Soll D R, Staebell M, Langtimm C, Pfaller M, Hicks J, Rao T V
Department of Biology, University of Iowa, Iowa City 52242.
J Clin Microbiol. 1988 Aug;26(8):1448-59. doi: 10.1128/jcm.26.8.1448-1459.1988.
Species and strain variabilities have been monitored during the history of a prolonged Candida infection in a single compromised bone marrow transplant patient by analyzing sugar assimilation patterns, high-frequency switching repertoires, and Southern blot hybridization patterns with two cloned mid-repeat sequences (Ca3 and Ca7) which are species specific for Candida albicans and one cloned mid-repeat sequence (Ct13-8) which is species specific for Candida tropicalis. Evidence is presented that during the course of this infection (i) two strains of C. albicans and three strains of C. tropicalis were distinguished by their switching repertoires, Southern blot hybridization patterns, and sugar assimilation patterns; (ii) the three C. tropicalis strains were in a high-frequency mode of switching; (iii) two C. tropicalis strains coexisted in the blood and three C. tropicalis strains coexisted in the throat at different times during the history of the infection; (iv) amphotericin B treatment selectively removed one of two C. tropicalis strains coexisting in the blood and this strain exhibited greater susceptibility to amphotericin B in vitro (the remaining strain was subsequently removed from the blood by flucytosine treatment); and (v) both the strain removed from the blood by amphotericin B and the strain removed from the blood by flucytosine reappeared several days later at another site of infection. It is demonstrated for the first time that C. tropicalis is capable of high-frequency switching of colony morphology just as C. albicans is, that there is more than one strain-specific switching repertoire in C. tropicalis, and that a C. tropicalis mid-repeat sequence can be used for discriminating species and assessing strain relatedness, as previously demonstrated for C. albicans mid-repeat sequences.
在一名骨髓移植受者发生的持续性念珠菌感染病程中,通过分析糖同化模式、高频转换谱以及用两个白色念珠菌特异性的克隆中重复序列(Ca3和Ca7)和一个热带念珠菌特异性的克隆中重复序列(Ct13-8)进行Southern印迹杂交模式,监测了菌种和菌株的变异性。有证据表明,在该感染过程中:(i)通过其转换谱、Southern印迹杂交模式和糖同化模式区分出两株白色念珠菌和三株热带念珠菌;(ii)三株热带念珠菌处于高频转换模式;(iii)在感染病程中的不同时间,两株热带念珠菌共存于血液中,三株热带念珠菌共存于咽喉部;(iv)两性霉素B治疗选择性地清除了血液中并存的两株热带念珠菌中的一株,该菌株在体外对两性霉素B表现出更高的敏感性(剩余菌株随后通过氟胞嘧啶治疗从血液中清除);(v)被两性霉素B从血液中清除的菌株和被氟胞嘧啶从血液中清除的菌株在几天后又重新出现在另一个感染部位。首次证明热带念珠菌能够像白色念珠菌一样进行菌落形态的高频转换,热带念珠菌存在不止一种菌株特异性的转换谱,并且热带念珠菌的一个中重复序列可用于区分菌种和评估菌株相关性,正如之前对白色念珠菌中重复序列所证明的那样。