Trypanosoma cruzi:: Ultrastructural studies of adhesion, lysis and biofilm formation by Serratia marcescens

被引:49
作者
Castro, Daniele P.
Seabra, Sergio H.
Garcia, Eloi S.
de Souza, Wanderley
Azambuja, Patricia
机构
[1] Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, Dept Bioquim & Biol Mol, BR-21045900 Rio De Janeiro, Brazil
[2] Ctr Univ Estadual Zona Oeste, Dept Pesquisa & Extensao, BR-21070200 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Lab Ultraestrut Celular Hertha Meyer, Ctr Ciencias Saude, BR-21941590 Rio De Janeiro, Brazil
关键词
trypanosoma cruzi; Serratia marcescens; adhesion; lysis; Biofilm formation;
D O I
10.1016/j.exppara.2007.04.014
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学]; 100103 [病原生物学];
摘要
A few days after blood meal the number of bacteria in the anterior midgut (stomach) of Rhodnius prolixus, a vector of Trypanosoma cruzi, the causative agent of Chagas' disease, increases dramatically. Many of the bloodstream trypomastigotes of the pathogenic protozoan as well as ingested erythrocytes are lysed in the stomach. Incubation of T cruzi with Serratia marcescens variant SM365, lead to parasite lysis. In the present study, this bacterium rapidly adhered to the protozoan surface through D-mannose recognizing fimbriae and rapidly induced its complete lysis. In contrast, the DB11 variant of the same bacterial species did not adhere and did not induce protozoan lysis. Scanning and transmission electron microscopy revealed that following bacteria-protozoan attachment there is an assembly of long filamentous structures, identified as a biofilm, which connect the protozoan to the bacteria forming bacterial clusters. We conclude that parasite lysis and biofilm formation mechanisms are important for understanding parasite microbiota interactions in the gut of insect vectors of trypanosomatids. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:201 / 207
页数:7
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