Background In the United States there have been recent outbreaksof multidrug-resistant tuberculosis. These outbreaks have primarilyinvolved persons infected with the human immunodeficiency virus(HIV).
Methods We collected clinical information on 17 patients seenat a New York City hospital who had repeatedly positive culturesfor Mycobacterium tuberculosis. Analysis of restriction-fragment-lengthpolymorphisms (RFLPs) was performed on serial isolates of M.tuberculosis obtained from these patients.
Results Six patients had isolates that remained drug-susceptible,and the RFLP patterns of these isolates did not change overtime. Eleven patients had isolates that became resistant toantimicrobial agents. The RFLP patterns of the isolates fromsix of these patients remained essentially unchanged (two strainsshowed one additional band) despite the development of drugresistance. In five other patients, however, the RFLP patternsof the isolates changed dramatically at the time that drug resistancewas detected. The change in the RFLP pattern of the isolatefrom one patient appeared to be the result of contaminationduring processing in the laboratory. In the remaining four patients,all of whom had advanced HIV disease, the clinical and microbiologicevidence was consistent with the presence of active tuberculosiscaused by a new strain of M. tuberculosis.
Conclusions Resistance to antituberculous drugs can developnot only in the strain that caused the initial disease, butalso as a result of reinfection with a new strain of M. tuberculosisthat is drug-resistant. Exogenous reinfection with multidrug-resistantM. tuberculosis can occur either during therapy for the originalinfection or after therapy has been completed.
Source Information
From the Department of Medicine, Division of Infectious Diseases and Geographic Medicine, and the Howard Hughes Medical Institute (P.M.S., S.P.S., G.K.S.) and the Department of Medicine, Centers for AIDS Research (R.W.S.), Stanford University, Stanford, Calif.; the Medical Service, San Francisco General Hospital and the University of California, San Francisco (P.C.H.); the Department of Medicine, Division of Infectious Diseases (M.J.M.), and the Department of Pathology (M.F.S.), State University of New York Health Sciences Center at Brooklyn, Brooklyn; and the California Department of Health Services Microbial Diseases Laboratory, Berkeley (E.D.).
Address reprint requests to Dr. Small at the Howard Hughes Medical Institute, Rm. 251, Beckman Ctr., Stanford, CA 94306.
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