THE EFFECT OF VIRGINIAMYCIN ON RUMEN FERM ENTATION IN-VITRO AFTER ADAPTATION OF INOCULUM DONORS

Citation
M. Marounek et al., THE EFFECT OF VIRGINIAMYCIN ON RUMEN FERM ENTATION IN-VITRO AFTER ADAPTATION OF INOCULUM DONORS, Veterinarni medicina, 40(5), 1995, pp. 129-132
Citations number
13
Categorie Soggetti
Veterinary Sciences
Journal title
ISSN journal
03758427
Volume
40
Issue
5
Year of publication
1995
Pages
129 - 132
Database
ISI
SICI code
0375-8427(1995)40:5<129:TEOVOR>2.0.ZU;2-M
Abstract
Virginiamycin is an antibiotic active against grampositive bacteria in the alimentary tract, which is also suitable for supplementation of d iets of growing and finishing ruminants. The aim of this work was to s pecify the effect of virginiamycin on some parameters of rumen ferment ation in vitro with inoculi taken from wethers adapted or non-adapted to the virginiamycin intake. Incubations were performed anaerobically at 39 degrees C in serum bottles closed with Bunsen valves. Virginiamy cin was added at 0 or 10 mg/l to the rumen fluid diluted with McDougal l buffer. Virginiamycin significantly decreased production and utiliza tion of lactic acid, production of methane and decomposition of casein when rumen fluid was taken from non-adapted wethers. Most of its effe cts disappeared when rumen fluid was sampled from wethers adapted to t he virginiamycin intake (100 mg per head daily for 2 months). Adaptati on of wethers to virginiamycin was further confirmed by analyses of th e rumen fluid which was used for inoculation of in vitro cultures. Mol ar percentages of acetate, propionate, butyrate and valerate were the same before and after the adaptation. Therefore it can be concluded th at the effects of virginiamycin on rumen parameters are not stable and its addition to ruminant diets cannot be recommended, with exception of the milk nutrition period. In the last experiment the stability of virginiamycin in the rumen fluid of adapted wethers was investigated. The rumen fluid was diluted with buffer containing glucose and virgini amycin (10 mg/l, final cone.) and incubated in the LF2 fermenter at pH = 6.5. Samples taken at 0, 3, 6 and 9 h were centrifuged and cell-fre e supernatant was added to the MRS nutrient broth inoculated with Baci llus stearothermophilus 794B. Inoculated cultures of this indicator or ganism were incubated overnight. It was found that the antibiotic acti vity was stable within 9h incubation interval and, thus, a resistance mechanism other than the direct inactivation of virginiamycin existed in virginiamycin-adapted wethers.