Vet Med - Czech, 2017, 62(1):1-9 | DOI: 10.17221/107/2016-VETMED

Gram-positive aerobic and microaerophilic microorganisms isolated from pathological processes and lesions of horsesOriginal Paper

J. Bzdil*,1, O. Holy2, D. Chmelar3
1 State Veterinary Institute in Olomouc, Olomouc, Czech Republic
2 Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic
3 Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic

The aim of this study was to characterise the genera and species of Gram-positive aerobic and microaerophilic microorganisms isolated from pathological processes and lesions in horses. In the period 2009-2014, 449 clinical samples from horses were examined. Of these, 229 (51%) were collected from the respiratory tract, 121 (26.9%) from the skin, 40 (8.9%) from the gastrointestinal tract, 40 (8.9%) from the eyes, 8 (1.8%) from the urinary tract, 6 (1.3%) from the musculoskeletal system, 4 (0.9%) from the lymphatic system and 1 (0.2%) from milk. The isolates were presumptively identified phenotypically, and identification was confirmed by molecular phenotypic MALDI-TOF. The most frequently detected strains (n = 330) were Staphylococcus spp., Streptococcus spp., Corynebacterium spp. with prevalence rates of 37.2%, 23.4% and 7.6%, respectively. In addition, 24 other taxa were identified, including Enterococcus spp., Bacillus spp., Trueperella pyogenes, Aerococcus viridans, Dermatophilus congolensis, Lysinibacillus fusiformis, Nocardiopsis alba and Streptomyces spp. Most of these are described as opportunistic pathogens of animals, including horses. Antibiotic susceptibility was tested using the disc diffusion method. Florfenicol and amoxycillin with clavulanic acid were the most effective antibiotics. The susceptibility to florfenicol was 100% for tested strains of Bacillus spp., Lysinibacillus spp., Corynebacterium spp., Dermatophilus congolensis, Streptococcus spp., Enterococcus spp., Aerococcus spp., Nocardiopsis alba and Trueperella pyogenes. The susceptibilities of Staphylococcus aureus and other staphylococci to florfenicol were 96.2% and 98.5% in tested strains, respectively. Amoxycillin with clavulanic acid exhibited 100% effectiveness against Corynebacterium spp., Dermatophilus congolensis, Streptococcus spp., Aerococcus spp., Enterococcus spp., Streptomyces spp., Nocardiopsis alba and Trueperella pyogenes tested strains. The susceptibilities of Staphylococcus aureus, other staphylococci and Bacillus/Lysinibacillus spp. to amoxycillin with clavulanic acid were 89.8%, 98.8% and 20.0% of tested strains, respectively.

Keywords: prevalence; pathogenicity; clinical; immunity; barrier; susceptibility

Published: January 31, 2017  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Bzdil J, Holy O, Chmelar D. Gram-positive aerobic and microaerophilic microorganisms isolated from pathological processes and lesions of horses. Vet Med - Czech. 2017;62(1):1-9. doi: 10.17221/107/2016-VETMED.
Download citation

