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. 2007 Mar 9;73(9):2911–2918. doi: 10.1128/AEM.02176-06

TABLE 1.

Phaeoacremonium isolates used in this study

Phaeoacremonium species No. of isolates GenBank accession no.a Origin Yr of isolation
P. parasiticum U31841 CBS860.73b,c,d 1973
CBS113591e
2 (1)f Plant nursery in Murcia, Spain 2004
2 (1) Plant nursery in Cataluña, Spain 2005
1 (1) Cataluña, Spain 2005
P. rubrigenum AF118139 CBS498.94c 1994
P. inflatipes AF197990 CBS391.71c,d 1966
CBS166.75e 1974
P. mortoniae AF295328 CBS211.97e
CBS101585c,d 1998
P. viticola AF118137 CBS113065e 2001
CBS101738c,d 1993
1 (1) Cataluña, Spain 2005
P. angustius AF197974g
CBS114992c,d 1992
CBS114991e
P. krajdenii CBS109479d 2001
P. venezuelense CBS651.85d 1974
P. scolyti CBS113593d
CBS113597e 1999
P. aleophilum AF017651 CBS246.91c,d 1996
CBS110753e 1998
1 Toscana, Italy
16 (1) Ciudad Real, Spain 2003
2 (2) Ciudad Real, Spain 2004
4 Cataluña, Spain 2005
2 Plant nursery in Portugal 2004
5 (1) Plant nursery in Valencia, Spain 2004
1 Plant nursery in Murcia, Spain 2004
2 Plant nursery in Cataluña, Spain 2005
a

GenBank accession numbers of the ITS sequences used to design the primers and the discriminant restriction enzyme digestion patterns.

b

CBS isolates are from the Centraalbureau voor Schimmelcultures, Baarn, The Netherlands.

c

Ex-type strains used to optimize PCR conditions.

d

Ex-type strains used to test PCR-RFLPs.

e

CBS isolates used to validate the identification by PCR-RFLP.

f

The numbers in parentheses are the numbers of field isolates identified by ITS sequences (and β-tubulin for P. viticola) used to validate the identification by PCR-RFLP.

g

ITS sequence of CBS isolate 249.95. This was the original holotype of P. angustius, which was replaced with CBS114992 when lethally contaminated.