Blackstock R, Buchanan K L, Cherniak R, Mitchell T G, Wong B, Bartiss A, Jackson L, Murphy J W
Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, USA.
Mycopathologia. 1999;147(1):1-11. doi: 10.1023/a:1007041401743.
Two isolates of Cryptococcus neoformans were previously described as being highly divergent in their level of capsule synthesis in vivo and in their virulence for mice. The highly virulent isolate (NU-2) produced more capsule than a weakly virulent isolate (184A) in vitro under tissue culture conditions and in vivo. This investigation was done to determine if there were differences between the two isolates in other factors that might also contribute to virulence. Growth rate was not a factor as NU-2 grew more slowly than 184A. Based on PCR fingerprinting the two isolates were genetically different providing an opportunity to examine differences in multiple virulence traits. Quantitative analysis revealed that NU-2 expressed significantly more melanin and mannitol than did 184A. Although the isolates expressed the same capsular chemotype, NU-2 produced an additional structure reporter group (SRG) under tissue culture conditions that was not present when grown in glucose salts/urea/basal medium (GSU). Capsular polysaccharide SRGs of 184A were unaffected by shifting the growth conditions from GSU to tissue culture conditions. Our results suggest that pathogenesis of a C. neoformans strain is dictated by the quantitative expression of the strain's combined virulence traits. Regulators of the expression of these genes may be playing key roles in virulence.
之前曾描述过两株新型隐球菌分离株,它们在体内荚膜合成水平以及对小鼠的毒力方面存在高度差异。在组织培养条件下和体内,高毒力分离株(NU-2)比弱毒力分离株(184A)产生更多的荚膜。开展这项研究是为了确定这两株分离株在其他可能也有助于毒力的因素方面是否存在差异。生长速率不是一个因素,因为NU-2的生长速度比184A慢。基于PCR指纹图谱分析,这两株分离株在基因上存在差异,这为研究多种毒力性状的差异提供了机会。定量分析表明,NU-2比184A表达更多的黑色素和甘露醇。尽管这些分离株表达相同的荚膜化学型,但在组织培养条件下,NU-2产生了一种在葡萄糖盐/尿素/基础培养基(GSU)中生长时不存在的额外结构报告基团(SRG)。将生长条件从GSU转变为组织培养条件时,184A的荚膜多糖SRG不受影响。我们的结果表明,新型隐球菌菌株的发病机制由该菌株综合毒力性状的定量表达所决定。这些基因表达的调节因子可能在毒力中发挥关键作用。