“…To identify viruses, RNA was extracted from isolates using a QIAampViral RNA mini kit (Qiagen, Germantown, MD, USA), eluted in a nal volume of 70 μl. A reverse transcription polymerase chain reaction (RT-PCR) was performed in a 25 μl reaction using a Titan onetube RT-PCR system (Roche Diagnostics, Indianapolis, IN, USA) with generic orthobunyavirus primers [10,12]. Ampli cation products of the appropriate size, were puri ed as per Eastwood et al [10], then commercially sequenced (Science Hill DNA Analysis Facility, Yale University, New Haven, CT, USA).…”