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. 1978 Oct;22(1):10–17. doi: 10.1128/iai.22.1.10-17.1978

Plasmid Carriage and the Serum Sensitivity of Enterobacteria

Peter W Taylor 1, Colin Hughes 1
PMCID: PMC422108  PMID: 365738

Abstract

The carriage of a range of plasmids by rough, serum-sensitive laboratory strains of Escherichia coli made no difference to their reactivity in human serum as determined by two methods. Plasmid-carrying enterobacteria isolated from polluted river water gave a variety of responses to serum. Smooth E. coli river isolate C8 was killed by serum but only after a delay of 1 h, and curing of antibiotic resistance and colicin determinants from this strain led to a small but significant increase in serum sensitivity. Plasmids from eight strains were transferred by conjugation to a cured derivative of C8 (C8NalR), and in six cases a significant increase in the serum resistance of the progeny was observed. Plasmid-mediated enhancement of resistance was particularly marked with plasmids R1 and NR1, and a round of replication mutant of NR1 conferred greater resistance than did the normal R factor. However, R1 and NR1 were unable to modify the serum response of a cured strain (P21NalR) derived from promptly serum-sensitive isolate P21. These findings suggest that lipopolysaccharide O-side chains, the cell surface components responsible for the delay in serum killing, are essential for the expression of plasmid factors that modify sensitivity to serum. Examination of K(A) variants of two isolates indicated that the K(A) antigen has only a marginal effect on the serum response.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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