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Identification of an Attenuated Substrain of Francisella tularensis SCHU S4 by Phenotypic and Genotypic Analyses

机译:通过表型和基因型分析鉴定Francisella Tularentensis Schu S4的减毒底板

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摘要

Pneumonic tularemia is a highly debilitating and potentially fatal disease caused by inhalation of Francisella tularensis. Most of our current understanding of its pathogenesis is based on the highly virulent F. tularensis subsp. tularensis strain SCHU S4. However, multiple sources of SCHU S4 have been maintained and propagated independently over the years, potentially generating genetic variants with altered virulence. In this study, the virulence of four SCHU S4 stocks (NR-10492, NR-28534, NR-643 from BEI Resources and FTS-635 from Battelle Memorial Institute) along with another virulent subsp. tularensis strain, MA00-2987, were assessed in parallel. In the Fischer 344 rat model of pneumonic tularemia, NR-643 and FTS-635 were found to be highly attenuated compared to NR-10492, NR-28534, and MA00-2987. In the NZW rabbit model of pneumonic tularemia, NR-643 caused morbidity but not mortality even at a dose equivalent to 500x the LD50 for NR-10492. Genetic analyses revealed that NR-10492 and NR-28534 were identical to each other, and nearly identical to the reference SCHU S4 sequence. NR-643 and FTS-635 were identical to each other but were found to have nine regions of difference in the genomic sequence when compared to the published reference SCHU S4 sequence. Given the genetic differences and decreased virulence, NR-643/FTS-635 should be clearly designated as a separate SCHU S4 substrain and no longer utilized in efficacy studies to evaluate potential vaccines and therapeutics against tularemia.
机译:肺炎术术是一种由吸入Francisella Tularensis引起的高度衰弱和潜在的致命疾病。我们目前对其发病机制的了解是基于高毒性的F. Tularensis Subsp。 Tularensis菌株SCHU S4。然而,多年来,Schu S4的多种来源是独立的,潜在地产生具有改变的毒力的遗传变异。在本研究中,四种舒S4股(NR-10492,NR-10492,NR-643,来自BEI资源的NR-643,FTS-635的NR-643)以及另一个毒性潜群。并联评估Tularensis菌株MA00-2987。在FIScher 344中,与NR-10492,NR-28534和MA00-2987相比,发现NR-643和FTS-635的NR-643和FTS-635高度衰减。在NZW兔模型的肺肺线血症模型中,NR-643甚至导致发病率,而不是死亡率,即使在等于NR-10492的LD50的剂量上也不会产生死亡率。遗传分析显示,NR-10492和NR-28534彼此相同,并且与参考SCHU S4序列几乎相同。与已发表的参考SCHU S4序列相比,NR-643和FTS-635彼此相同但被发现在基因组序列中具有九个差异区域。鉴于遗传差异和毒力减少,NR-643 / FTS-635应清楚地指定为单独的SCHU S4基底,不再用于评估潜在疫苗和治疗针对尖刻症的疗效研究。

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