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31.
Pili in gram-positive pathogens 总被引:1,自引:0,他引:1
Telford JL Barocchi MA Margarit I Rappuoli R Grandi G 《Nature reviews. Microbiology》2006,4(7):509-519
Most bacterial pathogens have long filamentous structures known as pili or fimbriae extending from their surface. These structures are often involved in the initial adhesion of the bacteria to host tissues during colonization. In gram-negative bacteria, pili are typically formed by non-covalent interactions between pilin subunits. By contrast, the recently discovered pili in gram-positive pathogens are formed by covalent polymerization of adhesive pilin subunits. Evidence from studies of pili in the three principal streptococcal pathogens of humans indicates that the genes that encode the pilin subunits and the enzymes that are required for the assembly of these subunits into pili have been acquired en bloc by the horizontal transfer of a pathogenicity island. 相似文献
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Dishonest signalling in a fiddler crab 总被引:5,自引:0,他引:5
Backwell PR Christy JH Telford SR Jennions MD Passmore NI 《Proceedings. Biological sciences / The Royal Society》2000,267(1444):719-724
Animal communication theory predicts that low-frequency cheating should be common in generally honest signalling systems. However, perhaps because cheats are designed to go undetected, there are few examples of dishonest signals in natural populations. Here we present what we believe is the first example of a dishonest signal which is used commonly by males to attract mates and fight sexual rivals. After losing their large claw male fiddler crabs (Uca annulipes) grow a new one which has less mass, is a less effective weapon and costs less to use in signalling than an equivalent-length claw of the original form. Males with original claws do not differentially fight males with regenerated claws even though they are likely to win. Regenerated claws effectively bluff fighting ability and deter potential opponents before they fight. During mate searching, females do not discriminate against males with low-mass, regenerated claws, indicating that they are deceived as to the true costs males pay to produce sexual signals. Up to 44% of males in natural populations have regenerated claws, a level unanticipated by current signalling theory. The apparent rarity of cheating may be an artefact of the usual difficulty of detecting cheats and dishonesty may be quite common. 相似文献
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The Australian skink Egernia stokesii is parasitized uncommonly by Plasmodium circularis n. sp. and by Plasmodium mackerrasae. Plasmodium circularis is distinguished from all other plasmodiids by immature schizonts that encircle host cell nuclei, forming an unbroken ring from apparent fusion of the attenuated ends. Mature schizonts contract into halteridial or dumbbell-shaped forms 15.6 x 4.3 microm, LW 66.2 microm2, with 19-52 nuclei. Rounded or oval gametocytes are 9.0 x 7.3 microm, LW 66.9 microm2, and L/W 1.24. Gametocyte LW is 2.63 x host erythrocyte nucleus size and 1.79X uninfected erythrocyte nuclei. Plasmodium mackerrasae occurs in high prevalence and often massive parasitemia in E. stokesii. Schizonts, often oblong, elongate, or oval, are 5.1 x 3.7 microm, LW 19.8 microm2, with 7.2 merozoites. Immature gametocytes, elongate with terminal nucleus, may produce multiple infections of 6 or more parasites. Mature gametocytes, usually rounded, are 5.8 x 4.6 microm, LW 26.7 microm2, and L/W 1.29. Gametocyte size is 0.98 x host erythrocyte nucleus size and 1.03 x uninfected erythrocyte nuclei. Phanerozoites, in endothelium or connective tissue of most organs, may appear in large numbers in circulating blood as seemingly intact bodies of regular form, similar to or larger than phanerozoites seen in sections. Previously unreported phenomena for hemosporidian parasites include extremely large, highly irregular exoerythrocytic schizonts, in circulating blood, perhaps torn from endothelial lining of blood vessels and sinuses, and a visible flooding of free merozoites into the blood stream. 相似文献
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PJS Amaral LFM Finotelo EHC De Oliveira A Pissinatti CY Nagamachi JC Pieczarka 《BMC evolutionary biology》2008,8(1):169