Bryan Eric J, Sagong Hye Yeon, Parhi Ajit K, Grier Mark C, Roberge Jacques Y, LaVoie Edmond J, Pilch Daniel S
Department of Pharmacology, Rutgers Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
TAXIS Pharmaceuticals, Inc., Monmouth Junction, NJ 08852, USA.
Antibiotics (Basel). 2022 May 20;11(5):693. doi: 10.3390/antibiotics11050693.
The emergence of multi-drug-resistant Gram-negative pathogens highlights an urgent clinical need to explore and develop new antibiotics with novel antibacterial targets. MreB is a promising antibacterial target that functions as an essential elongasome protein in most Gram-negative bacterial rods. Here, we describe a third-generation MreB inhibitor (TXH11106) with enhanced bactericidal activity versus the Gram-negative pathogens , , , and compared to the first- and second-generation compounds A22 and CBR-4830, respectively. Large inocula of these four pathogens are associated with a low frequency of resistance (FOR) to TXH11106. The enhanced bactericidal activity of TXH11106 relative to A22 and CBR-4830 correlates with a correspondingly enhanced capacity to inhibit MreB ATPase activity via a noncompetitive mechanism. Morphological changes induced by TXH11106 in , , , and provide further evidence supporting MreB as the bactericidal target of the compound. Taken together, our results highlight the potential of TXH11106 as an MreB inhibitor with activity against a broad spectrum of Gram-negative bacterial pathogens of acute clinical importance.
多重耐药革兰氏阴性病原体的出现凸显了探索和开发具有新型抗菌靶点的新型抗生素的迫切临床需求。MreB是一个有前景的抗菌靶点,在大多数革兰氏阴性菌杆状菌中作为一种必需的伸长体蛋白发挥作用。在此,我们描述了一种第三代MreB抑制剂(TXH11106),与第一代和第二代化合物A22和CBR - 4830相比,它对革兰氏阴性病原体、、、和具有更强的杀菌活性。这四种病原体的大量接种物对TXH11106的耐药频率较低。TXH11106相对于A22和CBR - 4830增强的杀菌活性与其通过非竞争性机制抑制MreB ATPase活性的相应增强能力相关。TXH11106在、、、和中诱导的形态变化提供了进一步的证据,支持MreB作为该化合物的杀菌靶点。综上所述,我们的结果突出了TXH11106作为一种MreB抑制剂的潜力,它对具有急性临床重要性的广泛革兰氏阴性细菌病原体具有活性。