References

  1. Bednarczyk A, Daczkowska-Kozon EG (2007): Pathogenic features of bacteria from the Bacillus cereus group (in Polish). Postepy Microbiologii 47, 51-63.
  2. Bek-Thomsen M, Tettelin H, Hance L, Nelson KE, Kilian M (2008): Population diversity and dynamics of Streptococcus mitis, Streptococcus oralis, and Streptococcus infantis in the upper respiratory tracts of adults, determined by a nonculture strategy. Infection and Immunity 76, 1889-1896. Go to original source... Go to PubMed...
  3. Bolin DC, Donahue JM, Vickers ML, Harrison L, Sells S, Giles RC, Hong CB, Poonacha KB, Roberts J, Sebastian MM, Swerczek TW, Tramontin R, Williams NM (2005): Microbiologic and pathologic findings in an epidemic of equine pericarditis. Journal of Veterinary Diagnostic Investigation 17, 38-44. Go to original source... Go to PubMed...
  4. Erol E, Locke SJ, Donahoe JK, Mackin MA, Carter CN (2012a): Beta-hemolytic Streptococcus spp. from horses: a retrospective study (2000-2010). Journal of Veterinary Diagnostic Investigation 24, 142-147. Go to original source... Go to PubMed...
  5. Erol E, Sells SF, Williams NM, Kennedy L, Locke SJ, Labeda DP, Donahue JM, Carter CN (2012b): An investigation of a recent outbreak of nocardioform placentitis caused abortions in horses. Veterinary Microbiology 158, 425-430. Go to original source... Go to PubMed...
  6. Freeman K, Woods E, Welsby S, Percival SL, Cochrane CA (2009): Biofilm evidence and the microbial diversity of horse wounds. Canadian Journal of Microbiology 55, 197-202. Go to original source... Go to PubMed...
  7. Funke G, Von Gravenitz A, Clarridge JE, Bernard KA (1997): Clinical microbiology of coryneform bacteria. Clinical Microbiology Reviews 10, 125-159. Go to original source... Go to PubMed...
  8. Herdan CL, Acke E, Dicken M, Archer RM, Forsyth SF, Gee EK, Pauwels FET (2012): Multi-drug-resistant Enterococcus spp. as a cause of non-responsive septic synovitis in three horses. New Zealand Veterinary Journal 60, 297- 304. Go to original source... Go to PubMed...
  9. Laus F, Preziuso S, Spaterna A, Beribe F, Tesei B, Cuteri V (2007): Clinical and epidemiological investigation of chronic upper respiratory diseases caused by betahaemolytic Streptococci in horses. Comparative Immunology, Microbiology and Infectious Diseases 30, 247-260. Go to original source... Go to PubMed...
  10. Leite A, Vinhas-Da-Silva A, Felicio L, Vilarinho AC, Ferreira G (2010): Aerococcus viridans urinary tract infection in a pediatric patient with secondary pseudohypoaldosteronism. Revista Argentina de Microbiologia 42, 269-270.
  11. Leon-Galvan MF, Barboza-Corona JE, Lechuga-Arana AA, Valencia-Posadas M, Aguayo DD, Cedillo-Pelaez C, Martinez-Ortega EA, Gutierrez-Chavez AJ (2015): Molecular detection and sensitivity to antibiotics and bacteriocins of pathogens isolated from bovine mastitis in family dairy herds of central Mexico. Biomed Research International, DOI: 10.1155/2015/615153. Go to original source... Go to PubMed...
  12. Liu G, Liu Y, Ali T, Ferreri M, Gao J, Chen W, Yin J, Su J, Fanning S, Han B (2015): Molecular and phenotypic characterization of Aerococcus viridans associated with subclinical bovine mastitis. Plos One 10, 1-14. Go to original source... Go to PubMed...
  13. Masoud W, Jakobsen M (2003): Surface ripened cheeses: the effects of Debaryomyces hansenii, NaCl and pH on the intensity of pigmentation produced by Brevibacterium linens and Corynebacterium flavescens. International Dairy Journal 13, 231-237. Go to original source...
  14. Minkin R, Shapiro JM (2004): Corynebacterium afermentans lung abscess and empyema in a patient with human immunodeficiency virus infection. Southern Medical Journal 97, 395-397. Go to original source... Go to PubMed...
  15. Papadimitriou K, Anastasiou R, Mavrogonatou E, Blom J, Papandreou NC, Hamodrakas SJ, Ferreira S, Renault P, Supply P, Pot B, Tsakalidou E (2014): Comparative genomics of the dairy isolate Streptococcus macedonicus ACA-DC 198 against related members of the Streptococcus bovis/Streptococcus equinus complex. BMC Genomics 15, 272. Go to original source... Go to PubMed...
  16. Pasciak M, Pawlik K, Gamian A, Szponar B, Skora J, Gutarowska B (2014): An airborne actinobacteria Nocardiopsis alba isolated from bioaerosol of a mushroom compost facility. Aerobiologia 30, 413-422. Go to original source... Go to PubMed...
  17. Peyrou M, Higgins R, Lavoie JP (2003): Evolution of bacterial resistance to certain antibacterial agents in horses in a veterinary hospital. Canadian Veterinary Journal 44, 978-981.
  18. Popescu GA, Benea E, Mitache E, Piper C, Horstkotte D (2005): An unusual bacterium, Aerococcus viridans, and four cases of infective endocarditis. The Journal of Heart Valve Disease 14, 317-319.
  19. Quinn PJ, Carter ME, Markey B, Carter GR (eds) (1994): Clinical Veterinary Microbiology. 1st edn. Wolfe, London. 648 pp.
  20. Rubin JE, Ball KR, Chirino-Trejo M (2011): Antimicrobial susceptibility of Staphylococcus aureus and Staphylococcus pseudintermedius isolated from various animals. Canadian Veterinary Journal 52, 153-157.
  21. Silva N (2001): Identification and antimicrobial susceptibility patterns of Staphylococcus spp. isolated from canine chronic otitis externa. Arquivo Brasileiro de Medicina Veterinaria e Zootecnia 53, 141-145. Go to original source...
  22. Songer JG, Post KW (eds) (2005): Veterinary Microbiology, Bacterial and Fungal Agents of Animal Disease. Elsevier Saunders, St Louis. 434 pp.
  23. Stull JW, Slavic D, Rousseau J, Weese JS (2014): Staphylococcus delphini and methicillin-resistant S. pseudintermedius in horses, Canada. Emerging Infectious Diseases 20, 485-487. Go to original source... Go to PubMed...
  24. Uwaezuoke JC, Aririatu LE (2004): A survey of antibiotic resistant Staphylococcus aureus strains from clinical sources in Owerri. Journal of Applied Sciences and Environmental Management 8, 67-69. Go to original source...
  25. Wenzler E, Kamboj K, Balada-Llasat JM (2015): Severe sepsis secondary to persistent Lysinibacillus sphaericus, Lysinibacillus fusiformis and Paenibacillus amylolyticus bacteremia. International Journal of Infectious Diseases 35, 93-95. Go to original source... Go to PubMed...
  26. Wintzer HJ (ed.) (1999): Horse Diseases, Study and Practice Guide (in Slovak). Slovak/Czech edition, Hajko and Hajkova, Bratislava. 538 pp.
  27. Yildirim A, Lammler C, Weiss R (2002): Identification and characterization of Streptococcus agalactiae isolated from horses. Veterinary Microbiology 85, 31-35. Go to original source... Go to PubMed...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.