01%) or on water agar with subsequent transfer to CPA (JKI method

01%) or on water agar with subsequent transfer to CPA (JKI method). For single zoospore cultures, 20 ml sterile water was added to a 10-day-old V8 culture. The sporangia suspension was then put at 2–8°C for 1 h to release zoospores. After 30 min at room temperature,

plating was carried out at a concentration of 50 zoospores per ml on V8. The plates were incubated overnight at 20–22°C in the dark, and single zoospore cultures were transferred to new plates. At CRAW, mycelium plugs from V8-cultures were stored in sterile water at 13°C. Between 2002 and 2007, isolates were transferred every 6 months onto fresh medium. From 2008 onwards, they were subcultured yearly. At JKI, long-term storage was carried out on oatmeal Vemurafenib datasheet agar (40 g/l), under paraffin PD-0332991 ic50 oil (16–17°C, in the dark) and on oatmeal agar with glycerine (50 ml/l of a 87% glycerine solution) in liquid nitrogen. New liquid nitrogen and paraffin oil storage cultures were prepared in 2004, 2007 and 2009. At ILVO, isolates were stored in sterile water as described for CRAW but at 4–8°C. Isolates kept under these long-term storage conditions were transferred every 1–3 years. At CRAW and ILVO, mating type determination was carried out using the method of Brasier and Kirk (2004) using

tester strains 2299 (A1) and 3237 (A2) at CRAW and PR/D/02/2084 (A1) and PRI480 (A2) at ILVO. At JKI, crossings were performed on CPA with complementary strains from four heterothallic species (Werres et al. 2001). In 2011, mating type determinations were replicated in each of the three laboratories. In 2006, during a mating type survey performed at CRAW, isolate 2545 (which was reisolated from A. glutinosa sapling inoculated

with the isolate 2338 in 2003) was found to have reverted to A1. In contrast, other isolates derived from isolate 2338 after inoculation on different tree species Pembrolizumab concentration (i.e. isolates 2531, 2533, 2546) were still A2. Isolate 3237 (derived from BBA26/02 and put in the CRAW collection in 2005) conserved its A2 mating type. Isolate 2386 (A1 in 2002) remained A1 (Table 1). In 2011, the mating type of all isolates was identified. Reference A1 isolates BBA27/02 and PR/D/02/2084 were still A1 (Table 1). Isolate 2338 (maintained for 9 years in the CRAW collection and originally A2) was found to be A1. Moreover, BBA26/02, an A2 isolate maintained at JKI since 2003, was also found to be A1. Isolates 3237, 2533, 2546 as well as the two other Belgian EU1 A2 isolates identified in 2003 at ILVO and the American isolates PRI480 and BBA Pr01 were still A2 (Table 1). Six single zoospore cultures were produced from isolate 2338 and from two other strains that conserved their initial A2 mating type (2546 and PR/D/02/2340). All single zoospore cultures displayed the same mating type as their corresponding parental isolate.

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