Development of an experimentally induced Streptococcus uberis subclinical mastitis in goats

Veterinary Microbiology

Volumn 154, Issue 3-4, 2012, Pages 376-383

  Lasagno, Mirta C ^a   Vissio, Claudina ^a   Reinoso, Elina B ^a   Raspanti, Claudia ^a   Yaciuk, Raúl ^a   Larriestra, Alejandro J ^a   Odierno, Liliana M ^a  

^a DEPARTAMENTO DE QUÍMICA   (Argentina)

Author keywords

Experimentally induced subclinical mastitis; Goat; Immunohistochemistry; Streptococcus uberis

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BACTERIAL GROWTH; BACTERIAL SHEDDING; BACTERIAL VIABILITY; BACTERIUM DETECTION; CELL COUNT; COLONY FORMING UNIT; CONTROLLED STUDY; EXPERIMENTALLY INDUCED SUBCLINICAL MASTITIS; FEMALE; GOAT; HISTOPATHOLOGY; IMMUNOHISTOCHEMISTRY; INFLAMMATION; INOCULATION; LACTATION; LYMPH NODE; MAMMARY GLAND; MASTITIS; MILK; NONHUMAN; PATHOGENESIS; RIGHT MAMMARY HALF; SOMATIC CELL; STREPTOCOCCUS UBERIS;

ANIMALS; FEMALE; GOATS; LACTATION; LEUKOCYTE COUNT; MASTITIS; MILK; RABBITS; STREPTOCOCCAL INFECTIONS; STREPTOCOCCUS;

BACTERIA (MICROORGANISMS); CAPRA HIRCUS; STREPTOCOCCUS UBERIS;

EID: 84855955166     PISSN: 03781135     EISSN: 18732542     Source Type: Journal    
DOI: 10.1016/j.vetmic.2011.07.031     Document Type: Article

References (25)

1. Almeida R.A., Gillespie B.E., Lewis M.J., Headrick S.J., Oliver S.P. Development of an experimental Streptococcus uberis intramammary infection model. NMC Annu. Meet. Proc. 2004, 282-283.
2. Bassam L.S., Hasso S.A. Mastitis in goats caused by Nocardia asteroids. Small Ruminant Res. 1997, 26:287-290.
3. Boutet P., Boulanger D., Gillet L., Vanderplasschen A., Closset R., Bureau F., Lekeux P. Delayed neutrophil apoptosis in bovine subclinical mastitis. J. Dairy Sci. 2004, 87:4104-4114.
4. Brouillette E., Malouin F. The pathogenesis and control of Staphylococcus aureus-induced mastitis: study models in the mouse. Microb. Inf. 2005, 7:560-568.
5. Bush B.M Interpretation of Laboratory Results for Small Animal Clinicians 1993, Blackwell, Oxford.
6. Castro-Alonso A., Rodríguez F., De la Fe C., Espinosa de los Monteros A., Poveda J.B., Andrada M., Herráez P. Correlating the immuneresponse with clinical-pathological course of persistent mastitis experimentally induced by Mycoplasma agalactiae in dairy goats. Res. Vet. Sci. 2009, 86:274-280.
7. Diker K.S., Haziroglu R., Diker F.S. Experimental infection of the mouse mammary gland with Campylobacter coli. Res. Vet. Sci. 1992, 52:123-125.
8. Directive 92/46ECC Council, 1992. Diario Official de las Comunidades Europeas, vol. L 268. European Council, Brussels, Belgium, pp. 1-34.
9. Fournier J., Vann W., Karakawa W. Purification and characterization of Staphylococcus aureus Type 8 capsular polysaccharide. Infect. Immun. 1984, 45:87-93.
10. Honkanen-Buzalski T., Anderson J.C., Bramley A.J. The virulence of strains of Corynebacterium bovis in the mammary gland of the mouse and the effect of corynebacterial mastitis on subsequent infection with Staphylococcus aureus. Br. Vet. J. 1985, 141:519-528.
11. Koul S., Singh J., Dhingra P.N., Khatra G.S. Studies on experimental chlamydial mastitis in goat histoenzymology. Comp. Immunol. Microbiol. 1993, 16:307-316.
12. Lasagno, M., Reinoso, E., Dieser, S., Calvinho, L., Buzzola, F., Vissio, C., Bogni, C., Odierno, L., 2011. Phenotypic and genotypic characteriz and genotypic characterization of Streptococcus uberis isolated from bovine subclinical mastitis in argentinean dairy farms. Revista Argentina de Microbiología 43.
13. Moroni P., Pisoni G., Ruffo G., Boettcher P.J. Risk factors for intramammary infections and relationship with somatic-cell counts in Italian dairy goats. Prev. Vet. Med. 2005, 69:163-173.
14. Paape M.J., Capuco A.V. Cellular defense mechanisms in the udder and lactation of goats. J. Anim. Sci. 1997, 75:556-565.
15. Paape M.J., Wiggans G.R., Bannerman D.D., Thomas D.L., Sanders A.H., Contreras A., Moroni P., Millar R.H. Monitoring goat and sheep milk somatic cell counts. Small Ruminant Res. 2007, 68:114-125.
16. Paape M.J., Shafer-Weaver K., Capuco A.V., Van Oostveldt K., Burvenich C. Immune surveillance of mammary tissue by phagocytic cells. Adv. Exp. Med. Biol. 2002, 480:259-277.
17. Pedersen L., Aalbaek B., Rontved C., Ingvarstsen K., Sorensen N., Heegaard P., Jensen H. Early pathogenesis and inflammatory response in experimental bovine mastitis due to Streptococcus uberis. J. Comp. Path. 2003, 128:156-164.
18. Rainard P., Riollet C. Mobilization of neutrophils and defense of the bovine mammary gland. Reprod. Nutr. Dev. 2003, 43:439-457.
19. Rambeaud M., Almeida R., Pighetti G., Oliver S. Dynamics of leukocytes and cytokines during experimentally induced Streptococcus uberis mastitis. Vet. Immun. Immunopath. 2003, 96:193-205.
20. Reid I.M., Harrison R.D., Anderson J.C. Experimental staphylococcal mastitis in the mouse. A morphometric study of early changes in mammary gland structure. J. Comp. Pathol. 1976, 86:329-336.
21. Reinoso E.B., Lasagno M.C., Dieser S.A., Odierno L.M. Distribution of virulence associated genes in Streptococcus uberis isolated from bovine mastitis. FEMS Microbiol. Lett. 2011, 318(2):183-188.
22. Reinoso E., Dieser S., Calvinho L., Bogni C., Odierno L. Phenotyping and genotyping of streptococci in bovine milk in Argentinean dairy herds. Acta Vet. Hung. 2010, 58:287-295. 10.1556/AVet.58.2010.3.2.
23. Schibler L., Vaiman D., Oustry A., Giraud-Delville C., Cribiu E.P. Comparative gene mapping: a fine-scale survey of chromosome rearrangements between ruminants and humans. Genome Res. 1998, 8:901-915.
24. Tamilselvam B., Almeida R.A., Dunlap J.R., Oliver S.P. Streptococcus uberis internalizes and persists in bovine mammary epithelial cells. Microb. Pathog. 2006, 40:279-285.
25. Thomas L.H., Haider W., Hill A.W., Cook R.S. Pathologic findings of experimentally induced Streptococcus uberis infection in the mammary gland of cows. Am. J. Vet. Res. 1994, 55:1723-1728.