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Published on: October 23, 2013
CHANGES IN MOUSE PNEUMONITIS AGENT ASSOCIATED WITH DEVELOPMENT OF RESISTANCE TO CHLORTETRACYCLINE
Abstract:
Moulder, James W. (University of Chicago, Chicago, Ill.), Dorothy L. Novosel, and Ilse I. E. Tribby. Changes in mouse pneumonitis agent associated with development of resistance to chlortetracycline. J. Bacteriol. 89:17-22. 1965.-A chlortetracycline-resistant mutant of mouse pneumonitis agent, a member of the psittacosis group of microorganisms, differed in several ways from the susceptible stock from which it had been derived by serial chick-embryo passage in the presence of the antibiotic. It was almost completely resistant to chlortetracycline, had a longer growth cycle, produced many more very large particles, was not neutralized by parent antiserum and vice versa, was 10 times as resistant to d-cycloserine, and was highly lethal to mice when inoculated intracerebrally. These changes probably do not occur independently of one another but are the reflection of some genetically controlled change in the surface structure of the mouse pneumonitis particle which enables the resistant mutant to multiply in the presence of chlortetracycline.
Insights
A chlortetracycline-resistant mutant of mouse pneumonitis agent exhibited altered characteristics, including resistance to other drugs and increased virulence. These changes suggest a genetically controlled modification in the microorganism
Area of Science:
- Microbiology
- Bacteriology
- Virology
Background:
- Mouse pneumonitis agent belongs to the psittacosis group of microorganisms.
- Antibiotic resistance is a significant challenge in microbial infections.
Purpose of the Study:
- To investigate the changes in mouse pneumonitis agent associated with the development of chlortetracycline resistance.
- To characterize the properties of a chlortetracycline-resistant mutant.
Main Methods:
- Serial passage of mouse pneumonitis agent in chick embryos with chlortetracycline.
- Characterization of the resistant mutant's properties, including antibiotic resistance, growth cycle, particle size, antigenicity, and virulence.
Main Results:
- The chlortetracycline-resistant mutant showed complete resistance to chlortetracycline and increased resistance to d-cycloserine.
- The mutant had a longer growth cycle and produced more large particles.
- The resistant mutant was not neutralized by parent antiserum and vice versa, indicating antigenic changes.
- The resistant mutant exhibited high lethality in mice upon intracerebral inoculation.
Conclusions:
- The observed changes in the resistant mutant are likely due to a genetically controlled alteration in the surface structure of the mouse pneumonitis particle.
- This surface modification enables the multiplication of the mutant in the presence of chlortetracycline.
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