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1.
Asian Pacific Journal of Tropical Medicine ; (12): 193-196, 2014.
Article in English | WPRIM | ID: wpr-819707

ABSTRACT

OBJECTIVE@#To determine the patterns of resistance to first line anti-tuberculosis (TB) drugs among a collection of Mycobacterium tuberculosis (MTB) isolates from 5 provinces of Iran.@*METHODS@#A total of the 6 426 clinical specimens from patients suspected of active TB were collected from March 2010 to June 2012. All specimens were subjected for microscopy and culture tests in the TB centers of studies provinces. Drug susceptibility testing to the first line anti-TB drugs for culture positive MTB was performed on Löwenstein-Jensen (LJ) medium using proportion method.@*RESULTS@#Of 6 426 clinical specimens, 261 were culture positive for mycobacteria, of which 252 were MTB and 9 were MOTT (mycobacteria other than tuberculosis). Of 252 MTB isolates, 211 (83.7%) were pan-susceptible and 41 (16.3%) were resistant to at least one drug. Resistance was most common to streptomycin, 30 isolates (12.0%), followed by isoniazid, 20 isolates (8.0%), rifampin, 15 isolates (6.0%) and ethambutol, 14 isolates (5.5%). Sixteen (6.3%) MTB isolates were MDR. A clear evidence of heterogeneity amongst the 5 provinces in the proportions with resistance to one or more drugs was observed [χ(2); = 12.209 (4 degrees of freedom), P values = 0.015 9].@*CONCLUSIONS@#The prevalence of drug resistance in this study area underscoring the need for further enforcement of TB control strategies in the Iran. Drug susceptibility testing for all TB cases to provide optimal treatment, establishing advanced diagnostic facilities for rapid detection of MDR-TB and continuous monitoring of drug resistance are recommended for prevention and control of drug-resistant TB.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Humans , Middle Aged , Young Adult , Antitubercular Agents , Pharmacology , Bronchoalveolar Lavage Fluid , Microbiology , Chi-Square Distribution , Cross-Sectional Studies , Iran , Microbial Sensitivity Tests , Mycobacterium tuberculosis , Sputum , Microbiology , Tuberculosis, Multidrug-Resistant , Microbiology
2.
Annals of Laboratory Medicine ; : 87-90, 2012.
Article in English | WPRIM | ID: wpr-43980

ABSTRACT

We herein report a case in which the recently characterized species Mycobacterium monacense was isolated from the sputum of an Iranian patient. This case represents the first isolation of M. monacense from Iran. The isolate was identified by conventional and molecular techniques. Our findings show that M. monacense infection is not restricted to developed countries.


Subject(s)
Female , Humans , Middle Aged , Bacterial Proteins/genetics , Chaperonin 60/genetics , Chronic Disease , Iran , Lung Diseases/diagnosis , Mycobacterium/classification , Mycobacterium Infections/microbiology , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , Sputum/microbiology
3.
Gastroenterology and Hepatology from Bed to Bench. 2012; 5 (2): 94-99
in English | IMEMR | ID: emr-116800

ABSTRACT

We intended to find out the diversity of EPEC isolates among asymptomatic or diarrheal children in Iran using ribotyping. Enteropathogenic Escherichia coli [EPEC] is responsible for gastroenteritis especially in young children. A total of 39 EPEC collected strains were serotyped and the presence of virulence genes as well as EAF plasmid among the strains was studied. Adherence assay was also performed. Clonal diversity of the isolates was investigated using ribotyping. Of 39 studied strains of E. coli, 6 serogroups of EPEC were represented. The presence of the stx gene was ascertained in 7 isolates and the eaeA, eaeB and bfpA genes were harbored by 5, 3 and 1 strains, respectively. Ribotyping yielded 9 different clusters. According to our results there was not a significant correlation between the results of serotyping and those of ribotyping. However, different serotypes of E. coli may belong to the same ribotype clusters and vice versa

