Year of detection | Strain name/GenBank accession number | Polymerase genotype | Capsid genotype | Breakpoint: SimPlot/x2 | Estimated P-value (x2) | GenBank accession number of most closely related NoV strain (%identity/%coverage)# | Worldwide detection# |
---|---|---|---|---|---|---|---|
2010 | Johannesburg 6108 KC962457 | GII.P21 | GII.3 | ā16/+56* | 2.154 Ć 10ā13 | JX439787 (98%/99%)a | China, India, Korea |
2010 | Bushbuckridge 6387 KC962458 | GII.P NA | GII.3 | ND | ND | KC597144 (89%/99%)b | Novel polymerase region |
2011 | Cape Town 6745 KJ710245 | GII.P4 New Orleans 2009 | GII.4 NA | ND | ND | JX448566 (96%/99%)c | Novel capsid region |
2011 | Cape Town 6799 KC962459 | GII.Pg | GII.1 | ā27/-88 | 1.608 Ć 10ā4 | JN797508 (93%/99%)a | Europe, US |
2011 | Empangeni 7299 KC962460 | GII.P16 | GII.17 | ā6/+17 | 1.610 Ć 10ā15 | JX683114 (93%/99%)a | Novel recombinant |
2011 | Cape Town 8179 KM025143 | GII.Pe | GII.4 Osaka 2007 | ND | ND | GQ845369 (97%/99%)c | Australia, India, Japan, US |
2011 | Pietermaritzburg 8412 KC962461 | GII.P21 | GII.2 | ā29/+14 | 1.846 Ć 10ā13 | AY682549 (96%/97%)a | France |
2012 | Empangeni 8491 KC962462 | GII.P4 New Orleans 2009 | GII.4 Sydney 2012 | ā15/-61 | 1.767 Ć 10ā3 | KF509947 (96%/99%)c | Australia, Canada, Europe, Asia, US |
2012 | Bushbuckridge 9306 KJ710246 | GII.Pg | GII.12 | ā29/+68 | 9.441 Ć 10ā9 | JQ613568 (98%/99%)a | Asia, Australia, Europe, US |
2012 | Johannesburg 9814 KJ710247 | GII.Pe | GII.4 Sydney 2012 | ā59/+20 | 8.515 Ć 10ā15 | KF145148 (98%/99%)c | Worldwide |
2013 | Johannesburg 130930 KJ710248 | GII.P7 | GII.6 | ā54/-36 | 8.238 Ć 10ā10 | KJ407072 (96%/98%)a | Japan, US |