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𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴 uses a surface protein of its spores to slow down the human immune system
The mold 𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴 produces an enzyme on the surface of its spores with which it can attenuate the human immune response. This makes it easier for for the fungus to colonize human tissue with severe courses of infection. An international research team has now published the results in 𝘕𝘢𝘵𝘶𝘳𝘦 𝘔𝘪𝘤𝘳𝘰𝘣𝘪𝘰𝘭𝘰𝘨𝘺.
𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴 is a mold that is found all over the world. Unlike closely related species, it can cause serious, often fatal infections in humans. What makes 𝘈. 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴 so dangerous? An international research team led by Gustavo Goldman from the University of São Paulo in Brazil has found clues to the cause: a special enzyme on the surface of the fungal spores – glycosylasparaginase – apparently suppresses the release of pro-inflammatory substances by immune cells, making it easier for the pathogen to spread unhindered in the tissue.
“Gustavo Goldman’s group was particularly interested in the surface proteins on the spores, as these are the first to come into contact with the immune system – usually through inhalation,” reports Olaf Kniemeyer from the Leibniz Institute for Natural Product Research and Infection Biology – Hans Knöll Institute (Leibniz-HKI), the German partner of the study. Kniemeyer is a proteomics expert. Together with his team, he analyzes all the proteins in a cell and assigns functions to them. This is how he finds potential targets for new active substances. The researchers from Jena also specialize in phagocytosis, a defence mechanism in which immune cells devour foreign invaders. This also enabled the international research team to study the interaction of the fungus with immune cells.
𝗔𝗻 𝗲𝗻𝘇𝘆𝗺𝗲 𝗶𝗻𝘁𝗲𝗿𝗳𝗲𝗿𝗲𝘀 𝘄𝗶𝘁𝗵 𝘁𝗵𝗲 𝘀𝗶𝗴𝗻𝗮𝗹
In the current study, they used an approach called trypsin shaving: with the help of trypsin, a protein-cleaving enzyme, they removed all proteins from the spore surface and analyzed their fragments in a mass spectrometer. Using database comparisons, they were able to identify 62 proteins that only occur on the spores of 𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴, but not on closely related species. Some of them could therefore play a role in the infection process. To test this, the researchers created a knockout library with 42 mutants of the fungus, in each of which a gene coding for one of these proteins was switched off. The mutant that lacked the glycosylasparaginase triggered an increased release of interleukin-1β in immune cells. Interleukins are highly effective proteins that trigger fever, inflammation and a range of other immune reactions even in the smallest of quantities, thus boosting the body’s defense against pathogens. If the glycosylasparaginase on the fungal spores is missing, the immune system can release more of this inflammatory substance. Immune cells are activated and are better able to fight off the fungus. Conversely, this indicates that the glycosylasparaginase produced by the fungus normally helps to dampen the immune response. This allows the fungus to infect the body almost unhindered.
The study in the mouse model supports this hypothesis: in mice with an intact immune system, the fungus was attacked more strongly by the immune system when the gene for glycosylasparaginase was previously switched off. “The glycosylasparaginase on the spores of 𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴 therefore plays a role in the fight against the immune system. However, we cannot yet say exactly how this mechanism works,” says Kniemeyer, summarizing the results of the study.
The findings can help to develop new therapies for infections with 𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴. This is urgently needed, as there are currently only a few effective drugs to combat fungal infections and resistance to them is gradually spreading.
The research work is a demonstration of successful cooperation between institutes and clinics in several countries. In addition to the Brazilian and German researchers, British and US colleagues also contributed significantly to the new findings.
The German side of the study was funded by the German Research Foundation (DFG) in the Collaborative Research Center/Transregio 124 FungiNet, among others.
𝗣𝗮𝗿𝘁𝗶𝗰𝗶𝗽𝗮𝘁𝗶𝗻𝗴 𝗶𝗻𝘀𝘁𝗶𝘁𝘂𝘁𝗶𝗼𝗻𝘀
University of São Paulo, Brazil
National Institute of Science and Technology in Human Pathogenic Fungi, São Paulo, Brazil
Leibniz Institute for Natural Product Research and Infection Biology – Hans Knöll Institute, Jena, Germany
Friedrich Schiller University Jena, Germany
University of Manchester, United Kingdom
Harbor-UCLA Medical Center, Torrance, USA
University of California, Berkeley, USA
Vanderbilt University, Nashville, USA
David Geffen School of Medicine at UCLA, Los Angeles, USA
Dr. Olaf Kniemeyer
Molecular and Applied Microbiology, Leibniz-HKI, Jena, Germany
Deputy head of Department
+49 3641 532-1071
olaf.kniemeyer@leibniz-hki.de
Pinzan CF, Valero C, de Castro PA, da Silva JL, Earle K, Liu H, Horta MAC, Kniemeyer O, Krüger T, Pschibul A, Cömert DN, Heinekamp T, Brakhage AA, Steenwyk JL, Mead ME, Hermsdorf N, Filler SG, da Rosa-Garzon NG, Delbaje E, Bromley MJ, Cabral H, Diehl C, Angeli CB, Palmisano G, Ibrahim AS, Rinker DC, Sauters TJC, Steffen K, Gumilang A, Rokas A, Gago S, Dos Reis TF, Goldman GH (2024) 𝘈𝘴𝘱𝘦𝘳𝘨𝘪𝘭𝘭𝘶𝘴 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴 conidial surface-associated proteome reveals factors for fungal evasion and host immunity modulation. 𝘕𝘢𝘵 𝘔𝘪𝘤𝘳𝘰𝘣𝘪𝘰𝘭, https://doi.org/10.1038/s41564-024-01782-y.
Scanning electron micrograph of a spore carrier of 𝘈. 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴. The numerous spherical spores are k ...
Jeannette Schmaler-Ripcke
Jeannette Schmaler-Ripcke/Leibniz-HKI
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Scanning electron micrograph of a spore carrier of 𝘈. 𝘧𝘶𝘮𝘪𝘨𝘢𝘵𝘶𝘴. The numerous spherical spores are k ...
Jeannette Schmaler-Ripcke
Jeannette Schmaler-Ripcke/Leibniz-HKI
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