Shieh M T, Brown R L, Whitehead M P, Cary J W, Cotty P J, Cleveland T E, Dean R A
Department of Plant Pathology and Physiology, Clemson University, South Carolina 29634-0377, USA.
Appl Environ Microbiol. 1997 Sep;63(9):3548-52. doi: 10.1128/aem.63.9.3548-3552.1997.
Isolates of Aspergillus flavus can be differentiated based on production of the polygalacturonase P2c. One group of isolates produces P2c, whereas the other group does not. In general, the group that produces P2c causes more damage and spreads to a greater extent in cotton bolls than those isolates that do not produce P2c. To determine whether P2c contributes to disease, the expression of pecA, the gene previously determined to encode P2c, was genetically altered. Adding the pecA gene to a strain previously lacking the gene resulted in the ability to cause significantly more damage to the intercarpellary membrane and the ability spread to a greater extent within the adjacent locule compared to the abilities of a control transformant. Conversely, eliminating the expression of pecA by targeted disruption caused a significant reduction in aggressiveness compared to that of a nondisrupted control transformant. These results provide direct evidence that P2c contributes to the invasion and spread of A. flavus during infection of cotton bolls. However, other factors not evaluated in this study also contribute to aggressiveness.
黄曲霉菌株可根据多聚半乳糖醛酸酶P2c的产生情况进行区分。一组菌株产生P2c,而另一组则不产生。一般来说,产生P2c的菌株比不产生P2c的菌株对棉铃造成的损害更大,传播范围更广。为了确定P2c是否与病害有关,对先前确定编码P2c的基因pecA的表达进行了基因改造。与对照转化体相比,将pecA基因添加到先前缺乏该基因的菌株中,导致对心皮间膜造成更大损害的能力以及在相邻子房室内更大范围传播的能力。相反,与未破坏的对照转化体相比,通过靶向破坏消除pecA的表达导致侵袭性显著降低。这些结果提供了直接证据,表明P2c在棉铃感染期间有助于黄曲霉的入侵和传播。然而,本研究中未评估的其他因素也会影响侵袭性。