TY - JOUR
T1 - Melanin deposition in two Cryptococcus species depends on cell-wall composition and flexibility
AU - Chrissian, Christine
AU - Camacho, Emma
AU - Fu, Man Shun
AU - Prados-Rosales, Rafael
AU - Chatterjee, Subhasish
AU - Cordero, Radames J.B.X.
AU - Lodge, Jennifer K.X.
AU - Casadevall, Arturo
AU - Stark, Ruth E.
N1 - Funding Information:
1 Recipient of a fellowship award from the United States Department of Edu-cation Graduate Assistance in Areas of National Need (GAANN) Program in Biochemistry, Biophysics, and Biodesign at The City College of New York (Grants PA200A120211 and PA200A150068).
Funding Information:
Acknowledgments—We thank Alexander Idnurm (Mycology Laboratory, University of Melbourne) for the kind gift of C. neoformans strain ST211A and Barbara Smith (Microscopy Facility, School of Medicine, Johns Hopkins University) for her expertise and technical assistance with transmission EM. We also thank Hsin Wang (City College, CUNY) and Van Chanh Phan (Hostos College, CUNY) for the development of NMR programs and technical support. The 600-MHz NMR facilities used in this work are operated by City College and the CUNY Institute for Macromolecular Assemblies, with additional infrastructural support provided by National Institutes of Health Grant 3G12MD007603-30S2 from the National Institute on Minority Health and Health Disparities of the National Institutes of Health.
Funding Information:
This work was supported by National Institutes of Health Grant R01-AI052733 (to A. C. and R. E. S.). The authors declare that they have no conflicts of interest with the contents of this article. The content is solely the respon-sibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2020 Chrissian et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2020
Y1 - 2020
N2 - Cryptococcus neoformans and Cryptococcus gattii are two species complexes in the large fungal genus Cryptococcus and are responsible for potentially lethal disseminated infections. These two complexes share several phenotypic traits, such as production of the protective compound melanin. In C. neoformans, the pigment associates with key cellular constituents that are essential for melanin deposition within the cell wall. Consequently, melanization is modulated by changes in cell-wall composition or ultrastructure. However, whether similar factors influence melanization in C. gattii is unknown. Herein, we used transmission EM, biochemical assays, and solid-state NMR spectroscopy of representative isolates and “leaky melanin” mutant strains from each species complex to examine the compositional and structural factors governing cell-wall pigment deposition in C. neoformans and C. gattii. The principal findings were the following. 1) C. gattii R265 had an exceptionally high chitosan content compared with C. neoformans H99; a rich chitosan composition promoted homogeneous melanin distribution throughout the cell wall but did not increase the propensity of pigment deposition. 2) Strains from both species manifesting the leaky melanin phenotype had reduced chitosan content, which was compensated for by the production of lipids and other nonpolysaccharide constituents that depended on the species or mutation. 3) Changes in the relative rigidity of cellwall chitin were associated with aberrant pigment retention, implicating cell-wall flexibility as an independent variable in cryptococcal melanin assembly. Overall, our results indicate that cell-wall composition and molecular architecture are critical factors for the anchoring and arrangement of melanin pigments in both C. neoformans and C. gattii species complexes.
AB - Cryptococcus neoformans and Cryptococcus gattii are two species complexes in the large fungal genus Cryptococcus and are responsible for potentially lethal disseminated infections. These two complexes share several phenotypic traits, such as production of the protective compound melanin. In C. neoformans, the pigment associates with key cellular constituents that are essential for melanin deposition within the cell wall. Consequently, melanization is modulated by changes in cell-wall composition or ultrastructure. However, whether similar factors influence melanization in C. gattii is unknown. Herein, we used transmission EM, biochemical assays, and solid-state NMR spectroscopy of representative isolates and “leaky melanin” mutant strains from each species complex to examine the compositional and structural factors governing cell-wall pigment deposition in C. neoformans and C. gattii. The principal findings were the following. 1) C. gattii R265 had an exceptionally high chitosan content compared with C. neoformans H99; a rich chitosan composition promoted homogeneous melanin distribution throughout the cell wall but did not increase the propensity of pigment deposition. 2) Strains from both species manifesting the leaky melanin phenotype had reduced chitosan content, which was compensated for by the production of lipids and other nonpolysaccharide constituents that depended on the species or mutation. 3) Changes in the relative rigidity of cellwall chitin were associated with aberrant pigment retention, implicating cell-wall flexibility as an independent variable in cryptococcal melanin assembly. Overall, our results indicate that cell-wall composition and molecular architecture are critical factors for the anchoring and arrangement of melanin pigments in both C. neoformans and C. gattii species complexes.
UR - http://www.scopus.com/inward/record.url?scp=85079472528&partnerID=8YFLogxK
U2 - 10.1074/jbc.RA119.011949
DO - 10.1074/jbc.RA119.011949
M3 - Article
C2 - 31896575
AN - SCOPUS:85079472528
SN - 0021-9258
VL - 295
SP - 1815
EP - 1828
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 7
ER -