Chunyu Wang

This study systematically evaluated insect resistance in transgenic poplar lines carrying three distinct Bacillus thuringiensis (Bt) gene vector architectures: a single-gene pb vector (Cry1Ac), a reverse-oriented double-gene n19 vector (Cry1Ac-Cry3A), and a forward-oriented double-gene n5 vector (Cry3A-Cry1Ac). The transgenic lines were accordingly designated as pb8/pb9, n19a/n19b, and DB7/DB16, respectively. Molecular analyses confirmed stable Bt gene integration, with the expression of Cry3A being consistently higher than that of Cry1Ac expression. Bioassays showed that dual-gene lines conferred broader insect resistance to pests than that of single-gene lines against both lepidopteran (Hyphantria cunea) and coleopteran (Plagiodera versicolora, Anoplophora glabripennis) pests. In contrast, the single-gene line pb9 exhibited specialized, high efficacy against H. cunea, achieving 100% mortality. Transcriptomic analysis of P. versicolora larvae fed the double-gene high-resistance n19a line and low-resistance DB16 line revealed multi-level molecular responses to Bt stress, including up-regulation of toxin-activating proteases, altered receptor expression, and suppression of growth-related genes. These changes were associated with significant developmental delay (8.33–20.83% reduction in the molting index). Our findings characterize the insect resistance and molecular profiles of the six transgenic poplar lines, as follows: multi-gene lines (n19a/n19b and DB7/DB16) confer broad-spectrum pest resistance, whereas single-gene lines (pb8/pb9) exhibit targeted efficacy. These results support the utility of these lines for pest-specific poplar breeding programs.

With the increasing severity of forest pest problems, breeding insect-resistant varieties has become a crucial task for the sustainable development of forestry. The highly insect-resistant triploid Populus line Pb29, genetically modified with BtCry1Ac, served as the maternal parent in controlled hybridization with three paternal Populus cultivars. Hybrid progenies were obtained through embryo rescue and tissue culture. Results showed that 4 °C storage was favorable for pollen preservation, with 84K poplar exhibiting superior pollen viability and embryo germination rates. All progenies displayed significantly lower seedling height and ground diameter growth than the maternal parent (p < 0.05), with some showing leaf shape and branching variations. Among the three crosses, the 84K-sired progeny exhibited the best growth performance but the highest variability. PCR analysis confirmed stable inheritance of the BtCry1Ac and Kan genes from Pb29, showing tight linkage. Progenies carrying BtCry1Ac exhibited detectable gene transcription and toxic protein accumulation, though expression levels varied due to copy number, insertion sites, and potential co-suppression effects. Ploidy analysis suggested all hybrids were aneuploid, with lower survival rates than the maternal parent. Insect-feeding assays confirmed high resistance in all BtCry1Ac-inheriting progenies, with an average larval mortality rate of 97.03%. Mortality rates and death indices significantly correlated with transcript abundance and toxin protein levels. These results demonstrate that BtCry1Ac insect resistance is stably inherited through hybridization. Transgene expression appears co-modulated by copy number, insertion sites, and ploidy status. Simultaneously, it was found that the aneuploid progeny derived from triploid hybridization exhibited growth disadvantages. This provides an important basis for subsequent poplar improvement breeding.