» Articles » PMID: 4564286

Immunogenicity of the Common Enterobacterial Antigen Produced by Smooth and Rough Strains

Overview
Journal Infect Immun
Date 1972 Oct 1
PMID 4564286
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Enterobacteriaceae share a common antigen (CA). This antigen exists as a powerful immunogen, when produced by Escherichia coli O14, and as a minimally effective immunogen, when present in cultures of most other smooth strains. The present study was directed toward the assessment of immunogenicity of this antigen produced by various rough mutants and their parent strains as well as that of viable and nonviable bacterial suspensions. Rabbits were immunized intravenously, and the passive hemagglutination test was used for the quantitation of CA antibodies. The following results were obtained. (i) Immunization of rabbits with viable or heat-killed (1 hr, 100 C) suspensions of smooth parent strains resulted in only slight or insignificant antibody production. Of seven additional smooth strains of Enterobacteriaceae tested, none induced CA antibodies upon immunization with killed (1 hr, 100 C) suspensions, and only two engendered antibodies in moderate titers when viable suspensions were used, possibly due to the presence of undetected R mutant cells. (ii) In contrast, administration of viable suspensions of the corresponding mutant strains, regardless of core types, including E. coli R1, R2, R3, and Salmonella Ra types, caused a significant antibody response. (iii) The immunogenicity of R mutants differed strikingly, inasmuch as mutants with the R1 core [E. coli O8(-):K27(-)(R) and Shigella boydii type 3(-)(R)] engendered CA antibodies when heated suspensions were administered, in contrast to heated suspensions of mutants with the R2, R3, and Ra cores. (iv) Viability per se is not an abolute requirement for immunogenicity of R2 mutants, since CA antibodies were engendered by suspensions killed at 60 C or by merthiolate or formaldehyde. (v) Ethanol fractionation revealed that immunogenic CA of the R1 mutant is ethanol-insoluble and that of the parental smooth strain is ethanol-soluble; thus, CA of R1 mutants resembles that of E. coli O14 in both immunogenicity and ethanol insolubility.

Citing Articles

ElyC and Cyclic Enterobacterial Common Antigen Regulate Synthesis of Phosphoglyceride-Linked Enterobacterial Common Antigen.

Rai A, Carr J, Bautista D, Wang W, Mitchell A mBio. 2021; 12(6):e0284621.

PMID: 34809459 PMC: 8609368. DOI: 10.1128/mBio.02846-21.


Lipopolysaccharide-Linked Enterobacterial Common Antigen (ECA) Occurs in Rough Strains of R1, R2, and R4.

Maciejewska A, Kaszowska M, Jachymek W, Lugowski C, Lukasiewicz J Int J Mol Sci. 2020; 21(17).

PMID: 32839412 PMC: 7504096. DOI: 10.3390/ijms21176038.


Enterobacterial Common Antigen: Synthesis and Function of an Enigmatic Molecule.

Rai A, Mitchell A mBio. 2020; 11(4).

PMID: 32788387 PMC: 7439462. DOI: 10.1128/mBio.01914-20.


The modality of enterobacterial common antigen polysaccharide chain lengths is regulated by o349 of the wec gene cluster of Escherichia coli K-12.

Barr K, Klena J, Rick P J Bacteriol. 1999; 181(20):6564-8.

PMID: 10515954 PMC: 103799. DOI: 10.1128/JB.181.20.6564-6568.1999.


Effect of proteins on the immunogenicity of enterobacterial common antigen.

KUHN H, Adamus G, Romanowska E, Mayer H Infect Immun. 1981; 34(2):373-7.

PMID: 7309231 PMC: 350876. DOI: 10.1128/iai.34.2.373-377.1981.


References
1.
DOMINGUE G, NETER E . Inhibition by lipopolysaccharide of immune phagocytosis of latex particles modified with common antigen of enteric bacteria. Proc Soc Exp Biol Med. 1966; 121(1):133-7. DOI: 10.3181/00379727-121-30717. View

2.
Aoki S, Merkel M, McCabe W . Immunofluorescent demonstration of the common enterobacterial antigen. Proc Soc Exp Biol Med. 1966; 121(1):230-4. DOI: 10.3181/00379727-121-30744. View

3.
LUDERITZ O, Galanos C, RISSE H, RUSCHMANN E, Schlecht S, Schmidt G . Structural relationship of Salmonella O and R antigens. Ann N Y Acad Sci. 1966; 133(2):349-74. DOI: 10.1111/j.1749-6632.1966.tb52376.x. View

4.
Whang H, NETER E . Further studies on effect of endotoxin on antibody response of rabbit to common antigen of Enterobacteriaceae. J Immunol. 1967; 98(5):948-57. View

5.
NETER E, Whang H, LUDERITZ O, Westphal O . Immunological priming without production of circulating bacterial antibodies conditioned by endotoxin and its lipoid A component. Nature. 1966; 212(5060):420-1. DOI: 10.1038/212420a0. View