PMID:
28702375
DOI:
10.3389/fcimb.2017.00270
Author(s):
Liang, Xudong, Zhu, Jin, Zhao, Zhongzhi, Zheng, Feng, Zhang, Enmin, Wei, Jianchun, Ji, Yon, Ji, Yinduo
Publisher(s):
Frontiers Media SA
Tags:
Immunology and Microbiology, Medicine
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article description
Anthrax toxins and capsules, which are encoded by genes located on pXO1 and pXO2, respectively, are major virulence factors of . Our previous studies demonstrated that exposure to high-temperatures is unable to abolish the pXO1 plasmid of the Pasteur II strain, but the growth of the strain was obviously slower than that of the Sterne strain and wild-type virulent strain. To elucidate a potential regulatory mechanism of slowing growth, we employed comparative genome and bioinformatic analysis and revealed a unique SNP (G to T) at the 143135 bp position in pXO1 that is possibly involved in the mediation of growth of Pasteur II. However, the T to G mutation in did not result in any change of the amino acid sequence. A predominant nucleotide G existed at the 143135 bp in pXO1 of 100 wild-type isolates and 9 isolates documented in GenBank, whereas T replaced G in pXO1 of the Pasteur II strain. Further analysis indicate that the SNP is located in a gene between 143042 and 143173 bp, and that it encodes a small protein of 43 amino acids and is termed as a growth regulator (GroR). Site-directed mutagenesis and gene deletion demonstrates that regulates the growth and spore formation of . Our results indicate that the pXO1 plasmid is involved in the regulation of growth and spore formation in .

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