Zhaohui Zhang

Zhaohui Zhang


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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Journal Article
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DXDandan Xi
Dandan Xi
LGLu Gao
Lu Gao
LMLiming Miao
Liming Miao
LGLi-Ao Ge
Li-Ao Ge
DZDing-Yu Zhang
Ding-Yu Zhang
HZHongfang Zhu
Hongfang Zhu
Plasmodiophora brassicae (P. brassicae) is a soil-born pathogen worldwide and can infect most cruciferous plants, which causes great yield decline and economic losses. It is not well known how microbial diversity and community composition change during P. brassicae infecting plant roots. Here, we employed a resistant and a susceptible pakchoi cultivar with and without inoculation with P. brassicae to analyze bacterial and fungal diversity using 16S rRNA V3-V4 and ITS_V1 regions, respectively. 16S rRNA V3-V4 and ITS_V1 regions were amplified and sequenced separately. Results revealed that both fungal and bacterial diversity increased, and composition was changed in the rhizosphere soil of the susceptible pakchoi compared with the resistant cultivar. In the four groups of R_mock, S_mock, R_10d, and S_10d, the most relatively abundant bacterium and fungus was Proteobacteria, accounting for 61.92%, 58.17%, 48.64%, and 50.00%, respectively, and Ascomycota, accounting for 75.11%, 63.69%, 72.10%, and 90.31%, respectively. A total of 9488 and 11,914 bacteria were observed uniquely in the rhizosphere soil of resistant and susceptible pakchoi, respectively, while only 80 and 103 fungi were observed uniquely in the correlated soil. LefSe analysis showed that 107 and 49 differentially abundant taxa were observed in bacteria and fungi. Overall, we concluded that different pakchoi cultivars affect microbial diversity and community composition, and microorganisms prefer to gather around the rhizosphere of susceptible pakchoi. These findings provide a new insight into plant–microorganism interactions.

19 May 2023 in Agronomy
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ZZZhaohui Zhang
Zhaohui Zhang
KWKuanhong Wang
Kuanhong Wang
CCChunhong Chen
Chunhong Chen
STShoubo Tian
Shoubo Tian
JWJue Wu
Jue Wu
DXDong Xiao
Dong Xiao
Powdery mildew (PM) is the main disease that afflicts bottle gourd. Previous studies on PM mainly focused on its effects on pumpkin, melon, and other crops; however, the exact molecular mechanism of bottle gourd resistance to PM remains unclear. RNA sequencing (RNA-Seq) technology was used to investigate the dynamic changes in leaf transcriptome profiles between resistant and susceptible gourd at 12, 24, 48, and 72 h post-inoculation with powdery mildew. Compared with a susceptible variety (G3), the expression levels of the differentially expressed genes of phenylpropanoid biosynthesis, starch, and sucrose metabolism, and plant–pathogen interaction pathways in disease-resistant plants were upregulated. We propose that disease resistance and tolerance in bottle gourd are enhanced via several pathways, including the antioxidant system, phenylalanine biosynthesis, and cell wall cellulose synthesis. Our research will provide an important basis for further screening and breeding PM resistance in bottle gourd.

SLShuangxi Li
Shuangxi Li
ZZZhaohui Zhang
Zhaohui Zhang
JZJuanqin Zhang
Juanqin Zhang
XZXianqing Zheng
Xianqing Zheng
Hanlin ZhangHanlin Zhang
Hanlin Zhang
WLWeiguang Lv
Weiguang Lv
The current fertilizer recommendations for melon plantation have many limitations and exhibit deficiencies regarding future development. Therefore, in this study, the optimal quantities of fertilizer, in terms of the effects of single factors and interaction effects, are studied. There were significant interaction effects between N and P, N and K, P and K; the contents of soluble protein, vitamin C (Vc), and soluble sugar in melon could be improved using the optimal fertilization ratios. The optimal ratio of N:P:K was 2.33:1:3.85, with the amounts of N, P2O5, and K2O, respectively, being 157.5, 67.58, and 260.38 kg/hm2, yielding 8.73 g/kg of soluble protein in melon. The optimal ratio of N:P:K was 2.03:1:3.36, with amounts of N, P2O5, and K2O being 157.50, 77.40, and 260.38 kg/hm2, respectively, yielding 25.32 g/kg Vc content in melon. Finally, the optimal ratio of N:P:K was 1.53:1:3.36, with the amounts of N, P2O5, and K2O being 118.07, 77.40, respectively, and 260.38 kg/hm2, yielding 13.34% soluble sugar content in melon.

