Fengyan Zhai

Dr. Fengyan Zhai


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

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1 March 2026 in Horticultural Plant Journal
Verified
Journal Article
Open access
LXLaixiang Xu
Laixiang Xu
WWWenhao Wang
Wenhao Wang
ZCZhaopeng Cai
Zhaopeng Cai
WHWenwen Huang
Wenwen Huang
FZFengyan Zhai
Fengyan Zhai
JZJunmin Zhao
Junmin Zhao

1 December 2019 in Plant Disease
Verified
Journal Article
Open access
FZFengyan Zhai
Fengyan Zhai
HLH. J. Lu
H. J. Lu
XXX. Y. Xie
X. Y. Xie
CLC. Q. Li
C. Q. Li
LZL. G. Zeng
L. G. Zeng

1 September 2021 in Plant Disease
Verified
Journal Article
Closed access
DWD. Wang
D. Wang
YZYabo Zhang
Yabo Zhang
JCJ. Chang
J. Chang
KMK. Meng
K. Meng
JSJin-ping Shu
Jin-ping Shu
FZFengyan Zhai
Fengyan Zhai

1 July 2022 in Plant Disease
Verified
Journal Article
Closed access
YGYan Gao
Yan Gao
FZFengyan Zhai
Fengyan Zhai
YZY. B. Zhang
Y. B. Zhang
JSJin-ping Shu
Jin-ping Shu
JCJun Chang
Jun Chang
HWHaojie Wang
Haojie Wang
Pecan (Carya illinoinensis K. Koch) is very productive and brings good economic returns for mountain dwellers. In recent years, symptoms were observed on both leaves and fruits of pecan in orchards, Fuyang, Anhui Province, and Jiande, Zhejiang Province. On the leaf, spots, rust-colored, long shuttle to irregular shaped, and 1–3 mm in size, firstly appeared between veins. The color of area around the spot gradually changed from green to yellow making a yellow halo. Then, some spots often merged in to a big lesion. On the fruit, symptoms firstly appear as irregular and black spots. The spots gradually spread to most part of the fruit and the core of the fruit turned black at the late stage of pathogenesis. Normally, the leaf infection rate was less than 10%, whereas infection rate of fruit could reach 5–15% which leads to drastic quality reduction and significant yield losses. To isolate the pathogens, fresh infected tissues were cut from samples, disinfected and cultured at 2% water agar at 28 oC till colony could be spotted. Fungal isolates were obtained by mycelia tip transferring. Similar cultural and morphological characters showed on 39 of the total 45 isolates. The mycelia grew rapidly in PDA plates, and colony diameter could reach 8.0 cm after culture at 25 oC in dark for 5 days. Mycelia on surface of the colony were cotton-like and showed obvious growth rings, and turn yellow from the middle on aged cultures. Pycnidia, brown to dark in color, began to form on PDA after 15 days’ culture in the dark. Conidia were fusoid, straight to slightly curved, 4-septate, 23.5–26.3×7.6–9.0μm, average 24.9×8.3μm (n=60) in size. The basal cell was hyaline, conic with a truncate base and thin-walled, average 4.4–5.1μm long (n=60). The three median cells were doliiform and brown with darker septa. The apical cell was hyaline, cylindrical, with 2–3 tubular apical appendages arising from the apical crest, unbranched, filiform, average 21.7–29.2 μm(n=60) long. The cultural and morphological characters of the strains matched the previous descriptions of Neopestalotiopsis sp. (Maharachchikumbura et al., 2014). Their 3 partial genes, ITS, β-tubulin (TUB) and translation elongation factor 1-alpha (TEF1-α), were amplified and sequenced with primers (Lee et al., 2006; Maharachchikumbura et al., 2014). These sequences were submitted in GenBank with accession number of MW504791 (ITS), MW633956 (TEF1-α), and MW633958 (TUB2), seperately. The BLAST results against the GenBank database showed more than 99% identity with sequences claimed from Neopestalotiopsis sp. The multilocus phylogenetic analysis of the three genes showed the isolate was closest with N. rosae. The strains were finally identified as N. rosae by morphological and molecular analysis. Pathogenicity testing was performed by spreading 20μl conidia suspension drop (1 × 106 conidia ml-1) on surface of wounded or unwounded leaves and fruits. The pecan variety MaHan was used for inoculation. Wounds were made by scratching with sterile needles, and then a drop of 20μl conidia suspension was spread on the wounded area. For unwounded inoculation, a drop of 20μl conidia suspension was spread without wound procedure. The same amount of water drops were spread on the surface of wounded and unwounded tissues as controls. The plant parts were wrapped with PE films to keep moisture after drop spreading. Ten trees were selected for inoculation, and 10 leaves and fruits were randomly selected separately for wounded and unwounded inoculation and corresponding controls in each tree. The similar symptoms appeared from 3 dpi on leaves and 9 dpi on fruits, and finally showed on more than 90% wounded inoculated leaves or fruits and on less than 50% after unwounded inoculation, while controls remained symptomless. N. rosae was consistently re-isolated from inoculated parts with symptoms, while not from the control. Therefore, N. rosae was confirmed as the pathogen causing black spot on leaf and fruit of pecan (C. illinoinensis). To the best of our knowledge, this is the first report of N. rosae causing black spot disease of pecan (C. illinoinensis). In recent years, both the infection area and severity of this disease grow rapidly, which means the potential of the disease to become a big problem in local orchards.

