Parasite can't survive without its tail.The parasite that causes African sleeping sickness Af·ri·can sleeping sickness n. African trypanosomiasis. can't survive in the mammalian bloodstream without its tail, scientists report. The finding could lead to novel ways to fight this disease. Trypanosoma brucei has a two-part life cycle in which it inhabits the tsetse fly tsetse fly (tsĕt`sē), name for any of several bloodsucking African flies of the genus Glossina, and in the same family as the housefly. and then a mammal. Although the parasite takes on slightly different forms in these two hosts, both forms have along, whiplike tail called a flagellum flagellum Hairlike structure that acts mainly as an organelle of movement in the cells of many living organisms. Characteristic of the protozoan group Mastigophora, flagella also occur on the sex cells of algae, fungi (see fungus), mosses, and slime molds. . While investigating how T. brucei's flagellum operates, microbiologist Keith Gull of the University of Oxford in England and his colleagues made an exhaustive catalog of the structure's 380 proteins. Then, to determine the proteins' functions, the researchers selectively prevented the parasite from making each one. Disabling any flagellum protein in the T. brucei form that inhabits the tsetse tsetse /tset·se/ (tset´se) an African fly of the genus Glossina, which transmits trypanosomiasis. tsetse an African fly of the genus glossina, which transmits trypanosomiasis. fiyprevented the protozoan protozoan (prō'təzō`ən), informal term for the unicellular heterotrophs of the kingdom Protista. Protozoans comprise a large, diverse assortment of microscopic or near-microscopic organisms that live as single cells or in simple from moving around in lab dishes but had little effect on its hardiness or reproductive success. However, when the researchers performed the same experiment on the form that inhabits mammals, they found that the parasite couldn't divide effectively. Rather than splitting, it formed abnormally large cells with multiple nuclei and then rapidly died. Developing drugs that have a similar effect on T. brucei's flagellum proteins could eventually be a strategy for attacking the parasite in people, Gull's team suggests in the March 9 Nature.--C.B. |
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