106 research outputs found

    Comparison of fermentation characteristics and bacterial diversity in the rumen of sheep and batch cultures of rumen microorganisms

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    The objective of the current study was to assess how closely batch cultures (BC) of rumen microorganisms can mimic the dietary differences in fermentation characteristics found in the rumen, and to analyse changes in bacterial diversity over the in vitro incubation period. Four ruminally and duodenally cannulated sheep were fed four diets having forage : concentrate ratios (FCR) of 70 : 30 or 30 : 70, with either alfalfa hay or grass hay as forage. Rumen fluid from each sheep was used to inoculate BC containing the same diet fed to the donor sheep, and the main rumen fermentation parameters were determined after 24 h of incubation. There were differences between BC and sheep in the magnitude of most measured parameters, but BC detected differences among diets due to forage type similar to those found in sheep. In contrast, BC did not reproduce the dietary differences due to FCR found in sheep for pH, degradability of neutral detergent fibre and total volatile fatty acid (VFA) concentrations. There were differences between systems in the magnitude of most determined parameters and BC showed higher pH values and NH3–N concentrations, but lower fibre degradability and VFA and lactate concentrations compared with sheep. There were significant relationships between in vivo and in vitro values for molar proportions of acetate, propionate and butyrate, and the acetate : propionate ratio. The automated ribosomal intergenic spacer analysis (ARISA) of 16S ribosomal deoxyribonucleic acid showed that FCR had no effect on bacterial diversity either in the sheep rumen fluid used as inoculum (IN) or in BC samples. In contrast, bacterial diversity was greater with alfalfa hay diets than those with grass hay in the IN, but was unaffected by forage type in the BC. Similarity index between the bacterial communities in the inocula and those in the BC ranged from 67·2 to 74·7%, and was unaffected by diet characteristics. Bacterial diversity was lower in BC than in the inocula with 14 peaks out of a total of 181 detected in the ARISA electropherograms never appearing in BC samples, which suggests that incubation conditions in the BC may have caused a selection of some bacterial strains. However, each BC sample showed the highest similarity index with its corresponding rumen IN, which highlights the importance of using rumen fluid from donors fed a diet similar to that being incubated in BC when conducting in vitro experiments

    Influence of processing method of rumen contents on microbial populations in the inoculum and in vitro fermentation of substrates of variable composition

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    The in vitro batch culture technique is being increasingly used to study rumen fermentation, but the results are affected by several factors, being the source of the inoculum one of the most relevant. This work was conducted to assess the effects of different processing methods of ruminal contents on microbial populations in the obtained fluid, and its influence on fermentation parameters when the fluid was used as inoculum for in vitro incubations. Rumen contents were obtained from four rumen-fistulated sheep fed a 2:1 alfalfa hay:concentrate diet and subjected to the following treatments: SQ: squeezed through four layers of cheesecloth; FL: SQ treatment and further filtration through a 100-μm nylon cloth; STO: blended for three min at 230 rev min−1 in a Stomacher® and further filtrations as in SQ. Microbial populations’ abundance and bacterial diversity in the ruminal fluids were analysed by quantitative PCR (qPCR) and automated ribosomal intergenic spacer analysis (ARISA), respectively. Three forages (alfalfa hay, grass hay and barley straw) were incubated in vitro, either alone or mixed with concentrate (1:1), using each of the ruminal fluids as inoculum. There were no differences between SQ and FL methods in any of the microbial populations analysed, but STO increased the relative abundance of Fibrobacter succinogenes and Ruminococcus albus (P 0.05) by the processing methods. There were no interactions (P > 0.05) between the processing method and the characteristics of the substrates for any of the fermentation parameters analysed. Compared with SQ, the STO method resulted in greater (P < 0.05) methane production and ammonia-N concentrations in 8 h incubations. After 24 h of incubation, the use of STO inoculum increased (P < 0.05) methane production and dry matter degradability compared with SQ, with no differences in the rest of the parameters. No differences between SQ and FL methods were detected in any parameter. The results show that stomaching the rumen contents prior to inoculation of in vitro cultures modified some microbial populations, but had only subtle effects on fermentation parameters

    Presente y perspectivas de futuro en la UE del empleo de probióticos en la alimentación de rumiantes

