Yanyan Liu’s research while affiliated with Chinese Center For Disease Control And Prevention and other places

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Publications (3)


Detection of Clostridium botulinum gene by quantitative Real-Time PCR (qPCR). A. qPCRfor the detection of C. botulinum. B. Detection of the neurotoxin gene encoding Clostridium botulinum type E (BoNT/E). Lane 1: Remaining marinated pig liver; Lane 2: Household garbage from the patient (mixed with vomit); Lane 3: Vomit from the patient; Lane 4: Positive control; Lane 5: Negative control
Circos genome circle map of KM001, the bacterial chromosome is 3.71 Mb in size. The distribution of the circle from the outside indicates the genome size, forward CDS, reverse CDS, GC ratio (blue and orange indicate regions where the GC ratio is higher than average and lower than average, respectively), and CG skew positive (blue) and negative (green)
Genome analysis results of KM001. A. Functional annotation of KEGG databases of KM001. B. Functional annotation of GO databases of KM001. C. Functional annotation of COG databases of KM001. D. Distribution of Predicted Virulence Factors in the Complete Genome of KM001
Dendrogram constructed by average nucleotide identification of published whole-genome assembly sequences and neighbor-joining tree methods
Comparative Genomic Analysis of Clostridium botulinum Strains. A. CCT map comparing the C. botulinum strain to other four type of C. botulinum genomes. This map starting from the outermost ring the feature rings depict: (1) COG functional categories for forward strand coding sequences; (2) Forward strand sequence features; (3) Reverse strand sequence features; (4) COG functional categories for reverse strand coding sequences. The next four rings show regions of sequence similarity detected by BLAST comparisons conducted between CDS translations from the reference genome and five C. botulinum comparison genomes. The 5 circles from inside to outside represent the genomes of 5 C. botulinum strains. The color of each of the 5 circles corresponds to the homology score of BLAST HIT. Red indicates the sites with homology score greater than 90%, and some blue and white sites have low homology scores even within the same species. Colored triangular arrows refer to the forward and reverse chains of coding regions, and the functional classification of cogs in the same region has cross and unique functions. B. A Mauve alignment of five C. botulinum strains. It shows collinear set of matched colored regions, Each sequence of identically colored blocks represents a collinear set of matching regions. One connecting line is drawn per collinear block. Most regions of C. botulinum species have common conserved segments. C. Petals of single copy genes and species-specific genes in each sample
Genomic characterisation and traceability analysis of a Clostridium botulinum strain involved in a food poisoning incident
  • Article
  • Full-text available

March 2025

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28 Reads

BMC Infectious Diseases

Guiman Li

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Huiwen Wang

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Yan Zhang

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[...]

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Yanyan Liu

Objective To identify the source of Clostridium botulinum (C. botulinum) involved in a food poisoning case in Kunming and analyze its molecular characteristics. Results This study examined samples from a clustered food poisoning incident, including pickled pig liver consumed by three patients, hospital vomit from a deceased patient, and household waste mixed with vomit. Enrichment culture, microscopic examination, and real-time quantitative PCR confirmed the presence of C. botulinum (designated KM001) with type E botulinum toxin. The full-length genomic sequence of this strain was obtained through second and third-generation sequencing, revealing a genome size of 3,713,470 bp. KEGG annotation indicated that 1,840 single genes were assigned to 44 KEGG pathways. Whole-genome sequencing revealed genetic diversity among toxin gene clusters, with 94.76% homology to C. botulinum E3 strain (Alaska E43) and 93.65% homology to C. botulinum B strain (Eklund 17B, NRP). Evolutionary analysis, incorporating complete genomes of foodborne and environmental C. botulinum strains worldwide along with KM001, showed stronger phylogenetic affinity of KM001 to other type E strains. Conclusion Overall, this study identified KM001 as the causative agent in a food poisoning incident, marking the first report of type E botulinum toxin poisoning in the region. Genomic analysis revealed the serotype and genetic diversity among toxin gene clusters, providing insights into its gene function, virulence, and evolutionary relationships. Understanding the genetic relationships and evolutionary pathways of different C. botulinum strains is crucial for predicting infection risks and implementing effective control measures.The findings contribute to the documentation of botulinum toxin incidents in Yunnan, China, but do not examine the antimicrobial resistance of C. botulinum or its interactions with other microorganisms; further research is needed to address these aspects.

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Computed tomography of lung. (A, B) Results on March 6, 2024 showed that multiple patchy and patchy increased density shadows were seen in both lungs, with unclear boundary and uneven density; (C, D) Results on March 23, 2024 showed a reduction in lesions compared to previous scans.
Phylogenetic trees of H10N3 strains based on nucleotide sequence. (A) Phylogenetic tree of HA; (B) Phylogenetic tree of NA. The Phylogenetic trees were downloaded from the GISAID database (https://gisaid.org) using the neighbor-joining method in MEGA X. The diamond indicates the H10N3 strain in this study, and the octagon indicates the H10N3 strain from the first case in Jiangsu.
Phylogenetic and mutational analysis of H10N3 avian influenza A virus in China: potential threats to human health

June 2024

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19 Reads

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2 Citations

In recent years, the avian influenza virus has emerged as a significant threat to both human and public health. This study focuses on a patient infected with the H10N3 subtype of avian influenza virus, admitted to the Third People’s Hospital of Kunming City on March 6, 2024. Metagenomic RNA sequencing and polymerase chain reaction (PCR) analysis were conducted on the patient’s sputum, confirming the H10N3 infection. The patient presented severe pneumonia symptoms such as fever, expectoration, chest tightness, shortness of breath, and cough. Phylogenetic analysis of the Haemagglutinin (HA) and neuraminidase (NA) genes of the virus showed that the virus was most closely related to a case of human infection with the H10N3 subtype of avian influenza virus found in Zhejiang Province, China. Analysis of amino acid mutation sites identified four mutations potentially hazardous to human health. Consequently, this underscores the importance of continuous and vigilant monitoring of the dynamics surrounding the H10N3 subtype of avian influenza virus, utilizing advanced genomic surveillance techniques.


First human case of avian influenza A (H10N3) in Southwest China

March 2024

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148 Reads

In recent years, the avian influenza virus has emerged as a significant threat to both human and public health. Despite this, only two cases of human infection with the H10N3 strain have been documented. Here, we present the initial instance of human infection with avian influenza virus H10N3 in Yunnan Province, Southwest China. The patient, a previously healthy 51-year-old male, presented with recurrent fever peaking at 39℃, accompanied by symptoms such as cough, expectoration, chest tightness, and shortness of breath. Diagnosis revealed severe pneumonia, type I respiratory failure, and infection with avian influenza virus H10N3. Additionally, the patient experienced complications from Candida albicans and Staphylococcus epidermidis infections. Following treatment with appropriate antiviral drugs and antibiotics, the patient's condition improved. Molecular analysis of the viral strain identified four mutations potentially hazardous to human health. This underscores the importance of continuous and vigilant monitoring of the dynamics surrounding the H10N3 subtype of avian influenza virus.

Citations (1)


... This alteration increases the affinity of avian influenza viruses to bind to human receptors [11][12][13]. Dai et al. also found genetic mutations in this case may increasing the likelihood of human infection avian influenza [14]. Furthermore, the H10N3 sub-type avian influenza virus is a recombinant virus with surface genes derived from the H7 and H9 sub-types of viruses circulating in chickens and ducks [12]. ...

Reference:

A case report of human infection with avian influenza H10N3 with a complex respiratory disease history
Phylogenetic and mutational analysis of H10N3 avian influenza A virus in China: potential threats to human health