Corrigendum to "Expression of immunoregulatory genes in peripheral blood mononuclear cells of European wild boar immunized with BCG" [Vet. Microbiol. 134 (3-4) (2009) 334-339] (DOI:10.1016/j.vetmic.2008.08.026);Expression of immunoregulatory genes in peripheral blood mononuclear cells of European wild boar immunized with BCG

Veterinary Microbiology

Volumn 134, Issue 3-4, 2009, Pages 334-339

  Lastra, José Manuel Pérez de la ^a   Galindo, Ruth C ^a   Gortázar, Christian ^a   Ruiz Fons, Francisco ^a   Aranaz, Alicia ^c   de la Fuente, José ^a,b  

^a INSTITUTO DE INVESTIGACIÓN EN RECURSOS CINEGÉTICOS IREC CSIC UCLM JCCM   (Spain)

^b OKLAHOMA STATE UNIVERSITY   (United States)

^c UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

Author keywords

BCG; Genomics; Immunization; Porcine; Real time RT PCR; Signature; Tuberculosis; Wild boar

Indexed keywords

BCG VACCINE; COMPLEMENT COMPONENT C3; GAMMA INTERFERON; MESSENGER RNA; RANTES;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BCG VACCINATION; BLOOD SAMPLING; BOVINE TUBERCULOSIS; CONTROLLED STUDY; FEMALE; GENE EXPRESSION; GENETIC TRANSCRIPTION; IMMUNE RESPONSE; IMMUNOREGULATION; MALE; MYCOBACTERIUM BOVIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PERIPHERAL BLOOD MONONUCLEAR CELL; QUANTITATIVE ANALYSIS; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALIA; BOVINAE; MYCOBACTERIUM BOVIS; SUS; SUS SCROFA;

EID: 58749108070     PISSN: 03781135     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetmic.2009.05.006     Document Type: Erratum

References (34)

