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多克隆抗体抑制瘤胃中关键纤维素分解细菌物种的生长。

Polyclonal antibodies inhibit growth of key cellulolytic rumen bacterial species.

作者信息

Tondini Sara M, Mackie Roderick I, McCann Joshua C

机构信息

Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, United States.

Carle R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, United States.

出版信息

Front Microbiol. 2023 Jun 20;14:1196492. doi: 10.3389/fmicb.2023.1196492. eCollection 2023.

Abstract

Antibodies targeting specific bacterial species could allow for modification of the rumen microbial population to enhance rumen fermentation. However, there is limited knowledge of targeted antibody effects on rumen bacteria. Therefore, our objective was to develop efficacious polyclonal antibodies to inhibit the growth of targeted cellulolytic bacteria from the rumen. Egg-derived, polyclonal antibodies were developed against pure cultures of 7 (), 8 (), and S85 (). Antibodies were added to a cellobiose-containing growth medium for each of the three targeted species. Antibody efficacy was determined via inoculation time (0 h and 4 h) and dose response. Antibody doses included: 0 (), 1.3 × 10 (), 0.013 (), and 1.3 () mg antibody per ml of medium. Each targeted species inoculated at 0 h with HI of their respective antibody had decreased ( < 0.01) final optical density and total acetate concentration after a 52 h growth period when compared with CON or LO. Live/dead stains of 7 and S85 dosed at 0 h with HI of their respective antibody indicated a decrease (≥ 96%; < 0.05) in live bacterial cells during the mid-log phase compared with CON or LO. Addition of HI of anti-FS85 at 0 h in S85 cultures reduced ( < 0.01) total substrate disappearance over 52 h by at least 48% when compared with CON or LO. Cross-reactivity was assessed by adding HI at 0 h to non-targeted bacterial species. Addition of anti-RA8 or anti-RA7 to S85 cultures did not affect ( ≥ 0.45) total acetate accumulation after 52 h incubation, indicating that antibodies have less of an inhibitory effect on non-target strains. Addition of anti-FS85 to non-cellulolytic strains did not affect ( ≥ 0.89) OD, substrate disappearance, or total VFA concentrations, providing further evidence of specificity against fiber-degrading bacteria. Western blotting with anti-FS85 indicated selective binding to S85 proteins. Identification by LC-MS/MS of 8 selected protein spots indicated 7 were outer membrane proteins. Overall, polyclonal antibodies were more efficacious at inhibiting the growth of targeted cellulolytic bacteria than non-targeted bacteria. Validated polyclonal antibodies could serve as an effective approach to modify rumen bacterial populations.

摘要

靶向特定细菌物种的抗体可用于改变瘤胃微生物种群,以增强瘤胃发酵。然而,关于靶向抗体对瘤胃细菌的影响,我们所知有限。因此,我们的目标是开发有效的多克隆抗体,以抑制瘤胃中靶向纤维素分解菌的生长。针对7种()、8种()和S85种()的纯培养物制备了鸡蛋源多克隆抗体。将抗体添加到三种靶向物种各自含纤维二糖的生长培养基中。通过接种时间(0小时和4小时)和剂量反应来确定抗体效力。抗体剂量包括:每毫升培养基0()、1.3×10()、0.013()和1.3()毫克抗体。与对照组或低剂量组相比,在0小时接种各自抗体高剂量的每种靶向物种,在52小时的生长周期后,最终光密度和总乙酸盐浓度均降低(<0.01)。在0小时用各自抗体高剂量处理的7种和S85种活/死染色显示,与对照组或低剂量组相比,在对数中期活细菌细胞减少(≥96%;<0.05)。在S85培养物中于0小时添加抗FS85高剂量,与对照组或低剂量组相比,52小时内总底物消失量减少(<0.01)至少48%。通过在0小时向非靶向细菌物种添加高剂量来评估交叉反应性。在S85培养物中添加抗RA8或抗RA7,在52小时孵育后对总乙酸盐积累没有影响(≥0.45),表明抗体对非靶向菌株的抑制作用较小。向非纤维素分解菌株添加抗FS85对光密度、底物消失或总挥发性脂肪酸浓度没有影响(≥0.89),这进一步证明了对纤维降解细菌的特异性。用抗FS85进行蛋白质印迹表明与S85蛋白有选择性结合。通过液相色谱-串联质谱对8个选定蛋白斑点的鉴定表明,7个是外膜蛋白。总体而言,多克隆抗体在抑制靶向纤维素分解菌生长方面比非靶向细菌更有效。经过验证的多克隆抗体可作为改变瘤胃细菌种群的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24e2/10318403/ed3297d84f94/fmicb-14-1196492-g0001.jpg

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