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1.
Antimicrob Agents Chemother ; 49(6): 2218-25, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15917515

ABSTRACT

In performing radiometric susceptibility testing on over 2,000 patient isolates of Mycobacterium tuberculosis during the past 6 years, we found that resistance to 7.5 microg/ml ethambutol (EMB) occurred only in isolates that are also resistant to 0.4 microg/ml isoniazid (INH). Using 157 selected isolates in the present study, we performed radiometric and agar proportion susceptibility tests and DNA sequencing of genetic regions associated with resistance to these two drugs. The goal was to study the occurrence of the common mutations associated with resistance to each drug and also to determine whether any particular INH-resistance-associated mutation occurred more often in combination with any particular EMB-resistance-associated mutation. In an analysis of 128 isolates resistant to 0.4 microg/ml INH, we found that a mutation at katG Ser315 was more common in isolates also resistant to 7.5 microg/ml EMB (61 of 67=91.0%) than in isolates either susceptible to EMB or resistant to 2.5 microg/ml EMB (39 of 60=65.0%). These observations suggest that INH-resistant strains with a mutation at katG Ser315 are more likely to acquire resistance to 7.5 microg/ml EMB than are isolates with INH-resistance-associated mutations at other sites. In addition, we found that 64 of 67 (95.5%) isolates resistant to 7.5 microg/ml EMB contained a mutation in either codon 306 or codon 406 of embB. Met306Val was the most common embB mutation, present in 52 (77.6%) of the 67 isolates. Most occurrences of this mutation (49 of 52=94.2%) were found in isolates that also contained the katG Ser315Thr mutation. Finally, sequencing this region of embB appears to be sufficiently sensitive for use as a rapid screening tool for detection of high-level resistance to EMB.


Subject(s)
Antitubercular Agents/pharmacology , Drug Resistance, Multiple, Bacterial/genetics , Ethambutol/pharmacology , Isoniazid/pharmacology , Mycobacterium tuberculosis/drug effects , Bacterial Proteins/genetics , Catalase/genetics , DNA, Bacterial/analysis , Genotype , Humans , Microbial Sensitivity Tests/methods , Mutation , Oligonucleotides/analysis , Pentosyltransferases/genetics , Phenotype , Polymerase Chain Reaction , Radiometry , Tuberculosis, Multidrug-Resistant/microbiology
2.
Emerg Infect Dis ; 8(11): 1306-9, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12453361

ABSTRACT

Spacer oligonucleotide (spoligotyping) analysis is a rapid polymerase chain reaction-based method of DNA fingerprinting the Mycobacterium tuberculosis complex. We examined spoligotype data using a bioinformatic tool (sequence logo analysis) to elucidate undisclosed phylogenetic relationships and gain insights into the global dissemination of strains of tuberculosis. Logo analysis of spoligotyping data provides a simple way to describe a fingerprint signature and may be useful in categorizing unique spoligotypes patterns as they are discovered. Large databases of DNA fingerprint information, such as those from the U.S. National Tuberculosis Genotyping and Surveillance Network and the European Concerted Action on Tuberculosis, contain information on thousands of strains from diverse regions. The description of related spoligotypes has depended on exhaustive listings of the individual spoligotyping patterns. Logo analysis may become another useful graphic method of visualizing and presenting spoligotyping clusters from these databases.


Subject(s)
Computational Biology/methods , DNA, Bacterial/analysis , Mycobacterium tuberculosis/genetics , Bacterial Typing Techniques , DNA Fingerprinting , DNA, Bacterial/genetics , DNA, Intergenic/analysis , Databases, Factual , Genotype , Humans , Oligonucleotides/genetics
3.
Emerg Infect Dis ; 8(11): 1264-70, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12453354

ABSTRACT

We estimated direct medical and nonmedical costs associated with a false diagnosis of tuberculosis (TB) caused by laboratory cross-contamination of Mycobacterium tuberculosis cultures in Massachusetts in 1998 and 1999. For three patients who received misdiagnoses of active TB disease on the basis of laboratory cross-contamination, the costs totaled U.S. dollars 32618. Of the total, 97% was attributed to the public sector (local and state health departments, public health hospital and laboratory, and county and state correctional facilities); 3% to the private sector (physicians, hospitals, and laboratories); and <1% to the patient. Hospitalizations and inpatient tests, procedures, and TB medications accounted for 69% of costs, and outpatient TB medications accounted for 18%. The average cost per patient was dollars 10873 (range, dollars 1033-dollars 21306). Reducing laboratory cross-contamination and quickly identifying patients with cross-contaminated cultures can prevent unnecessary and potentially dangerous treatment regimens and anguish for the patient and financial burden to the health-care system.


Subject(s)
Diagnostic Errors/economics , Health Care Costs , Laboratories/economics , Tuberculosis/diagnosis , Tuberculosis/economics , Adult , Antitubercular Agents/economics , Bacterial Typing Techniques , Contact Tracing/economics , Equipment Contamination , False Positive Reactions , Female , Humans , Laboratories/standards , Male , Massachusetts , Middle Aged , Mycobacterium tuberculosis/genetics , Mycobacterium tuberculosis/isolation & purification , Specimen Handling , Tuberculosis/drug therapy , Tuberculosis/microbiology
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