Department of Oral Biology, Rutgers School of Dental Medicine, Newark, NJ, 07103, USA.
Sci Rep. 2017 May 15;7(1):1887. doi: 10.1038/s41598-017-01692-6.
Aggregatibacter actinomycetemcomitans leukotoxin (LtxA) is a major virulence factor that kills leukocytes permitting it's escape from host immune surveillance. A. actinomycetemcomitans strains can produce high or low levels of toxin. Genetic differences reside in the "so called JP2" ltxA promoter region. These hyper-leukotoxin producing strains with the 530 bp deletion have been studied in detail. However, regions contained within the 530 bp deletion that could be responsible for modulation of leukotoxin production have not been defined. Here, we report, for the first time, on regions within the 530 bp that are responsible for high-levels of ltxA expression. We constructed a deletion of 530 bps in a primate isolate of A. actinomycetemcomitans, which produced leukotoxin equivalent to the JP2 strain. We then constructed sequential deletions in regions that span the 530 bps. Results indicated that expression of the ltxA transcript was reduced by a potential transcriptional terminator in promoter region 298 to 397 with a ΔG = -7.9 kcal/mol. We also confirmed previous findings that transcriptional fusion between the orfX region and ltxC increased ltxA expression. In conclusion, we constructed a hyper-leukotoxin producing A. actinomycetemcomitans strain and identified a terminator located in the promoter region extending from 298-397 that alters ltxA expression.
伴放线聚集杆菌白细胞毒素(LtxA)是一种主要的毒力因子,它能杀死白细胞,使其逃避宿主的免疫监视。伴放线聚集杆菌菌株可以产生高水平或低水平的毒素。遗传差异存在于所谓的 JP2"ltxA 启动子区域。这些高白细胞毒素产生菌株的 530bp 缺失已被详细研究。然而,导致白细胞毒素产生调节的 530bp 缺失内的区域尚未确定。在这里,我们首次报道了负责高水平 ltxA 表达的 530bp 内的区域。我们构建了一个 530bps 的缺失,在一个灵长类分离株的伴放线聚集杆菌中,该缺失产生了与 JP2 株相当的白细胞毒素。然后,我们构建了跨越 530bps 的区域的连续缺失。结果表明,在启动子区域 298 到 397 处存在一个潜在的转录终止子,导致 ltxA 转录本的表达减少,ΔG = -7.9 kcal/mol。我们还证实了先前的发现,即 orfX 区域和 ltxC 之间的转录融合增加了 ltxA 的表达。总之,我们构建了一个高白细胞毒素产生的伴放线聚集杆菌菌株,并鉴定出一个位于从 298 到 397 的启动子区域的终止子,该终止子改变了 ltxA 的表达。