RÉSUMÉ
The encephalitic alphaviruses encode nsP2 protease (nsP2pro), which because of its vital role in virus replication, represents an attractive target for therapeutic intervention. To facilitate the discovery of nsP2 inhibitors we have developed a novel assay for quantitative measurement of nsP2pro activity in a cell-based format. The assay is based on a substrate fusion protein consisting of eGFP and Gaussia luciferase (Gluc) linked together by a small peptide containing a VEEV nsp2pro cleavage sequence. The expression of the substrate protein in cells along with recombinant nsP2pro results in cleavage of the substrate protein resulting in extracellular release of free Gluc. The Gluc activity in supernatants corresponds to intracellular nsP2pro-mediated substrate cleavage; thus, providing a simple and convenient way to quantify nsP2pro activity. Here, we demonstrate potential utility of the assay in identification of nsP2pro inhibitors, as well as in investigations related to molecular characterization of nsP2pro.
Sujet(s)
Techniques de culture cellulaire , Cysteine endopeptidases/métabolisme , Virus de l'encéphalite équine du Venezuela/enzymologie , Dosages enzymatiques/méthodes , Séquence d'acides aminés , Antiviraux/pharmacologie , Lignée cellulaire , Cysteine endopeptidases/composition chimique , Cysteine endopeptidases/génétique , Découverte de médicament/méthodes , Virus de l'encéphalite équine du Venezuela/effets des médicaments et des substances chimiques , Activation enzymatique/effets des médicaments et des substances chimiques , Antienzymes/pharmacologie , Expression des gènes , Ordre des gènes , Gènes rapporteurs , Vecteurs génétiques , Tests de criblage à haut débit , Humains , Protéines de fusion recombinantes/génétique , Protéines de fusion recombinantes/métabolismeRÉSUMÉ
Oropouche (ORO) virus, a member of the Simbu serogroup, is one of the few human pathogens in the Orthobunyavirus genus in the family Bunyaviridae. Genetic analyses of ORO-like strains from Iquitos, Peru, identified a novel reassortant containing the S and L segments of ORO virus and the M segment of a novel Simbu serogroup virus. This new pathogen, which we named Iquitos (IQT) virus, was first isolated during 1999 from a febrile patient in Iquitos, an Amazonian city in Peru. Subsequently, the virus was identified as the cause of outbreaks of "Oropouche fever" during 2005 and 2006 in Iquitos. In addition to the identification of 17 isolates of IQT virus between 1999 and 2006, surveys for neutralizing antibody among Iquitos residents revealed prevalence rates of 14.9% for ORO virus and 15.4% for IQT virus. Limited studies indicate that prior infection with ORO virus does not seem to protect against disease caused with the IQT virus infection. Identification of a new Orthobunyavirus human pathogen in the Amazon region of Peru highlights the need for strengthening surveillance activities and laboratory capabilities, and investigating the emergence of new pathogens in tropical regions of South America.