The 861 nucleotides (nt) consensus sequence for MrNV using Sri Widada et al.’s (2003) primers was generated from 12 overlapping reads. With Yoganandhan et al.’s (2006) primers, the 682 nt consensus sequence was generated from 5 reads. The 508 nt consensus sequence for XSV using
Sri Widada et al.’s (2004) primers was from 8 reads. MrNV sequences from GenBank were trimmed to be the same number of nt as the Australian isolate, and ClustalW2 with a neighbour-joining
algorithm was then used to produce the phylograms