I |
Ia, Ib, Ic |
Australia, Africa, Europe, US, Asia |
Low virulence, Ulster, V4 |
II |
- |
North and South America, Africa, Asia, and Europe |
Avirulent, lentogenic, Lasota, B1 |
III |
- |
Japan and Australia, Taiwan, Zimbabwe |
Ancient strains but still emerging, mesogenic Mukteshwar |
IV |
- |
Europe, Africa, Asia |
Virulent, Herts/33 (UK) |
V |
Va, Vb, Vc, Vd |
South America, Europe, and Africa |
Virulent, Anhinga (US) |
VI |
VIa, VIb, VIc, VId, VIe, VIf, VIg, VIh, |
Europe, Asia, Africa, South America |
Pigeon paramyxoviruses |
VII |
VIIa, VIIb, VIIc,, VIId, VIIe, VIIf, VIIg, VIIh, VIIi |
Emerged in Far East in 1990, spread to Europe and Asia, Africa. |
Virulent, 4th Newcastle disease panzootic virus, 5th panzootic virus |
VIII |
- |
South Africa, Asia |
Highly virulent, AF22440 |
IX |
- |
First isolated in China in 1948 |
Highly virulent |
X |
- |
Taiwan, Argentina, USA |
Virulent |
XI |
- |
Madagascar |
Virulent, restricted distribution |
XII |
- |
South America and China |
Virulent |
XIII |
XIIIa, XIIIb, XIIIc |
Asia, Europe, and Africa |
Virulent, continuously emerging |
XIV |
XIVa, XIVb |
West Africa |
Highly virulent, recovered from domestic birds only |
XV |
- |
China |
Originated from mixed virulent and vaccine viruses |
XVI |
- |
Europe in the 1940s, Africa and Asia in 1980s |
Highly related to genotype IV |
XVII |
XVIIa, XVIIb |
West and Central Africa |
Highly virulent, continuously emerging evolving |
XVIII |
XVIIIa, XVIIIb |
West Africa |
Highly virulent |