ABSTRACT
Holospora obtusa is a Gram-negative bacterium inhabiting the macronucleus of the ciliate Paramecium caudatum. Experimental infection with H. obtusa was carried out under nocodazole treatment. Nocodazole has been shown to cause disassembly of the cytoplasmic microtubules radiating from the cytopharynx and postoral fibers in P. caudatum. Treatment with this drug did not prevent the ingestion of both prey bacteria and H. obtusa, but it reduced the phagosome number and affected cyclosis. In situ hybridization revealed infectious forms of this endobiont very close to the macronucleus, but never inside it. These results indicate that disassembly of microtubules does not impair transportation of the infectious forms of H. obtusa in the cytoplasm, but that it completely blocks the invasion of the nucleus by the bacteria.
Subject(s)
Holosporaceae/drug effects , Macronucleus/microbiology , Nocodazole/pharmacology , Paramecium caudatum/microbiology , Actin Cytoskeleton/drug effects , Actin Cytoskeleton/microbiology , Animals , Cytoplasmic Streaming/drug effects , Holosporaceae/isolation & purification , Immunohistochemistry , In Situ Hybridization , Macronucleus/ultrastructure , Microtubules/drug effects , Microtubules/microbiology , Paramecium caudatum/ultrastructure , Phagocytosis/drug effects , Phagosomes/drug effectsABSTRACT
New light and electron microscope data on the initial steps of endocytobiosis establishment between the ciliate Paramecium and specific intranuclear bacteria Holospora are provided. At the cytoplasmic step of infection bacteria of all Holospora species are found in a vesicle originating from the membrane of the host cell phagosome. The association between host cell microfilaments and the bacterium bearing vesicle may suggest a possible involvement of the ciliate cytoskeleton in the transportation of bacteria to the host cell nucleus. The authors subdivide the process of infection into 6 steps. Some strains of P. caudatum never take up infectious Holospora bacteria in the course of phagocytosis.