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BASI74, a Virulence-Related sRNA in . | LitMetric

BASI74, a Virulence-Related sRNA in .

Front Microbiol

Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, China.

Published: September 2018

AI Article Synopsis

Article Abstract

spp. are intracellular pathogens that infect a wide variety of mammals including humans, posing threats to the livestock industry and human health in developing countries. A number of genes associated with the intracellular trafficking and multiplication have so far been identified in spp. However, the sophisticated post-transcriptional regulation and coordination of gene expression that enable spp. to adapt to changes in environment and to evade host cell defenses are not fully understood. Bacteria small RNAs (sRNAs) play a significant role in post-transcriptional regulation, which has already been confirmed in a number of bacteria but the role of sRNAs in remains elusive. In this study, we identified several different sRNAs in spp., and found that over-expression of a sRNA, tentatively termed BASI74, led to alternation in virulence of in macrophage infection model. The expression level of BASI74 increased while 2308 was grown in acidic media. In addition, BASI74 affected the growth ratio of the cells in minimal media and iron limiting medium. Using a two-plasmid reporter system, we identified four genes as the target of BASI74. One target gene, BABI1154, was predicted to encode a cytosine-N4-specific DNA methyltransferase, which protects cellular DNA from the restriction endonuclease in . These results show that BASI74 plays an important role in survival in macrophage infection model, speculatively by its connection with stress response or impact on restriction-modification system. Our study promotes the understanding of sRNAs, as well as the mechanism by which sRNAs use to influence physiology and pathogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146029PMC
http://dx.doi.org/10.3389/fmicb.2018.02173DOI Listing

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