“…The widespread pathological findings in skin, subcutaneous tissue, and multiple internal organs were in line with the observation of high viral loads, with a median of 5.11 ϫ 10 6 copies of AnaPV RNA per mg of tissue, in skin, kidney, liver, thyroid, lung, heart, pancreas, and gastrointestinal specimens obtained from the dead green anaconda juveniles (Table 2), and the in vitro characteristic of the virus to replicate in a large variety of cell lines from various organs and tissues (see Table S1 in the supplemental material). This pathogenic characteristic of AnaPV is similar to that observed for FDLV, which was originally discovered in a common lancehead snake during a disease outbreak in a snake farm in Zurich, Switzerland, in 1972, as well as other paramyxovirus-like agents isolated from a variety of reptile species causing epizootics with high mortality rates in snakes and other reptiles (26)(27)(28)(29)(30). Notably, the internal organs that showed the most serious pathologies in the anaconda juveniles infected by AnaPV were the kidneys, whereas the organs that were most severely affected by FDLV were the lungs (18,31,32).…”