Kitano K, Tomasz A
J Bacteriol. 1979 Dec;140(3):955-63. doi: 10.1128/jb.140.3.955-963.1979.
Two types of Escherichia coli mutants tolerant to beta-lactam antibiotics were isolated. One is E. coli chi2452, which showed a tolerant response against beta-lactam antibiotics when grown at 42 degrees C, and the others are the mutants C-80 and C-254, selected from mutagenized E. coli chi1776 by cycles of exposure to ampicillin, cephaloridine, and starvation of the nutritionally required diaminopimelic acid. Beta-lactam antibiotics caused rapid loss of viability and lysis in cultures of chi1776 or in chi2452 grown at 32 degrees C. In contrast, the same antibiotics caused only a reversible inhibition of growth in mutants C-80 and C-254 or in cultures of chi2452 grown at 42 degrees C. Beta-lactam antibiotics that show high affinity for penicillin-binding proteins 2 or 3 (mecillinam and cephalexin, respectively) induced similar morphological effects (ovoid cell formation and filament formation) in both parent and mutant strains. In contrast, beta-lactam antibiotics which have a high affinity for penicillin-binding protein 1 (e.g., cephaloridine or cefoxitin), which cause rapid lysis in the parental strains, caused cell elongation in the tolerant bacteria. In contrast to the parental cells, autolytic cell wall degradation was not triggered by beta-lactam treatment of chi2452 cells grown at 42 degrees C or in mutants C-80 and C-254. The total autolytic activity of mutants C-80 and C-254 was less than 30% that of the parent strain. However, virtually identical autolytic activities were found in cells of chi2452 grown either at 42 or 32 degrees C. Possible mechanisms for the penicillin tolerance of E. coli are considered on the basis of these findings.
分离出了两种对β-内酰胺抗生素耐受的大肠杆菌突变体。一种是大肠杆菌chi2452,当在42℃生长时,它对β-内酰胺抗生素表现出耐受反应,其他的是突变体C-80和C-254,它们是通过对大肠杆菌chi1776进行诱变处理,经反复暴露于氨苄青霉素、头孢菌素以及营养必需的二氨基庚二酸饥饿处理后筛选出来的。β-内酰胺抗生素会导致chi1776培养物或在32℃生长的chi2452培养物中细菌活力迅速丧失并发生裂解。相比之下,相同的抗生素在突变体C-80和C-254培养物或在42℃生长的chi2452培养物中仅引起生长的可逆抑制。对青霉素结合蛋白2或3具有高亲和力的β-内酰胺抗生素(分别为美西林和头孢氨苄)在亲本菌株和突变菌株中诱导了相似的形态学效应(卵形细胞形成和丝状形成)。相比之下,对青霉素结合蛋白1具有高亲和力的β-内酰胺抗生素(例如头孢菌素或头孢西丁),它们在亲本菌株中会导致快速裂解,但在耐受细菌中却导致细胞伸长。与亲本细胞不同,对在42℃生长的chi2452细胞或突变体C-80和C-254进行β-内酰胺处理不会引发自溶细胞壁降解。突变体C-80和C-254的总自溶活性不到亲本菌株的30%。然而,在42℃或32℃生长的chi2452细胞中发现了几乎相同的自溶活性。基于这些发现,探讨了大肠杆菌对青霉素耐受的可能机制。