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M B Esteves

Publications and source records attributed to M B Esteves.

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Genetic parameters of the polygenic regulation of antibody responsiveness to flagellar and somatic antigens of salmonellae.

Selective breedings of mice were carried out for quantitative antibody responsiveness to flagellar Ag., f (Selection III) or somatic Ag., s (Selection IV) of two non cross-reacting Salmonellae (Salm. tm., Salm. or.) alternated for immunization of consecutive generations. At the selection limit, these selections produced homozygous high (H) and low (L) responder lines for the character investigated: peak agglutinin response to optimal secondary immunization. The responsiveness to both f and s Ags. is submitted to polygenic regulation. The heritability (h2) realized during the selective breeding was 0.37 +/- 0.07 for the response to fAg. and 0.40 +/- 0.1 for the response to s Ag. The respective part of genetic and environmental variance in F2 hybrids was 64% and 36% in selection III and 61% and 39% in selection IV. In the two selections, the dominance variance is negligible (less than 1%), therefore the genetic variance is essentially additive. The additive variance calculated as the heritable fraction of the F2 hybrid variance is somewhat lower, the reason for this difference is discussed. The quantitative antibody response to f Ag. in selection III is controlled by about seven independent loci. The antibody response to s Ag. in selection IV is controlled by about four independent loci. A possible association of relevant genes with the H-2 locus was investigated. In selection III, no significant participation if H-2 linked genes, in the regulation of responses to f and s Ags. of Salm. tm and Salm. or. could be demonstrated. In selection IV a partial contribution of H-2 linked genes was observed concerning responsiveness to both f and s Ags. of Salm. tm. but not Salm. or. Ags. The H-2 effect accounts for 25% of the total interline difference.

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Nonspecific genetic regulation of antibody responsiveness in the mouse.

Four lines of mice were produced by selective breeding for quantitative agglutinin responsiveness to flagellar (f) or somatic (s) antigens (Ags) of Salmonellae: high (H) or low (L) responder lines to fAg and H and L responder lines to sAg. The Salmonellae contained both f and sAgs, the Ag used to perform the selection was the Selection Ag and the other was the Associated Ag. The selective breeding produced a progressive interline separation with an equivalent effect for both Ags. After 15 generations (F15) the level of agglutinin response was about 60 times higher in H than in L responders. About 50% of the phenotypic variation of the character investigated is determined by a group of immune response genes, the rest is due to environmental factors. The nonspecific effect of this group of immune response genes was investigated by measuring the responses to three independent antigens: Sheep erythrocytes (SE), dinitrophenyl-conjugated human IgG (DNP-HGG) and bovine IgG (BGG). The selection for fAg response produced an equivalent modification in the respnsiveness to the Associated Ag (97%) and to BGG (130%). This nonspecific effect was smaller for responsiveness to SE and DNP-HGG, 58% and 41% of the Selection Ag response, respectively. The selection for sAg response produced a nonspecific modification of responsiveness of 94% for the Associated Ag of 74% for BGG and 63% for DNP-HGG. An important exception concerned SE to which an equal antibody response is produced in high and low lines of sAg selection.

Animals

[Non-specific polygenic regulation of antibody synthesis].

Four two-way genetic selections of outbred mice for the quantitative character "agglutinin production" to heterologous erythrocytes and flagellar or somatic antigens of Salmonella are briefly described. The principal genetic parameters regulating the quantitative antibody response are the following: 1) the character is polygenic; the number of independent loci is estimated between 7 and 16; 2) the heritability of the character (h2) is comprised between 0.17 and 0.21; 3) the maximal interline separation RT (4.8-7.8 log2) is reached after about 15 consecutive generations of selective breeding; (4) the rate of interline separation/generation RG is 0.32-0.48 log2. 5) The phenotypic variance V(P) of the foundation populations is due for 52%-63% to genetic factors V(G) and for 37%-48% to environmental factors V(E); 6) The effect of the selective breeding is essentially non-specific; it modifies the antibody responsiveness to many unrelated complex immunogens.

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