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    En este artículo se describe, en primer lugar, la situación legal actual de los probióticos como aditivos en la alimentación de los animales rumiantes en la Unión Europea (UE). A continuación se repasan sus mecanismos de acción, considerando especialmente los últimos avances científicos en referencia a sus acciones sobre las poblaciones microbianas ruminales, y se analizan los factores que influyen en la respuesta de los animales a la administración de estos aditivos. Finalmente, se detallan brevemente las perspectivas de futuro de los probióticos en el ámbito de la ganadería de rumiantes europea

    Perspectivas y retos de los extractos vegetales como aditivos alimentarios en rumiantes

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    Algunas plantas producen y almacenan compuestos secundarios que ejercen actividades beneficiosas en el organismo humano y animal. En lo que se refiere a su uso en alimentación animal, constituyen una alternativa natural a los aditivos antibióticos promotores del crecimiento, cuyo uso en rumiantes se ha centrado fundamentalmente en sus efectos sobre la fermentación rumial

    Influence of essential oils (cinnamaldehyde and garlic oil) on rumen fermentation, feeding 1 behavior and performance of lactating dairy cattle

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    Two experiments were conducted to study the effects of Next Enhance® 300 (NE300; cinnamaldehyde and garlic oil encapsulated product) on rumen fermentation and milk production of dairy cows. In experiment 1, batch cultures of mixed rumen micro-organisms were used to study the effects of increasing concentrations of NE300 (0, 200, 300, and 400 mg/L) on ruminal fermentation in 24 h in vitro incubations. All tested doses decreased (P < 0.05) methane production, but the dose of 400 mg/L also reduced the production of volatile fatty acid (VFA). The addition of NE300 at 300 mg/L produced the most beneficial effects, reducing methane production, acetate proportion, and ammonia-N concentration, and increasing propionate proportion compared with CON, without affecting total VFA production. These results would indicate a potentially greater supply of energy for the host animal. In experiment 2, sixteen lactating dairy cows (8 rumen-cannulated) participated in a switch-back design with three 4-wk periods and 2 treatments: control (CON, unsupplemented) and NE300 (300 mg NE300/cow/d). Milk yield response was affected by a 3-way interaction among treatment, parity, and days on treatment; after 15 d on treatment, multiparous cows on NE300 produced more milk (approximately additional 3 kg/d) than multiparous cows on CON. Total rumen VFA concentrations tended (P = 0.06) to be greater in NE300 than in CON when rumen fermentation kinetics were evaluated at the end of each period (day 28). It is concluded that NE300 modifies ruminal fermentation resulting in increased milk yield in multiparous lactating dairy cows after 15 d of adaptation

    Evolución temporal de las comunidades microbianas ruminales y los parámetros fermentativos en fermentadores Rusitec

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    Los fermentadores Rusitec (Czerkawski y Breckenridge, 1977) son uno de los tipos de fermentadores más ampliamente utilizados para simular in vitro la fermentación ruminal y permiten realizar estudios de larga duración (semanas). Sin embargo, debido a la prolongada extensión en el tiempo de este tipo de estudios se producen cambios cuantitativos y cualitativos en las poblaciones de microorganismos. Existen algunos estudios que han puesto de manifiesto la disminución de la población de protozoos a lo largo del período de incubación (Carro et al., 1995; Martínez et al., 2011), pero no existe información sobre otras poblaciones microbianas, a pesar de que uno de los requisitos que deberían cumplir los sistemas in vitro es mantener poblaciones microbianas representativas de las existentes en el rumen de los animales. Por ello, el objetivo del presente trabajo fue estudiar la evolución en el tiempo de la abundancia de bacterias, hongos, protozoos y arqueas, así como de los parámetros ruminales en fermentadores Rusitec

    Treatment of tropical forages with exogenous fibrolytiic enzymes: effects on chemical composition and in vitro rumen fermentation

