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. 2011 Apr;157(1-4):111–115. doi: 10.1016/j.virusres.2011.01.010

Table 1.

Sweet potato chlorotic stunt virus isolates used in this study and sequence accession numbers. Strain was determined by serology using antiserum MAb mix 1 and mix 2 (Gutierrez et al., 2003) for isolates 1–19 and by sequence analysis of hsp70h for isolates 20 and 21. Presence or absence of p22 was determined by PCR-RFLP as described in materials and methods and confirmed by sequencing in selected cases.

SPCSV Isolate Origin Strain p22 RNA1 3′-UTR RNA2 3′-UTR RNA2 5′-UTR
(1) m2-47 Cañete, Peru EA NO HQ291259 HQ291260 HQ291260
(2) Set2 San Ramon, Peru EA NO
(3) Set4 San Ramon, Peru EA NO
(4) Pelotas Pelotas, Brazil WA NO
(5) EL El Indio, Argentina WA NO HQ847524
(6) Arg Cordoba, Argentina WA NO HQ847529 HQ847534
(7) Africa10 Kenya EA NO HQ847523
(8) SR San Ramon, Peru EA NO
(9) Fe Ferreñafe, Peru EA NO
(10) Fio Cañete, Peru EA NO HQ847528 HQ847533 HQ847522
(11) KmtMil Cañete, Peru EA NO
(11) m2-41 Cañete, Peru EA NO
(12) m2-44 Cañete, Peru EA NO
(13) m2-63 Cañete, Peru EA NO
(14) C14 Cañete, Peru EA NO
(15) C18 Cañete, Peru EA NO
(16) C21 Cañete, Peru EA NO
(17) Hua Huaral, Peru EA NO HQ847520
(18) Chi4 Chimbote, Peru EA NO HQ847527 HQ847532 HQ847521
(19) Chi2 Chimbote, Peru EA NO
(20) KSR675 Kisoro, Uganda EA YES HQ847530 HQ847535 HQ847525
(21) Bitambi Masaka, Uganda EA YES HQ847531 HQ847536 HQ847526