A Quadruplex qPCR for Detection and Differentiation of Classic and Natural Recombinant Myxoma Virus Strains of Leporids

• Published in: International journal of molecular sciences 2021-11, Vol.22 (21), p.12052
• Main Authors: Abade Dos Santos, Fábio A, Carvalho, Carina L, Parra, Francisco, Dalton, Kevin P, Peleteiro, Maria C, Duarte, Margarida D
• Format: Article
• Language: English
• Subjects: Animals; Animals, Wild; Diagnosis, Differential; Differential diagnosis; Gene Transfer, Horizontal - genetics; Genes; Genomes; Infections; Laboratories; Lagomorpha - virology; Molecular Typing - methods; Molecular Typing - veterinary; Multiplexing; Myxoma; Myxoma virus - classification; Myxoma virus - genetics; Myxomatosis; Myxomatosis, Infectious - diagnosis; Myxomatosis, Infectious - virology; Pathogens; Polymerase chain reaction; Rabbits; Real time; Real-Time Polymerase Chain Reaction - methods; Real-Time Polymerase Chain Reaction - veterinary; Reproducibility of Results; rRNA 18S; Sensitivity and Specificity; Spain; Strains (organisms); Viruses
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms222112052

A natural recombinant myxoma virus (referred to as ha-MYXV or MYXV-Tol08/18) emerged in the Iberian hare ( ) and the European rabbit ( ) in late 2018 and mid-2020, respectively. This new virus is genetically distinct from classic myxoma virus (MYXV) strains that caused myxomatosis in rabbits until then, by acquiring an additional 2.8 Kbp insert within the gene that disrupted it into ORFs and . To distinguish ha-MYXV from classic MYXV strains, we developed a robust qPCR multiplex technique that combines the amplification of the m000.5L/R duplicated gene, conserved in all myxoma virus strains including ha-MYXV, with the amplification of two other genes targeted by the real-time PCR systems designed during this study, specific either for classic MYXV or ha-MYXV strains. The first system targets the boundaries between ORFs and , only contiguous in classic strains, while the second amplifies a fragment within gene , only present in recombinant MYXV strains. All amplification reactions were validated and normalized by a fourth PCR system directed to a housekeeping gene ( ) conserved in eukaryotic organisms, including hares and rabbits. The multiplex PCR (mPCR) technique described here was optimized for and systems allowing the detection of as few as nine copies of viral DNA in the sample with an efficiency > 93%. This real-time multiplex is the first fast method available for the differential diagnosis between classic and recombinant MYXV strains, also allowing the detection of co-infections. The system proves to be an essential and effective tool for monitoring the geographical spread of ha-MYXV in the hare and wild rabbit populations, supporting the management of both species in the field.