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2012 | 15 | 4 |

Tytuł artykułu

Antimicrobial resistance and genotypes of staphylococci from bovine milk and the cowshed environment

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Investigation of antimicrobial resistance and genetic relatedness of staphylococci from milk of cows with mastitis and cowshed environment was the aim of this study. Antimicrobial resistance against 14 antimicrobials were determined by using a disc diffusion method. Genetic similarity between the most frequently isolated species was analysed by PFGE (pulsed-field gel electrophoresis). Haemolytic activity, DNase, protease and esterase production was also investigated. Coagulase-negative Staphylococcus species were isolated from 30.8% of milk samples from cows with mastitis. The most frequently isolated species was Staphylococcus xylosus and yield of these organisms was significantly associated with milk of mastitis cows. S. epidermidis was a predominant penicillin-resistant species. High frequency of resistance to lincomycin was observed among isolates of S. sciuri (54.2%) and S. xylosus (25.9%) from cows with mastitis. PFGE (pulsed-field gel electrophoresis) analysis of 29 Staphylococcus aureus isolates showed the presence of 17 PFGE pulsotypes. Isolates of S. sciuri (n=36) had unique PFGE patterns. Some S. xylosus isolates from milk and milker’s hands had the same PFGE pulsotypes, and this observation could indicate that dairyman may be a potential source of the infection. The pulsotype of each of the remaining isolates of S. xylosus suggested that they might have come from common environmental sources; however, these isolates differed in antibiotic resistance pattern or virulence traits. Therefore, knowledge about antibiotic sensitivity pattern and virulence factors of a CNS isolate, besides its genotype, may be informative in tracking the source of the infection.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

15

Numer

4

Opis fizyczny

p.741-749,fig.,ref.

Twórcy

autor
  • Department of Microbiology, Institute of Biology, Siedlce University of Natural Sciences and Humanities, Bolesława Prusa 12, 08-110 Siedlce, Poland
autor
  • Department of Microbiology, Institute of Biology, Siedlce University of Natural Sciences and Humanities, Bolesława Prusa 12, 08-110 Siedlce, Poland
  • Department of Microbiology, Military Institute of Hygiene and Epidemiology, Kozielska 4, 01-163 Warsaw, Poland
autor
  • Department of Microbiology, Institute of Biology, Siedlce University of Natural Sciences and Humanities, Bolesława Prusa 12, 08-110 Siedlce, Poland
autor
  • Department of Microbiology, Institute of Biology, Siedlce University of Natural Sciences and Humanities, Bolesława Prusa 12, 08-110 Siedlce, Poland
autor
  • Department of Microbiology, Institute of Biology, Siedlce University of Natural Sciences and Humanities, Bolesława Prusa 12, 08-110 Siedlce, Poland
autor
  • Department of Microbiology, Military Institute of Hygiene and Epidemiology, Kozielska 4, 01-163 Warsaw, Poland
autor
  • Department of Cattle Breeding and Milk Testing, Siedlce University of Natural Sciences and Humanities, Bolesława Prusa 14, 08-110 Siedlce, Poland
autor
  • Department of Microbiology, Military Institute of Hygiene and Epidemiology, Kozielska 4, 01-163 Warsaw, Poland