4.
Iranian Journal of Basic Medical Sciences. 2010; 13 (1): 210-215
in English | IMEMR | ID: emr-93114

ABSTRACT

Rapidly growing mycobacteria [RGM] are capable of producing diseases in humans. Since mycobacteria vary in their susceptibility, precise identification is critical for adoption of correct drug therapy. The main aim of this study was molecular identification and evaluation of antimicrobial susceptibility pattern of Iranian clinically isolated Myocbacterium fortuitum. A total of 72 presumptively identified isolates of clinical atypical mycobacteria collected by Isfahan Research Center for Infectious Diseases and Tropical Medicine during 2006-2008 were included in the current study. A combination of conventional and molecular tests was applied to identify the isolates. Molecular methods including genus and group specific PCR and PCR-Restriction Algorithm [PRA] based on hsp65 gene were applied to achieve exact identification of mycobacterial strains. Antimicrobial susceptibility testing on M. fortidtum isolates was performed by in-house prepared broth microdilution test. Out of 72 collected atypical mycobacteria isolates, we identified 25 strains of M. fortuitum. All strains had the specific molecular markers of mycobacterial identity and similar species specific PRA pattern of the international type strain of M fortuitum. Drug susceptibility testing showed that the M. fortidtum isolates are sensitive to amikacin, sulfamethoxazole and ciprofloxacin [100%], imipenem [92%], clarithromycin [76%], cefoxitin [56%] and doxycycline [16%]. Molecular identification of atypical mycobacteria based on PRA is a reliable and rapid approach which can identify mycobacterial strains to the species level. Our study showed that M. fortuitum plays a significant role in pulmonary and extrapulmonary infection in patients and should be given proper considerations when clinical samples are processed


Subject(s)
Mycobacterium fortuitum/isolation & purification , Heat-Shock Proteins , Polymerase Chain Reaction , Microbial Sensitivity Tests
5.
Iranian Journal of Basic Medical Sciences. 2008; 11 (3): 174-182
in English | IMEMR | ID: emr-103253

ABSTRACT

Resistance to antimicrobial agents, particularly metronidazole and clarithromycin, is frequently observed in Helicobacter pylori and may be associated with treatment failure. This resistance rate varies according to the population studied. The aim of this study was to assess the pattern of antimicrobial resistance of H. pylori isolates from dyspeptic patients in Isfahan. Antral gastric biopsies from 230 dyspeptic patients were cultured. Susceptibility testing to commonly used antibiotics performed on pure cultures of 80 H. pylori-positive isolates by Modified Disk Diffusion Method [MDDM]. Genomic DNA extracted and subjected for study of entire genomic pattern using Random Amplified Polymorphic DNA- Polymerase Chain Reaction [RAPD-PCR]. The overall rates of primary resistance were 30.0%, 8.75%, 6.25%, 3.75%, 3.75%, and 2.50% for metronidazole, ciprofloxacin, clarithromycin, azithromycin, tetracycline, and amoxicillin, respectively. Multiple antibiotic resistances were observed in 8 of 27 resistant isolates [29.6%] that mainly were double resistance with the prevalence of 6.25%. No association between antimicrobial resistance and either the gender, age or clinical presentation of the patients were detected. In RAPD-PCR, great diversity observed in 27 resistant strains isolated from different patients and this heterogeneity was not significantly different from susceptible strains. Primary H, pylori resistance to metronidazole in our population was lower than the developing world and even other parts of Iran, to ciprofloxacin was considerable in comparison with results in most other countries. Moreover, antibiotic resistance had no effect on genomic pattern of H. pylori isolates. Finally, pretreatment H. pylori isolates susceptibility testing is highly recommended


Subject(s)
Drug Resistance, Bacterial/genetics , Prevalence , Helicobacter pylori/genetics , Clarithromycin/pharmacology , Metronidazole/pharmacology , Disk Diffusion Antimicrobial Tests , Random Amplified Polymorphic DNA Technique , Polymerase Chain Reaction
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