Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients

Author:

Nguyen M. Hong12,Kaul Drishti3,Muto Carlene412,Cheng Shaoji J.2,Richter R. Alex3,Bruno Vincent M.5,Liu Guojun2,Beyhan Sinem3ORCID,Sundermann Alexander J.61ORCID,Mounaud Stephanie7ORCID,Pasculle A. William12,Nierman William C.7,Driscoll Eileen2,Cumbie Richard1,Clancy Cornelius J.2,Dupont Christopher L.3ORCID

Affiliation:

1. University of Pittsburgh Medical Center, Pittsburgh, PA, USA

2. University of Pittsburgh School of Medicine, Pittsburgh, PA, USA

3. J. Craig Venter Institute, La Jolla, CA, USA

4. Present address: Department of Medicine, University of Virginia, Charlottesville, VA, USA

5. University of Maryland School of Medicine, Baltimore, MD, USA

6. University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, USA

7. J. Craig Venter Institute, Rockville, MD, USA

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.

Funder

National Science Foundation

Medical Center, University of Pittsburgh

Publisher

Microbiology Society

Subject

General Medicine

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