首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Efficacy of chlorine and heat treatment in killing Salmonella stanley inoculated onto alfalfa seeds and growth and survival of the pathogen during sprouting and storage.
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Efficacy of chlorine and heat treatment in killing Salmonella stanley inoculated onto alfalfa seeds and growth and survival of the pathogen during sprouting and storage.

机译:氯和热处理在杀灭接种到苜蓿种子上的斯坦史氏沙门氏菌以及在发芽​​和贮藏过程中病原体的生长和存活的功效。

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摘要

The efficacy of chlorine and hot water treatments in killing Salmonella stanley inoculated onto alfalfa seeds was determined. Treatment of seeds containing 10(2) to 10(3) CFU/g in 100-micrograms/ml active chlorine solution for 5 or 10 min caused a significant (P < or = 0.05) reduction in population, and treatment in 290-micrograms/ml chlorine solution resulted in a significant reduction compared with treatment in 100 micrograms of chlorine per ml. However, concentrations of chlorine of up to 1,010 micrograms/ml failed to result in further significant reductions. Treatment of seeds containing 10(1) to 10(2) CFU of S. stanley per g for 5 min in a solution containing 2,040 micrograms of chlorine per ml reduced the population to undetectable levels (< 1 CFU/g). Treatment of seeds in water for 5 or 10 min at 54 degrees C caused a significant reduction in the S. stanley population, and treatment at > or = 57 degrees C reduced populations to < or = 1 CFU/g. However, treatment at > or = 54 degrees C for 10 min caused a substantial reduction in viability of the seeds. Treatment at 57 or 60 degrees C for 5 min appears to be effective in killing S. stanley without substantially decreasing germinability of seeds. Storage of seeds for 8 to 9 weeks at 8 and 21 degrees C resulted in reductions in populations of S. stanley of about 1 log10 and 2 log10 CFU/g, respectively. The behavior of S. stanley on seeds during soaking germination, sprouting, and refrigerated storage of sprouts was determined. An initial population of 3.29 log10 CFU/g increased slightly during 6 h of soaking, by about 10(3) CFU/g during a 24-h germination period, and by an additional 10 CFU/g during a 72-h sprouting stage. A population of 10(7) CFU/g of mature alfalfa sprouts was detected throughout a subsequent 10-day storage period at 5 degrees C. These studies indicate that while populations of S. stanley can be greatly reduced, elimination of this organism from alfalfa seeds may not be reliably achieved with traditional disinfection procedures. If S. stanley is present on seeds at the initiation of the sprout production process, populations exceeding 10(7) CFU/g can develop and survive on mature sprouts exposed to handling practices used in commercial production and marketing.
机译:确定了氯和热水处理在杀死接种到苜蓿种子上的斯坦沙门氏菌的功效。处理100毫克/毫升活性氯溶液中含10(2)至10(3)CFU / g的种子持续5或10分钟,可导致种群显着减少(P <或= 0.05),处理290毫克与每毫升100微克氯的处理相比,每毫升氯溶液的处理量显着降低。但是,高达1010微克/毫升的氯气浓度无法进一步降低。在每毫升含2,040微克氯的溶液中处理每克含10(1)至10(2)CFU斯坦链霉菌的种子5分钟,可将种群减少到不可检测的水平(<1 CFU / g)。在54摄氏度下在水中处理种子5到10分钟会导致S.stanley种群显着减少,在>或= 57摄氏度下进行处理会使种群减少到<或= 1 CFU / g。但是,在>或= 54摄氏度下处理10分钟会导致种子活力大大降低。在57或60摄氏度下处理5分钟似乎可以有效杀死S.stanley,而不会显着降低种子的发芽率。将种子在8和21摄氏度下保存8至9周可导致斯坦链球菌种群分别减少约1 log10和2 log10 CFU / g。确定了斯坦利链球菌在种子发芽,浸泡和冷藏后的行为。在浸泡6小时后,初始种群为3.29 log10 CFU / g,在发芽的24小时内略有增加,增加了10(3)CFU / g,在发芽72小时的过程中,又增加了10 CFU / g。在随后的5摄氏度下的10天存储期中,检测到10(7)CFU / g成熟的苜蓿芽。这些研究表明,虽然可以大大减少S.stanley种群,但从苜蓿中消除了这种生物传统的消毒程序可能无法可靠地获得种子。如果在芽苗生产过程开始时种子中存在S.stanley,则暴露于商业生产和销售中使用的处理方法的成熟芽苗上,超过10(7)CFU / g的种群就会发育并存活。

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