Xiang-Dang Du

Prof. Xiang-Dang Du

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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2 June 2021 in Clinical Microbiology Reviews
Verified
Journal Article
Closed access
Stefan SchwarzStefan Schwarz
Stefan Schwarz
WZWanjiang Zhang
Wanjiang Zhang
XDXiang-Dang Du
Xiang-Dang Du
HKHenrike Krüger
Henrike Krüger
AFAndrea T. Feßler
Andrea T. Feßler
YWYang Wang
Yang Wang
Seven mobile oxazolidinone resistance genes, including cfr , cfr (B), cfr (C), cfr (D), cfr (E), optrA , and poxtA , have been identified to date. The cfr genes code for 23S rRNA methylases, which confer a multiresistance phenotype that includes resistance to phenicols, lincosamides, oxazolidinones, pleuromutilins, and streptogramin A compounds. The optrA and poxtA genes code for ABC-F proteins that protect the bacterial ribosomes from the inhibitory effects of oxazolidinones.

1 January 2018 in The Lancet Infectious Diseases
Verified
Journal Article
Closed access
HYHong Yao
Hong Yao
SQShangshang Qin
Shangshang Qin
SCSheng Chen
Sheng Chen
JSJianzhong Shen
Jianzhong Shen
XDXiang-Dang Du
Xiang-Dang Du

1 September 2019 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Closed access
PDF file
DLDexi Li
Dexi Li
XLXing-Yun Li
Xing-Yun Li
SSStefan Schwarz
Stefan Schwarz
MYMengyan Yang
Mengyan Yang
SZSu-Mei Zhang
Su-Mei Zhang
XDXiang-Dang Du
Xiang-Dang Du
The novel 12,932-bp nonconjugative multiresistance transposon Tn 6674 was identified in the chromosomal DNA of a porcine Enterococcus faecalis strain. Tn 6674 belongs to the Tn 554 family of transposons. It shares the same arrangement of the transposase genes tnpA , tnpB, and tnpC with Tn 554 . However, in addition to the Tn 554 -associated resistance genes spc and erm (A), Tn 6674 harbored the resistance genes fexA and optrA .

17 July 2019 in Journal of Antimicrobial Chemotherapy
Verified
Journal Article
Open access
PDF file
YSYanhong Shang
Yanhong Shang
DLDexi Li
Dexi Li
WHWenbo Hao
Wenbo Hao
SSStefan Schwarz
Stefan Schwarz
XSXinxin Shan
Xinxin Shan
XDXiang-Dang Du
Xiang-Dang Du
To investigate the presence and transfer of the oxazolidinone/phenicol resistance gene optrA and identify the genetic elements involved in the horizontal transfer of the optrA gene in Streptococcus suis. A total of 237 S. suis isolates were screened for the presence of the optrA gene by PCR. Whole-genome DNA of three optrA-positive strains was completely sequenced using the Illumina MiSeq and Pacbio RSII platforms. MICs were determined by broth microdilution. Transferability of the optrA gene in S. suis was investigated by conjugation. The presence of circular intermediates was examined by inverse PCR. The optrA gene was present in 11.8% (28/237) of the S. suis strains. In three strains, the optrA gene was flanked by two copies of IS1216 elements in the same orientation, located either on a prophage or on ICESa2603-family integrative and conjugative elements (ICEs), including one tandem ICE. In one isolate, the optrA-carrying ICE transferred with a frequency of 2.1 × 10−8. After the transfer, the transconjugant displayed elevated MICs of the respective antimicrobial agents. Inverse PCRs revealed that circular intermediates of different sizes were formed in the three optrA-carrying strains, containing one copy of the IS1216E element and the optrA gene alone or in combination with other resistance genes. A prophage and two ICESa2603-family ICEs (including one tandem ICE) associated with the optrA gene were identified in S. suis. The association of the optrA gene with the IS1216E elements and its location on either a prophage or ICEs will aid its horizontal transfer.

21 March 2025 in Science Advances
Verified
Journal Article
Open access
XCXueyan Chen
Xueyan Chen
MSMeirong Song
Meirong Song
LTLei Tian
Lei Tian
XSXinxin Shan
Xinxin Shan
CMChangsi Mao
Changsi Mao
LWLiuji Wu
Liuji Wu
Multidrug-resistant (MDR) bacteria pose a major threat to public health, and additional sources of antibacterial candidates are urgently needed. Noncanonical peptides (NCPs), derived from noncanonical small open reading frames, represent small biological molecules with important roles in biology. However, the antibacterial activity of NCPs remains largely unknown. Here, we discovered a plant-derived noncanonical antibacterial peptide (NCBP1) against both Gram-positive and Gram-negative bacteria. NCBP1 is composed of 11 amino acid residues with cationic surface potential and favorable safety and stability. Mechanistic studies revealed that NCBP1 displayed antibacterial activity by targeting phosphatidylglycerol and cardiolipin in bacterial membrane, resulting in membrane damage and dysfunction. Notably, NCBP1 showed promising efficacy in mice. Furthermore, NCBP1 effectively inhibited the growth of plant fungal pathogens and enhanced disease resistance in maize. Our results demonstrate the unexplored antimicrobial potential of plant-derived NCPs and provide an accessible source for the discovery of antimicrobial substances against MDR bacterial and fungal pathogens.

23 September 2023 in Environmental Pollution
Verified
Journal Article
Closed access
WHWen-Bo Hao
Wen-Bo Hao
XGXiaodan Gu
Xiaodan Gu
XYXiaohu Yu
Xiaohu Yu
YZYoubao Zhao
Youbao Zhao
CLChenglong Li
Chenglong Li
XDXiang-Dang Du
Xiang-Dang Du