Hu Li

Dr. Hu Li

Department of Entomology, China Agricultural University, Beijing 100193, China
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

View All Publications
1 January 2018 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
YLYingqi Liu
Yingqi Liu
FSFan Song
Fan Song
PJPei Jiang
Pei Jiang
JWJohn-James Wilson
John-James Wilson
WCWanzhi Cai
Wanzhi Cai
HLHu Li
Hu Li

21 March 2019 in Systematic Entomology
Verified
Journal Article
Closed access
PDF file
YLYingqi Liu
Yingqi Liu
HLHu Li
Hu Li
FSFan Song
Fan Song
YZYisheng Zhao
Yisheng Zhao
JWJohn‐James Wilson
John‐James Wilson
Wanzhi CaiWanzhi Cai
Wanzhi Cai

8 March 2019 in Molecular Biology and Evolution
Verified
Journal Article
Open access
PDF file
ZDZhenyong Du
Zhenyong Du
HHHiroki Hasegawa
Hiroki Hasegawa
JCJohn R Cooley
John R Cooley
CSChris Simon
Chris Simon
JYJin Yoshimura
Jin Yoshimura
HLHu Li
Hu Li
The mass application of whole mitogenome (MG) sequencing has great potential for resolving complex phylogeographic patterns that cannot be resolved by partial mitogenomic sequences or nuclear markers. North American periodical cicadas (Magicicada) are well known for their periodical mass emergence at 17- and 13-year intervals in the north and south, respectively. Magicicada comprises three species groups, each containing one 17-year species and one or two 13-year species. Within each life cycle, single-aged cohorts, called broods, of periodical cicadas emerge in different years, and most broods contain members of all three species groups. There are 12 and three extant broods of 17- and 13-year cicadas, respectively. The phylogeographic relationships among the populations and broods within the species groups have not been clearly resolved. We analyzed 125 whole MG sequences from all broods and seven species within three species groups to ascertain the divergence history of the geographic and allochronic populations and their life cycles. Our mitogenomic phylogeny analysis clearly revealed that each of the three species groups had largely similar phylogeographic subdivisions (east, middle, and west) and demographic histories (rapid population expansion after the last glacial period). The mitogenomic phylogeny also partly resolved the brood diversification process, which could be explained by hypothetical temporary life cycle shifts, and showed that none of the 13- and 17-year species within the species groups was monophyletic, possibly due to gene flow between them. Our findings clearly reveal phylogeographic structures in the three Magicicada species groups, demonstrating the advantage of whole MG sequence data in phylogeographic studies.

29 February 2024 in Nutrients
Verified
Journal Article
Open access
PDF file
HSHuihui Sun
Huihui Sun
YYYu Wenzhen Yu
Yu Wenzhen Yu
HLHu Li
Hu Li
XHXiaosong Hu
Xiaosong Hu
Xiaofei WangXiaofei Wang
Xiaofei Wang
Areca catechu L. is a widely cultivated tropical crop in Southeast Asia, and its fruit, areca nut, has been consumed as a traditional Chinese medicinal material for more than 10,000 years, although it has recently attracted widespread attention due to potential hazards. Areca nut holds a significant position in traditional medicine in many areas and ranks first among the four southern medicines in China. Numerous bioactive compounds have been identified in areca nuts, including alkaloids, polyphenols, polysaccharides, and fatty acids, which exhibit diverse bioactive functions, such as anti-bacterial, deworming, anti-viral, anti-oxidant, anti-inflammatory, and anti-tumor effects. Furthermore, they also display beneficial impacts targeting the nervous, digestive, and endocrine systems. This review summarizes the pharmacological functions and underlying mechanisms of the bioactive ingredients in areca nut. This helps to ascertain the beneficial components of areca nut, discover its medicinal potential, and guide the utilization of the areca nut.

17 November 2020 in Evolutionary Applications
Verified
Journal Article
Open access
PDF file
Zhenyong DuZhenyong Du
Zhenyong Du
YWYunfei Wu
Yunfei Wu
ZCZhuo Chen
Zhuo Chen
LCLiangming Cao
Liangming Cao
TITadashi Ishikawa
Tadashi Ishikawa
HLHu Li
Hu Li
Biological invasion has been a serious global threat due to increasing international trade and population movements. Tracking the source and route of invasive species and evaluating the genetic differences in their native regions have great significance for the effective monitoring and management, and further resolving the invasive mechanism. The spotted lanternflyLycorma delicatulais native to China and invaded South Korea, Japan, and the United States during the last decade, causing severe damages to the fruits and timber industries. However, its global phylogeographic pattern and invasion history are not clearly understood. We applied high‐throughput sequencing to obtain 392 whole mitochondrial genome sequences from four countries to ascertain the origin, dispersal, and invasion history of the spotted lanternfly. Phylogenomic analyses revealed that the spotted lanternfly originated from southwestern China, diverged into six phylogeographic lineages, and experienced northward expansion across the Yangtze River in the late Pleistocene. South Korea populations were derived from multiple invasions from eastern China and Japan with two different genetic sources of northwestern (Loess Plateau) and eastern (East Plain) lineages in China, whereas the each of Japan and the United States had only one. The United States populations originated through single invasive event from South Korea, which served as a bridgehead of invasion. The environmental conditions, especially the distribution of host Ailanthus trees, and adaptability possibly account for the rapid spread of the spotted lanternfly in the native and introduced regions.

Verified
Journal Article
Open access
PDF file
PJPei Jiang
Pei Jiang
HLHu Li
Hu Li
FSFan Song
Fan Song
YCYao Cai
Yao Cai
JWJianyun Wang
Jianyun Wang
Wanzhi CaiWanzhi Cai
Wanzhi Cai
Most assassin bugs are predators that act as important natural enemies of insect pests. Mitochondrial (mt) genomes of these insects are double-strand circular DNAs that encode 37 genes. In the present study, we explore the duplication and rearrangement of tRNA genes in the mt genome of Reduvius tenebrosus, the first mt genome from the subfamily Reduviinae. The gene order rearranges from CR (control region)-trnI-trnQ-trnM-ND2 to CR-trnQ-trnI2-trnI1-trnM-ND2. We identified 23 tRNA genes, including 22 tRNAs commonly found in insects and an additional trnI (trnI2), which has high sequence similarity to trnM. We found several pseudo genes, such as pseudo-trnI, pseudo-CR, and pseudo-ND2, in the hotspot region of gene rearrangement (between the control region and ND2). These features provided evidence that this novel gene order could be explained by the tandem duplication/random loss (TDRL) model. The tRNA duplication/anticodon mutation mechanism further explains the presence of trnI2, which is remolded from a duplicated trnM in the TDRL process (through an anticodon mutation of CAT to GAT). Our study also raises new questions as to whether the two events proceed simultaneously and if the remolded tRNA gene is fully functional. Significantly, the duplicated tRNA gene in the mitochondrial genome has evolved independently at least two times within assassin bugs.