, Pages 74-86

  Zhao, Shanshan ^a   Gao, Qi ^a   Qin, Tao ^a   Yin, Yinyan ^a   Lin, Jian ^a   Yu, Qinghua ^a   Yang, Qian ^a  

^a NANJING AGRICULTURAL UNIVERSITY   (China)

Author keywords

Intestinal DCs; Major histocompatibility complex classes II (SLA II DR); Monocyte derived dendritic cells (Mo DCs); T cell proliferation; Virulent and attenuated transmissible gastroenteritis virus (TGEV)

Indexed keywords

CELL SURFACE MARKER; GAMMA INTERFERON; INTERLEUKIN 10; INTERLEUKIN 12; VIRUS ANTIGEN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIGEN PRESENTATION; ARTICLE; CONTROLLED STUDY; CORONAVIRUS INFECTION; CYTOKINE RELEASE; DENDRITIC CELL; DISEASE PREDISPOSITION; DOWN REGULATION; IN VITRO STUDY; IN VIVO STUDY; LYMPHOCYTE PROLIFERATION; MONOCYTE; NONHUMAN; PIGLET; PROTEIN EXPRESSION; T LYMPHOCYTE; T LYMPHOCYTE ACTIVATION; TRANSMISSIBLE GASTROENTERITIS VIRUS; VIRUS ATTENUATION; VIRUS PATHOGENESIS; VIRUS VIRULENCE;

SUS; TRANSMISSIBLE GASTROENTERITIS VIRUS;

INTESTINAL DCS; MAJOR HISTOCOMPATIBILITY COMPLEX CLASSES II (SLA-II-DR); MONOCYTE-DERIVED DENDRITIC CELLS (MO-DCS); T-CELL PROLIFERATION; VIRULENT AND ATTENUATED TRANSMISSIBLE GASTROENTERITIS VIRUS (TGEV);

ANIMALS; ANTIGENS, VIRAL; CELL PROLIFERATION; CYTOKINES; DENDRITIC CELLS; GASTROENTERITIS, TRANSMISSIBLE, OF SWINE; GENE EXPRESSION REGULATION; INTESTINES; SWINE; T-LYMPHOCYTES; TRANSMISSIBLE GASTROENTERITIS VIRUS;

EID: 84899920031     PISSN: 03781135     EISSN: 18732542     Source Type: Journal    
DOI: 10.1016/j.vetmic.2014.03.017     Document Type: Article

References (35)

