MAPK基因MaHog1影响绿僵菌的逆境敏感性和毒力
MaHog1, a Hog1-type MAP kinase gene, contributes to stress tolerance and virulence of the entomopathogenic fungus, Metarhizium acridum
真菌杀虫剂在害虫综合防治应用中具有较大潜力。但防效低对环境敏感等不足限制了其广泛应用。研究表明,Hog1激酶在细胞应对逆境过程中起重要作用。MaHog1(EFY85878)是从绿僵菌中克隆得到的一个编码Hog1的基因,序列分析表明该基因属于Hog1/Sty1/p38 MAPK家族。将该基因敲除后发现,突变体对高温、高渗、氧胁迫等敏感性增加,而对细胞壁破坏剂敏感性降低,暗示MaHog1与绿僵菌的细胞壁合成相关。生物测定结果表明MaHog1突变体毒力显著低于野生型菌株,进一步研究发现MaHog1突变体在蝗虫翅膀上的萌发率及附着胞形成率显著降低,在蝗虫血淋巴中的生长速率显著下降,推测可能与侵染寄主过程中MaHog1突变体对逆境的耐受性降低有关。
Fungal biocontrol agents have great potential in integrated pest management. However, the poor efficacy and secnsitiveness to various adversities have hampered their wide application. In eukaryotic cells, Hog1 kinase play a critical role in stress responses. In this study, MaHog1 (GenBank accession number EFY85878) encodeing a member of the Hog1/Sty1/p38 MAPK family was identified from M. acridum. Targeted gene disruption was adopted to analyze the role of MaHog1 in virulence and tolerance to adverse factors. Mutant depleted for MaHog1 showed increased sensitivity to high osmotic stress, high temperature and oxidative stress and exhibited remarkable resistance to the cell wall disturbing agents. These results suggested that Hog1 kinase has conserved function in regulating multistress responses among fungi, and that MaHog1 might influence the cell wall biogenesis in M. acridum. Bioassays conducted with topical inoculation and intrahaemocoel injection revealed that MaHog1 is required for both the penetration and the postpenetration development of M. acridum. Disruption of MaHog1 resulted in a signi?cant reduction in virulence, likely due to the combination of a decrease in conidial germination, a reduction in appressorium formation, and a decline in growth rate in insect haemolymph, which might be caused by impairing the fungal tolerance to various stresses during infection.
金凯、夏玉先、明月
微生物学分子生物学遗传学
微生物学昆虫病原真菌MaHog1抗逆性毒力
Microbiologyentomopathogenic fungusMaHog1stress tolerancevirulence
金凯,夏玉先,明月.MAPK基因MaHog1影响绿僵菌的逆境敏感性和毒力[EB/OL].(2012-09-10)[2025-08-10].http://www.paper.edu.cn/releasepaper/content/201209-84.点此复制
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