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Recent findings regarding maintenance of enzootic variants of Yersinia pestis in sylvatic reservoirs and their significance in the evolution of epidemic plague.

机译:有关在鼠疫性水库中维持鼠疫耶尔森氏菌的变种的最新发现以及它们在流行瘟疫演变中的意义。

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Despite the widespread presence of bubonic plague in sylvatic reservoirs throughout the world, the causative agent (Yersinia pestis) evolved in its present form within the last 20,000 years from enteropathogenic Yersinia pseudotuberculosis. Comparison of the genomes from the two species revealed that Y. pestis possesses only a few unique plasmid-encoded genes that contribute to acute disease, whereas this organism has lost about 13% of the chromosomal genes that remain active in Y. pseudotuberculosis. These losses reflect readily detectable additions, deletions, transpositions, inversions, and acquisition of about 70 insertion sequence (IS) inserts, none of which are likely to promote increased virulence. In contrast, major enzymes of intermediary metabolism, including glucose 6-phosphate dehydrogenase (Zwf ) and aspartase, are present but not catalytically functional due to the presence of missense mutations. The latter are generally not detectable by the technology of bioinformatics and, in the case of Y. pestis, result in radical changes in the metabolic flow of carbon. As an important consequence, plague bacilli exhibit a stringent low-calcium response characterized by conversion of L-glutamate (and metabolically related amino acids) to L-aspartate with secretion of the latter into supernatant fluid at 37 degrees C in culture media containing Na(+) but lacking added Ca(2+). This phenomenon also occurs in vivo and likely adversely affects the bioenergetics of host amino acid pools. Curiously, aspartase is functional in all tested enzootic (pestoides) strains of Y. pestis. These isolates are typically restricted to the ancient plague reservoirs of Central Asia and Africa and are fully virulent in members of the rodent Superfamily Muroidea but avirulent in guinea pigs and man. The implications of these findings for the distribution and ecology of Y. pestis could be significant.
机译:尽管在世界各地的sylvatic储库中广泛存在鼠疫鼠疫,但病原体(鼠疫耶尔森氏菌)在过去的20,000年来仍从肠致病性耶尔森氏菌假结核病演变成现在的形式。两种物种的基因组比较表明,鼠疫耶尔森氏菌仅具有少数独特的质粒编码基因,这些基因可导致急性疾病,而该生物损失了约13%的在假结核耶尔森氏菌中保持活性的染色体基因。这些损失反映了约70个插入序列(IS)插入片段的容易检测到的添加,缺失,转座,倒置和获取,这些插入片段均不可能促进增加的毒力。相反,存在中间代谢的主要酶,包括葡萄糖6-磷酸脱氢酶(Zwf)和天冬氨酸酶,但由于存在错义突变而没有催化功能。后者通常无法通过生物信息学技术检测到,并且在鼠疫耶尔森氏菌的情况下,会导致碳代谢流的根本变化。重要的结果是,鼠疫杆菌表现出严格的低钙反应,其特征是L-谷氨酸(和代谢相关氨基酸)转化为L-天冬氨酸,并在37°C的条件下在含有Na( +),但缺乏添加的Ca(2+)。这种现象也发生在体内,并且可能对宿主氨基酸库的生物能产生不利影响。奇怪的是,天冬氨酸酶在所有测试的鼠疫耶尔森氏菌的生(毒)菌株中都起作用。这些分离物通常仅限于中亚和非洲的古老鼠疫水库,在啮齿动物超纲鼠科Muroidea的成员中具有完全毒性,但对豚鼠和人无毒。这些发现对鼠疫耶尔森氏菌的分布和生态学的意义可能很大。

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