# Genomic-based genotype and drug susceptibility profile of Mycobacterium kansasii in China

**Authors:** Yiting Wang, Xichao Ou, Bing Zhao, Hui Xia, Yang Zheng, Yang Zhou, Ruida Xing, Yuanyuan Song, Shengfen Wang, Yanlin Zhao, Huiwen Zheng

PMC · DOI: 10.3389/fmicb.2025.1573448 · Frontiers in Microbiology · 2025-04-29

## TL;DR

This study analyzed the genetic and drug susceptibility profiles of Mycobacterium kansasii in China, finding that rifabutin and clarithromycin are most effective, while new tuberculosis drugs show potential for treating M. kansasii infections.

## Contribution

The study provides the first comprehensive genomic and drug susceptibility analysis of M. kansasii in China, highlighting novel insights into drug resistance patterns and potential treatment options.

## Key findings

- M. kansasii type I is the predominant genotype in China, with 153 isolates classified into 3 clusters.
- Rifabutin and clarithromycin showed 100% and 99.35% susceptibility, respectively, while new drugs like bedaquiline and delamanid had very low MIC values.
- Cluster 3 showed higher resistance rates compared to clusters 1 and 2, suggesting a link between clustering and drug resistance.

## Abstract

To analyze subtypes, microbiological characteristics and antimicrobial susceptibility of Mycobacterium kansasii in China, a total of 153 M. kansasii isolates, collected from national drug resistance surveillance, were genotyped with whole genome sequencing and explored the antimicrobial susceptibility with broth microdilution. All isolates were classified as M. kansasii type I based on Average Nucleotide Identity(ANI). The 153 M. kansasii representatives were differentiated into 3 clusters with 141 genotypes, including 17 isolates from a cluster and 136 isolates with unique patterns. The EXS-1, EXS-3 and EXS-5 regions were involved in all isolates. Rifabutin and clarithromycin were the most highly active against M. kansasii strains, with the susceptible rate of 100 and 99.35%, respectively. Followed by amikacin and linezolid, the resistance rate was 5.88 and 7.19%, respectively. The resistance rate to rifampin (RIF) was 22.22%. As for the antibiotics without the breakpoint values, all isolates had very low MIC50 (0.03 μg/mL) and MIC90 (≤0.06 μg/mL) values against bedaquiline, sutezolid, delamanid, and clofazimine. Except for ciprofloxacin and moxifloxacin, the resistance rate of other drugs in cluster 3 was higher than that in cluster 1 and cluster 2. In conclusion, M. kansasii type I was the predominant genotype in China, and rifabutin and clarithromycin presented strong activities. The new drugs, used for the treatment of multidrug - resistant tuberculosis, have the potential to be potent agents in the treatment of M. kansasii infection. The clustering might contribute to the high resistance rate of M. kansasii.

## Linked entities

- **Chemicals:** Clarithromycin (PubChem CID 84029), Amikacin (PubChem CID 37768), Linezolid (PubChem CID 3929), Rifampin (PubChem CID 135398735), Bedaquiline (PubChem CID 5388906), Sutezolid (PubChem CID 465951), Delamanid (PubChem CID 6480466), Clofazimine (PubChem CID 2794), Ciprofloxacin (PubChem CID 2764), Moxifloxacin (PubChem CID 152946)
- **Diseases:** multidrug-resistant tuberculosis (MONDO:0005861)
- **Species:** Mycobacterium kansasii (taxon 1768)

## Full-text entities

- **Diseases:** M. kansasii infection (MESH:C566367), multidrug - resistant tuberculosis (MESH:D018088)
- **Chemicals:** RIF (MESH:D012293), linezolid (MESH:D000069349), moxifloxacin (MESH:D000077266), Rifabutin (MESH:D017828), amikacin (MESH:D000583), ciprofloxacin (MESH:D002939), bedaquiline (MESH:C493870), clarithromycin (MESH:D017291), delamanid (MESH:C516022), sutezolid (MESH:C543015), clofazimine (MESH:D002991)
- **Species:** Mycobacterium kansasii (species) [taxon 1768]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12069364/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12069364/full.md

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Source: https://tomesphere.com/paper/PMC12069364