Treatment of Pseudomonas aeruginosa infections is challenging due to its antibiotic resistance. Polymyxins are considered last-resort options for treating serious infections caused by multidrug-resistant P. aeruginosa. Understanding the molecular mechanisms of polymyxin resistance may provide clues for the development of new therapeutic strategies against P. aeruginosa. In this study, we demonstrated that the phosphatidic acid-phosphatase family (PAP2) protein LpxT interacts with L-Ara4N transferase ArnT and controls polymyxin B resistance in P. aeruginosa. Our findings reveal a novel role for lpxT and its molecular mechanism to defend against polymyxin B in P. aeruginosa.
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Bai et al. (Mon,) studied this question.
synapsesocial.com/papers/69c37b41b34aaaeb1a67d8d4 — DOI: https://doi.org/10.1128/spectrum.01852-25
Yuxi Bai
Nankai University
Yue Zhao
Nankai University
Yuan Yu
Nanjing University of Chinese Medicine
Microbiology Spectrum
Korea University
Nankai University
State Key Laboratory of Medicinal Chemical Biology
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