We have investigated the mitotic and meiotic transmission of chromosom
e-length polymorphisms in Ophiostoma ulmi s.l., the causal agent of Du
tch elm disease. The North-American aggressive (NAN) strain CESS16K ha
s an atypical electrophoretic karyotype, carrying two chromosome-sized
DNAs (chDNAs) that have not been observed in other members of the NAN
biotype. Independent CESS 16K chDNA preparations, even after repeated
inoculation and recovery from the elm host, and analysis of 16 progen
y strains after a cross between the NAN strains FG245B(r)-O and CESS 1
6K, demonstrated that these unique chDNAs are integral components of t
he CESS 16K genome. Analysis of the progeny, by electrophoretic karyot
yping and hybridizations with probes specific to individual chDNAs, pr
esented evidence that genome rearrangements can occur as a consequence
of meiosis. Even though novel electrophoretic karyotypes and a novel-
sized chromosome were observed in the karyotypes of the progeny strain
s, the low level of reassortment between the chromosomes carrying leng
th polymorphisms presented evidence that there are constraints to geno
me plasticity for this fungus.