Development of polymerase chain reaction for detection of predominant streptococcal isolates causing subclinical bovine mastitis

Indian Journal of Biotechnology

Volumn 12, Issue 2, 2013, Pages 208-212

  Prabhu, K Nithin ^a   Isloor, S ^a   Hegde, Raveendra ^a   Rathnamma, D ^a   Veeregowda, B M ^a   Murthy, H N Narasimha ^b   Shome, Rajeswari ^c   Suryanarayana, V V S ^d  

^a Department of Veterinary Microbiology ^*  (India)

^b VETERINARY COLLEGE   (India)

^c ICAR NATIONAL INSTITUTE OF VETERINARY EPIDEMIOLOGY AND DISEASE INFORMATICS   (India)

^d INDIAN VETERINARY RESEARCH INSTITUTE   (India)

Author keywords

16S rRNA; Mastitis; PCR; Streptococcus

Indexed keywords

BACTERIAL RNA; RNA 16S;

ARTICLE; BACTERIUM DETECTION; BOVINE MASTITIS; CELL COUNT; CONTROLLED STUDY; DAIRY CATTLE; INDIA; MILK; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SOMATIC CELL; STREPTOCOCCUS AGALACTIAE; STREPTOCOCCUS DYSGALACTIAE; STREPTOCOCCUS INFECTION; STREPTOCOCCUS UBERIS;

EID: 84881502882     PISSN: 09725849     EISSN: 09750967     Source Type: Journal    
DOI: None     Document Type: Article

References (27)

1. Anonymous, India reference annual 2009, 53rd edn (Ministry of Information and Broadcasting, Government of India, New Delhi) 2009, 38-39.
2. Watts J L, Etiological agents of bovine mastitis, Vet Microbiol, 16 (1988) 41-66.
3. Sharma A & Prasad B, Prevalence and therapy of mastitis in dairy animals of Kangra valley of Himachal Pradesh, Proc 4th Round Table Conf on Mastitis (Indian Veterinary Research Institute, Izatnagar, India) 2003, 204-213.
4. Oncel T, Ica T & Akan M, Betalactamase detection rate and antimicrobial susceptibility of S. aureus isolated from clinical and sub-clinical mastitis cases in Turkey, Rev Med Vet, 155 (2004) 385-388.
5. Joshi S & Gokhale S, Status of mastitis as an emerging disease in improved and periurban dairy farms in India, Ann N Y Acad Sci, 1081 (2006) 74-83.
6. Bramley A J, Cullor J S, Erskine R J, Fox L K, Harmon R J et al, Current concepts of bovine mastitis, 4th edn (National Mastitis Council, Madison, WI, USA) 1996, 1-3.
7. Smith K L, Environmental mastitis: Cause, prevalence, prevention, J Dairy Sci, 68 (1996) 1531-1553.
8. Forsman E J, Alatossava T & Spratt B G, Recombination and the population structures of bacterial pathogens, Ann Rev Microbiol, 55 (1997) 561-590.
9. Ghadershoi A, Coelen R J & Hirst R G, Development of a species specific DNA probe and PCR for detection of Mycoplasma bovis, Vet Microbiol, 56 (1997) 87-98.
10. Khan U, Kim C H, Koma I, Morin E, Hansen R D et al, Detection of S. uberis in milk by use of polymerase chain reaction analysis, Am J Vet Res, 59 (1998) 807-813.
11. Pheuktes P, Mansell P D & Browning G F, Multiplex polymerase chain reaction assay for simultaneous detection of Staphylococcus aureus and streptococcal causes of bovine mastitis, J Dairy Sci, 84 (2001)1140-1148.
12. Riffon R, Sayasith H, Khalil H, Dubreuil P, Drolet M et al, Development of a rapid and sensitive test for identification of major pathogens in bovine mastitis by PCR, J Clin Microbiol, 39 (2001) 2584-2589.
13. Meiri-Bendek I, Lipkin E, Friedman A, Leitner G, Saran A et al, A PCR based method for the detection of Streptococcus agalactiae in milk, J Dairy Sci, 85 (2002) 1717-1723.
14. Phuektes P, Browning G F, Anderson G & Mansell P, Multiplex polymerase chain reaction as a mastitis screening test for Staphylococcus aureus, Streptococcus agalactiae, Streptococcus dysgalactiae and Streptococcus uberis in bulk milk samples, J Dairy Res, 70 (2003) 149-155.
15. Cremonesi P, Castiglioni B, Malferrari G, Biunno I, Vimercati C et al, Technical note: Improved method for rapid DNA extraction of mastitis pathogens directly from milk, J Dairy Sci, 89 (2006) 163-169.
16. Paape M, Mehrzad J, Zhao X, Detilleux J & Burvenich C, Defense of the bovine mammary gland by polymorphonuclear neutrophil leukocytes, J Mammary Gland Biol Neoplasia, 7 (2002) 109-121.
17. Collee J G, Fraser A G, Marimon B P & Simmons A, Practical medical microbiology, 14th edn (Churchil Livingstone, New York USA) 1996, 813-834.
18. Odierno L, Calvinho L P, Traverssa M, Lasagno C, Bogni C et al, Conventional identification of Streptococcus uberis isolated from bovine mastitis in Argentinean dairy herds, J Dairy Sci, 89 (2006) 3886-3890
19. Freney J, Bland S, Etienne J, Desmonceaux M, Boeufgras J M et al, Description and evaluation of the semi automated 4-hour rapid ID 32 Strep method for identification of streptococci and members of related genera, J Clin Microbiol, 30 (1992) 2657-2661
20. Olive J C, Norberg M, Schukken Y H & Brand A, Detection of subclinical mastitis from on-line milking parlor data, J Dairy Sci, 78 (2004) 1039-1049
21. Picard F J, Ke D, Boudreau D K, Boissinot M, Huletsky A et al, Use of tuf sequences for genus-specific PCR detection and phylogenetic analysis of 28 streptococcal species, J Clin Microbiol, 42 (2004) 3686-3695.
22. Facklam R, What happened to the streptococci: Overview of taxonomic and nomenclature changes, Clin Microbiol Rev, 15 (2002) 613-630.
23. Ke D, Picard F J, Martineau F, MéNard C, Roy P H et al, Development of a PCR assay for rapid detection of enterococci, J Clin Microbiol, 37 (2000) 3497-3503.
24. Martineau F, Picard F J, Ke D, Paradis S, Roy P H et al, Development of PCR assay for identification of staphylococci at genus and species levels, J Clin Microbiol, 39 (2001) 2541-2547.
25. Hall L M C, Duke B & Urwin G, An approach to the identification of the pathogens of bacterial meningitis by the polymerase chain reaction, Eur J Clin Microbiol Infect Dis, 14 (1995) 1090-1094.
26. Ahmet Z, Stanier P, Harvey D & Holt D, New PCR primers for sensitive detection and specific identification of group B -hemolytic streptococci in cerebrospinal fluid, Mol Cell Probes, 13 (1999) 349-357.
27. BäCkman A, Lants P G, RaodströM P & Olcé N P, Evaluation of an extended diagnostic PCR assay for detection and verification of the common causes of bacterial meningitis in CSF and other biological samples, Mol Cell Probes, 13 (1999) 49-60.