3 results match your criteria: "Institute of Animal and Veterinary Medicine[Affiliation]"

Responses of nutrient utilization, rumen fermentation and microorganisms to different roughage of dairy buffaloes.

BMC Microbiol

May 2024

Yunnan Provincial Key Laboratory of Animal Nutrition and Feed Science, Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming, 650201, China.

Article Synopsis
  • Dairy buffaloes are commonly fed low-quality, high-fiber diets, which leads to inefficiencies in energy and protein utilization.
  • This study investigated how different types of roughage affect the nutrient digestibility, ruminal fermentation, and microbiology in dairy buffaloes using three buffaloes with rumen fistulas.
  • The findings indicated that whole corn silage resulted in the highest digestibility, while sugarcane shoot silage had the lowest, and that rumen fermentation parameters varied significantly among the different roughages tested.
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The lip gene contributes to the virulence of Aeromonas veronii strain TH0426.

Microb Pathog

June 2022

College of Animal Science and Technology, Jilin Agricultural University, Changchun, 130118, China. Electronic address:

Aeromonas veronii (A. veronii) is a pathogen that can infect aquatic organisms and mammals and has caused irrecoverable economic losses to the aquaculture industry. The results of an epidemiological investigation showed that the number of cases of A.

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[Soluble expression of chicken interferon-gamma and antiviral activity of purified expression product].

Wei Sheng Wu Xue Bao

January 2009

Institute of Animal and Veterinary Medicine, Shandong Academy of Agricultural Sciences, Shandong Key Laboratory of Animal Disease Control and Breeding, Jinan 250100, China.

Objective: We cloned and expressed chicken interferon-gamma gene (chIFN-gamma), and detected the bioactivity of chIFN-gamma expressed in Escherichia coli (E. coli).

Methods: The chIFN-gamma mature protein gene was amplified by RT-PCR from spleen lymphocytes of chicken which were stimulated with concanavalin A (ConA) and then cloned into the prokaryotic expression vector pET-32a ( + ).

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