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Inducing Meningococcal Meningitis Serogroup C in Mice via Intracisternal Delivery
Published on: November 5, 2019
Cryptococcus neoformans hyperfilamentous strain is hypervirulent in a murine model of cryptococcal
Marianna Feretzaki1, Sarah E Hardison2, Floyd L Wormley2
1Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America.
Abstract:
Cryptococcus neoformans is a human fungal pathogen that causes lethal infections of the lung and central nervous system in immunocompromised individuals. C. neoformans has a defined bipolar sexual life cycle with a and α mating types. During the sexual cycle, which can occur between cells of opposite mating types (bisexual reproduction) or cells of one mating type (unisexual reproduction), a dimorphic transition from yeast to hyphal growth occurs. Hyphal development and meiosis generate abundant spores that, following inhalation, penetrate deep into the lung to enter the alveoli, germinate, and establish a pulmonary infection growing as budding yeast cells. Unisexual reproduction has been directly observed only in the Cryptococcus var. neoformans (serotype D) lineage under laboratory conditions. However, hyphal development has been previously associated with reduced virulence and the serotype D lineage exhibits limited pathogenicity in the murine model. In this study we show that the serotype D hyperfilamentous strain XL280α is hypervirulent in an animal model. It can grow inside the lung of the host, establish a pulmonary infection, and then disseminate to the brain to cause cryptococcal meningoencephalitis. Surprisingly, this hyperfilamentous strain triggers an immune response polarized towards Th2-type immunity, which is usually observed in the highly virulent sibling species C. gattii, responsible for the Pacific Northwest outbreak. These studies provide a technological advance that will facilitate analysis of virulence genes and attributes in C. neoformans var. neoformans, and reveal the virulence potential of serotype D as broader and more dynamic than previously appreciated.
Insights
The hypervirulent Cryptococcus neoformans serotype D strain XL280α causes lethal meningoencephalitis in animal models. This strain triggers a Th2 immune response, broadening our understanding of fungal pathogen virulence.
Area of Science:
- Mycology
- Immunology
- Infectious Diseases
Background:
- Cryptococcus neoformans is a fungal pathogen causing life-threatening infections in immunocompromised individuals.
- Sexual reproduction in C. neoformans involves a dimorphic transition from yeast to hyphal growth, producing infectious spores.
- Serotype D strains, particularly those undergoing hyphal development, were previously considered less virulent.
Purpose of the Study:
- To investigate the virulence of the serotype D hyperfilamentous strain XL280α in an animal model.
- To characterize the immune response elicited by this hypervirulent strain.
- To advance the analysis of virulence factors in C. neoformans var. neoformans.
Main Methods:
- Infection of an animal model with the hypervirulent C. neoformans serotype D strain XL280α.
- Assessment of pulmonary infection establishment and dissemination to the brain.
- Analysis of the host immune response, specifically T-helper cell polarization.
Main Results:
- The hyperfilamentous serotype D strain XL280α demonstrated hypervirulence, causing pulmonary infection and cryptococcal meningoencephalitis.
- This strain induced a Th2-type immune response, typically associated with more virulent fungal species.
- The study revealed a broader and more dynamic virulence potential for serotype D strains than previously recognized.
Conclusions:
- The serotype D lineage of C. neoformans possesses significant, previously underestimated, virulence potential.
- Hyperfilamentous growth in serotype D strains can lead to severe disease and is associated with a Th2 immune bias.
- These findings necessitate a re-evaluation of C. neoformans serotype D pathogenicity and offer new avenues for studying fungal virulence mechanisms.

