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siRNA Electroporation to Modulate Autophagy in Herpes Simplex Virus Type 1-Infected Monocyte-Derived Dendritic Cells
Published on: October 28, 2019
The putative autophagy regulator Atg7 affects the physiology and pathogenic mechanisms of Cryptococcus neoformans
Debora L Oliveira1, Fernanda L Fonseca1, Daniel Zamith-Miranda2
1Fundação Oswaldo Cruz (Fiocruz), Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Rio de Janeiro, Brazil.
Aim:
We investigated the involvement of the autophagy protein 7 (Atg7) in physiology and pathogenic potential of Cryptococcus neoformans.
Materials & Methods:
The C. neoformans gene encoding Atg7 was deleted by biolistic transformation for characterization of autophagy mechanisms, pigment formation, cell dimensions, interaction with phagocytes and pathogenic potential in vivo.
Results & Conclusion:
ATG7 deletion resulted in defective autophagy mechanisms, enhanced pigmentation and increased cellular size both in vitro and in vivo. The atg7Δ mutant had decreased survival in the lung of infected mice, higher susceptibility to the killing machinery of different host phagocytes and reduced ability to kill an invertebrate host. These results connect Atg7 with mechanisms of pathogenicity in the C. neoformans model.
Insights
Autophagy protein 7 (Atg7) in Cryptococcus neoformans impacts virulence. Deleting Atg7 impaired autophagy but increased pigmentation and cell size, leading to reduced survival and host interaction.
Area of Science:
- Microbiology
- Molecular Biology
- Pathogenesis
Background:
- Autophagy is a crucial cellular process.
- Cryptococcus neoformans is an opportunistic fungal pathogen.
Purpose of the Study:
- To investigate the role of autophagy protein 7 (Atg7) in Cryptococcus neoformans.
Main Methods:
- Gene deletion of Atg7 in C. neoformans via biolistic transformation.
- Characterization of autophagy, pigmentation, cell size, and host interactions.
Main Results:
- Atg7 deletion resulted in defective autophagy, enhanced pigmentation, and increased cell size.
- The atg7Δ mutant showed decreased survival in mice and increased susceptibility to phagocytes.
Conclusions:
- Atg7 is implicated in the pathogenicity mechanisms of Cryptococcus neoformans.
- Atg7 influences fungal physiology and host-pathogen interactions.
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