Phenotypic and Genotypic Analysis of Multidrug-ResistantMycobacterium tuberculosisIsolates from Sudanese Patients

Author:

Sabeel Solima M. A.12ORCID,Salih Mohamed Ahmed3,Ali Manasik4,EL-Zaki Salah-Eldin5,Abuzeid Nadir6,Elgadi Zeinab Abubaker Mohammed7,Altayb Hisham N.8,Elegail Asrar M. A.9,Ibrahim Nuha Y.9,Elamin Bahaeldin K.110

Affiliation:

1. Department of Microbiology, Faculty of Medical Laboratory Sciences, University of Khartoum, Khartoum, Sudan

2. Microbiology Department, Faculty of Medical Laboratory Sciences, Ibn Sina University, Khartoum, Sudan

3. Department of Bioinformatics, Africa City of Technology, Khartoum, Sudan

4. Sudan Academy of Sciences, Khartoum, Sudan

5. Department of Epidemiology, Tropical Medicine Research Institute, National Center for Research, Khartoum, Sudan

6. Department of Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Khartoum, Sudan

7. Veterinary Research Institute, Khartoum, Sudan

8. Microbiology Department, College of Medical Laboratory Sciences, Sudan University of Science and Technology, Khartoum, Sudan

9. National Reference Laboratory-Tuberculosis (NRL-TB), National Public Health Laboratory, Khartoum, Sudan

10. Department of Microbiology and Parasitology, College of Medicine, University of Bisha, Bisha, Saudi Arabia

Abstract

Background.Currently, mutations inrpoB,KatG, andrrsgenes andinhApromoter were considered to be involved in conferring resistance to rifampicin, isoniazid, and streptomycin inMycobacterium tuberculosis(MTB).Objective.The aims of this study were to detect the prevalence of first-line tuberculosis (TB) drug resistance among a group of previously treated and newly detected TB patients, to determine the association between prevalence of multidrug resistance (MDR) and demographic information (age and sex), to explain genes correlated with MDRMycobacterium tuberculosis, and to characterize MTB via 16S ribosomal RNA (16S rRNA) analysis.Methods.A hundred MTB isolates from Sudanese pulmonary TB patients were included in the study. The proportional method of drug susceptibility test was carried out on Löwenstein-Jensen media. Multiplex PCR ofrpoBandKatGgenes andinhApromoter was conducted; thenrrsgenes were amplified by conventional PCR and were sequenced. The sequences of the PCR product were compared with knownrrsgene sequences in the GenBank database by multiple sequence alignment tools.Result.The prevalence of MDR was 14.7% among old cases and 5.3% among newly diagnosed cases.Conclusion.Mutations inrrscould be considered as a diagnostic marker.

Publisher

Hindawi Limited

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