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Suresh Mahalingam

Researcher at Griffith University

Publications -  130
Citations -  5650

Suresh Mahalingam is an academic researcher from Griffith University. The author has contributed to research in topics: Virus & Chikungunya. The author has an hindex of 37, co-authored 116 publications receiving 4683 citations. Previous affiliations of Suresh Mahalingam include Indian Institute of Technology Madras & RMIT University.

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Arthritogenic alphaviruses: new insights into arthritis and bone pathology

TL;DR: This review aims to provide insights into alphavirus-induced bone loss and focuses on aspects of disease exacerbation in patients with underlying arthritis and on possible therapeutic targets.
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Pentosan Polysulfate: a Novel Glycosaminoglycan-Like Molecule for Effective Treatment of Alphavirus-Induced Cartilage Destruction and Inflammatory Disease

TL;DR: PPS is a promising new therapy for alphvirus-induced arthritis, acting to preserve the cartilage matrix, which is damaged during alphavirus infection, and demonstrates the potential of glycotherapeutics as a new class of treatment for infectious arthritis.
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The Immunobiology of viral arthritides

TL;DR: Evidence from mouse models suggests targeting MCP-1 or complement may emerge as viable new treatment options for viral arthritides, and the challenge for new treatments is to target excessive inflammation without compromising anti-viral immunity.
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Alphavirus-induced hyperactivation of PI3K/AKT directs pro-viral metabolic changes.

TL;DR: This work investigates how two alphaviruses, Semliki Forest virus and Ross River virus, reprogram host metabolism and defines the molecular mechanisms responsible and demonstrates that in both cases the presence of a YXXM motif in the viral protein nsP3 is necessary for binding to the PI3K regulatory subunit p85 and for activating AKT.
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Lower temperatures reduce type I interferon activity and promote alphaviral arthritis.

TL;DR: It is shown that CHIKV replication and the ensuing foot arthropathy were dramatically reduced when mice were housed at 30°C, rather than the conventional 22°C; this may provide an explanation for why alphaviral arthropathies are largely restricted to joints of the limbs and the extremities.