Nisbet David J, Callaway Todd R, Edrington T S, Anderson Robin C, Krueger N
Food and Feed Safety Research Unit, Southern Plains Agricultural Research Center, Agricultural Research Service, USDA, College Station, TX 77845, USA.
Curr Microbiol. 2009 May;58(5):488-92. doi: 10.1007/s00284-008-9351-1. Epub 2009 Feb 5.
The dicarboxylic acids malate and fumarate increase ruminal pH, reduce methane production, increase propionate and total volatile fatty acid (VFA) production, and reduce lactic acid accumulation in a manner similar to ionophores. These acids stimulate the ruminal bacterium Selenomonas ruminantium to ferment lactate to produce propionate. Thus, dicarboxylic acids have been suggested as nonantibiotic modifiers of the ruminal fermentation, but their impact on ruminal microbial ecology remains unknown. This study was designed to examine what effects these modifiers may have on intestinal pathogen populations such as Escherichia coli O157:H7 and S. enterica Typhimurium prior to their widespread incorporation into cattle rations. Pure cultures of E. coli O157:H7 strain 933 and S. enterica Typhimurium were grown with malate and fumarate added at 0, 1, 5, 10, and 20 mM (v/v; n = 3). Neither dicarboxylic acid inhibited (p > 0.1) the growth rate or final populations of E. coli O157:H7 or S. enterica Typhimurium. Ruminal fluid was collected from cattle (n = 2) and E. coli O157:H7 and S. enterica Typhimurium were added to separate ruminal fermentations incubated for 24 h at 39 degrees C. Fumarate and malate were added at concentrations of 0, 5, 10, and 20 mM (v/v; n = 2) and incubated for 24 h at 39 degrees C. Malate or fumarate addition did not affect (p > 0.1) populations of E. coli O157:H7 or S. enterica Typhimurium. However, the final pH was increased (p < 0.05), the acetate:propionate ratio was decreased (p < 0.05), and the total VFA production was increased (p < 0.05) by > or =10 mM dicarboxylic acid addition. These results confirm that dicarboxylic acids can modify ruminal fermentation, but they do not affect populations of critical foodborne pathogens.
二羧酸苹果酸和富马酸可提高瘤胃pH值,减少甲烷生成,增加丙酸和总挥发性脂肪酸(VFA)的生成,并以类似于离子载体的方式减少乳酸积累。这些酸刺激瘤胃细菌反刍月形单胞菌发酵乳酸以产生丙酸。因此,二羧酸被认为是瘤胃发酵的非抗生素调节剂,但其对瘤胃微生物生态的影响尚不清楚。本研究旨在检验在这些调节剂广泛应用于牛日粮之前,它们可能对诸如大肠杆菌O157:H7和鼠伤寒沙门氏菌等肠道病原菌种群产生何种影响。将大肠杆菌O157:H7菌株933和鼠伤寒沙门氏菌的纯培养物分别在添加了0、1、5、10和20 mM(体积/体积;n = 3)苹果酸和富马酸的条件下培养。两种二羧酸均未抑制(p > 0.1)大肠杆菌O157:H7或鼠伤寒沙门氏菌的生长速率或最终菌量。从牛(n = 2)采集瘤胃液,并将大肠杆菌O157:H7和鼠伤寒沙门氏菌分别添加到单独的瘤胃发酵液中,在39℃下培养24小时。分别添加浓度为0、5、10和20 mM(体积/体积;n = 2)的富马酸和苹果酸,并在39℃下培养24小时。添加苹果酸或富马酸对大肠杆菌O157:H7或鼠伤寒沙门氏菌的菌量没有影响(p > 0.1)。然而,添加≥10 mM二羧酸可使最终pH值升高(p < 0.05),乙酸:丙酸比值降低(p < 0.05),总挥发性脂肪酸生成量增加(p < 0.05)。这些结果证实二羧酸可改变瘤胃发酵,但不影响关键食源性病原体的菌量。