Chávez-Munguía Bibiana, Salazar-Villatoro Lizbeth, Omaña-Molina Maritza, Espinosa-Cantellano Martha, Ramírez-Flores Elizabeth, Lorenzo-Morales Jacob, Martínez-Palomo Adolfo
Department of Infectomics and Molecular Pathogenesis, Center for Research and Advanced Studies, Mexico City, 07360, Mexico.
School of Superior Studies Iztacala, National Autonomous University of Mexico, Mexico City, 54090, Mexico.
J Eukaryot Microbiol. 2016 Nov;63(6):744-750. doi: 10.1111/jeu.12321. Epub 2016 May 6.
The virulence of various amoebic parasites has been correlated with the presence of electron-dense granules (EDGs) in the cytoplasm of trophozoites. Here, we report the finding by transmission electron microscopy of a large number of EDGs in a recent culture of Acanthamoeba culbertsoni, isolated from a severe case of human keratitis. When this isolate was maintained in culture for 6 mo, the granules almost disappeared. However, after induction of mice brain lesions with the long-term cultured isolate, recovered amoebas had abundant EDGs. Trophozoites of the original isolate, or those recovered from experimental lesions, secreted EDGs into the medium when incubated with MDCK cells. To analyze a possible cytotoxic effect the conditioned medium was incubated with MDCK monolayers. After 5 h, the media containing EDGs produced opening of the tight junctions; at 24 h, cell viability was compromised, and at 48 h most of the cells were detached from the monolayer. In contrast, trophozoites in long-term cultures did not release EDGs to the medium during incubation with MDCK cells, and the corresponding conditioned medium did not have any effect on MDCK monolayers. Our observations further support the hypothesis that EDGs play a role in the cytopathogenic mechanisms of A. culbertsoni.
多种阿米巴寄生虫的毒力与滋养体细胞质中电子致密颗粒(EDGs)的存在有关。在此,我们报告通过透射电子显微镜在最近从一例严重人类角膜炎病例中分离出的库氏棘阿米巴培养物中发现大量EDGs。当该分离株在培养物中保存6个月时,这些颗粒几乎消失。然而,在用长期培养的分离株诱导小鼠脑部病变后,回收的阿米巴具有丰富的EDGs。原始分离株的滋养体或从实验性病变中回收的滋养体在与MDCK细胞一起孵育时会将EDGs分泌到培养基中。为了分析可能的细胞毒性作用,将条件培养基与MDCK单层细胞一起孵育。5小时后,含有EDGs的培养基导致紧密连接开放;24小时后,细胞活力受损,48小时时大多数细胞从单层上脱落。相比之下,长期培养的滋养体在与MDCK细胞孵育期间不会向培养基中释放EDGs,相应的条件培养基对MDCK单层细胞没有任何影响。我们的观察结果进一步支持了EDGs在库氏棘阿米巴细胞致病机制中起作用的假说。