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肺炎支原体和生殖支原体中转座子Tn4001产生的细胞黏附缺陷转化体的分离与鉴定

Isolation and characterization of transposon Tn4001-generated, cytadherence-deficient transformants of Mycoplasma pneumoniae and Mycoplasma genitalium.

作者信息

Reddy S P, Rasmussen W G, Baseman J B

机构信息

Department of Microbiology, University of Texas Health Science Center, San Antonio 78249-7758, USA.

出版信息

FEMS Immunol Med Microbiol. 1996 Oct;15(4):199-211. doi: 10.1111/j.1574-695X.1996.tb00086.x.

Abstract

Cytadherence and subsequent parasitism of host cells by the human pathogens, Mycoplasma pneumoniae and Mycoplasma genitalium, are mediated by adhesins and adherence-related accessory proteins. In this report we demonstrate the use of transposon Tn4001 to generate Tn-induced transformants displaying cytadherence-deficient characteristics. Mycoplasma pneumoniae Tn-generated transformant, designated 8R, lacked the high-molecular weight adherence-accessory proteins HMW1/4 and was deficient in hemadsorption and cytadherence capabilities. In transformant 8R, Tn4001 was not localized in or near the hmw1 gene or in the upstream adhesin (p30/hmw3) locus, suggesting an alternate site associated with the regulation of hmw1 gene expression. Sequence analysis identified the transposon insertion site at the crl locus previously reported, although the protein characteristics of transformant 8R differed from the earlier described transformants. The M. genitalium Tn-transformant, designated G26, was also defective in hemadsorption and cytadherence. However, transformant G26 synthesized adhesins P140 and P32 suggesting that Tn4001 transposed into a new gene or site previously unlinked to cytadherence, namely ORF MG032. This study demonstrates the utility of Tn4001 mutagenesis for both M. pneumoniae and M. genitalium which, in the latter case, has special relevance in light of the recent complete characterization of its continuous total genomic sequence.

摘要

人类病原体肺炎支原体和生殖支原体对宿主细胞的细胞黏附及随后的寄生作用是由黏附素和与黏附相关的辅助蛋白介导的。在本报告中,我们展示了利用转座子Tn4001来产生表现出细胞黏附缺陷特征的Tn诱导转化体。肺炎支原体Tn诱导的转化体,命名为8R,缺乏高分子量黏附辅助蛋白HMW1/4,并且血细胞吸附和细胞黏附能力存在缺陷。在转化体8R中,Tn4001并不定位于hmw1基因内部或附近,也不在上游黏附素(p30/hmw3)基因座中,这表明存在一个与hmw1基因表达调控相关的替代位点。序列分析确定转座子插入位点在先前报道的crl基因座处,尽管转化体8R的蛋白质特征与先前描述的转化体不同。生殖支原体Tn转化体,命名为G26,在血细胞吸附和细胞黏附方面也存在缺陷。然而,转化体G26合成了黏附素P140和P32,这表明Tn4001转座到了一个先前与细胞黏附无关的新基因或位点,即开放阅读框MG032。本研究证明了Tn4001诱变对肺炎支原体和生殖支原体均有用,对于后者而言,鉴于其连续全基因组序列最近已被完全表征,具有特殊的意义。

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