Abstract:A total of 397 Trichoderma isolates were obtained from the different soil samples collected from some greenhouse vegetable fields of Hebei Province. Using traditional morphological classification and ITS sequences analysis methods, eleven Trichoderma species, Trichoderma longibrachiatum, T.atroviride, T.harzianum, T.viren, T.minutisporum, T.pseudokoningii, T.aureoviride, T.inhamatum, T.asperellum, T.longipile and T.helicum, were identified. Twenty strains were clustered into 5 groups based on rDNA-ITS sequences on phylogenetic tree. Additionally, genetic diversity of Trichoderma isolates was analyzed using universally primed PCR (UP-PCR). The result indicated that a total of 46 bands appeared after amplification by using 5 primers, 43 bands (93.5%) of which were polymorphic. Twenty-four Trichoderma isolates were classified into 9 groups at the similarity coefficient of 0.80 by UP-PCR cluster analysis. Our results indicated that UP-PCR could reflect the genetic relationships and differences of Trichoderma species, and could be used as an assistant method for Trichoderma classification.