Sullivan D, Bennett D, Henman M, Harwood P, Flint S, Mulcahy F, Shanley D, Coleman D
Moyne Institute, Department of Microbiology, School of Dental Science, University of Dublin, Republic of Ireland.
J Clin Microbiol. 1993 Aug;31(8):2124-33. doi: 10.1128/jcm.31.8.2124-2133.1993.
Oligonucleotide fingerprinting of genomic DNA from oral isolates of four different Candida species other than C. albicans and atypical chlamydospore-positive isolates from human immunodeficiency virus (HIV)-positive individuals and AIDS patients was investigated as a means for differentiating between isolates within individual species. Oligonucleotides composed of simple repetitive sequence motifs, including (GACA)4, (GATA)4, (GGAT)4, (GTG)5, and (GT)8, all yielded fingerprints suitable for strain segregation of 8 C. tropicalis isolates, 12 Torulopsis (Candida) glabrata isolates, 8 atypical Candida isolates, and, except for (GATA)4, 2 C. krusei probe in turn and so generate several distinct DNA fingerprints of the same DNA sample. However, none of the probes yielded fingerprints suitable for strain segregation with three C. parapsilosis isolates. The (GATA)4 probe was also used to detect restriction fragment length polymorphisms among a genetically closely related group of atypical Candida isolates on primary isolation from an additional HIV-infected patient. These chlamydospore-positive atypical Candida isolates were sucrose positive, were of C. albicans serotype A, hybridized weakly with the C. albicans-specific mid-repeat sequence probe 27A, and yielded fingerprint profiles by random polymorphic DNA analysis that were distinct from those derived from C. albicans isolates. The C. stellatoidea ex-type strain NCPF 3108 was indistinguishable from the atypical Candida isolates in all these tests and also yielded an identical carbohydrate and nitrogen source assimilation profile by using the ID 32C yeast identification system.
对除白色念珠菌外的四种不同念珠菌口腔分离株以及来自人类免疫缺陷病毒(HIV)阳性个体和艾滋病患者的非典型厚壁孢子阳性分离株的基因组DNA进行寡核苷酸指纹分析,作为区分单个物种内分离株的一种方法。由简单重复序列基序组成的寡核苷酸,包括(GACA)4、(GATA)4、(GGAT)4、(GTG)5和(GT)8,依次对8株热带念珠菌分离株、12株光滑念珠菌(假丝酵母)分离株、8株非典型念珠菌分离株进行指纹分析,除(GATA)4外,还对2株克鲁斯念珠菌进行指纹分析,从而产生同一DNA样本的几个不同的DNA指纹。然而,没有一种探针能产生适用于3株近平滑念珠菌分离株菌株分离的指纹。(GATA)4探针还用于检测从另一名HIV感染患者初次分离的一组遗传关系密切的非典型念珠菌分离株中的限制性片段长度多态性。这些厚壁孢子阳性的非典型念珠菌分离株蔗糖阳性,为白色念珠菌血清型A,与白色念珠菌特异性中重复序列探针27A杂交较弱,通过随机多态性DNA分析产生的指纹图谱与白色念珠菌分离株的不同。在所有这些测试中,星状念珠菌模式菌株NCPF 3108与非典型念珠菌分离株无法区分,并且使用ID 32C酵母鉴定系统也产生相同的碳水化合物和氮源同化图谱。