4.5 Article

Transcriptional landscape of Burkholderia pseudomallei cultured under environmental and clinical conditions

Journal

MICROBIAL GENOMICS
Volume 9, Issue 4, Pages -

Publisher

MICROBIOLOGY SOC
DOI: 10.1099/mgen.0.000982

Keywords

Burkholderia pseudomallei; comparative transcriptomics; biofilm; environmental niche; human plasma

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This study conducted a comparative transcriptome analysis of B. pseudomallei in human plasma and soil extract media, revealing gene expression patterns related to bacterial adaptation and infectivity in the host. The results showed upregulation of genes involved in energy metabolism and cellular processes, and downregulation of genes related to fatty acid and phospholipid metabolism, amino acid biosynthesis, and regulatory function proteins in B. pseudomallei grown in human plasma. The induction of biofilm formation and overexpression of virulence factors in human plasma suggest an enhanced virulence potential of B. pseudomallei in the host.
Burkholderia pseudomallei, a Gram-negative pathogen, is the causative agent of melioidosis in humans. This bacterium can be isolated from the soil, stagnant and salt -water bodies, and human and animal clinical specimens. While extensive studies have contributed to our understanding of B. pseudomallei pathogenesis, little is known about how a harmless soil bacterium adapts when it shifts to a human host and exhibits its virulence. The bacterium's large genome encodes an array of factors that support the pathogen's ability to survive under stressful conditions, including the host's internal milieu. In this study, we performed comparative transcriptome analysis of B. pseudomallei cultured in human plasma versus soil extract media to provide insights into B. pseudomal-lei gene expression that governs bacterial adaptation and infectivity in the host. A total of 455 genes were differentially regulated; genes upregulated in B. pseudomallei grown in human plasma are involved in energy metabolism and cellular processes, whilst the downregulated genes mostly include fatty acid and phospholipid metabolism, amino acid biosynthesis and regulatory function proteins. Further analysis identified a significant upregulation of biofilm-related genes in plasma, which was validated using the biofilm-forming assay and scanning electron microscopy. In addition, genes encoding known virulence factors such as capsular polysaccharide and flagella were also overexpressed, suggesting an overall enhancement of B. pseudomallei virulence potential when present in human plasma. This ex vivo gene expression profile provides comprehensive information on B. pseudomallei's adaptation when shifted from the environment to the host. The induction of biofilm formation under host conditions may explain the difficulty in treating septic melioidosis.

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