食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2015年
1期
119-123
,共5页
晚观生%倪长鹏%那晗%吴远高%郑秋月%曹际娟
晚觀生%倪長鵬%那晗%吳遠高%鄭鞦月%曹際娟
만관생%예장붕%나함%오원고%정추월%조제연
致泻大肠埃希氏菌O157%O111%能力验证%样品制备
緻瀉大腸埃希氏菌O157%O111%能力驗證%樣品製備
치사대장애희씨균O157%O111%능력험증%양품제비
Escherichia coliO157,O111%proficiency test%sample preparation
目的:研制植物源性成分绿豆基质中 O157和 O111检测能力验证样品,建立有效的样品制备流程来考核实验室检测致泻大肠埃希氏菌 O157和 O111的能力,根据参加实验室检测结果是否准确及可靠来评价实验室检测水平,并促进实验室检测体系进一步完善。方法选用O157和O111的ATCC标准菌株制备样品,以绿豆粉为基质,真空冷冻干燥技术制备样品。采用显色培养基、荧光定量PCR、全自动细菌生化鉴定仪、VIDAS全自动免疫荧光分析仪和血清型鉴定进行定性检测,并进行菌落计数。结果随机选取每一批阳性样品中的30个样品,每个样品中目标菌数在21~60 CFU之间,并且A组与B组阳性样品中均检测出目标菌,而阴性样品中均没有出现目标菌。结论表明采用本方法制备的能力验证样品均一稳定,能较好地评价实验室致泻大肠埃希氏菌O157和O111的检测能力。
目的:研製植物源性成分綠豆基質中 O157和 O111檢測能力驗證樣品,建立有效的樣品製備流程來攷覈實驗室檢測緻瀉大腸埃希氏菌 O157和 O111的能力,根據參加實驗室檢測結果是否準確及可靠來評價實驗室檢測水平,併促進實驗室檢測體繫進一步完善。方法選用O157和O111的ATCC標準菌株製備樣品,以綠豆粉為基質,真空冷凍榦燥技術製備樣品。採用顯色培養基、熒光定量PCR、全自動細菌生化鑒定儀、VIDAS全自動免疫熒光分析儀和血清型鑒定進行定性檢測,併進行菌落計數。結果隨機選取每一批暘性樣品中的30箇樣品,每箇樣品中目標菌數在21~60 CFU之間,併且A組與B組暘性樣品中均檢測齣目標菌,而陰性樣品中均沒有齣現目標菌。結論錶明採用本方法製備的能力驗證樣品均一穩定,能較好地評價實驗室緻瀉大腸埃希氏菌O157和O111的檢測能力。
목적:연제식물원성성분록두기질중 O157화 O111검측능력험증양품,건립유효적양품제비류정래고핵실험실검측치사대장애희씨균 O157화 O111적능력,근거삼가실험실검측결과시부준학급가고래평개실험실검측수평,병촉진실험실검측체계진일보완선。방법선용O157화O111적ATCC표준균주제비양품,이록두분위기질,진공냉동간조기술제비양품。채용현색배양기、형광정량PCR、전자동세균생화감정의、VIDAS전자동면역형광분석의화혈청형감정진행정성검측,병진행균락계수。결과수궤선취매일비양성양품중적30개양품,매개양품중목표균수재21~60 CFU지간,병차A조여B조양성양품중균검측출목표균,이음성양품중균몰유출현목표균。결론표명채용본방법제비적능력험증양품균일은정,능교호지평개실험실치사대장애희씨균O157화O111적검측능력。
Objective To develop O157 and O111 proficiency testing samples of plant-derived ingredients of mung matrix, and an effective sample preparation process was established to assess the ability of the laboratories to detect diarrheogenic Escherichia coli O157 and O111. According to the accuracy and reliability of test results of laboratories participate in the test to evaluate the detectable levels of laboratories, and to promote the laboratory testing system to get a further improvement. Methods The O157 and O111 ATCC standard strain were used for sample preparation, with mung bean powder as matrix, the samples were made by using vacuum freeze drying technology. The chromogenic medium, fluorescence quantitative PCR, full automatic bacterial biochemical identification instrument, VIDAS automatic immune fluorescence analyzer and serotype identification were used for qualitative detection, and the number of colonies were counted. Results Totally 30 samples were selected randomly in each batch of positive samples, the target bacteria number of each sample should be between the 21~60 CFU. Target bacteria was detected in the positive samples of both group A and group B, while no target bacteria were detected in the negative samples. Conclusion Proficiency testing samples were uniform and stable, and the ability of laboratories to detect diarrheogenic Escherichia coli O157 and O111 got a better evaluation.