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J Clin Microbiol. 1985 Nov;22(5):789-92. doi: 10.1128/jcm.22.5.789-792.1985.
2
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J Clin Microbiol. 1986 Sep;24(3):377-9. doi: 10.1128/jcm.24.3.377-379.1986.
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Comparison of media for isolation of Ureaplasma urealyticum and genital Mycoplasma species.用于解脲脲原体和生殖支原体分离培养的培养基比较
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J Clin Microbiol. 1978 Feb;7(2):127-32. doi: 10.1128/jcm.7.2.127-132.1978.

引用本文的文献

1
Isolation of Mycoplasma species and Ureaplasma urealyticum from obstetrical and gynecological patients by using commercially available medium formulations.使用市售培养基配方从妇产科患者中分离支原体和解脲脲原体。
J Clin Microbiol. 1986 Sep;24(3):377-9. doi: 10.1128/jcm.24.3.377-379.1986.
2
Comparison of commercially available media for detection and isolation of Ureaplasma urealyticum and Mycoplasma hominis.用于检测和解脲脲原体及人型支原体分离的市售培养基的比较
J Clin Microbiol. 1992 May;30(5):1335-7. doi: 10.1128/jcm.30.5.1335-1337.1992.

本文引用的文献

1
Comparative evaluation of media for isolation of ureaplasma urealyticum and genital mycoplasma species.用于解脲脲原体和生殖支原体分离培养的培养基的比较评估
J Clin Microbiol. 1982 Oct;16(4):709-14. doi: 10.1128/jcm.16.4.709-714.1982.
2
The genital mycoplasmas (second of two parts).生殖支原体(两部分中的第二部分)。
N Engl J Med. 1980 May 8;302(19):1063-7. doi: 10.1056/NEJM198005083021905.
3
The genital mycoplasmas (first of two parts).生殖支原体(两部分中的第一部分)
N Engl J Med. 1980 May 1;302(18):1003-10. doi: 10.1056/NEJM198005013021805.
4
Evaluation of PPLO, A7B, E, and NYC agar media for the isolation of Ureaplasma urealyticum and Mycoplasma species from the genital tract.评估PPLO、A7B、E和NYC琼脂培养基用于从生殖道分离解脲脲原体和支原体的效果。
J Clin Microbiol. 1984 Jan;19(1):73-6. doi: 10.1128/jcm.19.1.73-76.1984.
5
Comparison of media for isolation of Ureaplasma urealyticum and genital Mycoplasma species.用于解脲脲原体和生殖支原体分离培养的培养基比较
J Clin Microbiol. 1984 Nov;20(5):862-5. doi: 10.1128/jcm.20.5.862-865.1984.
6
Effects of manganese on the growth and morphology of Ureaplasma urealyticum.锰对解脲脲原体生长及形态的影响。
J Clin Microbiol. 1984 Jun;19(6):857-64. doi: 10.1128/jcm.19.6.857-864.1984.
7
Urease color test medium U-9 for the detection and identification of "T" mycoplasms in clinical material.用于检测和鉴定临床材料中“T”支原体的脲酶颜色试验培养基U-9
Appl Microbiol. 1970 Oct;20(4):539-43. doi: 10.1128/am.20.4.539-543.1970.
8
Differential agar medium (A7) for identification of Ureaplasma urealyticum (human T mycoplasmas) in primary cultures of clinical material.用于在临床材料原代培养物中鉴定解脲脲原体(人T支原体)的鉴别琼脂培养基(A7)。
J Clin Microbiol. 1976 Jun;3(6):613-25. doi: 10.1128/jcm.3.6.613-625.1976.
9
Bromothymol blue broth: improved medium for detection of Ureaplasma urealyticum (T-strain mycoplasma).溴麝香草酚蓝肉汤:用于检测解脲脲原体(T株支原体)的改良培养基。
J Clin Microbiol. 1978 Feb;7(2):127-32. doi: 10.1128/jcm.7.2.127-132.1978.
10
Significance of appropriate techniques and media for isolation and identification of Ureaplasma urealyticum from clinical specimens.从临床标本中分离和鉴定解脲脲原体的适当技术和培养基的意义。
J Clin Microbiol. 1978 Oct;8(4):445-53. doi: 10.1128/jcm.8.4.445-453.1978.

评估用于分离支原体属和人型支原体的霉菌三嗪-GU。

Evaluation of Mycotrim-GU for isolation of Mycoplasma species and Ureaplasma urealyticum.

作者信息

Wood J C, Lu R M, Peterson E M, de la Maza L M

出版信息

J Clin Microbiol. 1985 Nov;22(5):789-92. doi: 10.1128/jcm.22.5.789-792.1985.

DOI:10.1128/jcm.22.5.789-792.1985
PMID:4056004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC268528/
Abstract

The Mycotrim-GU (Hana Biologics, Berkeley, Calif.) biphasic culture system and a conventional system were compared for their ability to detect Ureaplasma urealyticum and Mycoplasma species in 100 clinical specimens. Both systems detected 18 Mycoplasma spp. isolates. The average colony detection time was 1.9 days with the Mycotrim-GU and 2.3 days with the conventional system. The Mycotrim-GU agar detected all 33 U. urealyticum isolates recovered in the study, and the conventional agar detected 31. In addition to the U. urealyticum isolates recovered from the agar, there were several specimens that, although they did not grow colonies on the agar, gave an alkaline broth change. Of these specimens, two were found with the conventional system and seven were found with the Mycotrim-GU. The average detection time of U. urealyticum colonies was 2.0 days for the conventional agar and 1.7 days for the Mycotrim-GU. The Mycotrim-GU offers several advantages over the conventional system: it is commercially available, consists of a one-flask system which is ready to use, has a significantly longer shelf life, and is cost competitive. This study showed the Mycotrim-GU to be an effective system for detecting the genital mycoplasmas.

摘要

比较了Mycotrim-GU(加利福尼亚州伯克利市哈纳生物制品公司)双相培养系统和传统系统在100份临床标本中检测解脲脲原体和支原体属的能力。两种系统均检测到18株支原体分离株。使用Mycotrim-GU时平均菌落检测时间为1.9天,使用传统系统时为2.3天。Mycotrim-GU琼脂检测到了研究中回收的所有33株解脲脲原体分离株,而传统琼脂检测到31株。除了从琼脂中回收的解脲脲原体分离株外,还有几个标本,虽然它们在琼脂上没有长出菌落,但肉汤发生了碱性变化。在这些标本中,传统系统发现了2个,Mycotrim-GU发现了7个。传统琼脂检测解脲脲原体菌落的平均时间为2.0天,Mycotrim-GU为1.7天。Mycotrim-GU比传统系统具有几个优点:它有商业产品,由即用型单瓶系统组成,保质期显著更长,且具有成本竞争力。这项研究表明Mycotrim-GU是检测生殖道支原体的有效系统。