RT Journal Article SR Electronic(1) A1 Roantree, R. J. A1 Kuo, T.-T. A1 Macphee, D. G.YR 1977 T1 The Effect of Defined Lipopolysaccharide Core Defects upon Antibiotic Resistances of Salmonella typhimurium JF Microbiology, VO 103 IS 2 SP 223 OP 234 DO https://doi.org/10.1099/00221287-103-2-223 PB Microbiology Society, SN 1465-2080, AB Antibiotic resistances of two sets of Salmonella typhimurium rfa transductants (along with those of their smooth pyrE + and cysE + sister transductants) were measured. One set was derived from a pyrE smooth LT2 parent and the other from a cysE smooth LT7 parent. Results showed that strains with defects at the rfa(R-res-2) level and deeper were more susceptible to bacitracin, novobiocin and polymyxin. Those with defects at the rfaG level or deeper were in addition more sensitive to vancomycin, erythromycin, oxacillin and nafcillin. At these levels the presence or absence of galactose I or glucose I from the lipopolysaccharide core made a considerable difference. A heptose-less rfaE mutant was the most sensitive of the strains tested to the above named antibiotics. Strains with rfa lesions at several levels of defect showed slight increases in resistances to tetracycline, cephalothin, ampicillin and penicillin. One would expect strains with galE mutations to be similar to rfa(R-res-2) strains and those with galU mutations to be similar to rfaG strains if the core defects accounted for the differing antibiotic resistances. They proved to be so except that the galE and galU strains in the S. typhimurium FIRN line were as resistant to novobiocin as were smooth strains. The results are interpreted in respect to Nikaido's hypothesis that hydrophilic antibiotics with molecular weights of less than about 650 can gain access to the periplasmic space through protein-lined, water-filled pores and that hydrophobic ones can gain access in deep rough strains when phospholipid patches appear on the surface due to absence of polysaccharides and proteins., UL https://www.microbiologyresearch.org/content/journal/micro/10.1099/00221287-103-2-223