AI Article Synopsis

  • Staphylococcus xylosus, a gram-positive bacterium, is increasingly linked to serious drug resistance issues, making its study significant.
  • The research investigates the role of L-lactate dehydrogenase (LDH) in multidrug resistance using genetically modified S. xylosus strains, where LDH was knocked out and complemented.
  • Findings reveal that knocking out LDH increases antibiotic resistance, particularly to lincomycin, and alters key metabolic pathways, indicating that LDH deficiency enhances drug resistance by disrupting the TCA cycle and thioredoxin system.

Article Abstract

Staphylococcus xylosus is a gram-positive bacterium that has attracted much attention due to its increasing clinical appearance, frequently associated with serious multidrug resistance cases. L-lactate dehydrogenase (LDH) has been related to drug resistance in several bacterial species. However, the mechanism of multidrug resistance in S. xylosus remains unclear as well as the involvement of LDH in such resistance. To explore the relationship between multidrug resistance and LDH in S. xylosus, we used tylosin-resistant S. xylosus as the parent strain to construct ldh knockout and complemented strains. Then, we tested their resistance to macrolides, lincosamides, tetracyclines, and aminoglycosides. In addition, the enzyme activity, metabolite content, and transcriptional level of key genes involved in the TCA cycle and thioredoxin system were determined to clarify the mechanism of resistance. We observed that the resistance to multiple antibiotics increased significantly after ldh knockout, especially that to lincomycin, whereas antibiotic sensitivity was partially restored in the complemented strain. The levels of pyruvate, nicotinamide adenine dinucleotide, and reactive oxygen species decreased significantly upon ldh knockout, and the activity of isocitrate dehydrogenase and malate dehydrogenase decreased. These results indicate that the lack of LDH promotes multidrug resistance in S. xylosus by inhibiting the TCA cycle and regulating the thioredoxin system.

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Source
http://dx.doi.org/10.1007/s00203-021-02625-8DOI Listing

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