Signatures of transposon-mediated genome inflation, host specialization, and photoentrainment in Entomophthora muscae and allied entomophthoralean fungi

Author:

Stajich Jason E1ORCID,Lovett Brian2ORCID,Lee Emily3,Macias Angie M4,Hajek Ann E5,de Bivort Benjamin L3ORCID,Kasson Matt T4ORCID,De Fine Licht Henrik H6ORCID,Elya Carolyn37ORCID

Affiliation:

1. Department of Microbiology and Plant Pathology, University of California-Riverside

2. Emerging Pests and Pathogens Research Unit, USDA-ARS

3. Department of Organismic and Evolutionary Biology, Harvard University

4. Division of Plant and Soil Sciences, West Virginia University

5. Department of Entomology, Cornell University

6. Section for Organismal Biology, Department of Plant and Environmental Sciences, University of Copenhagen

7. Department of Molecular and Cellular Biology, Harvard University

Abstract

Despite over a century of observations, the obligate insect parasites within the order Entomophthorales remain poorly characterized at the genetic level. In this manuscript, we present a genome for a laboratory-tractable Entomophthora muscae isolate that infects fruit flies. Our E. muscae assembly is 1.03 Gb, consists of 7810 contigs and contains 81.3% complete fungal BUSCOs. Using a comparative approach with recent datasets from entomophthoralean fungi, we show that giant genomes are the norm within Entomophthoraceae owing to extensive, but not recent, Ty3 retrotransposon activity. In addition, we find that E. muscae and its closest allies possess genes that are likely homologs to the blue-light sensor white-collar 1, a Neurospora crassa gene that has a well-established role in maintaining circadian rhythms. We uncover evidence that E. muscae diverged from other entomophthoralean fungi by expansion of existing families, rather than loss of particular domains, and possesses a potentially unique suite of secreted catabolic enzymes, consistent with E. muscae’s species-specific, biotrophic lifestyle. Finally, we offer a head-to-head comparison of morphological and molecular data for species within the E. muscae species complex that support the need for taxonomic revision within this group. Altogether, we provide a genetic and molecular foundation that we hope will provide a platform for the continued study of the unique biology of entomophthoralean fungi.

Funder

National Science Foundation

National Institute of Food and Agriculture

National Institutes of Health

West Virginia University

United States Department of Agriculture

Alfred P. Sloan Foundation

Richard and Susan Smith Family Foundation

Esther A. and Joseph Klingenstein Fund

National Institute of Neurological Disorders and Stroke

USDA Forest Service

Independent Research Fund Denmark

Carlsberg Foundation

Howard Hughes Medical Institute

Publisher

eLife Sciences Publications, Ltd

Reference155 articles.

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