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Effect of manganese and enzymatic deoxyribonucleic acid digests on population changes and respiration of Pneumococci
Abstract:
Firshein, William (Wesleyan University, Middletown, Conn.). Effect of manganese and enzymatic deoxyribonucleic acid digests on population changes and respiration of pneumococci. J. Bacteriol. 84:478-484. 1962.-Deoxyribonucleic acid (DNA; Na salt) treated with deoxyribonuclease and Mn(++) (as MnSO(4)) stimulated R (avirulent) to S (virulent) population changes in vitro. Under certain environmental conditions and with certain strains, Mn(++) alone elicited these changes, but, in most cases, both digested DNA and Mn(++) were necessary for maximal effect. These population changes were due to a selective stimulation of the multiplication of S cells and a delay in S-cell lysis, with either a slight inhibitory effect or no effect against the multiplication of R cells. The magnitude of the population change depended upon the presence of digested DNA, the level of Mn(++), the strain, and the concentration of basal medium. Mn(++) enhanced respiration of S cells while inhibiting that of R cells.
Insights
Manganese (Mn++) and digested deoxyribonucleic acid (DNA) promote the transformation of avirulent (R) to virulent (S) pneumococci. This transformation involves stimulating virulent cell multiplication and delaying lysis, with manganese also affecting bacterial respiration.
Area of Science:
- Microbiology
- Molecular Biology
- Bacteriology
Background:
- Pneumococci exist in virulent (S) and avirulent (R) forms.
- Understanding factors influencing pneumococcal population dynamics is crucial for infectious disease research.
Purpose of the Study:
- To investigate the effects of manganese (Mn++) and enzymatically digested deoxyribonucleic acid (DNA) on pneumococcal population changes.
- To determine the impact of these factors on bacterial respiration.
Main Methods:
- In vitro experiments using pneumococcal cultures.
- Treatment of deoxyribonucleic acid (DNA) with deoxyribonuclease and manganese (Mn++) ions.
- Monitoring population shifts between R and S forms.
- Measuring bacterial respiration rates.
Main Results:
- Digested DNA and Mn++ significantly stimulated the transformation of R to S pneumococci.
- Mn++ alone could induce changes under specific conditions, but combined treatment yielded maximal effects.
- Population changes resulted from stimulated S-cell multiplication and delayed S-cell lysis.
- Mn++ enhanced respiration in S cells while inhibiting it in R cells.
Conclusions:
- Enzymatically digested DNA in the presence of manganese is a potent stimulator of pneumococcal virulence.
- Manganese plays a dual role, influencing both bacterial transformation and respiration.
- The findings highlight the complex interplay between DNA, metal ions, and bacterial physiology in determining virulence.
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