Min Xiao

Dr. Min Xiao

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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1 June 2021 in The Journal of Molecular Diagnostics
Verified
Journal Article
Closed access
MXMin Xiao
Min Xiao
CLCai-Xia Lei
Cai-Xia Lei
YXYan-Ping Xi
Yan-Ping Xi
YLYu-Lin Lu
Yu-Lin Lu
JWJun-Ping Wu
Jun-Ping Wu
XSXi xiao Sun
Xi xiao Sun

8 November 2022 in BMC Veterinary Research
Verified
Journal Article
Open access
PDF file
HZHong Zhuang
Hong Zhuang
LSLeilei Sun
Leilei Sun
XWXiaobo Wang
Xiaobo Wang
MXMin Xiao
Min Xiao
LZLong Zeng
Long Zeng
CWChengbao Wang
Chengbao Wang
Background: Porcine epidemic diarrhea virus (PEDV), an enteric coronavirus, has become the major causative agent of acute gastroenteritis in piglets since 2010 in China.Results: In the current study, 91 complete spike (S) gene sequences were obtained from PEDV positive samples collected from 17 provinces in China from March 2020 to March 2021. A phylogenetic analysis showed that 92.3% (84 out of 91) of the identified strains belonged to GII subtype, while 7.7% (7 out of 91) were categorized as S-INDEL like strains and grouped within GI-c clade. Based on a recombination analysis, six of S-INDEL like strains were recombinant strains originated from S-INDEL strain FR/001/2014 and virulent strain AJ1102. In addition, PEDV variant strains (CH/GDMM/202012, CH/GXDX/202010 et al) carrying novel insertions (360QGRKS364 and 1278VDVF1281) in the S protein were observed. Furthermore, the deduced amino acid sequences for the S protein showed that multiple amino acid substitutions in the antigenic epitopes in comparison with the vaccine strains.Conclusions: In conclusion, these data provide novel molecular evidence on the epidemiology and molecular diversity of PEDV in 2020–2021. This information may help design a strategy for controlling and preventing the prevalence of PEDV variant strains in China.

11 June 2016 in Archives of Microbiology
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AAArshia Amin
Arshia Amin
Iftikhar AhmedIftikhar Ahmed
Iftikhar Ahmed
NHNeeli Habib
Neeli Habib
SASaira Abbas
Saira Abbas
FHFariha Hasan
Fariha Hasan
Wen-Jun LiWen-Jun Li
Wen-Jun Li

1 October 2016 in International Journal of Systematic and Evolutionary Microbiology
Verified
Journal Article
Open access
BLBing-Bing Liu
Bing-Bing Liu
HWHongfei Wang
Hongfei Wang
QLQiuli Li
Qiuli Li
XZXing-Kui Zhou
Xing-Kui Zhou
YZYongguang Zhang
Yongguang Zhang
Wen-Jun LiWen-Jun Li
Wen-Jun Li
An orange-coloured, aerobic, motile and short-rods bacterial strain, designated EGI 6500337T, was isolated from the surface-sterilized root of a halophyte Anabasis elatior (C. A. Mey.) Schischk collected from Urumqi, Xinjiang province, north-west China. Growth occurred at 5-35 °C (optimum 30 °C), at pH 6.0-9.0 (optimum pH 7.0), and in the presence of 0-6 % NaCl (w/v) (optimum 0-1 %). Phylogenetic tree based on 16S rRNA gene sequences indicated that strain EGI 6500337T formed a distinct lineage in the cluster that comprised the genera Aurantimonas and Aureimonas in the family Aurantimonadaceae. The 16S rRNA gene sequence of strain EGI 6500337T shared the highest similarities to those of Aurantimonas coralicida DSM 14790T (97.15 %) and Aurantimonas manganoxydans DSM 21871T (97.15 %). Strain EGI 6500337T contained Q-10 as the dominant isoprenoid quinone. The major cellular fatty acids were C18:1 7c (66.4 %) and C19:0 8c cyclo (23.3 %). The polar lipid profile of strain EGI 6500337T contained diphosphatidylglycerol, phosphatidylglycerol, phosphatidylcholine, phosphatidylethanolamine as major components, similarly to the members of the genus Aurantimonas. The DNA G+C content of strain EGI 6500337T was 66.8 mol%. The DNA-DNA relatedness between strain EGI 6500337T and Aurantimonas coralicida DSM 14790T was 24.7 ± 2.9 %. On the basis of the phylogenetic analysis, chemotaxonomic data and phenotypic characteristics, strain EGI 6500337T represents a novel species of the genus Aurantimonas, for which the name Aurantimonas endophytica sp. nov. is proposed. The type strain is EGI 6500337T (=KCTC 52296T =CPCC 100904T).

1 August 2019 in International Journal of Systematic and Evolutionary Microbiology
Verified
Journal Article
Open access
MRManik Prabhu Narsing Rao
Manik Prabhu Narsing Rao
ZDZhouyan Dong
Zhouyan Dong
Hui ZhangHui Zhang
Hui Zhang
XNXue-Ke Niu
Xue-Ke Niu
KZKun Zhang
Kun Zhang
Wen-Jun LiWen-Jun Li
Wen-Jun Li
A Gram-stain-positive, strictly aerobic, rod-shaped, motile, endospore-forming strain, SYSU K30001T, was isolated from a soil sample collected from a cave in Xingyi county, Guizhou province, south-west China. Phylogenetic analysis based on 16S rRNA gene sequences indicated that strain SYSU K30001T belonged to the genus Bacillus , with the highest sequence similarity to the type strain of Bacillus panaciterrae (98.1 %). Growth occurred at pH 6.0–9.0 (optimum, pH 7.0), at 28–55 °C (optimum, 28 °C) and in the presence of 0–3 % (w/v) NaCl (optimum in the absence of NaCl). Strain SYSU K30001T contained meso-2,6-diaminopimelic acid in the cell-wall peptidoglycan and MK-7 as the only isoprenoid quinone present. The polar lipids consisted of diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine and an unidentified glycolipid. The major fatty acids were iso-C15 : 0, iso-C17 : 1 ω10c, anteiso-C14 : 0 and iso-C17 : 0. The genome G+C content was 39.8 mol%. The average nucleotide identity values between SYSU K30001T and B. panaciterrae DSM 19096T were 72.1 % (ANIb) and 83.1 % (ANIm), which were below the cut-off level (95–96 %) for species delineation. Based on phenotypic, chemotaxonomic and molecular characterizations, strain SYSU K30001T represents a novel species of the genus Bacillus , for which the name Bacillus antri sp. nov. is proposed. The type strain is SYSU K30001T (=KCTC 33954T=CGMCC 1.13871T).