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Published on: November 11, 2012
[Mucous (M) mutants of enteropathogenic, septicemic and saprophytic E. coli (author's transl)]
Abstract:
Mucoid M mutants of enteropathogenic (for suckling pigs), septicemic (for calves), and saprophytic E. Coli were subject of the study. The characteristics of the M colonies have been listed in Table 1. Both spontaneously occurring M mutants which had been isolated by culturing of E. coli strains (S form) in normal horse serum (undiluted) for several weeks were observed. Enzymatic-biochemical tests revealed the existence of M mutants with full enzmatic activity which are identical with the homologous S and R forms. There were also M mutants exhibiting a considerably reduced enzymatic activity. Antigenic-serological analysis (agglutination) exhibited M mutants which were agglutinated by the homologous sera, at low and high titres. In contrast to this, one group of M mutants was found not to be agglutinable, despite autoclaving at 120 degrees C for 2 hours. Some mutants cultured in broth for several weeks were re-exhibiting S colonies of full biochemical activity and full antigen reactivity against homologous agglutinating sera.
Insights
This study investigated Mucoid M mutants of Escherichia coli (E. coli), finding variations in enzymatic activity and antigen reactivity. Some mutants reverted to their original S form, indicating potential instability in these E. coli mutants.
Area of Science:
- Microbiology
- Bacteriology
- Molecular Biology
Background:
- Escherichia coli (E. coli) exists in various forms, including Smooth (S), Rough (R), and Mucoid (M) mutants.
- Understanding the characteristics of E. coli mutants is crucial for studying bacterial pathogenesis and host-pathogen interactions.
Purpose of the Study:
- To characterize Mucoid M mutants of E. coli isolated from different sources (enteropathogenic, septicemic, saprophytic).
- To investigate the enzymatic activity, biochemical properties, and antigenic-serological behavior of these E. coli M mutants.
Main Methods:
- Isolation of M mutants through prolonged culturing of E. coli strains in normal horse serum.
- Enzymatic-biochemical testing to assess enzyme activity.
- Antigenic-serological analysis using agglutination tests with homologous sera.
- Observation of colony morphology and reversion characteristics.
Main Results:
- Identified M mutants with full enzymatic activity, comparable to S and R forms.
- Observed M mutants with significantly reduced enzymatic activity.
- Found M mutants agglutinable by homologous sera at varying titers.
- Discovered a group of non-agglutinable M mutants, even after autoclaving.
- Noted reversion of some M mutants to S colonies with full biochemical and antigenic activity after extended broth culturing.
Conclusions:
- E. coli M mutants display diverse enzymatic and antigenic profiles.
- Some M mutants exhibit instability, capable of reverting to the S form.
- The non-agglutinable nature of certain M mutants suggests alterations in surface antigens.
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