1. Ardavin C. Origin, precursors and differentiation of mouse dendritic cellsNature reviews. Nat. Rev. Immunol. 2003, 3:582-590.
2. Baize S., Kaplon J., Faure C., Pannetier D., Georges-Courbot M.C., Deubel V. Lassa virus infection of human dendritic cells and macrophages is productive but fails to activate cells. J. Immunol. 2004, 172:2861-2869.
3. Barchet W., Price J.D., Cella M., Colonna M., MacMillan S.K., Cobb J.P., Thompson P.A., Murphy K.M., Atkinson J.P., Kemper C. Complement-induced regulatory T cells suppress T-cell responses but allow for dendritic-cell maturation. Blood 2006, 107:1497-1504.
4. Bertram E.M., Dawicki W., Watts T.H. Role of T cell costimulation in anti-viral immunity. Semin. Immunol.16 2004, 185-196.
5. Bogunovic M., Ginhoux F., Helft J., Shang L., Hashimoto D., Greter M., Liu K., Jakubzick C., Ingersoll M.A., Leboeuf M., Stanley E.R., Nussenzweig M., Lira S.A., Randolph G.J., Merad M. Origin of the lamina propria dendritic cell network. Immunity 2009, 31:513-525.
6. Carrasco C.P., Rigden R.C., Schaffner R., Gerber H., Neuhaus V., Inumaru S., Takamatsu H., Bertoni G., McCullough K.C., Summerfield A. Porcine dendritic cells generated in vitro: morphological, phenotypic and functional properties. Immunology 2001, 104:175-184.
7. Carrasco C.P., Rigden R.C., Vincent I.E., Balmelli C., Ceppi M., Bauhofer O., Tache V., Hjertner B., McNeilly F., van Gennip H.G., McCullough K.C., Summerfield A. Interaction of classical swine fever virus with dendritic cells. J. Gen. Virol. 2004, 85:1633-1641.
8. Chen Y., Khanna S., Goodyear C.S., Park Y.B., Raz E., Thiel S., Gronwall C., Vas J., Boyle D.L., Corr M., Kono D.H., Silverman G.J. Regulation of dendritic cells and macrophages by an anti-apoptotic cell natural antibody that suppresses TLR responses and inhibits inflammatory arthritis. J. Immunol. 2009, 183:1346-1359.
9. Chetty R., Gatter K. CD3: structure, function, and role of immunostaining in clinical practice. J. Pathol. 1994, 173:303-307.
10. Dejnirattisai W., Duangchinda T., Lin C.L., Vasanawathana S., Jones M., Jacobs M., Malasit P., Xu X.N., Screaton G., Mongkolsapaya J. A complex interplay among virus, dendritic cells, T cells, and cytokines in dengue virus infections. J. Immunol. 2008, 181:5865-5874.
11. Frederick G., Bohl E., Cross R. Pathogenicity of an attenuated strain of transmissible gastroenteritis virus for newborn pigs. Am. J. Vet. Res. 1976, 37:165.
12. Gutzeit C., Raftery M.J., Peiser M., Tischer K.B., Ulrich M., Eberhardt M., Stockfleth E., Giese T., Sauerbrei A., Morita C.T., Schonrich G. Identification of an important immunological difference between virulent varicella-zoster virus and its avirulent vaccine: viral disruption of dendritic cell instruction. J. Immunol. 2010, 185:488-497.
13. Haggett P., Gunawardena K. Determination of population thresholds for settlement functions by the Reed-Muench method. Prof. Geogr. 1964, 16:6-9.
14. Haverson K., Singha S., Stokes C.R., Bailey M. Professional and non-professional antigen-presenting cells in the porcine small intestine. Immunology 2000, 101:492-500.
15. He K.w., Lin J.H., Huan H.H., Ni Y.X., Qian Y.Q., He J.H., Hou J.B. Studies on cell cultivation and pathogenicity of attenuated transmissible gastroenteritis virus STC3 [J]. Chin. J. Vet. Sci. Technol. 2001, 31:8-9.
16. Kim B., Chae C. Experimental infection of piglets with transmissible gastroenteritis virus: a comparison of three strains (Korean, Purdue and Miller). J. Comp. Pathol. 2002, 126:30-37.
17. Krempl C., Herrler G. Sialic acid binding activity of transmissible gastroenteritis coronavirus affects sedimentation behavior of virions and solubilized glycoproteins. J. Virol. 2001, 75:844-849.
18. Lancaster K.Z., Pfeiffer J.K. Viral population dynamics and virulence thresholds. Curr. Opin. Microbiol. 2012, 15:525-530.
19. Laude H., Charley B., Gelfi J. Replication of transmissible gastroenteritis coronavirus (TGEV) in swine alveolar macrophages. J. Gen. Virol. 1984, 65(Pt 2):327-332.
20. Law H.K., Cheung C.Y., Ng H.Y., Sia S.F., Chan Y.O., Luk W., Nicholls J.M., Peiris J.S., Lau Y.L. Chemokine up-regulation in SARS-coronavirus-infected, monocyte-derived human dendritic cells. Blood 2005, 106:2366-2374.
21. Masters P.S. The molecular biology of coronaviruses. Adv. Virus Res. 2006, 66:193-292.
22. Mosmann T.R., Li L., Sad S. Functions of CD8 T-cell subsets secreting different cytokine patterns. Semin. Immunol. 1997, 9:87-92.
23. Narvaez C.F., Angel J., Franco M.A. Interaction of rotavirus with human myeloid dendritic cells. J. Virol. 2005, 79:14526-14535.
24. Nielsen N.O., Sautter J.H. Infection of ligated intestinal loops with hemolytic Escherichia coli in the pig. Can. Vet. J.[nl]La revue veterinaire canadienne 1968, 9:90-97.
25. Pannetier D., Reynard S., Russier M., Journeaux A., Tordo N., Deubel V., Baize S. Human dendritic cells infected with the nonpathogenic Mopeia virus induce stronger T-cell responses than those infected with Lassa virus. J. Virol. 2011, 85:8293-8306.
26. Peng Y.T., Chaung H.C., Chang H.L., Chang H.C., Chung W.B. Modulations of phenotype and cytokine expression of porcine bone marrow-derived dendritic cells by porcine reproductive and respiratory syndrome virus. Vet. Microbiol. 2009, 136:359-365.
27. Poltorak A., He X., Smirnova I., Liu M.-Y., Van Huffel C., Du X., Birdwell D., Alejos E., Silva M., Galanos C. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science 1998, 282:2085-2088.
28. Rescigno M., Urbano M., Valzasina B., Francolini M., Rotta G., Bonasio R., Granucci F., Kraehenbuhl J.P., Ricciardi-Castagnoli P. Dendritic cells express tight junction proteins and penetrate gut epithelial monolayers to sample bacteria. Nat. Immunol. 2001, 2:361-367.
29. Stenger S., Mazzaccaro R.J., Uyemura K., Cho S., Barnes P.F., Rosat J.P., Sette A., Brenner M.B., Porcelli S.A., Bloom B.R., Modlin R.L. Differential effects of cytolytic T cell subsets on intracellular infection. Science 1997, 276:1684-1687.
30. Summerfield A., McCullough K.C. The porcine dendritic cell family. Dev. Comp. Immunol. 2009, 33:299-309.
31. Vervelde L., Reemers S.S., van Haarlem D.A., Post J., Claassen E., Rebel J.M., Jansen C.A. Chicken dendritic cells are susceptible to highly pathogenic avian influenza viruses which induce strong cytokine responses. Dev. Comp. Immunol. 2012, 39:198-206.
32. Woods R.D. Efficacy of a transmissible gastroenteritis coronavirus with an altered ORF-3 gene. Can. J. Vet. Res. 2001, 65:28.
33. Yang Z.F., Ho D.W., Ngai P., Lau C.K., Zhao Y., Poon R.T., Fan S.T. Antiinflammatory properties of IL-10 rescue small-for-size liver grafts. Liver Transpl. 2007, 13:558-565. (official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society).
34. Zhou W., Peng Q., Li K., Sacks S.H. Role of dendritic cell synthesis of complement in the allospecific T cell response. Mol. Immunol. 2007, 44:57-63.
35. Zhu J., Paul W.E. CD4 T cells: fates, functions, and faults. Blood 2008, 112:1557-1569.