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    The effects of three treatments of fibrolytic enzymes (cellulase from Trichoderma longibrachiatum (CEL), xylanase from rumen micro-organisms (XYL) and a 1:1 mixture of CEL and XYL (MIX) on the in vitro fermentation of two samples of Pennisetum clandestinum (P1 and P2), two samples of Dichanthium aristatum (D1 and D2) and one sample of each Acacia decurrens and Acacia mangium (A1 and A2) were investigated. The first experiment compared the effects of two methods of applying the enzymes to forages, either at the time of incubation or 24 h before, on the in vitro gas production. In general, the 24 h pre-treatment resulted in higher values of gas production rate, and this application method was chosen for a second study investigating the effects of enzymes on chemical composition and in vitro fermentation of forages. The pre-treatment with CEL for 24 h reduced (p < 0.05) the content of neutral detergent fibre (NDF) of P1, P2, D1 and D2, and that of MIX reduced the NDF content of P1 and D1, but XYL had no effect on any forage. The CEL treatment increased (p < 0.05) total volatile fatty acid (VFA) production for all forages (ranging from 8.6% to 22.7%), but in general, no effects of MIX and XYL were observed. For both P. clandestinum samples, CEL treatment reduced (p < 0.05) the molar proportion of acetate and increased (p < 0.05) that of butyrate, but only subtle changes in VFA profile were observed for the rest of forages. Under the conditions of the present experiment, the treatment of tropical forages with CEL stimulated their in vitro ruminal fermentation, but XYL did not produce any positive effect. These results showed clearly that effectiveness of enzymes varied with the incubated forage and further study is warranted to investigate specific, optimal enzyme-substrate combinations

    Utilización de enzimas fibrolíticas para mejorar la digestión de forrajes tropicales. I. Influencia del método de aplciacion en la producción de gas in vitro y la composición química

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    Los forrajes tropicales presentan, en general, un menor valor nutritivo que los forrajes de zonas templadas. Sin embargo, su disponibilidad suele ser elevada y en numerosas ocasiones son el único recurso alimenticio disponible para los animales rumiantes. Esta situación limita la productividad de estos animales y por ello se han investigado diferentes estrategias para aumentar el valor nutritivo de los forrajes tropicales. Una de las metodologías propuestas para incrementar la utilización digestiva de los forrajes es el tratamiento de los mismos con enzimas fibrolíticas (Carro y Ranilla, 2001), pero todavía son escasos los estudios realizados con forrajes tropicales. El objetivo de este trabajo fue evaluar el efecto de tres preparados enzimáticos en la fermentación ruminal in vitro y la degradabilidad de tres forrajes tropicales

    Utilización de enzimas fibrolíticas para mejorar la digestión de forrajes tropicales. II. Efectos en la fermetación ruminal in vitro y la degradabilidad

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    En muchos países tropicales los sistemas productivos de animales rumiantes se basan en una amplia utilización de recursos forrajeros. Sin embargo, estos recursos suelen tener una baja calidad, por lo que cualquier mejora de su valor nutritivo tendrá una repercusión positiva en la productividad de los animales. En los últimos años se han realizado numerosos estudios para evaluar diferentes enzimas fibrolíticas como aditivos para mejorar el valor nutritivo de forrajes, pero la mayoría de ellos han utilizado forrajes de elevada calidad y apenas existen estudios con forrajes de baja calidad. Por otra parte, los resultados han sido muy variables, ya que la efectividad de las enzimas se ve afectada por numerosos factores, siendo el tipo de forraje y el método de aplicación de las enzimas dos de los más importantes (Giraldo et al., 2008). El objetivo del presente estudio fue evaluar el efecto de tres enzimas fibrolíticas exógenas en la fermentación ruminal in vitro de tres forrajes tropicales cuando las enzimas se aplicaron 24 h antes o en el momento de la incubación

    Influencia del tipo de filtrado y tratamiento con Stomacher del fluido ruminal de ovejas en las poblaciones microbianas del inóculo

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    Four rumen-fistulated sheep fed a 66:34 alfalfa hay:concentrate diet were used as donors to investigate the effect of rumen contents’ treatment on microbial populations in the resulting fluid. Rumen contents were sampled from each individual sheep and subjected to the following treatments: SQ: squeezed through 4 layers of cheesecloth; FIL: SQ treatment and further filtration through a 100-μm nylon cloth; STO: reated with a Stomacher® for 3 min at 230 rev min-1 and followed by SQ. Microbial populations in the fluid were analysed by real-time PCR and bacterial diversity was assessed by the automated ribosomal intergenic spacer analysis (ARISA) of the 16S ribosomal DNA. Bacterial DNA concentrations and relative abundance of Ruminococcus flavefaciens, arqueal and fungal DNA did not differ (P>0.05) between treatments. In contrast, STO treatment decreased (P0.05) between treatments either in the Shannon index or in the number of peaks in the ARISA electropherograms, indicating no effect on bacterial diversity. Studies analyzing the influence on the tested methods on fermentation characteristics of different substrates when the fluid is used as inoculum is required
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