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2015 | 71 | 10 |

Tytuł artykułu

Aktualny stan badań choroby Glassera świń

Warianty tytułu

EN
Present state of research on Glasser’s disease of swine

Języki publikacji

PL

Abstrakty

EN
The introduction of this review of literature contains basic data of Glässer’s disease occurring in swine and boar. This is followed by the characterization of the properties of Haemophilus (H.) parasuis and the pathogenesis. Information about at least 15 classified serovars, using immunodiffusion testing or passive hemagglutination, is given. Potentially pathoghenic strains belong to serovar: 1, 5, 10, 12, 13 and 14. However, this classification shows exceptions, indicating that not all strains of the mentioned serovars, even of serovar 5, are pathogenic. On the other side strains, not belonging to the so called pathogenic serovars, cause Glässer’s disease. The recent developments of genomic information and genetic manipulation systems have improved the selection of virulent H. parasuis strains, contributing to better understanding of the pathogenesis of H. parasuis infection. Some data are presented how the pathogen overcomes host immune responses, with participation of virulence factors coded by defined genes. The cited results, concerning genes and pathogenicity factors of H. parasuis contribute also to improvement of the efficacy of the vaccine against Glässer’s disease. Finally prevention and control of Glässer’s disease is presented.

Wydawca

-

Rocznik

Tom

71

Numer

10

Opis fizyczny

s.595-598,bibliogr.

Twórcy

  • Zakład Chorób Świń, Państwowy Instytut Weterynaryjny - Państwowy Instytut Badawczy w Puławach, Al. Partyzantów 57, 24-100 Puławy
autor
  • Zakład Chorób Świń, Państwowy Instytut Weterynaryjny - Państwowy Instytut Badawczy w Puławach, Al. Partyzantów 57, 24-100 Puławy

