Live Imaging of Host-Parasite Interactions in a Zebrafish Infection Model Reveals Cryptococcal Determinants of Virulence and Central Nervous System Invasion.
Abstract
UNLABELLED: The human fungal pathogen Cryptococcus neoformans is capable of infecting
a broad range of hosts, from invertebrates like amoebas and nematodes to standard
vertebrate models such as mice and rabbits. Here we have taken advantage of a zebrafish
model to investigate host-pathogen interactions of Cryptococcus with the zebrafish
innate immune system, which shares a highly conserved framework with that of mammals.
Through live-imaging observations and genetic knockdown, we establish that macrophages
are the primary immune cells responsible for responding to and containing acute cryptococcal
infections. By interrogating survival and cryptococcal burden following infection
with a panel of Cryptococcus mutants, we find that virulence factors initially identified
as important in causing disease in mice are also necessary for pathogenesis in zebrafish
larvae. Live imaging of the cranial blood vessels of infected larvae reveals that
C. neoformans is able to penetrate the zebrafish brain following intravenous infection.
By studying a C. neoformans FNX1 gene mutant, we find that blood-brain barrier invasion
is dependent on a known cryptococcal invasion-promoting pathway previously identified
in a murine model of central nervous system invasion. The zebrafish-C. neoformans
platform provides a visually and genetically accessible vertebrate model system for
cryptococcal pathogenesis with many of the advantages of small invertebrates. This
model is well suited for higher-throughput screening of mutants, mechanistic dissection
of cryptococcal pathogenesis in live animals, and use in the evaluation of therapeutic
agents. IMPORTANCE: Cryptococcus neoformans is an important opportunistic pathogen
that is estimated to be responsible for more than 600,000 deaths worldwide annually.
Existing mammalian models of cryptococcal pathogenesis are costly, and the analysis
of important pathogenic processes such as meningitis is laborious and remains a challenge
to visualize. Conversely, although invertebrate models of cryptococcal infection allow
high-throughput assays, they fail to replicate the anatomical complexity found in
vertebrates and, specifically, cryptococcal stages of disease. Here we have utilized
larval zebrafish as a platform that overcomes many of these limitations. We demonstrate
that the pathogenesis of C. neoformans infection in zebrafish involves factors identical
to those in mammalian and invertebrate infections. We then utilize the live-imaging
capacity of zebrafish larvae to follow the progression of cryptococcal infection in
real time and establish a relevant model of the critical central nervous system infection
phase of disease in a nonmammalian model.
Type
Journal articleSubject
AnimalsCentral Nervous System
Cryptococcosis
Cryptococcus neoformans
DNA Mutational Analysis
Disease Models, Animal
Gene Knockdown Techniques
Host-Parasite Interactions
Larva
Macrophages
Optical Imaging
Survival Analysis
Virulence
Virulence Factors
Zebrafish
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https://hdl.handle.net/10161/11177Published Version (Please cite this version)
10.1128/mBio.01425-15Publication Info
Tenor, Jennifer L; Oehlers, Stefan H; Yang, Jialu L; Tobin, David M; & Perfect, John
R (2015). Live Imaging of Host-Parasite Interactions in a Zebrafish Infection Model Reveals
Cryptococcal Determinants of Virulence and Central Nervous System Invasion. MBio, 6(5). pp. e01425-e01415. 10.1128/mBio.01425-15. Retrieved from https://hdl.handle.net/10161/11177.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
John Robert Perfect
James B. Duke Distinguished Professor of Medicine
Research in my laboratory focuses around several aspects of medical mycology. We
are investigating antifungal agents (new and old) in animal models of candida and
cryptococcal infections. We have examined clinical correlation of in vitro antifungal
susceptibility testing and with in vivo outcome. Our basic science project examines
the molecular pathogenesis of cryptococcal infections. We have developed a molecular
foundation for C. neoformans, including transformation systems, gene disr
Jennifer L Tenor
Assistant Professor in Medicine
David M. Tobin
Professor of Molecular Genetics and Microbiology
Tuberculosis: Mycobacterial Pathogenesis and Host Susceptibility
Tuberculosis kills 1.5 million people annually. Our laboratory aims to understand
the intricate interplay between mycobacteria and their hosts using a combination of
model organism genetics, human genetics, pharmacology and high-resolution microscopy.
By identifying key pathways utilized by the infecting bacteria and the host innate
immune system, we hope to discover new therapeutic targets and interventi
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