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Establishment of a linear regression equation for quantification of beta-hemolytic Escherichia coli in different media and survival of hemolytic Escherichia coli after blending with three different media

机译:建立线性回归方程以定量不同培养基中的β-溶血性大肠杆菌和三种溶媒混合后溶血性大肠杆菌的存活率

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摘要

Pathogenic E. coli associated post-weaning diarrhea (PWD) and edema disease are common diseases in commercially-housed weanling pigs. An enterotoxigenic E. coli (ETEC) oral challenge model has been used to mimic the physiological responses observed in commercial conditions. However, an oral challenge procedure has two major limitations: (1) the ETEC cell density is unknown at the point of oral inoculation, and (2) blending ETEC with traditional TSB (trypticase soy broth) is not palatable and hence decreases acceptability by piglets. Therefore, the purposes of this study were to (1) establish a regression equation that can be used for estimation of ETEC concentration in dilution media using the spectrophotometric measurement of cell density; and (2) examine survival of ETEC after blending either with TSB, sweetener or dextrose. A strain of ETEC (serogroup beta-hemolytic E. coli O149; K91; F4; toxins LT, STa, STb) was grown in TSB for 3.5 hours, centrifuged, the supernatant was discarded, and the ETEC pellet was then blended either with TSB (100 mL), sweetener (60 mL TSB + 40 mL fruit flavored concentrate), or dextrose (50 mL TSB + 50 mL dextrose; 0.5g/mL dextrose). Cell density was measured using the colorimetric method and also plated on a 5% sheep blood agar for counting of ETEC colony forming units at 0, 5, 35, 65 and 125 min after blending. The optical density at 600 nm explained 83% of ETEC colony forming units, indicating that the established linear equation (y= 6E+08x – 4E+07, P<0.004) can be used for robust quantification of ETEC cell density in TSB, sweetener and dextrose media. When ETEC was blended with sweetener and dextrose, survival of ETEC was decreased by 45% and 72% within 5 min post-blending. Therefore, further research is required to find out the suitable medium that has potential to improve palatability without compromising survival of ETEC.
机译:致病性大肠杆菌相关的断奶后腹泻(PWD)和水肿病是商业饲养的断奶猪的常见疾病。产肠毒素的大肠杆菌(ETEC)口服攻击模型已用于模拟在商业条件下观察到的生理反应。但是,口服攻击程序有两个主要局限性:(1)口服接种时ETEC细胞密度未知,(2)ETEC与传统TSB(胰蛋白酶大豆肉汤)混合不宜用,因此降低了仔猪的可接受性。因此,本研究的目的是(1)建立一个回归方程,该方程可用于通过分光光度法测量细胞密度来估计稀释培养基中的ETEC浓度; (2)与TSB,甜味剂或葡萄糖混合后,检查ETEC的存活率。将ETEC菌株(β-溶血性大肠杆菌O149血清群; K91; F4;毒素LT,STa,STb)在TSB中生长3.5小时,离心,弃去上清液,然后将ETEC沉淀与TSB混合(100毫升),甜味剂(60毫升TSB + 40毫升水果调味浓缩物)或葡萄糖(50毫升TSB + 50毫升葡萄糖; 0.5克/毫升葡萄糖)。使用比色法测量细胞密度,并且在混合后0、5、35、65和125分钟,将其铺板在5%羊血琼脂上以计数ETEC集落形成单位。 600 nm处的光密度解释了83%的ETEC集落形成单位,表明建立的线性方程式(y = 6E + 08x – 4E + 07,P <0.004)可用于可靠地定量甜味剂TSB中ETEC细胞的密度和葡萄糖培养基。当ETEC与甜味剂和葡萄糖混合后,在混合后5分钟内ETEC的存活率分别降低了45%和72%。因此,需要进行进一步的研究以找到合适的培养基,该培养基在不损害ETEC存活的情况下具有改善适口性的潜力。

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