Bibliografia

  • Bannerman TL (2003) Staphylococcus, micrococcus, and other catalase-positive cocci that grow aerobically. In: Murray PR, Baron EJ, Jorgensen JH, Pfaller MA, Yolken RH (eds) Manual of clinical microbiology, American Society Microbiology, Washington, pp 384-404.
  • Bjorklind A, Arvidson S (1977) Occurrence of an extracellular serine-proteinase among Staphylococcus aureus strains. Acta Pathol Microbiol Scand B 85: 277-280.
  • Bochniarz M, Wawron W (2011) Antibiotic susceptibility of methicillin-resistant and methicillin-susceptible coagulase- negative staphylococci isolated from bovine mastitis. Pol J Vet Sci 14: 405-410.
  • Capurro A, Aspän A, Artursson K, Waller KP (2010) Genotypic variation among Staphylococcus aureus isolates from cases of clinical mastitis in Swedish dairy cows. Vet J 185: 188-192.
  • Capurro A, Concha C, Nilsson L, O¨ stensson K (1999) Identification of coagulase-positive staphylococci isolated from bovine milk. Acta Vet Scan 40: 315-321.
  • Casadevall A, Pirofski LA (2000) Host-pathogens interactions: basic concepts of microbial commensalism, colonization, infection and disease. Infect Immun 8: 6511-6518.
  • Chapin KC, Murray PR (1999) Media. In: Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken RH (eds), Manual of Clinical Microbiology. American Society for Microbiology, Washington, pp 1687-1707.
  • Clinical and Laboratory Standards Institute (CLSI) (2011) Performance standards for antimicrobial susceptibility testing; 21st Informational Supplement. CLSI, Wayne, M100-S21, 31, 1.
  • Dordet-Frisoni E, Dorchies G, De Araujo C, Talon R, Leroy S (2007) Genomic diversity in Staphylococcus xylosus. Appl Environ Microbiol 73: 7199-7209.
  • Downes FP, Ito K (2001) Compendium of methods for the microbiological examination of foods. 4th ed., APHA, Washington, pp 391.
  • Gentilini E, Denamiel G, Betancor A, Rebuelto M, Rodriguez FM, De Torrest RA (2002) Antimicrobial susceptibility of coagulase-negative staphylococci isolated from bovine mastitis in Argentina. J Dairy Sci 85: 1913-1917.
  • Gillespie BE, Headrick SI, Boonyayatra S, Oliver SP (2009) Prevalence and persistence of coagulase-negative Staphylococcus species in three dairy research herds. Vet Microbiol 134: 65-72.
  • Halasa T, Huijps K, Østeras O, Hogeveen H (2007) Economic effects of bovine mastitis and mastitis management: a review. Vet Q 29: 18-31.
  • Konemam EW, Allen SD, Janda WM, Schreckenberger PC, Winn Jr WC (1997) Color atlas and textbook of diagnostic microbiology. Lippincott-Raven Pulishers, Philadelphia.
  • Lüthje P, Schwarz S (2006) Antimicrobial resistance of coagulase-negative staphylococci from bovine subclinical mastitis with particular reference to macrolide-lincosamide resistance phenotypes and genotypes. J Antimicrob Chemother 57: 966-969.
  • Malinowski E, Lassa H, Kłossowska A, Smulski S, Markiewicz H, Kaczmarowski M (2006) Etiological agents of dairy cows’ mastitis in western part of Poland. Pol J Vet Sci 9: 191-194.
  • Resch M, Nagel V, Hertel C (2008) Antibiotic resistance of coagulase-negative staphylococci associated with food and used in starter cultures. Int J Food Microbiol 127: 99-104.
  • Sampimon OC, Barkema HW, Berends IM, Sol J, Lam TJ (2009) Prevalence and herd-level risk factors for intramammary infection with coagulase-negative staphylococci in Dutch dairy herds. Vet Microbiol 134: 37-44.
  • Sampimon OC, Lam TJ, Mevius DJ, Schukken YH, Zadoks RN (2011) Antimicrobial susceptibility of coagulase-negative staphylococci isolated from bovine milk samples. Vet Microbiol 150: 173-179.
  • Sawant AA, Gillespie BE, Oliver SP (2009) Antimicrobial susceptibility of coagulase-negative Staphylococcus species isolated from bovine milk. Vet Microbiol 134: 73-81.
  • Siqueira JF Jr, Lima KC (2002) Staphylococcus epidermidis and Staphylococcus xylosus in a secondary root canal infection with persistent symptoms: a case report. Aust Endod J 28: 61-63.
  • Taponen S, Simojoki H, Haveri M, Larsen HD, Pyörälä S (2006) Clinical characteristics and persistence of bovine mastitis caused by different species of coagulase-negative staphylococci identified with API or AFLP. Vet Microbiol 115: 199-207.
  • Thorberg BM, Kühn I, Aarestrup FM, Brändström B, Jonsson P, Danielson-Tham ML (2006) Pheno- and genotyping of Staphylococcus epidermidis isolated from bovine milk and human skin. Vet Microbiol 115: 163-172

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Bibliografia

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