XWXiaofang Wu

Xiaofang Wu

*This is an algorithmically generated author record based on publicly available information.

Xiaofang Wu has a total of 9 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Outbreak of multidrug-resistant Salmonella typhimurium monophasic variant 1,4,[5],12:i:- sequence type 34 linked to food, in China

    by Wei Yan, Deshun Xu, Peng Zhang, Liping Chen, Xiaofang Wu

    The monophasic Salmonella Typhimurium variant (1,4,[5],12:i:-) is a growing global public health and food safety concern. This study analyzed 60 such isolates collected in Huzhou (2023–2025), including 16 outbreak strains. All isolates belonged to ST34 and carried 211 virulence genes. Antimicrobial susceptibility testing showed universal resistance to tetracycline (100%) and a high multidrug resistance rate (96.67% resistant to ≥ 3 antibiotic classes). Whole-genome sequencing identified 39 resistance genes; aac(6´)-Iaa was present in all strains, and 48.33% carried ≥ 4 resistance genes. Phylogenetic analysis revealed high overall homology with localized evolutionary traits. Notably, clinical outbreak and food-derived isolates were clonally identical (0 SNP difference).

  • Open Access

    Molecular typing and epidemiologic profiles of human metapneumovirus infection among children with severe acute respiratory infection in Huzhou, China

    by Lei Ji, Liping Chen, Deshun Xu, Xiaofang Wu

    Background: Human metapneumovirus (hMPV) is one of the important pathogens in infant respiratory tract infection. However, the molecular epidemiology of hMPV among children < 14 years of age hospitalized with severe acute respiratory infection (SARI) is unclear. We investigated the hMPV infection status and genotypes of children hospitalized with SARI from January 2016 to December 2020 in Huzhou, China. Methods: A nasopharyngeal flocked swab, nasal wash, or nasopharyngeal swab/or opharyngeal swab combination sample was collected from children with SARI in Huzhou from January 2016 to December 2020. Quantitative reverse transcription-polymerase chain reaction was performed to detect hMPV RNA. The hMPV F gene was amplified and sequenced, followed by analysis using MEGA software (ver. 7.0). Epidemiological data were analyzed using Microsoft Excel 2010 and SPSS (ver. 22.0) software. Results: A total of 1133 children with SARI were recruited from 2016 to 2020. Among them, 56 (4.94%) were positive for hMPV-RNA. Children < 5 years of age accounted for 85.71% of the positive cases. The hMPV incidence was high in spring and winter, especially in December and January to March. Phylogenetic analysis of the F-gene sequences of 28 hMPV strains showed that the A1, B1, and B2 genotypes were prevalent in Huzhou, and the dominant hMPV genotype varied according to surveillance year. Conclusions: HMPV is an important respiratory pathogen in children in Huzhou, with a high incidence in winter and spring in children < 5 years of age. In this study, genotypes A1, B1, and B2 were the most prevalent.


  • Open Access

    Bioinformatics analysis of the epitope regions for norovirus capsid protein

    by Liping Chen, Di Wu, Lei Ji, Xiaofang Wu, Deshun Xu, Zhiwei Cao, Jiankang Han

    Background: Norovirus is the major cause of nonbacterial epidemic gastroenteritis, being highly prevalent in both developing and developed countries. Despite of the available monoclonal antibodies (MAbs) for different sub-genogroups, a comprehensive epitope analysis based on various bioinformatics technology is highly desired for future potential antibody development in clinical diagonosis and treatment. Methods: A total of 18 full-length human norovirus capsid protein sequences were downloaded from GenBank. Protein modeling was performed with program Modeller 9.9. The modeled 3D structures of capsid protein of norovirus were submitted to the protein antigen spatial epitope prediction webserver (SEPPA) for predicting the possible spatial epitopes with the default threshold. The results were processed using the Biosoftware. Results: Compared with GI, we found that the GII genogroup had four deletions and two special insertions in the VP1 region. The predicted conformational epitope regions mainly concentrated on N-terminal (1~96), Middle Part (298~305, 355~375) and C-terminal (560~570). We find two common epitope regions on sequences for GI and GII genogroup, and also found an exclusive epitope region for GII genogroup. Conclusions: The predicted conformational epitope regions of norovirus VP1 mainly concentrated on N-terminal, Middle Part and C-terminal. We find two common epitope regions on sequences for GI and GII genogroup, and also found an exclusive epitope region for GII genogroup. The overlapping with experimental epitopes indicates the important role of latest computational technologies. With the fast development of computational immunology tools, the bioinformatics pipeline will be more and more critical to vaccine design.