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Conjugative Mating Assays for Sequence-specific Analysis of Transfer Proteins Involved in Bacterial Conjugation
Published on: January 4, 2017
Pathogenic Determinants of the Mycobacterium kansasii Complex: An Unsuspected Role for Distributive Conjugal Transfer
Florian Tagini1, Trestan Pillonel1, Claire Bertelli1
1Department of Laboratory Medicine, Institute of Microbiology, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland.
Abstract:
The Mycobacterium kansasii species comprises six subtypes that were recently classified into six closely related species; Mycobacterium kansasii (formerly M. kansasii subtype 1), Mycobacterium persicum (subtype 2), Mycobacterium pseudokansasii (subtype 3), Mycobacterium ostraviense (subtype 4), Mycobacterium innocens (subtype 5) and Mycobacterium attenuatum (subtype 6). Together with Mycobacterium gastri, they form the M. kansasii complex. M. kansasii is the most frequent and most pathogenic species of the complex. M. persicum is classically associated with diseases in immunosuppressed patients, and the other species are mostly colonizers, and are only very rarely reported in ill patients. Comparative genomics was used to assess the genetic determinants leading to the pathogenicity of members of the M. kansasii complex. The genomes of 51 isolates collected from patients with and without disease were sequenced and compared with 24 publicly available genomes. The pathogenicity of each isolate was determined based on the clinical records or public metadata. A comparative genomic analysis showed that all M. persicum, M. ostraviense, M innocens and M. gastri isolates lacked the ESX-1-associated EspACD locus that is thought to play a crucial role in the pathogenicity of M. tuberculosis and other non-tuberculous mycobacteria. Furthermore, M. kansasii was the only species exhibiting a 25-Kb-large genomic island encoding for 17 type-VII secretion system-associated proteins. Finally, a genome-wide association analysis revealed that two consecutive genes encoding a hemerythrin-like protein and a nitroreductase-like protein were significantly associated with pathogenicity. These two genes may be involved in the resistance to reactive oxygen and nitrogen species, a required mechanism for the intracellular survival of bacteria. Three non-pathogenic M. kansasii lacked these genes likely due to two distinct distributive conjugal transfers (DCTs) between M. attenuatum and M. kansasii, and one DCT between M. persicum and M. kansasii. To our knowledge, this is the first study linking DCT to reduced pathogenicity.
Insights
Comparative genomics reveals genetic factors influencing pathogenicity in the Mycobacterium kansasii complex. Loss of specific genes via distributive conjugal transfers (DCTs) is linked to reduced pathogenicity in these mycobacteria.
Area of Science:
- Genomics and Microbiology
- Pathogen Evolution
- Bacterial Pathogenesis
Background:
- The Mycobacterium kansasii complex includes six species, with M. kansasii being the most pathogenic.
- Understanding the genetic basis of pathogenicity is crucial for distinguishing between pathogenic and colonizing species.
- Previous studies highlighted the role of the ESX-1-associated EspACD locus in mycobacterial pathogenicity.
Purpose of the Study:
- To identify genetic determinants associated with pathogenicity within the M. kansasii complex using comparative genomics.
- To investigate the role of specific genomic features and gene loss in the reduced pathogenicity of certain species.
Main Methods:
- Sequencing and comparative genomic analysis of 51 M. kansasii complex isolates from patients.
- Comparison with 24 publicly available genomes to identify genetic variations.
- Genome-wide association analysis to pinpoint genes linked to pathogenicity.
Main Results:
- Species like M. persicum, M. ostraviense, M. innocens, and M. gastri lack the ESX-1-associated EspACD locus.
- M. kansasii uniquely possesses a 25-Kb genomic island encoding type-VII secretion system proteins.
- A hemerythrin-like protein and nitroreductase-like protein genes were significantly associated with pathogenicity, potentially aiding in oxidative stress resistance.
- Three non-pathogenic M. kansasii isolates lacked these key genes, suggesting acquisition via distributive conjugal transfers (DCTs).
Conclusions:
- The presence of the ESX-1-associated EspACD locus and a specific genomic island contributes to M. kansasii pathogenicity.
- Loss of genes involved in oxidative stress resistance, likely through DCTs, is associated with reduced pathogenicity in the M. kansasii complex.
- This study provides the first evidence linking DCTs to decreased pathogenicity in mycobacteria.
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