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LXLi Xiaofeng
Li Xiaofeng
DXDandan Xi
Dandan Xi
LGLu Gao
Lu Gao
HZHongfang Zhu
Hongfang Zhu
XYXiuke Yang
Xiuke Yang
MWMin Wei
Min Wei
Hypocotyl length is a critical determinant for the efficiency of mechanical harvesting in pakchoi production, but the knowledge on the molecular regulation of hypocotyl growth is very limited. Here, we report a spontaneous mutant of pakchoi, lhy7.1, and identified its characteristics. We found that it has an elongated hypocotyl phenotype compared to the wild type caused by the longitudinal growth of hypocotyl cells. Different light quality treatments, transcriptome, and proteomic analyses were performed to reveal the molecular mechanisms of hypocotyl elongation. The data showed that the hypocotyl length of lhy7.1 was significantly longer than that of WT under red, blue, and white lights but there was no significant difference under dark conditions. Furthermore, we used transcriptome and label-free proteome analyses to investigate differences in gene and protein expression levels between lhy7.1 and WT. At the transcript level, 4568 differentially expressed genes (DEGs) were identified, which were mainly enriched in “plant hormone signal transduction”, “photosynthesis”, “photosynthesis–antenna proteins”, and “carbon fixation in photosynthetic organisms” pathways. At the protein level, 1007 differentially expressed proteins (DEPs) were identified and were mainly enriched in photosynthesis-related pathways. The comprehensive transcriptome and proteome analyses revealed a regulatory network of hypocotyl elongation involving plant hormone signal transduction and photosynthesis-related pathways. The findings of this study help elucidate the regulatory mechanisms of hypocotyl elongation in lhy7.1.

27 August 2022 in Agronomy
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DXDandan Xi
Dandan Xi
LXLi Xiaofeng
Li Xiaofeng
Changwei ZhangChangwei Zhang
Changwei Zhang
LGLu Gao
Lu Gao
YZYuying Zhu
Yuying Zhu
ZZZhaohui Zhang
Zhaohui Zhang
Background: Arugula is an essential oil crop of cruciferous species worldwide and serves as a salad vegetable. Purple plant leaves provide nutrients benefiting human beings and are mainly attributed to high anthocyanins. In this study, we collected a purple arugula cultivar with purple leaves and a green arugula with green leaves. The genetic bases and mechanisms underlying purple leaf formation in arugula remain unclear. Therefore, we conducted integrative metabolomics and transcriptomics of two arugula cultivars with different leaf colors. Methods: To study the underlying mechanisms, transcriptomic and metabolomic analyses were carried out. Results: Metabolomic analysis revealed that 84 of 747 metabolites were significantly differentially expressed, comprising 30 depleted and 49 enriched metabolites. Further analysis showed that cyanidin is the main components responsible for the purple color. A total of 144,790 unigenes were obtained by transcriptomic analysis, with 13,204 unigenes differentially expressed, comprising 8120 downregulated and 5084 upregulated unigenes. Seven structural genes, PAL, C4H, 4CL, CHS, CCoAOMT, LDOX, and UFGT, were identified as candidate genes associated with anthocyanin accumulation through combined analysis of transcriptome and metabolome. Conclusions: Collectively, the differences in the expression levels of PAL, C4H, 4CL, CHS, CCoAOMT, LDOX, and UFGT might be responsible for purple leaf coloration, providing important data for the discovery of candidate genes and molecular bases controlling the purple leaves in arugula.

7 October 2026 in Horticulturae
Verified
Journal Article
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KWKuanhong Wang
Kuanhong Wang
YZYongxue Zhang
Yongxue Zhang
.L.panling Lu
.panling Lu
STShoubo Tian
Shoubo Tian
HZHongmei Zhang
Hongmei Zhang
ZZZhaohui Zhang
Zhaohui Zhang
Powdery mildew is one of the most destructive fungal diseases of bottle gourd (Lagenaria siceraria), severely threatening yield and quality, yet the genetic basis of its resistance remains poorly understood. In this study, an F2 segregating population derived from a cross between the resistant inbred line G6 and the susceptible inbred line G3 was used, and BSA-seq, integrated RNA-seq analysis, qRT-PCR validation, and KASP marker development were comprehensively employed. SNP-index and InDel-index analyses independently mapped and converged on a candidate interval of 1,898,234–8,241,294 bp (~6.34 Mb) on chromosome 2. By comparing differentially expressed genes (DEGs) at 12, 24, 48, and 72 h post-inoculation with the BSA candidate interval, one candidate resistance gene, Lsi02G006660, was identified, and a KASP marker (Chr2_5941698, G/T) was successfully developed. This study provides a candidate gene and marker resources for molecular breeding of powdery mildew resistance in bottle gourd.