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PMID: 8751922 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Elimination of the listeriolysin O-directed immune response by conservative alteration of the immunodominant listeriolysin O amino acid 91 to 99 epitope.

Infection and immunity ·Vol. 64 ·No. 9 ·1996-09-00 ·Pages 3728-35

Bouwer HG, Moors M, Hinrichs DJ

Abstract

A major H2-Kd-presented epitope for antilisterial cytotoxic T lymphocytes (CTLs) is the nanomer peptide which corresponds to the amino acid 91 to 99 (aa91-99) sequence from listeriolysin O (LLO). Although the LLO sequence contains at least five additional nanomer peptides which also satisfy the H2-Kd binding motif, aa91-99 is the only LLO-derived target peptide that is recognized by antilisterial CTLs following infection of BALB/c mice with Listeria monocytogenes. In order to investigate further the immunodominance of the LLO aa91-99 epitope following endogenous processing of LLO, we introduced a point mutation in hly (the gene for LLO) which results in a conservative Y-to-F substitution for the anchor residue at position 2 within the aa91-99 sequence. This "92F" L. monocytogenes mutant produces biologically active LLO and is phenotypically indistinct from wild-type L. monocytogenes in terms of intracellular growth in vitro and virulence in vivo. BALB/c mice actively immunized with the 92F L. monocytogenes mutant are protected against challenge with wild-type L. monocytogenes. Antilisterial CTLs from mice immunized with the 92F mutant lyse targets infected with L. monocytogenes; however, these CTLs do not lyse target cells pulsed with either the LLO aa91-99 peptide, other LLO-derived peptides which satisfy the H2-Kd binding motif, or a peptide corresponding to the LLO aa91-92F-99 sequence. Target cells pulsed with the LLO aa91-92F-99 peptide are, however, lysed by wild-type LLO aa91-99-specific cytotoxic cells. Thus, a conservative amino acid change in the first anchor residue of the immunodominant aa91-99 sequence of LLO eliminates the induction of the cytotoxic cell response to this epitope as well as to any of the other candidate LLO-derived peptides which fit the H2-Kd binding motif. The lack of anti-LLO-specific CTLs following immunization with the 92F mutant does not appear, however, to influence the protective antilisterial immune response.

MeSH Terms
Amino Acid Sequence Animals Bacterial Toxins Base Sequence Cytotoxicity, Immunologic DNA Primers/chemistry Epitopes H-2 Antigens/immunology Heat-Shock Proteins/immunology Hemolysin Proteins Listeria monocytogenes/genetics,immunology,pathogenicity Mice Mice, Inbred BALB C Molecular Sequence Data Peptides/immunology Point Mutation T-Lymphocytes, Cytotoxic/immunology
Chemicals
Bacterial Toxins DNA Primers Epitopes H-2 Antigens Heat-Shock Proteins Hemolysin Proteins Peptides hlyA protein, Listeria monocytogenes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bouwer H G
Veterans Affairs Medical Center, Portland, Oregon 97201, USA.
Moors M
Hinrichs D J
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1996-09-00
Pages
3728-35
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC174286
Subset
IM
Grants
NIAID NIH HHS · AI23455 · United States
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