Genomics and transcriptomics yields a system-level view of the biology of the pathogen Naegleria fowleri

Author:

Herman Emily K.,Greninger Alex,van der Giezen Mark,Ginger Michael L.,Ramirez-Macias Inmaculada,Miller Haylea C.,Morgan Matthew J.,Tsaousis Anastasios D.,Velle Katrina,Vargová Romana,Záhonová Kristína,Najle Sebastian Rodrigo,MacIntyre Georgina,Muller Norbert,Wittwer Mattias,Zysset-Burri Denise C.,Eliáš Marek,Slamovits Claudio H.,Weirauch Matthew T.,Fritz-Laylin Lillian,Marciano-Cabral Francine,Puzon Geoffrey J.,Walsh Tom,Chiu Charles,Dacks Joel B.ORCID

Abstract

Abstract Background The opportunistic pathogen Naegleria fowleri establishes infection in the human brain, killing almost invariably within 2 weeks. The amoeba performs piece-meal ingestion, or trogocytosis, of brain material causing direct tissue damage and massive inflammation. The cellular basis distinguishing N. fowleri from other Naegleria species, which are all non-pathogenic, is not known. Yet, with the geographic range of N. fowleri advancing, potentially due to climate change, understanding how this pathogen invades and kills is both important and timely. Results Here, we report an -omics approach to understanding N. fowleri biology and infection at the system level. We sequenced two new strains of N. fowleri and performed a transcriptomic analysis of low- versus high-pathogenicity N. fowleri cultured in a mouse infection model. Comparative analysis provides an in-depth assessment of encoded protein complement between strains, finding high conservation. Molecular evolutionary analyses of multiple diverse cellular systems demonstrate that the N. fowleri genome encodes a similarly complete cellular repertoire to that found in free-living N. gruberi. From transcriptomics, neither stress responses nor traits conferred from lateral gene transfer are suggested as critical for pathogenicity. By contrast, cellular systems such as proteases, lysosomal machinery, and motility, together with metabolic reprogramming and novel N. fowleri proteins, are all implicated in facilitating pathogenicity within the host. Upregulation in mouse-passaged N. fowleri of genes associated with glutamate metabolism and ammonia transport suggests adaptation to available carbon sources in the central nervous system. Conclusions In-depth analysis of Naegleria genomes and transcriptomes provides a model of cellular systems involved in opportunistic pathogenicity, uncovering new angles to understanding the biology of a rare but highly fatal pathogen.

Funder

CePaViP

Czech Science Foundation

CSIRO

Canada Research Chairs

Vanier Canada Graduate Scholarship

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Developmental Biology,Plant Science,General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,Physiology,Ecology, Evolution, Behavior and Systematics,Structural Biology,Biotechnology

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