Abstract

Mycobacterium avium comprises four subspecies that contain both human and veterinary pathogens. At the inception of this study, twenty-eight M. avium genomes had been annotated as RefSeq genomes, facilitating direct comparisons. These genomes represent strains from around the world and provided a unique opportunity to examine genome dynamics in this species. Each genome was confirmed to be classified correctly based on SNP genotyping, nucleotide identity and presence/absence of repetitive elements or other typing methods. The Mycobacterium avium subspecies paratuberculosis (Map) genome size and organization was remarkably consistent, averaging 4.8 Mb with a variance of only 29.6 kb among the 13 strains. Comparing recombination events along with the larger genome size and variance observed among Mycobacterium avium subspecies avium (Maa) and Mycobacterium avium subspecies hominissuis (Mah) strains (collectively termed non-Map) suggests horizontal gene transfer occurs in non-Map, but not in Map strains. Overall, M. avium subspecies could be divided into two major sub-divisions, with the Map type II (bovine strains) clustering tightly on one end of a phylogenetic spectrum and Mah strains clustering more loosely together on the other end. The most evolutionarily distinct Map strain was an ovine strain, designated Telford, which had >1,000 SNPs and showed large rearrangements compared to the bovine type II strains. The Telford strain clustered with Maa strains as an intermediate between Map type II and Mah. SNP analysis and genome organization analyses repeatedly demonstrated the conserved nature of Map versus the mosaic nature of non-Map M. avium strains. Finally, core and pangenomes were developed for Map and non-Map strains. A total of 80% Map genes belonged to the Map core genome, while only 40% of non-Map genes belonged to the non-Map core genome. These genomes provide a more complete and detailed comparison of these subspecies strains as well as a blueprint for how genetic diversity originated.

Highlights

  • The Mycobacterium avium complex (MAC) comprises three species which include M. avium, M. intracellulare, and more recently, M. chimaera (Tortoli et al, 2004)

  • Insufficient numbers of complete genomes had been a limitation in earlier studies, but recently a similar number of M. avium subspecies paratuberculosis (Map) and non-Map M. avium genomes have emerged

  • We show that among the three M. avium subspecies studied, Map is a relatively stable, closed genome while Mycobacterium avium subspecies hominissuis (Mah) and Mycobacterium avium subspecies avium (Maa) show more horizontal gene transfer and accessory genome components

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Summary

Introduction

The Mycobacterium avium complex (MAC) comprises three species which include M. avium, M. intracellulare, and more recently, M. chimaera (Tortoli et al, 2004). There currently exist four subspecies within M. avium, which are the focus of this study. These include: avium, hominissuis, paratuberculosis, and silvaticum. Through genome sequencing, differences have been identified and highlighted, especially for M. avium subspecies paratuberculosis (Map), which is the causative agent of Johne’s disease in cattle, sheep and other ruminant animals. This disease is endemic in the United States and is a problem worldwide due to the severe economic consequences to dairy cattle as well as goat and sheep industries. As more complete genome sequences accumulate, the opportunity to understand the pathological and genetic distinctions between the subspecies of M. avium will become more apparent

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