26 The Effect of Feeding Ferric Citrate on Rumen Microbial Communities and Methanogenesis in Growing Beef Steers.

2018 ◽  
Vol 96 (suppl_1) ◽  
pp. 14-14
Author(s):  
E A Melchior ◽  
K E Hales ◽  
A K Lindholm-Perry ◽  
J E Wells ◽  
P R Myer
2019 ◽  
Vol 3 (2) ◽  
pp. 162-162
Author(s):  
S. D. Nath ◽  
A. Ward ◽  
E. Knutson ◽  
X. Sun ◽  
W. Keller ◽  
...  

1981 ◽  
Vol 21 (108) ◽  
pp. 12
Author(s):  
GR Saul ◽  
AJ Clark

Each year from 1975 to 1977, three groups of six beef steers, 9 months old, were stocked at 2.6 ha-l and managed under one of the following treatments: (1 ) Pasture only (PO), no supplementary feeding, (2) Winter feeding (WF) ; pasture hay was cut from 33% of the grazed area, stored and fed back the following winter while the steers were at pasture. (3) Autumn deferment (AD) ; 33% of the grazed area was cut for hay and rolled using an Econ fodder roller. For 8-11 weeks after the opening rains, the steers were fed a complete hay ration of fodder rolls while confined to a tenth of the grazed area. Thereafter the steers grazed the whole area. The AD and WF hay averaged 11% crude protein, and 56% digestible organic matter. The growth rate of all groups during autumn was similar and averaged 0.1 5 kg day-1. During winter, the average growth rates of the PO, WF and AD groups were 0.26, 0.44 and 0.61 kg day-1, respectively. In spring the respective growth rates were 1.09, 0.81 and 0.77 kg day1 and the overall growth rates were 0.40, 0.37 and 0.42 kg day-1. The results show that when using average quality hay produced within the grazing system, AD is more effective than WF in increasing the winter liveweight gains of steers. However, the yearly beef production from each system was similar due mainly to compensatory growth by the PO steers in spring.


2021 ◽  
Vol 99 (Supplement_3) ◽  
pp. 339-340
Author(s):  
Zhe Pan ◽  
Yanhong Chen ◽  
Tim A McAllister

Abstract This study aimed to identify whether microbial interactions in the rectum contribute to Shiga toxin producing bacteria colonization. In total, 12 rectal digesta samples based on the previously identified Shiga toxin 2 gene (stx2) abundance (DNA) and expression (RNA) in Shiga toxin-producing bacteria (Stx2- group: detectable DNA, n=6; Stx2+ group: detectable DNA and RNA, n = 6) were subjected to microbial profiling using amplicon sequencing. Firmicutes (72.7 ± 2.0 %) and Bacteroidetes (24.6 ± 1.9 %) are the most predominant phyla of rectal microbiota, and no compositional differences were identified between two groups at the phylum level. The Shannon and Chao1 indices weren’t different in rectal digesta microbial communities between two groups. Twenty-four and thirteen taxa were identified to be group-specific genera in microbial communities from Stx2- and Stx2+ group, respectively (2 out of 6, average relative abundance >0.1%). The network analysis indicated 12 and 14 keystone taxa (Generalists, densely connected with other taxa) in microbial communities between Stx2- and Stx2+ groups, respectively. Eight out of 12 and six out of 14 generalists in the Stx2- and Stx2+ group are belonging to group-specific genera, respectively. Generalists belonging to group-specific genera were broadly distributed in Stx2- network while centralized distributed in the Stx2+ network, suggesting the higher stability of the Stx2- network structure in comparison of Stx2+ network computed by the natural connectivity measurement. However, 66 core genera shared by microbial communities between two groups were not classified into network generalists. Overall, our results indicate microbial crosstalks and keystone taxa in microbial communities between two groups differed, suggesting that the microbial interactions rather than the shifts in taxa abundance may be more important affecting host. Moreover, group-specific genera play a vital ecological role in the microbial interactions, indicating the potential for being microbial markers to differentiate Shiga toxin-producing bacteria colonization in beef cattle.


2005 ◽  
Vol 2005 ◽  
pp. 71-71
Author(s):  
M.R.F. Lee ◽  
J.K.S. Tweed ◽  
N. D. Scollan

Data on ruminal metabolism of lipids from forages have shown extensive biohydrogenation of C18 polyunsaturated fatty acids (Lee et al. 2003). Recent studies have noted a reduction in biohydrogenation an increase in duodenal flow of C18:1 trans- 11 and a shift in the ruminal production of CLA from cis- 9 trans- 11 CLA towards trans- 10 cis- 12 CLA with increasing amounts of concentrate in the diet (Kucuk et al. 2001, Loor et al. 2004). The study assessed the effect of feeding steers on isonitrogenous and isolipid diets differing in forage concentration and supplemented with linseed oil on ruminal lipid metabolism.


2020 ◽  
Vol 48 (2) ◽  
pp. 399-409
Author(s):  
Baizhen Gao ◽  
Rushant Sabnis ◽  
Tommaso Costantini ◽  
Robert Jinkerson ◽  
Qing Sun

Microbial communities drive diverse processes that impact nearly everything on this planet, from global biogeochemical cycles to human health. Harnessing the power of these microorganisms could provide solutions to many of the challenges that face society. However, naturally occurring microbial communities are not optimized for anthropogenic use. An emerging area of research is focusing on engineering synthetic microbial communities to carry out predefined functions. Microbial community engineers are applying design principles like top-down and bottom-up approaches to create synthetic microbial communities having a myriad of real-life applications in health care, disease prevention, and environmental remediation. Multiple genetic engineering tools and delivery approaches can be used to ‘knock-in' new gene functions into microbial communities. A systematic study of the microbial interactions, community assembling principles, and engineering tools are necessary for us to understand the microbial community and to better utilize them. Continued analysis and effort are required to further the current and potential applications of synthetic microbial communities.


1970 ◽  
Vol 70 (3, Pt.1) ◽  
pp. 431-436 ◽  
Author(s):  
Elvie H. Wilson ◽  
James A. Dinsmoor

Pneumologie ◽  
2009 ◽  
Vol 63 (S 01) ◽  
Author(s):  
T Zakharkina ◽  
C Herr ◽  
A Yildirim ◽  
M Friedrich ◽  
R Bals

Planta Medica ◽  
2015 ◽  
Vol 81 (11) ◽  
Author(s):  
JJ Araya ◽  
M Chavarría ◽  
A Pinto-Tomás ◽  
C Murillo ◽  
L Uribe ◽  
...  

EDIS ◽  
2017 ◽  
Vol 2017 (4) ◽  
Author(s):  
Philipe Moriel

Calves can be preconditioned using a wide variety of supplemental feed ingredients. However, feed ingredient selection is not the only factor to consider during a preconditioning process. Increasing the protein supply to stressed, preconditioning beef steers led to greater growth performance, and increased immune response to vaccination during a 42-day preconditioning period. Producers should not reduce the frequency of concentrate supplementation during the entire preconditioning period as it might lead to poorer vaccine response and average daily gain (consequently, less calf value at sale). However, a gradual reduction of frequency of supplementation is a supplementation strategy that can overcome these negative effects on growth and immunity, and allows producers to save on feeding and labor costs without producing lighter calves that have weaker immune responses.  


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