Abstract
BackgroundMycobacterium pinnipedii, a member of the Mycobacterium tuberculosis Complex (MTBC), is capable of infecting several host species, including humans. Recently, ancient DNA from this organism was recovered from pre-Columbian mummies of Peru, sparking debate over the origin and frequency of tuberculosis in the Americas prior to European colonization.ResultsWe present the first comparative genomic study of this bacterial species, starting from the genome sequencing of two M. pinnipedii isolates (MP1 and MP2) obtained from different organs of a stranded South American sea lion. Our results indicate that MP1 and MP2 differ by 113 SNPs (single nucleotide polymorphisms) and 46 indels, constituting the first report of a mixed-strain infection in a sea lion. SNP annotation analyses indicate that genes of the VapBC family, a toxin-antitoxin system, and genes related to cell wall remodeling are under evolutionary pressure for protein sequence change in these strains. OrthoMCL analysis with seven modern isolates of M. pinnipedii shows that these strains have highly similar proteomes. Gene variations were only marginally associated with hypothetical proteins and PE/PPE (proline-glutamate and proline-proline-glutamate, respectively) gene families. We also detected large deletions in ancient and modern M. pinnipedii strains, including a few occurring only in modern strains, indicating a process of genome reduction occurring over the past one thousand years. Our phylogenomic analyses suggest the existence of two modern clusters of M. pinnipedii associated with geographic location, and possibly host species, and one basal node associated with the ancient M. pinnipedii strains. Previously described MiD3 and MiD4 deletions may have occurred independently, twice, over the evolutionary course of the MTBC.ConclusionThe presence of superinfection (i.e. mixed-strain infection) in this sea lion suggests that M. pinnipedii is highly endemic in this population. Mycobacterium pinnipedii proteomes of the studied isolates showed a high degree of conservation, despite being under genomic decay when compared to M. tuberculosis. This finding indicates that further genomes need to be sequenced and analyzed to increase the chances of finding variably present genes among strains or that M. pinnipedii genome remodeling occurred prior to bacterial speciation.
Highlights
Mycobacterium pinnipedii, a member of the Mycobacterium tuberculosis Complex (MTBC), is capable of infecting several host species, including humans
MTBC is a clonal bacterial group composed of 11 species that can be divided into two major groups: those highly adapted to human beings, named Mycobacterium tuberculosis and Mycobacterium africanum L5 and L6, and those adapted to animal hosts, named Mycobacterium bovis, Mycobacterium caprae, Mycobacterium microti, Mycobacterium pinnipedii, Mycobacterium origys, Mycobacterium mungi, Mycobacterium suricattae, “dassie bacillus”, and “chimpanzee bacillus” [1,2,3]
Mapping of the M. pinnipedii MP1 and MP2 reads with the genome of the M. tuberculosis strain H37Rv resulted in a reference coverage of 99.08 and 99.03%, and 2312 and 2350 variants, respectively
Summary
Mycobacterium pinnipedii, a member of the Mycobacterium tuberculosis Complex (MTBC), is capable of infecting several host species, including humans. MTBC is a clonal bacterial group composed of 11 species that can be divided into two major groups: those highly adapted to human beings, named Mycobacterium tuberculosis and Mycobacterium africanum L5 and L6, and those adapted to animal hosts, named Mycobacterium bovis, Mycobacterium caprae, Mycobacterium microti, Mycobacterium pinnipedii, Mycobacterium origys, Mycobacterium mungi, Mycobacterium suricattae, “dassie bacillus”, and “chimpanzee bacillus” [1,2,3] These species share great genomic similarity, with more than 99.95% nucleotide identity over alignable regions, and no evidence of horizontal gene transfer or major recombination events [4]. The actual impact, of tuberculosis in pinniped species remains largely unknown, mainly because its prevalence in free-ranging seals and sea lions is completely unexplored
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