Department of Bioengineering, Division of Bioscience and Bioindustry, Graduate School of Technology, Industrial and Social Sciences, Tokushima University Graduate School, Tokushima, Japan; Department of Biological Science and Technology, Life System, Institute of Technology and Science, Tokushima University Graduate School, Tokushima, Japan.
Department of Biological Science and Technology, Life System, Institute of Technology and Science, Tokushima University Graduate School, Tokushima, Japan.
J Microbiol Methods. 2023 Apr;207:106696. doi: 10.1016/j.mimet.2023.106696. Epub 2023 Mar 9.
Cholesterol-dependent cytolysins (CDCs) are proteinaceous toxins widely distributed in gram-positive pathogenic bacteria. CDCs can be classified into three groups (I-III) based on the mode of receptor recognition. Group I CDCs recognize cholesterol as their receptor. Group II CDC specifically recognizes human CD59 as the primary receptor on the cell membrane. Only intermedilysin from Streptococcus intermedius has been reported as a group II CDC. Group III CDCs recognize both human CD59 and cholesterol as receptors. CD59 contains five disulfide bridges in its tertiary structure. Therefore, we treated human erythrocytes with dithiothreitol (DTT) to inactivate CD59 on membranes. Our data showed that DTT treatment caused a complete loss of recognition of intermedilysin and an anti-human CD59 monoclonal antibody. In contrast, this treatment did not affect the recognition of group I CDCs, judging from the fact that DTT-treated erythrocytes were lysed with the same efficiency as mock-treated human erythrocytes. The recognition of group III CDCs toward DTT-treated erythrocytes was partially reduced, and these results are likely due to the loss of human CD59 recognition. Therefore, the degree of human CD59 and cholesterol requirements of uncharacterized group III CDCs frequently found in Mitis group streptococci can be easily estimated by comparing the amounts of hemolysis between DTT-treated and mock-treated erythrocytes.
胆固醇依赖性细胞溶素(CDCs)是广泛分布于革兰氏阳性致病细菌中的蛋白毒素。根据受体识别模式,CDCs 可分为三组(I-III)。组 I CDC 以胆固醇为受体。组 II CDC 特异性识别细胞膜上的人类 CD59 作为主要受体。只有中间链球菌中介素被报道为组 II CDC。组 III CDC 同时识别人类 CD59 和胆固醇作为受体。CD59 在其三级结构中含有五个二硫键。因此,我们用二硫苏糖醇(DTT)处理人红细胞以灭活细胞膜上的 CD59。我们的数据表明,DTT 处理导致中介素和抗人 CD59 单克隆抗体的完全丧失识别。相比之下,从 DTT 处理的红细胞与未经处理的人红细胞以相同的效率被裂解这一事实判断,这种处理不影响组 I CDC 的识别。组 III CDC 对 DTT 处理的红细胞的识别部分减少,这可能是由于人类 CD59 识别的丧失。因此,通过比较 DTT 处理和未经处理的红细胞之间溶血的量,很容易估计米蒂斯组链球菌中经常发现的未鉴定的组 III CDC 对人类 CD59 和胆固醇的需求程度。