Hai-Li Qiao

Dr. Hai-Li Qiao

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100193, China

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
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MYMeng Ke Yang
Meng Ke Yang
HLHuanle Li
Huanle Li
Hai-Li QiaoHai-Li Qiao
Hai-Li Qiao
KGKun Guo
Kun Guo
RXRong Xu
Rong Xu
CXChang-Qing Xu
Chang-Qing Xu
Galls have become the best model for exploring plant–gall inducer relationships, with most studies focusing on gall-inducing insects but few on gall mites. The gall mite Aceria pallida is a major pest of wolfberry, usually inducing galls on its leaves. For a better understanding of gall mite growth and development, the dynamics of the morphological and molecular characteristics and phytohormones of galls induced by A. pallida were studied by histological observation, transcriptomics and metabolomics. The galls developed from cell elongation of the epidermis and cell hyperplasia of mesophylls. The galls grew quickly, within 9 days, and the mite population increased rapidly within 18 days. The genes involved in chlorophyll biosynthesis, photosynthesis and phytohormone synthesis were significantly downregulated in galled tissues, but the genes associated with mitochondrial energy metabolism, transmembrane transport, carbohydrates and amino acid synthesis were distinctly upregulated. The levels of carbohydrates, amino acids and their derivatives, and indole-3-acetic acid (IAA) and cytokinins (CKs), were markedly enhanced in galled tissues. Interestingly, much higher contents of IAA and CKs were detected in gall mites than in plant tissues. These results suggest that galls act as nutrient sinks and favor increased accumulation of nutrients for mites, and that gall mites may contribute IAA and CKs during gall formation.

13 July 2023 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
EHEnhua Hao
Enhua Hao
XYXi Yang
Xi Yang
MMMei Ma
Mei Ma
Pengfei LuPengfei Lu
Pengfei Lu
Hai-Li QiaoHai-Li Qiao
Hai-Li Qiao

Verified
Journal Article
Open access
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RFRu Feng
Ru Feng
HWHongshuang Wei
Hongshuang Wei
RXRong Xu
Rong Xu
SLSai Liu
Sai Liu
JWJian he Wei
Jian he Wei
CXChang-Qing Xu
Chang-Qing Xu
The medicinal plant Cistanche deserticola Ma (Orobanchaceae) is a holoparasitic angiosperm that takes life-essential materials from Haloxylon ammodendron (C. A. Mey.) Bunge (Amaranthaceae) roots. Although many experiments have been conducted to improve the quality of C. deserticola, little attention has been paid to the host’s influence on metabolite accumulation. In this study, transcriptomic and metabolomic analyses were performed to unveil the host’s role in C. deserticola’s metabolite accumulation, especially of phenylethanoid glycosides (PhGs). The results indicate that parasitism by C. deserticola causes significant changes in H. ammodendron roots in relation to metabolites and genes linked to phenylalanine metabolism, tryptophan metabolism and phenylpropanoid biosynthesis pathways, which provide precursors for PhGs. Correlation analysis of genes and metabolites further confirms that C. deserticola’s parasitism affects PhG biosynthesis in H. ammodendron roots. Then we found specific upregulation of glycosyltransferases in haustoria which connect the parasites and hosts. It was shown that C. deserticola absorbs PhG precursors from the host and that glycosylation takes place in the haustorium. We mainly discuss how the host resists C. deserticola parasitism and how this medicinal parasite exploits its unfavorable position and takes advantage of host-derived metabolites. Our study highlights that the status of the host plant affects not only the production but also the quality of Cistanches Herba, which provides a practical direction for medicinal plant cultivation.

7 March 2023 in Arthropod Structure & Development
Verified
Journal Article
Closed access
EHEnhua Hao
Enhua Hao
RLRui Liu
Rui Liu
RXRuirui Xu
Ruirui Xu
Pengfei LuPengfei Lu
Pengfei Lu
Hai-Li QiaoHai-Li Qiao
Hai-Li Qiao

16 May 2023 in Insects
Verified
Journal Article
Open access
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KSKe-Xin Song
Ke-Xin Song
JWJiang-Yue Wang
Jiang-Yue Wang
Hai-Li QiaoHai-Li Qiao
Hai-Li Qiao
HWHongshuang Wei
Hongshuang Wei
KGKun Guo
Kun Guo
CXChang-Qing Xu
Chang-Qing Xu
Sexual generation is an important generation in the life cycle of host-alternating aphids, and its population size determines the intensity of the peak in the next spring. Although male trapping techniques based on olfactory stimuli have been successfully established in the field, the biological basis of olfactory perception in males is unclear. In this study, we compared the morphology of antennae and the types, sizes, numbers, and distribution of sensilla between males and sexual females in the host-alternating aphid Semiaphis heraclei (Hemiptera: Aphididae). We found that flagellum length differentiation contributed to the majority of the sexual dimorphism of antennae. Most sensillum types or subtypes, including trichoid sensilla subtype I, campaniform sensilla, and primary rhinaria subtypes I and II, were enlarged in males. In addition, males bore more trichoid sensilla subtype I than sexual females. In particular, secondary rhinaria were present in males only and could not be detected in sexual females. These results revealed the structural basis of male olfactory perception. Our findings provide insight into the mechanism underlying chemical communication between sexual aphids and could thus be useful for pest control.

21 October 2022 in Insects
Verified
Journal Article
Open access
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Pengfei LuPengfei Lu
Pengfei Lu
EHEnhua Hao
Enhua Hao
MBMin Bao
Min Bao
RLRui Liu
Rui Liu
CGCiyuan Gao
Ciyuan Gao
Hai-Li QiaoHai-Li Qiao
Hai-Li Qiao
To protect vulnerable trees from native and invasive wood wasps, the mating behavior of these two woodwasp species (S. noctilio and S. nitobei, respectively) and factors influencing this behavior were investigated in cages outdoors. Male-produced pheromones were identified in both woodwasp species. Compared with the native species S. nitobei, the invasive species S. noctilio showed stronger mating ability, including mating frequency, time, and duration. The mating behavior of both species mainly occurred from 9:00 to 17:00 each day, peaking at 11:00 and 12:00. The daily mating behavior of both species was most directly related to light intensity. Both female and male S. noctilio and S. nitobei were capable of mating upon emergence, and most individuals mated at 2 days of age. For both species, a female-to-male ratio of 5:15 was most conducive to mating, and individuals with a larger body size were preferred as mates by males and females. (Z)-3-decenol was present in solid-phase microextraction extracts of both species. Two reported minor reference components, (Z)-4-decen-1-ol and (E, E)-2,4-decadienal, were not identified in either woodwasp species. The peak of male pheromone release occurred from 11:00–12:00 for 2-day-old individuals.