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however, their toxicities and the availability of better agents means they are not normally considered as suitable antimycoplasmal agents, with the exception of occasional use of chloramphenicol for treatment of systemic infections in neonates caused by m hominis or ureaplasma species in the setting of tetracycline resistance or clinical failure with other agents.
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these results are consistent with the fact that streptomycin and chloramphenicol are h- and c-group antibiotics, respectively vanbogelen neidhardt, 1990 , and that cold-shock and heat-shock genes are regulated antagonistically in y.
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chloramphenicol is a potent, broad-spectrum antibiotic drug and a potential carcinogen used only at therapeutic doses for treatment of serious infections in humans.
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