1. Buddle B.M., Skinner M.A., and Chambers M.A. Immunological approaches to the control of tuberculosis in wildlife reservoirs. Vet. Immunol. Immunopathol. 74 (2000) 1-16
2. Buddle B.M., Wedlock D.N., and Denis M. Progress in the development of tuberculosis vaccines for cattle and wildlife. Vet. Microbiol. 112 (2006) 191-200
3. Corner L.A. The role of wild animal populations in the epidemiology of tuberculosis in domestic animals: how to assess the risk. Vet. Microbiol. 112 (2006) 303-312
4. Costello E., Doherty M.L., Monaghan M.L., Quigley F.C., and O'Reilly P.F. A study of cattle-to-cattle transmission of Mycobacterium bovis infection. Vet. J. 155 (1998) 245-250
5. de Lisle G.W., Bengis R.G., Schmitt S.M., and O'Brien D.J. Tuberculosis in free-ranging wildlife: detection, diagnosis and management. Rev. Sci. Technol. 21 (2002) 317-334
6. Ehrt S., Schnappinger D., Bekiranov S., Drenkow J., Shi S., Gingeras T.R., Gaasterland T., Schoolnik G., and Nathan C. Reprogramming of the macrophage transcriptome in response to interferon-gamma and Mycobacterium tuberculosis: signaling roles of nitric oxide synthase-2 and phagocyte oxidase. J. Exp. Med. 194 (2001) 1123-1140
7. Gordon S.V., Eiglmeier K., Garnier T., Brosch R., Parkhill J., Barrell B., Cole S.T., and Hewinson R.G. Genomics of Mycobacterium bovis. Tuberculosis (Edinb) 81 (2001) 157-163
8. Gortazar C., Vicente J., Samper S., Garrido J.M., Fernandez-De-Mera I.G., Gavin P., Juste R.A., Martin C., Acevedo P., De La Puente M., and Hofle U. Molecular characterization of Mycobacterium tuberculosis complex isolates from wild ungulates in south-central Spain. Vet. Res. 36 (2005) 43-52
9. Howard M., and Paul W.E. Interleukins for B lymphocytes. Lymphokine Res. 1 (1982) 1-4
10. Kawahara M., Nakasone T., and Honda M. Dynamics of gamma interferon, interleukin-12 (IL-12), IL-10, and transforming growth factor beta mRNA expression in primary Mycobacterium bovis BCG infection in guinea pigs measured by a real-time fluorogenic reverse transcription-PCR assay. Infect. Immun. 70 (2002) 6614-6620
11. Keller C., Hoffmann R., Lang R., Brandau S., Hermann C., and Ehlers S. Genetically determined susceptibility to tuberculosis in mice causally involves accelerated and enhanced recruitment of granulocytes. Infect. Immun. 74 (2006) 4295-4309
12. Koul A., Herget T., Klebl B., and Ullrich A. Interplay between mycobacteria and host signalling pathways. Nat. Rev. Microbiol. 2 (2004) 189-202
13. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods 25 (2001) 402-408
14. Lyashchenko K.P., Greenwald R., Esfandiari J., Meylan M., Burri I.H., and Zanolari P. Antibody responses in New World camelids with tuberculosis caused by Mycobacterium microti. Vet. Microbiol. 125 (2007) 265-273
15. Lyashchenko K.P., Greenwald R., Esfandiari J., Olsen J.H., Ball R., Dumonceaux G., Dunker F., Buckley C., Richard M., Murray S., Payeur J.B., Andersen P., Pollock J.M., Mikota S., Miller M., Sofranko D., and Waters W.R. Tuberculosis in elephants: antibody responses to defined antigens of Mycobacterium tuberculosis, potential for early diagnosis, and monitoring of treatment. Clin. Vaccine Immunol. 13 (2006) 722-732
16. Maghazachi A.A., Al-Aoukaty A., and Schall T.J. CC chemokines induce the generation of killer cells from CD56 + cells. Eur. J. Immunol. 26 (1996) 315-319
17. McMurray D.N., Allen S.S., Jeevan A., Lasco T., Cho H., Skwor T., Yamamoto T., McFarland C., and Yoshimura T. Vaccine-induced cytokine responses in a guinea pig model of pulmonary tuberculosis. Tuberculosis (Edinb) 85 (2005) 295-301
18. Meadus W.J. A semi-quantitative RT-PCR method to measure the in vivo effect of dietary conjugated linoleic acid on porcine muscle PPAR gene expression. Biol. Proc. Online 5 (2003) 20-28
19. Murphy D., Corner L.A., and Gormley E. Adverse reactions to Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccination against tuberculosis in humans, veterinary animals and wildlife species. Tuberculosis (Edinb) (2008)
20. Naranjo V., Gortazar C., Vicente J., and de la Fuente J. Evidence of the role of European wild boar as a reservoir of Mycobacterium tuberculosis complex. Vet. Microbiol. 127 (2008) 1-9
21. Naranjo V., Gortazar C., Villar M., and de la Fuente J. Comparative genomics and proteomics to study tissue-specific response and function in natural Mycobacterium bovis infections. Anim. Health Res. Rev. 8 (2007) 81-88
22. Naranjo V., Hofle U., Vicente J., Martin M.P., Ruiz-Fons F., Gortazar C., Kocan K.M., and de la Fuente J. Genes differentially expressed in oropharyngeal tonsils and mandibular lymph nodes of tuberculous and nontuberculous European wild boars naturally exposed to Mycobacterium bovis. FEMS Immunol. Med. Microbiol. 46 (2006) 298-312
23. Naranjo V., Villar M., Martin-Hernando M.P., Vidal D., Hofle U., Gortazar C., Kocan K.M., Vazquez J., and de la Fuente J. Proteomic and transcriptomic analyses of differential stress/inflammatory responses in mandibular lymph nodes and oropharyngeal tonsils of European wild boars naturally infected with Mycobacterium bovis. Proteomics 7 (2007) 220-231
24. Neill S.D., Skuce R.A., and Pollock J.M. Tuberculosis-new light from an old window. J. Appl. Microbiol. 98 (2005) 1261-1269
25. Pavlik I. The experience of new European Union Member States concerning the control of bovine tuberculosis. Vet. Microbiol. 112 (2006) 221-230
26. Pollock J.M., Rodgers J.D., Welsh M.D., and McNair J. Pathogenesis of bovine tuberculosis: the role of experimental models of infection. Vet. Microbiol. 112 (2006) 141-150
27. Ragno S., Romano M., Howell S., Pappin D.J., Jenner P.J., and Colston M.J. Changes in gene expression in macrophages infected with Mycobacterium tuberculosis: a combined transcriptomic and proteomic approach. Immunology 104 (2001) 99-108
28. Raja A. Immunology of tuberculosis. Indian J. Med. Res. 120 (2004) 213-232
29. Ririe K.M., Rasmussen R.P., and Wittwer C.T. Product differentiation by analysis of DNA melting curves during the polymerase chain reaction. Anal. Biochem. 245 (1997) 154-160
30. Rozen S., and Skaletsky H. Primer3 on the WWW for general users and for biologist programmers. Methods Mol. Biol. 132 (2000) 365-386
31. Seah G.T., and Rook G.A. High levels of mRNA encoding IL-4 in unstimulated peripheral blood mononuclear cells from tuberculosis patients revealed by quantitative nested reverse transcriptase-polymerase chain reaction; correlations with serum IgE levels. Scand. J. Infect. Dis. 33 (2001) 106-109
32. Sugisaki K., Dannenberg Jr. A.M., Abe Y., Tsuruta J., Su W.J., Said W., Feng L., Yoshimura T., Converse P.J., and Mounts P. Nonspecific and immune-specific up-regulation of cytokines in rabbit dermal tuberculous (BCG) lesions. J. Leukoc. Biol. 63 (1998) 440-450
33. Tree J.A., Elmore M.J., Javed S., Williams A., and Marsh P.D. Development of a guinea pig immune response-related microarray and its use to define the host response following Mycobacterium bovis BCG vaccination. Infect. Immun. 74 (2006) 1436-1441
34. Waters W.R., Palmer M.V., Thacker T.C., Bannantine J.P., Vordermeier H.M., Hewinson R.G., Greenwald R., Esfandiari J., McNair J., Pollock J.M., Andersen P., and Lyashchenko K.P. Early antibody responses to experimental Mycobacterium bovis infection of cattle. Clin. Vaccine Immunol. 13 (2006) 648-654