Hsieh P C, Siegel S A, Rogers B, Davis D, Lewis K
Biotechnology Center, Tufts University, 4 Colby Street, Medford, MA 02155, USA.
Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6602-6. doi: 10.1073/pnas.95.12.6602.
Microorganisms express multidrug resistance pumps (MDRs) that can confound antibiotic discovery. We propose the use of mutants deficient in MDRs to overcome this problem. Sensitivity to quinolones and to amphipathic cations (norfloxacin, benzalkonium chloride, cetrimide, pentamidine, etc.) was increased 5- to 30-fold in a Staphylococcus aureus mutant with a disrupted chromosomal copy of the NorA MDR. NorA was required both for increased sensitivity to drugs in the presence of an MDR inhibitor and for increased rate of cation efflux. This requirement suggests that NorA is the major MDR protecting S. aureus from the antimicrobials studied. A 15- to 60-fold increase in sensitivity to antimicrobials also was observed in wild-type cells at an alkaline pH that favors accumulation of cations and weak bases. This effect was synergistic with a norA mutation, resulting in an increase up to 1,000-fold in sensitivity to antimicrobials. The usefulness of applying MDR mutants for natural product screening was demonstrated further by increased sensitivity of the norA- strain to plant alkaloid antimicrobials, which might be natural MDR substrates.
微生物表达的多药耐药泵(MDRs)会干扰抗生素的发现。我们建议使用MDRs缺陷型突变体来克服这一问题。在一株染色体上NorA MDR拷贝被破坏的金黄色葡萄球菌突变体中,其对喹诺酮类药物和两亲性阳离子(诺氟沙星、苯扎氯铵、西曲溴铵、喷他脒等)的敏感性提高了5至30倍。在存在MDR抑制剂的情况下,NorA对于提高对药物的敏感性以及提高阳离子外排速率都是必需的。这一需求表明NorA是保护金黄色葡萄球菌免受所研究抗菌药物影响的主要MDR。在有利于阳离子和弱碱积累的碱性pH条件下,野生型细胞对抗菌药物的敏感性也提高了15至60倍。这种效应与norA突变具有协同作用,导致对抗菌药物的敏感性提高了1000倍。norA菌株对可能是天然MDR底物的植物生物碱抗菌药物敏感性增加,进一步证明了应用MDR突变体进行天然产物筛选的实用性。