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      Broiler chicken response to xylanase and fermentable xylooligosaccharide supplementation

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          Abstract

          A study was conducted to determine the effect of dietary fiber ( DF), xylanase ( XYL), xylooligosaccharides ( XOS), and a combination of XYL and xylooligosaccharides ( STBIO) on chicken growth performance, N-corrected apparent metabolizable energy ( AMEn), and nutrient availability, characteristics of the gastrointestinal tract ( GIT), and cecal content of short-chain fatty acids ( SCFA). A 35-day experiment was performed on 1,920 as hatched Ross 308 broiler chicks, reared in 96 pens and fed ad libitum. Experimental diets were split into 2 phases: starter (0–21 d) and finisher (22–35 d). There were 2 basal diets, first contained 54% maize and in the second, 5% of the maize was replaced by wheat bran as DF. The diets were split into 4 batches: one of them was used as a control, and each of the others were supplemented either with XYL or XOS or with the STBIO. Each diet was fed to 12 pens following randomization. The data were analyzed in GenStat (20th edition) by ANOVA using a 2 × 4 factorial design. The addition of STBIO improved feed conversion ratio ( FCR) and increased weight gain ( WG) from 21 to 35 d and from 0 to 35 d ( P < 0.05). The inclusion of DF had a negative effect on N and fat retention coefficients at 35 d as well as AMEn and dry matter retention at 21 and 35 d. At 21 d, neutral detergent fiber ( NDF) retention was increased when xylanase and STBIO were added to the diet ( P < 0.001) and at d 35 the highest retention was noted when the diet was supplemented with DF and XYL or STBIO ( P = 0.001). There was no dietary effect on jejunum histomorphometry ( P > 0.05). The addition of DF increased the concentration of cecal SCFA in particular valeric and propionic acid at 35-day-old birds ( P < 0.05). It can be concluded that addition of STBIO in diet could provide benefits in terms of fiber degradation, WG, and feed efficiency.

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          The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research

          Reproducible science requires transparent reporting. The ARRIVE guidelines (Animal Research: Reporting of In Vivo Experiments) were originally developed in 2010 to improve the reporting of animal research. They consist of a checklist of information to include in publications describing in vivo experiments to enable others to scrutinise the work adequately, evaluate its methodological rigour, and reproduce the methods and results. Despite considerable levels of endorsement by funders and journals over the years, adherence to the guidelines has been inconsistent, and the anticipated improvements in the quality of reporting in animal research publications have not been achieved. Here, we introduce ARRIVE 2.0. The guidelines have been updated and information reorganised to facilitate their use in practice. We used a Delphi exercise to prioritise and divide the items of the guidelines into 2 sets, the “ARRIVE Essential 10,” which constitutes the minimum requirement, and the “Recommended Set,” which describes the research context. This division facilitates improved reporting of animal research by supporting a stepwise approach to implementation. This helps journal editors and reviewers verify that the most important items are being reported in manuscripts. We have also developed the accompanying Explanation and Elaboration (E&E) document, which serves (1) to explain the rationale behind each item in the guidelines, (2) to clarify key concepts, and (3) to provide illustrative examples. We aim, through these changes, to help ensure that researchers, reviewers, and journal editors are better equipped to improve the rigour and transparency of the scientific process and thus reproducibility.
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            Evaluation of Acid-Insoluble Ash as a Natural Marker in Ruminant Digestibility Studies

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              Lactate-utilizing bacteria, isolated from human feces, that produce butyrate as a major fermentation product.

              The microbial community of the human colon contains many bacteria that produce lactic acid, but lactate is normally detected only at low concentrations (<5 mM) in feces from healthy individuals. It is not clear, however, which bacteria are mainly responsible for lactate utilization in the human colon. Here, bacteria able to utilize lactate and produce butyrate were identified among isolates obtained from 10(-8) dilutions of fecal samples from five different subjects. Out of nine such strains identified, four were found to be related to Eubacterium hallii and two to Anaerostipes caccae, while the remaining three represent a new species within clostridial cluster XIVa based on their 16S rRNA sequences. Significant ability to utilize lactate was not detected in the butyrate-producing species Roseburia intestinalis, Eubacterium rectale, or Faecalibacterium prausnitzii. Whereas E. hallii and A. caccae strains used both D- and L-lactate, the remaining strains used only the d form. Addition of glucose to batch cultures prevented lactate utilization until the glucose became exhausted. However, when two E. hallii strains and one A. caccae strain were grown in separate cocultures with a starch-utilizing Bifidobacterium adolescentis isolate, with starch as the carbohydrate energy source, the L-lactate produced by B. adolescentis became undetectable and butyrate was formed. Such cross-feeding may help to explain the reported butyrogenic effect of certain dietary substrates, including resistant starch. The abundance of E. hallii in particular in the colonic ecosystem suggests that these bacteria play important roles in preventing lactate accumulation.
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                Author and article information

                Contributors
                Journal
                Poult Sci
                Poult Sci
                Poultry Science
                Elsevier
                0032-5791
                1525-3171
                04 August 2023
                November 2023
                04 August 2023
                : 102
                : 11
                : 103000
                Affiliations
                [* ]The National Institute of Poultry Husbandry, Harper Adams University, Edgmond, Newport, Shropshire TF10 8NB, United Kingdom
                []AB Vista, Woodstock Court, Marlborough, Wiltshire SN8 4AN, United Kingdom
                []Faculty of Veterinary Medicine, Trakia University, Stara Zagora 6000, Bulgaria
                Author notes
                [1 ]Corresponding author: ASimic@ 123456live.harper.ac.uk
                Article
                S0032-5791(23)00519-9 103000
                10.1016/j.psj.2023.103000
                10474081
                37639756
                88fb6c98-5348-4e5c-8d28-0506f6a02967
                © 2023 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 7 June 2023
                : 31 July 2023
                Categories
                METABOLISM AND NUTRITION

                broiler,xylanase,fermentable oligosaccharide,stimbiotic
                broiler, xylanase, fermentable oligosaccharide, stimbiotic

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