Bibliografia

  • 1. Amano H., Shibata M., Takahashi K., Sasaki Y.: Effects on endotoxin pathogenicity in pigs with acute septicemia of Haemophilus parasuis infection. J. Vet. Med. Sci. 1997, 59, 451-455.
  • 2. Aragon V., Cerdá-Cuéllar M., Fraile L., Mombarg M., Nofrarías M., Olvera A., Sibila M., Solanes D., Segalés J.: Correlation between clinico-pathological outcome and typing of Haemophilus parasuis field strains.Vet. Microbiol. 2010, 142, 387-393.
  • 3. Aragon V., Segars J., Oliveira S.: Glässer’s Disease, [w:] Zimmerman J. J., Karriker L. A., Ramírez A., Shwartz K. J., Stevenson G. W. (Eds.): Diseases of Swine. 10th Edition. Wiley-Blackwell 2012, s. 760-769.
  • 4. Bouchet B., Vanier G., Jacques M., Auger E., Gottschalk M.: Studies on the interactions of Haemophilus parasuis with porcine epithalial tracheal cells: limited role of LOS in apoptosis and pro-inflammatory cytokine release. Microb. Pathog. 2009, 46, 108-113.
  • 5. Bouchet B., Vanier G., Jacques M., Gottschalk M.: Interactions of Haemophilus parasuis and its LOS with porcine brain microvascular endothelial cells. Vet. Res. 2008, 39, 42.
  • 6. Cerda-Cuellar M., Aragon V.: Serum-resistance in Haemophilus parasuis is associated with systemic disease in swine. Vet. J. 2008, 175, 384-389.
  • 7. Cerdà-Cuéllar M., Naranjo J. F., Verge A., Nofrarias M., Cortey M., Olvera A., Segalés J.: Sow vaccination modulates the colonization of piglets by Haemophilus parasuis. Vet. Microbiol. 2010, 145, 315-320.
  • 8. Costa-Hurtado M., Ballester M., Galofre-Mila N., Darji A., Aragon V.: VtaA8 and VtaA9 from Haemophilus parasuis delay phagocytosis by alveolar macrophages. Vet. Res. 2012, 43, 57.
  • 9. Frandoloso R., Martinez-Martinez S., Gutierrez-Martin C. B., Rodriguez-Ferri E. F.: Haemophilus parasuis serovar 5 Nagasaki strain adheres and invades PK-15 cells. Vet. Microbiol. 2012, 154, 347-352.
  • 10. Goodman R. B., Pugin J., Lee J. S., Matthay M. A.: Cytokine-mediated inflammation in acute lung injury. Cytokine Growth Factor Rev. 2003, 14, 523-535.
  • 11. Kielstein P., Rapp-Gabrielson V. J.: Designation of 15 serovars of Haemophilus parasuis on the basis of immunodiffusion using heat-stable antigen extracts. J. Clin. Microbiol. 1992, 30, 862-865.
  • 12. Kielstein P., Wohlfarth E.: Schweinekrankheiten. VEB Gustav Fischer Verlag Jena 1987, 3. Aufl., s. 406-408.
  • 13. Mullins M. A., Register K. B., Bayles D. O., Butler J. E.: Haemophilus parasuis exhibits IgA protease activity but lacks homologs of the IgA protease genes of Haemophilus influernzae. Vet. Microbiol. 2011, 153, 407-412.
  • 14. Oliveira S., Pijoan C.: Haemophilus parasuis: new trends on diagnosis, epidemiology and control. Vet. Microbiol. 2004, 99, 1-12.
  • 15. Olvera A., Ballester M., Nofrarias M., Sibila M., Aragon V.: Differences in phagocytosis susceptibility in Haemophilus parasuis strains. Vet. Res. 2009, 40, 24.
  • 16. Peet R. L., Fry J., Lloyd J., Henderson J., Curran J., Moir D.: Haemophilus parasuis septicaemia in pigs. Aust. Vet. J. 1983, 60, 187.
  • 17. Pejsak Z., Żmudzki J., Wałachowski M.: Ostry przypadek choroby Glässera w wielkotowarowej fermie świń. Med. Weter. 2002, 58, 192-196.
  • 18. Pina S., Olvera A., Barcelo A., Bensaid A.: Trimeric autotransporters od Haemophilus parasuis: gheneratioon of an extensive passenger domain repertoire specific for pathogenic strains. J. Bacteriol. 2009, 191, 576-587.
  • 19. Ruiz A., Oliveira S., Torremorell M., Pijoan C.: Outer membrane proteins and DNA profiles in strains of Haemophilus parasuis recovered from systemic and respiratory sites. J. Clin. Microbiol. 2001, 39, 1757-1762.
  • 20. Sandal I., Corbeil L. B., Inzana T. J.: Haemophilus, [w:] Gyles C. L., Prescott J. F., Songer J. G., Thoen C. O.: Pathogenesis of Bacterial Infections in Animals. Wiley-Blackwell 2010, 4. Ed., s. 387-409.
  • 21. Serruto D., Rappuoli R., Scarselli M., Gros P., van Strijp J. A.: Molecular mechanisms of complement evasion: learning from staphylococci and meningococci. Nat. Rev. Microbiol. 2010, 8, 393-399.
  • 22. Smart N. L., Hurnik D., Macinnes J. I.: An investigation of enzootic Glässer’s disease in a specific-pathogen-free grower-finisher facility using restriction endonuclease analysis. Can. Vet. J. 1993, 34, 487-490.
  • 23. Vahle J. L., Haynes J. S., Andrews J. J.: Interaction of Haemophilus parasuis with nasal and tracheal mucosa following intranasal inoculation of cesarean derived colostrum deprived (CDCD) swne. Can. J. Vet. Res. 1997, 61, 200-206.
  • 24. Vanier G., Szczotka A., Friedl P., Lacouture S., Jacques M., Gottschalk M.: Haemophilus parasuis invades porcine brain microvascular endothelial cells. Microbiol. 2006, 152, 135-1452.
  • 25. Wang Y., Liu C., Fang Y., Liu X., Li W., Liu S., Liu Y, Charreyre C., Audonnet J. C., Chen P., He Q.: Transcription analysis on response of porcine alverolar macrophages to Haemophilus parasuis. BMC Genomics 2012, 13, 68.
  • 26. Yue M., Yang F., Yang J., Bei W., Cai X., Chen L., Dong J., Zhou R., Jin M., Jin Q., Chen H.: Complete Genome Sequence of Haemophilus parasuis SH0165. J. Bacteriol. 2008, 191, 1359-1360.
  • 27. Zhang B., Feng S., Xu C., Zhou S., He Y., Zhang L., Zhang J., Guo L., Liao M.: Serum resistance in Haemophilus parasuis SC096 strain requires outer membrane protein P2 ecpression. FEMS Microbiol. Lett. 2012, 326, 109-115.
  • 28. Zhang B., He Y., Xu C., Xu L., Feng S., Liao M., Ren T.: Cytolethal distending toxin (CDT) of the Haemophilus parasuis SC096 strain contributes to serum resistance and adherence to and invasion of PK-15 and PUVEC cells. Vet. Microbiol. 2012, 157, 237-242.
  • 29. Zhang B., Tang C., Liao M., Yue H.: Update on the pathogenesis of Haemophilus parasuis infection and virulence factors. Vet. Microbiol. 2014, 168, 1-7.
  • 30. Zhou H., Yang B., Xu F., Chen X., Wang J., Blackall P. J., Zhang P., Xia Y., Zhang J., Ma R.: Identification of putative virulence-associated genes of Haemophilus parasuis through suppression subtractive hybridization. Vet. Microbiol. 2010, 144, 377-383.
  • 31. Zhou M., Zhang Q., Zhao J., Jin M.: Haemophilus parasuis encodes two functional cytolethal distending toxins: CdtC contains an atypical cholesterol recognition/interaction region. PloS One 2012, 7, e32580.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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