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首页> 外文期刊>Diagnostic microbiology and infectious disease >Evaluation of pyrrolidonyl arylamidase for the identification of nonfermenting Gram-negative rods.
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Evaluation of pyrrolidonyl arylamidase for the identification of nonfermenting Gram-negative rods.

机译:评价吡咯烷酮芳基酰胺酶以鉴定非发酵革兰氏阴性棒。

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To evaluate the activity of pyrrolidonyl arylamidase (PYR) for the differentiation and identification of nonfermenting gram negative rods (NFGNR), 293 isolates were tested. A 24 h culture of each test organism was prepared. From this a 108-109 cfu/mL suspension was added to 0.25 mL of sterile physiologic solution. A PYR disk was then added and the test was incubated for 30 minutes at 35-37 degrees C, at environmental atmosphere. Reading was done by adding 1 drop of cinnamaldehyde reagent. Strains of Acinetobacter baumannii, Acinetobacter haemolyticus, Alcaligenes faecalis, Bergeyella zoohelcum, Bordetella bronchiseptica, Bordetella hinzii, Brevundimonas diminuta, Brevundimonas vesicularis, Brucella ovis, Brucella spp., Brucella suis, Burkholderia cepacia complex, Moraxella catarrhalis, Moraxella lacunata, Moraxella nonliquefaciens, Moraxella osloensis, Oligella ureolytica, Pseudomonas alcaligenes, Pseudomonas mendocina, Pseudomonas pseudoalcaligenes, Pseudomonas putida, Pseudomonas stutzeri, Pseudomonas Vb3, Psychrobacter phenylpyruvicus, and Stenotrophomonas maltophilia were PYR negative. On the other hand Achromobacter piechaudii, Achromobacter denitrificans, Achromobacter xylosoxidans, Burkholderia gladioli, Chryseobacterium gleum-indologenes, Comamonas testosroni, Cupriavidus pauculus, Delftia acidovorans, Elizabethkingia meningoseptica, Myroides spp., Ochrobactrum anthropi, Pseudomonas oryzihabitans, Ralstonia pickettii, Rhizobium radiobacter, Shewanella spp., Sphingobacterium multivorum, Sphingobacterium spiritivorum, and Weeksella virosa were PYR positive. Finally, Acinetobacter lwoffii, Pseudomonas aeruginosa, Pseudomonas fluorescens, Roseomonas spp., and Sphingomonas paucimobilis-parapaucimobilis were PYR variable. PYR testing should be considered as a useful tool to facilitate the identification of NFGNR.
机译:为了评估吡咯烷酮芳基酰胺酶(PYR)对非发酵革兰氏阴性棒(NFGNR)的分化和鉴定的活性,测试了293个分离株。制备每种测试生物的24小时培养物。由此将108-109 cfu / mL的悬浮液加入到0.25mL的无菌生理溶液中。然后添加PYR盘,并且将测试在环境气氛下在35-37℃下孵育30分钟。通过加入1滴肉桂醛试剂进行读取。鲍曼不动杆菌,溶血不动杆菌,粪产碱菌,游动性贝氏杆菌,支气管博德特氏菌,细小鲍氏杆菌,小肠布鲁氏菌,小肠布鲁氏菌,巴氏杆菌,莫拉氏杆菌,卡氏菌,波状杆菌osloensis,Oligella ureolytica,产碱假单胞菌,mendocina假单胞菌,Pseudomonas pseudoalcaligenes,恶臭假单胞菌,Pseudomonas stutzeri,假单胞菌Vb3,苯丙酮丙酮酸杆菌和嗜麦芽单胞菌嗜麦芽孢杆菌均为PYR。另一方面,匹氏无色杆菌,反硝化无色杆菌,木氧化无色杆菌,格氏伯克霍尔德氏菌,产油性灰霉,睾丸细单胞菌,铜杯菌,嗜酸Delftia嗜酸菌,伊丽莎白金菌,脑膜炎单胞菌,波状芽孢杆菌,R。 spp。,多重涡旋杆菌,精神食管Sphingobacterium spiritivorum和维氏霉菌Weeksella virosa均为PYR阳性。最后,lwoffii不动杆菌,铜绿假单胞菌,荧光假单胞菌,迷迭香属和小鞘氨醇单胞菌是PYR变量。 PYR测试应被视为有助于识别NFGNR的有用工具。

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