10 April 2026 in Journal of Agriculture and Food Research
Verified
Journal Article
Open access
YWYanfen Wang
Yanfen Wang
XGXupeng Gao
Xupeng Gao
ZZZhibo Zhang
Zhibo Zhang
LWLiuhao Wang
Liuhao Wang
HZHongwei Zhang
Hongwei Zhang
HYHao Yu
Hao Yu

15 March 2026 in Plant Disease
Verified
Journal Article
Closed access
DWDi Wang
Di Wang
JCJun Chang
Jun Chang
WZWei Zhang
Wei Zhang
JSJin-ping Shu
Jin-ping Shu
YZYabo Zhang
Yabo Zhang
FZFengyan Zhai
Fengyan Zhai
Anthracnose fruit rot and leaf blight caused by Colletotrichum species, are significant diseases affecting pecan in the subtropical regions of China. From 2018 to 2021, disease surveys were conducted in the provinces of Zhejiang, Anhui, Shandong, Yunnan, Jiangsu, Sichuan, Jiangxi, and Guangxi, leading to the isolation of 108 Colletotrichum isolates from symptomatic samples. Species identification was performed through multigene phylogenetic analysis of the ITS, ACT, CAL, GAPDH, TUB2, and CHS-1 DNA regions. The isolates were classified within the C. gloeosporioides, C. acutatum, C. gigasporum, and C. orchidearum species complexes, with over 52% belonging to the C. gloeosporioides complex. Twelve Colletotrichum species were identified: C. fructicola (n=48), C. fioriniae (n=18), C. siamense (n=15), C. gloeosporioides (n=5), C. nymphaeae (n=5), C. aenigma (n=4), C. jiangxiense (n=4), C. henanense (n=2), C. gigasporum (n=2), C. conoides (n=1), C. sojae (n=1), and C. cliviicola (n=1). Pathogenicity tests via point inoculations confirmed that C. fioriniae, C. fructicola, and C. siamense showed higher virulence. In wound inoculation assays, leaves inoculated with C. fioriniae, C. conoides, C. fructicola, C. siamense, and Colletotrichum sp. developed larger lesions (diameters ranging from 4.0 to 8.3 mm) compared to those inoculated with C. gigasporum, C. jiangxiense, C. sojae, C. nymphaeae, C. cliviicola, and C. henanense (lesion diameters from 2.0 to 2.5 mm). The prevalence and diversity of Colletotrichum species associated with pecan anthracnose varied among the eight provinces, with relatively greater diversity observed in Yunnan, Jiangsu, Zhejiang, and Anhui. C. fructicola (50.3 %) was the most prevalent species across most pecan-growing regions studied in China, followed by C. fioriniae (15.5 %). This study provides the first report of C. conoides, C. aenigma, C. henanense, C. jiangxiense, C. gigasporum, C. sojae, and C. cliviicola infecting Carya illinoinensis in China.