Delamanid and bedaquiline resistance patterns in Mycobacterium tuberculosis in Iran: A cross-sectional analysis

被引:4
作者
Aghababa, AmirHossein Akbari [1 ]
Nasiri, Mohammad Javad [1 ,2 ]
Pakzad, Parviz [1 ]
Mirsamadi, Elnaz Sadat [3 ]
机构
[1] Islamic Azad Univ, Fac Biol Sci, Dept Microbiol, North Tehran Branch, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
[3] Islamic Azad Univ, Fac Med, Dept Microbiol, Tehran Med Sci, Tehran, Iran
关键词
Mycobacterium tuberculosis; Antimicrobial resistance; Bedaquiline; Delamanid; Multidrug-resistance; MULTIDRUG-RESISTANT; PREVALENCE; DRUG; SUSCEPTIBILITY;
D O I
10.1016/j.nmni.2024.101437
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: The surge of multidrug-resistant TB (MDR-TB) in Iran poses a significant challenge to global healthcare. The introduction of delamanid (DLM) and bedaquiline (BDQ), two potent antimycobacterial drugs, marks a crucial advance. Nevertheless, as resistance in Mycobacterium tuberculosis is on the rise in Iran and resistance to these newer medications is emerging, investigations in this field are of utmost importance. Methods: In this cross-sectional study, 38 MDR-TB strains were collected from five distinct regional TB laboratories in Iran. The clinical isolates were confirmed as M. tuberculosis using the phenotypic tests and IS6110-based PCR assay. Drug susceptibility testing (DST) for isoniazid, rifampicin, ethambutol, DLM, and BDQ was performed using WHO-approved methods. Sequencing was used to investigate genetic mutations in DLM ( ddn , fgd1 ) and BDQ ( Rv0678 , atpE , pepQ ) genes associated with resistance. Results: Among the 38 collected MDR-TB isolates, 7 (18.5 %) exhibited resistance to DLM, while all remained susceptible to BDQ. Analysis of the sequencing data revealed that the ddn gene exhibited the highest number of mutations in DLM-resistant isolates, including 18 nonsynonymous mutations and 1 indel leading to frameshift mutations. A common mutation, Gly81Ser, was present in 4 of the DLM-resistant isolates (4/7; 57.1 %). A synonymous mutation, T960C, in the fgd1 gene was uniformly found in DLM-resistant samples. Notably, no significant mutations were observed in the atpE , Rv0678 , or pepQ genes in any of the BDQ-susceptible isolates. Conclusions: Our study underscores the emergence of DLM resistance in a subset of MDR-TB isolates in Iran, primarily associated with mutations in the ddn gene. This emphasizes the ongoing necessity for TB drug resistance surveillance and research. While BDQ remains efficacious, the emergence of DLM resistance is a concerning development, warranting further exploration into resistance mechanisms and the formulation of effective TB control strategies.
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共 34 条
[1]   High prevalence of multidrug-resistant TB among household contacts in a high burden setting [J].
Ahmed, S. ;
Lotia-Farrukh, I. ;
Khan, P. Y. ;
Adnan, S. ;
Sodho, J. S. ;
Bano, S. ;
Siddiqui, M. R. ;
Ghafoor, A. ;
Isani, A. K. ;
Salahuddin, N. ;
Khan, U. .
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2023, 27 (08) :646-648
[2]  
Ahmed SH, 2023, Indian J Tubercul, V71, P79
[3]   High-resolution melt curve analysis for rapid detection of rifampicin resistance in Mycobacterium tuberculosis: a single-centre study in Iran [J].
Arefzadeh, S. ;
Azimi, T. ;
Nasiri, M. J. ;
Nikpor, Z. ;
Dabiri, H. ;
Doustdar, F. ;
Goudarzi, H. ;
Allahyartorkaman, M. .
NEW MICROBES AND NEW INFECTIONS, 2020, 35
[4]   Characterization of Genomic Variants Associated with Resistance to Bedaquiline and Delamanid in Naive Mycobacterium tuberculosis Clinical Strains [J].
Battaglia, S. ;
Spitaleri, A. ;
Cabibbe, A. M. ;
Meehan, C. J. ;
Utpatel, C. ;
Ismail, N. ;
Tahseen, S. ;
Skrahina, A. ;
Alikhanova, N. ;
Kamal, S. M. Mostofa ;
Barbova, A. ;
Niemann, S. ;
Groenheit, R. ;
Dean, A. S. ;
Zignol, M. ;
Rigouts, L. ;
Cirillo, D. M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2020, 58 (11)
[5]   Best drug treatment for multidrug-resistant and extensively drug-resistant tuberculosis [J].
Caminero, Jose A. ;
Sotgiu, Giovanni ;
Zumla, Alimuddin ;
Migliori, Giovanni Battista .
LANCET INFECTIOUS DISEASES, 2010, 10 (09) :621-629
[6]   Treatment of Highly Drug-Resistant Pulmonary Tuberculosis [J].
Conradie, Francesca ;
Diacon, Andreas H. ;
Ngubane, Nosipho ;
Howell, Pauline ;
Everitt, Daniel ;
Crook, Angela M. ;
Mendel, Carl M. ;
Egizi, Erica ;
Moreira, Joanna ;
Timm, Juliano ;
McHugh, Timothy D. ;
Wills, Genevieve H. ;
Bateson, Anna ;
Hunt, Robert ;
Van Niekerk, Christo ;
Li, Mengchun ;
Olugbosi, Morounfolu ;
Spigelman, Melvin .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 382 (10) :893-902
[7]   Impact of fgd1 and ddn Diversity in Mycobacterium tuberculosis Complex on In Vitro Susceptibility to PA-824 [J].
Feuerriegel, Silke ;
Koeser, Claudio U. ;
Bau, Davide ;
Ruesch-Gerdes, Sabine ;
Summers, David K. ;
Archer, John A. C. ;
Marti-Renom, Marc A. ;
Niemann, Stefan .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (12) :5718-5722
[8]   Mechanisms of resistance to delamanid, a drug for Mycobacterium tuberculosis [J].
Fujiwara, Mamoru ;
Kawasaki, Masanori ;
Hariguchi, Norimitsu ;
Liu, Yongge ;
Matsumoto, Makoto .
TUBERCULOSIS, 2018, 108 :186-194
[9]  
Gler MT, 2012, NEW ENGL J MED, V366, P2151, DOI 10.1056/NEJMoa1112433
[10]   Genetic diversity of candidate loci linked to Mycobacterium tuberculosis resistance to bedaquiline, delamanid and pretomanid [J].
Gomez-Gonzalez, Paula J. ;
Perdigao, Joao ;
Gomes, Pedro ;
Puyen, Zully M. ;
Santos-Lazaro, David ;
Napier, Gary ;
Hibberd, Martin L. ;
Viveiros, Miguel ;
Portugal, Isabel ;
Campino, Susana ;
Phelan, Jody E. ;
Clark, Taane G. .
SCIENTIFIC REPORTS, 2021, 11 (01)