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1.
Microb Genom ; 6(12)2020 12.
Article in English | MEDLINE | ID: mdl-33245689

ABSTRACT

Mucormycoses are invasive infections by Rhizopus species and other Mucorales. Over 10 months, four solid organ transplant (SOT) recipients at our centre developed mucormycosis due to Rhizopus microsporus (n=2), R. arrhizus (n=1) or Lichtheimia corymbifera (n=1), at a median 31.5 days (range: 13-34) post-admission. We performed whole genome sequencing (WGS) on 72 Mucorales isolates (45 R. arrhizus, 19 R. delemar, six R. microsporus, two Lichtheimia species) from these patients, from five patients with community-acquired mucormycosis, and from hospital and regional environments. Isolates were compared by core protein phylogeny and global genomic features, including genome size, guanine-cytosine percentages, shared protein families and paralogue expansions. Patient isolates fell into six core phylogenetic lineages (clades). Phylogenetic and genomic similarities of R. microsporus isolates recovered 7 months apart from two SOT recipients in adjoining hospitals suggested a potential common source exposure. However, isolates from other patients and environmental sites had unique genomes. Many isolates that were indistinguishable by core phylogeny were distinct by one or more global genomic comparisons. Certain clades were recovered throughout the study period, whereas others were found at particular time points. In conclusion, mucormycosis cases could not be genetically linked to a definitive environmental source. Comprehensive genomic analyses eliminated false associations between Mucorales isolates that would have been assigned using core phylogenetic or less extensive genomic comparisons. The genomic diversity of Mucorales mandates that multiple isolates from individual patients and environmental sites undergo WGS during epidemiological investigations. However, exhaustive surveillance of fungal populations in a hospital and surrounding community is probably infeasible.


Subject(s)
Community-Acquired Infections/microbiology , Cross Infection/microbiology , Mucorales/classification , Mucormycosis/diagnosis , Transplants/microbiology , Whole Genome Sequencing/methods , Base Composition , Female , Genetic Variation , Genome Size , High-Throughput Nucleotide Sequencing , Humans , Male , Mucorales/genetics , Mucorales/isolation & purification , Mucormycosis/microbiology , Phylogeny
2.
Proc Natl Acad Sci U S A ; 112(4): 1173-8, 2015 Jan 27.
Article in English | MEDLINE | ID: mdl-25587132

ABSTRACT

Thaumarchaeota are among the most abundant microbial cells in the ocean, but difficulty in cultivating marine Thaumarchaeota has hindered investigation into the physiological and evolutionary basis of their success. We report here a closed genome assembled from a highly enriched culture of the ammonia-oxidizing pelagic thaumarchaeon CN25, originating from the open ocean. The CN25 genome exhibits strong evidence of genome streamlining, including a 1.23-Mbp genome, a high coding density, and a low number of paralogous genes. Proteomic analysis recovered nearly 70% of the predicted proteins encoded by the genome, demonstrating that a high fraction of the genome is translated. In contrast to other minimal marine microbes that acquire, rather than synthesize, cofactors, CN25 encodes and expresses near-complete biosynthetic pathways for multiple vitamins. Metagenomic fragment recruitment indicated the presence of DNA sequences >90% identical to the CN25 genome throughout the oligotrophic ocean. We propose the provisional name "Candidatus Nitrosopelagicus brevis" str. CN25 for this minimalist marine thaumarchaeon and suggest it as a potential model system for understanding archaeal adaptation to the open ocean.


Subject(s)
Archaea , Archaeal Proteins , Gene Expression Regulation, Archaeal/physiology , Proteome , Proteomics , Water Microbiology , Amino Acid Sequence , Archaea/classification , Archaea/genetics , Archaea/metabolism , Archaeal Proteins/biosynthesis , Archaeal Proteins/genetics , Metagenomics , Molecular Sequence Data , Oceans and Seas , Proteome/biosynthesis , Proteome/genetics
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