Yinfeng Wang, Biqian Wei, Guanhua Xuan, Linhui Qin, Hong Lin, Jingxue Wang
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引用次数: 0
Abstract
Phage adsorption, genome injection, and immediate activation of host genes are critical steps that determine whether phages can complete their infection cycle. Elucidating the early molecular dynamic network of phage-host interactions is essential for understanding the dynamic balance between phage invasion and bacterial defense. In this study, Pseudomonas aeruginosa PAO1 was used as a model to investigate the early transcriptional responses during infection by lytic phage vB_Pae_QDWS, which features an extremely short latent period. Transcriptomic analysis at 0, 3, 6, and 20 min postinfection revealed a transient expression of early phage genes (gp01-gp08, gp13). Concurrently, the host exhibited broad transcriptional reprogramming, particularly in genes related to receptors such as flagella, pili, and lipopolysaccharide (LPS) biosynthesis, as well as quorum-sensing (QS) regulators including lasI, lasR, and rhlI. Correlation analyses revealed strong associations between specific early phage genes and host QS-related genes. Notably, the early phage gene gp08 exhibited a strong negative correlation with the QS regulator lasR, implying a potential inhibitory interaction. This study highlights the critical role of early phage gene expression in the initial takeover of the host and demonstrates the host's rapid transcriptional response under phage pressure, offering new insights into phage-host interactions and phage-based control strategies.
期刊介绍:
The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions.
Papers published deal with:
microbial interactions (pathogenic, mutualistic, environmental),
ecology,
physiology,
genetics and cell biology/development,
new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications)
novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).