Abstract
It has been reported by Mitsuhashi (1965) that transfer of one R-factor was completely inhibited by anaerobic transfer conditions. In contrast, several workers have observed R-factor transfer, although at a reduced rate, in the animal intestines, a largely anaerobic environment. It is shown here that in vitro transfer of the R-factor R1 (F-type pilus, fi-+) in Escherichia coli K-12 is severely depressed, whereas transfer of R64 (I-type pilus, fi-minus) is slightly stimulated by anaerobiosis. Inhibition of R1 fertility is dependent on anaerobic conditions during pregrowth of the donor cells, whereas the oxygen tension during recipient pregrowth, transfer, and plating is of little importance. Anaerobic pregrowth has a less inhibitory effect on the fertility of R1drd19, a mutant of R1 having a defective sex repressor. The fi-+ property of R1 when introduced into F' or Hfr bacteria is amplified during anaerobic growth. These observations strongly indicate that the sex repressor is the mediator of the anaerobic fertility inhibition of the R-factor R1. This hypothesis was supported by studies of the formation of sex pili, the only gene product identified that is controlled by the sex repressor of R1. Using propagation of the F-type pilus-specific phage MS2 as a measure of the degree of sex piliation of a bacterial population, it is shown that in anaerobic cultures sex piliation due to R1 is strongly repressed, whereas piliation due to R1drd19 is repressed to a lesser extent. The possible survival value of the response of R1 towards oxygen tension is discussed.
MeSH Terms
Anaerobiosis
Conjugation, Genetic
Drug Resistance, Microbial
Escherichia coli/metabolism
F Factor
Genes, Regulator
Mutation
Plasmids
R Factors
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Burman L G
References (14)
14 references, click to expand
-
Phylogenetic relationships of drug-resistance factors and other transmissible bacterial plasmids.
Bacteriol Rev. 1968 Mar;32(1):55-83
PMID: 4869941
-
Formation of merodiploids in matings with a class of Rec- recipient strains of Escherichia coli K12.
Proc Natl Acad Sci U S A. 1968 May;60(1):160-7
PMID: 4873517
-
The relationship of F type piliation and F phage sensitivity to drug resistance transfer in R+F- Escherichia coli K 12.
J Gen Microbiol. 1966 Nov;45(2):365-76
PMID: 5338981
-
Functional homology of the sex-factor and resistance transfer factors.
Nature. 1965 Aug 21;207(999):884-5
PMID: 5328609
-
Mutant drug resistant factors of high transmissibility.
Nature. 1967 May 27;214(5091):885-7
PMID: 6054969
-
Resistance of Escherichia coli to Penicillins I. Genetic Study of Some Ampicillin-Resistant Mutants.
J Bacteriol. 1965 Jul;90(1):54-62
PMID: 16562043
-
EPISOME-MEDIATED TRANSFER OF DRUG RESISTANCE IN ENTEROBACTERIACEAE. VI. HIGH-FREQUENCY RESISTANCE TRANSFER SYSTEM IN ESCHERICHIA COLI.
J Bacteriol. 1963 Apr;85:788-94
PMID: 14044944
-
Investigations on the influence of diet on the quantity and composition of intestinal gas in humans.
Scand J Clin Lab Invest. 1956;8(2):87-94
PMID: 13351540
-
Acetylornithinase of Escherichia coli: partial purification and some properties.
J Biol Chem. 1956 Jan;218(1):97-106
PMID: 13278318
-
Some observations on linkage effects in genetic recombination in Escherichia coli K-12.
J Gen Microbiol. 1954 Oct;11(2):250-60
PMID: 13211981
-
Studies on lysogenesis. I. The mode of phage liberation by lysogenic Escherichia coli.
J Bacteriol. 1951 Sep;62(3):293-300
PMID: 14888646
-
Non-chromosomal antibiotic resistance in bacteria. II. Molecular nature of R-factors isolated from Proteus mirabilis and Escherichia coli.
J Mol Biol. 1970 Jun 28;50(3):671-87
PMID: 4920496
-
Early stages of conjugation in Escherichia coli.
J Bacteriol. 1969 Nov;100(2):1091-104
PMID: 4902383
-
Anaerobic bacteria of the gastrointestinal flora and their occurrence in clinical infections.
J Infect Dis. 1969 Jun;119(6):641-9
PMID: 4893893