TY - JOUR
T1 - Effect of Isolation Ruminal Yeast from Ruminants on In Vitro Ruminal Fermentation
AU - Wilachai, Krung
AU - Paengkoum, Pramote
AU - Taethaisong, Nittaya
AU - Thitisak, Pirat
AU - Poonsuk, Kriengsak
AU - Loor, Juan J.
AU - Paengkoum, Siwaporn
N1 - This work was supported by Thailand Research Fund (TRF) though the Research and Researcher for Industrial (RRi) Ph.D. scholarship program for providing financial support to research (grant number PHD58I0067), (5811014), awarded to Krung Wilachai and Pramote Paengkoum as a source of funding. The authors would like to thanks Suranaree University of Technology supported on farm and nutrition laboratory. The K.M.P. BIOTECH Co., Ltd. for trained and used micro biology laboratory, and also that is cooperates scholarship. This research was also supported by Suranaree University of Technology (SUT; contract no. Full-time Doctoral Researcher Full-time 66/03/2568). This work was supported by (i) Suranaree University of Technology (SUT), (ii) Thailand Science Research and Innovation (TSRI), and (iii) National Science, Research and Innovation Fund (NSRF); project codes: 4776018; FF3-303-68-24-08(F). National Research Council of Thailand (NRCT; project code: NRCT5-RSA63009-01).
The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by Thailand Research Fund (TRF) though the Research and Researcher for Industrial (RRi) Ph.D. scholarship program for providing financial support to research (grant number PHD58I0067), (5811014). This research was also supported by Suranaree University of Technology (SUT; contract no. Full-time Doctoral Researcher Full-time 66/03/2568), Thailand Science Research and Innovation (TSRI), National Science Research and Innovation Fund (NSRF; project codes: 90464; 160368; FF3-303-65-36-17(B). This work was supported by (i) Suranaree University of Technology (SUT), (ii) Thailand Science Research and Innovation (TSRI), and (iii) National Science, Research and Innovation Fund (NSRF); project codes: 4776018; FF3-303-68-24-08(F). National Research Council of Thailand (NRCT; project code: 900105), National Research Council of Thailand (NRCT; project code: NRCT5-RSA63009-01).
PY - 2025/2
Y1 - 2025/2
N2 - In order to obtain high-performing yeast strains from ruminants, it is necessary to select them from species such as beef cattle, dairy cows, goats, and buffalo. A total of 91 isolated yeasts were collected using the standard methods of microbial culture on agar medium followed by streaking on a plate at least three times until pure yeast colonies were formed. The API 20C AUX Kit and sequencing of the D1/D2 domain of the 26S rRNA gene were used to identify the genera Candida spp., namely, C. glabrata (99% identification), C. tropicallis (99%), C. rugosa (98%), and Issatchenkia orientalis (99%). A total of 12 yeast strains (Dc4, 14, 18; Be1, 2, 7; Bu3, 4, 7; and Go10, 16, 19) were chosen for further analyses. The performance criteria included the ability to tolerate pH values between 3.5 and 7.5, total volatile fatty acids (TVFAs, 0, 0.25, 0.5, 1, 2, and 4% of broth medium), anaerobic growth rate, and in vitro gas production efficiency. First, when all strains were grown at pH values between 3.5 and 7.5, Bu3 and Dc18 performed better than the other strains. Second, at a ruminal pH of 6.5 and a TVFA concentration of between 2 and 4% of the broth medium, strain Bu3 was more resistant than the other strains. Under anaerobic conditions, all strains experienced a decline in viable cell counts when compared with those under aerobic conditions. However, compared to strains Dc14, Be1, Be2, Be7, and Bu3, strain Dc18 exhibited more viable cells under anaerobic conditions in broth medium. The response of strain Dc18 did not differ from those of strains Dc4, Bu4, Bu7, or G16. Strains Be7, Bu3, and Dc18 were used for an in vitro fermentation experiment involving incubation for 2, 4, 6, 8, 10, 12, 24, 36, 48, and 72 h. Three ruminal cannulated dairy cows were used as donors of ruminal fluid. The treatments were run in triplicate. The addition of yeast culture had no effect on gas kinetics, gas accumulation, or the ratio of acetic acid and propionic acid, but led to significantly greater butyric acid concentrations at 24 h of incubation. In conclusion, strain Dc18 isolated from dairy cows is suitable for future studies of probiotic yeast development.
AB - In order to obtain high-performing yeast strains from ruminants, it is necessary to select them from species such as beef cattle, dairy cows, goats, and buffalo. A total of 91 isolated yeasts were collected using the standard methods of microbial culture on agar medium followed by streaking on a plate at least three times until pure yeast colonies were formed. The API 20C AUX Kit and sequencing of the D1/D2 domain of the 26S rRNA gene were used to identify the genera Candida spp., namely, C. glabrata (99% identification), C. tropicallis (99%), C. rugosa (98%), and Issatchenkia orientalis (99%). A total of 12 yeast strains (Dc4, 14, 18; Be1, 2, 7; Bu3, 4, 7; and Go10, 16, 19) were chosen for further analyses. The performance criteria included the ability to tolerate pH values between 3.5 and 7.5, total volatile fatty acids (TVFAs, 0, 0.25, 0.5, 1, 2, and 4% of broth medium), anaerobic growth rate, and in vitro gas production efficiency. First, when all strains were grown at pH values between 3.5 and 7.5, Bu3 and Dc18 performed better than the other strains. Second, at a ruminal pH of 6.5 and a TVFA concentration of between 2 and 4% of the broth medium, strain Bu3 was more resistant than the other strains. Under anaerobic conditions, all strains experienced a decline in viable cell counts when compared with those under aerobic conditions. However, compared to strains Dc14, Be1, Be2, Be7, and Bu3, strain Dc18 exhibited more viable cells under anaerobic conditions in broth medium. The response of strain Dc18 did not differ from those of strains Dc4, Bu4, Bu7, or G16. Strains Be7, Bu3, and Dc18 were used for an in vitro fermentation experiment involving incubation for 2, 4, 6, 8, 10, 12, 24, 36, 48, and 72 h. Three ruminal cannulated dairy cows were used as donors of ruminal fluid. The treatments were run in triplicate. The addition of yeast culture had no effect on gas kinetics, gas accumulation, or the ratio of acetic acid and propionic acid, but led to significantly greater butyric acid concentrations at 24 h of incubation. In conclusion, strain Dc18 isolated from dairy cows is suitable for future studies of probiotic yeast development.
KW - yeast selection
KW - rumen fermentation
KW - probiotic yeast
KW - ruminants
KW - plate method
KW - yeast strains
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U2 - 10.3390/vetsci12020155
DO - 10.3390/vetsci12020155
M3 - Article
C2 - 40005915
SN - 2306-7381
VL - 12
JO - Veterinary Sciences
JF - Veterinary Sciences
IS - 2
M1 - 155
ER -