Perera Lab

The research of Dr. Rushika Perera’s laboratory in the Center for Vector-Borne Infectious Diseases (CVID), is focused on understanding the impact of cellular metabolism on the replication of mosquito- and tick-borne flaviviruses within their vertebrate hosts and Arthropod vectors. Specifically, we use a systems biology approach including metabolomics and proteomics combined with molecular virology, cell biology, biochemistry and structural biology to study flavivirus-host interactions. Similar to other positive strand RNA viruses, flaviviruses cause significant perturbations to the host metabolome to facilitate the formation of replication factories within specialized membrane structures. These structures are required for viral genome replication, assembly and egress. The host metabolome also fulfills the energy requirements for virus replication. Therefore, it is a key avenue to understand the dynamics of virus-host interactions and provides a novel avenue to identify targets for antiviral intervention. The goal of her research is to identify control points in cellular metabolic pathways that are required for virus replication, and evaluate these control points as novel targets for antiviral intervention.

The Perera Lab supports ‘Diversity’, practices ‘Equity & Inclusion’, ensures ‘Social Justice’.

The Perera Lab abides by Colorado State University’s Principles of Community.

research project

COVID-19: Developing platforms to test antivirals against SARS-CoV-2

The Perera lab (in collaboration with the Geiss Laboratory and the CSU OVPR) has mobilized testing of FDA-approved antiviral drugs that can be repurposed and rapidly driven into clinical trials, as well as new compounds that can be evaluated for efficacy against SARS-CoV-2. We are currently working with collaborators and partners from around the world to screen their drug and compound inventories.

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research project

Metabolite biomarkers of severe disease, resolution and therapeutic efficacy

We utilize Systems Biology based-metabolomics to develop small molecule biosignatures of severe disease. These biosignatures can be utilized for early detection and triaging of patients, to better assist clinical management of those at greater risk. They are also powerful indicators of disease resolution, recurrence and/or therapeutic efficacy.

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research project

Metabolic basis of mosquito-endosymbiont-virus interactions

These studies will identify biochemical pathways that change in the mosquito following infection with arboviruses, and how the endosymbiont Wolbachia used to control virus transmission in Aedes aegypti may be metabolically competing with the virus. Identifying these pathways that are integral to mosquito biology, provide a novel avenue to interfere with vector transmission of the virus.

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research project

Exploiting Vulnerabilities in Mosquito Metabolism for Prevention of Human Arboviral Transmissions

Zika, dengue, chikungunya and yellow fever viruses are spread by the same mosquito vector, Aedes aegypti. The Perera lab studies specific metabolic processes in mosquitos required for successful viral replication. These studies will identify metabolic “choke-points” that can be exploited to develop interventions and thus block mosquito-human viral transmission.

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research project

Metabolic basis of insecticide resistance

We are investigating the metabolic basis of insecticide resistance in Aedes aegypti. We have developed capability to trace the metabolites of insecticides and measure the enzymatic activities responsible for insecticide break down and development of resistance. These studies will assist in driving improvements in insecticide design and informed use of insecticides.

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The 22nd Annual Meeting of the Rocky Mountain Virology Association.
Ratnayake OC, Gendler P, Swartzwelter B, Keene A, Brehm AL, Quackenbush SL, Rovnak J, Perera R.Viruses. 2022 Dec 29;15(1):98. doi: 10.3390/v15010098.PMID: 36680138

Electrochemical Capillary Driven Immunoassay for Detection of SARS-CoV-2.
Clark KM, Schenkel MS, Pittman TW, Samper IC, Anderson LBR, Khamcharoen W, Elmegerhi S, Perera R, Siangproh W, Kennan AJ, Geiss BJ, Dandy DS, Henry CS.ACS Meas Sci Au. 2022 Dec 21;2(6):584-594. doi: 10.1021/acsmeasuresciau.2c00037. Epub 2022 Aug 30.PMID: 36570470

RNase L activation in the cytoplasm induces aberrant processing of mRNAs in the nucleus.
urke JM, Ripin N, Ferretti MB, St Clair LA, Worden-Sapper ER, Salgado F, Sawyer SL, Perera R, Lynch KW, Parker R.
PLoS Pathog. 2022 Nov 1;18(11):e1010930. doi: 10.1371/journal.ppat.1010930. eCollection 2022 Nov. PMID: 36318584

Expression of fatty acid synthase genes and their role in development and arboviral infection of Aedes aegypti.
Chotiwan N, Brito-Sierra CA, Ramirez G, Lian E, Grabowski JM, Graham B, Hill CA, Perera R.
Parasit Vectors. 2022 Jun 27;15(1):233. doi: 10.1186/s13071-022-05336-1. PMID: 35761349

Acyl-Coa Thioesterases: A Rheostat That Controls Activated Fatty Acids Modulates Dengue Virus Serotype 2 Replication.
St Clair LA, Mills SA, Lian E, Soma PS, Nag A, Montgomery C, Ramirez G, Chotiwan N, Gullberg RC, Perera R.
Viruses. 2022 Jan 25;14(2):240. doi: 10.3390/v14020240. PMID: 35215835

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Rushika Perera, Ph.D.

Lab Principal Investigator (PI)
Associate Professor
Director, Antiviral Testing Laboratory
Co-Director, Center for Metabolism of Infectious Diseases (

Paul Soma, Ph.D.

Research Scientist I
Mass Spectrometist

Hannah Laurence, D.V.M., D.A.C.V.P.

Graduate Research Assistant

Oshani Ratnayaka

Graduate Research Assistant

Jared Goldberg

Student Researcher

Samantha Pinto

Undergraduate Student Researcher

Ryan Thompson

Student Researcher

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