Publications by authors named "Gui-xia Li"

Neisseria sicca, a Gram-negative diplococcus commonly found in the nasopharynx as part of normal bacterial flora, is typically non-pathogenic but has been associated with various diseases including endocarditis, conjunctivitis, pneumonia and meningitis (Jeurissen et al., 2006; Kozlova et al., 2020; Alcid, 1980; Carter et al.

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Nav1.8, a tetrodotoxin-resistant voltage-gated sodium channels (VGSCs) subtype encoded by SCN10A, which plays an important role in the production and transmission of peripheral neuropathic pain signals. Studies have shown that VGSCs may be key targets of MicroRNAs (miRNAs) in the regulation of neuropathic pain.

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Timely identification of respiratory pathogens guides specific treatment, reduces hospital costs and minimizes the excessive use of antibiotics. A new multiplex real-time PCR panel was developed based on an automatic molecular detection and analysis system (AutoMolec system), consisting of three separate internally controlled assays. Mycoplasma pneumoniae, Chlamydia pneumoniae, adenovirus, human metapneumovirus, influenza B virus, respiratory syncytial virus and human parainfluenza virus 1-3 may be directly detected in original samples.

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Objectives: Bordetella pertussis is a highly contagious respiratory agent and is the causative pathogen of pertussis, which primarily affects children. Current diagnostic techniques for this pathogen have a variety of limitations including a long culture time, low bacterial load, and lack of specificity.

Methods: This article reports the development of a one-tube nested quantitative real-time PCR assay using the locked nucleic acid (LNA) technique (LNA-OTN-q-PCR), targeting the BP485 gene and using a simple inexpensive extraction method.

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Multiplex real-time quantitative polymerase chain reaction (mRT-qPCR) assay is commonly used to detect respiratory viruses, however, the sensitivity is limited for most reports. A panel of locked nucleic acid based multiplex closed one-tube nested real-time PCR (mOTNRT-PCR) assay consisting of five separate internally controlled RT-qPCR assays was developed for detection of 14 respiratory viruses. The sensitivity and reproducibility of mOTNRT-PCR panel were evaluated using plasmid standards and the specificity was evaluated using clinical samples.

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Background: Human adenovirus (HAdV) is a common pathogen in children that can cause acute respiratory tract infection (ARTI), but the molecular epidemiological and clinical information relating to HAdV among hospitalized children with ARTI are few reported in China.

Objectives: To evaluate the epidemiological, clinical, and molecular characteristics of HAdV infections among hospitalized children with ARTI in Hebei, Northern China from June 2017 to May 2018.

Study Design: A 12-month longitudinal, retrospective study on HAdV, typed by nested polymerase chain reaction targeting the hexon gene's hypervariable region (typing was merely performed by sequencing of the hexon neutralization epitope and thus genotypes could not be identified unequivocally), associated with ARTI was performed.

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Article Synopsis
  • A study of 4,148 hospitalized children with community-acquired pneumonia (CAP) revealed that 38.18% of those with Mycoplasma pneumoniae (Mp) were also co-detected with other pathogens, notably more in younger children (≤3 years).
  • Most clinical symptoms and disease severity showed no significant differences between children with Mp alone and those with co-detection, although some specific symptoms like prolonged fever and runny nose were more common in those with Mp-viral co-detection.
  • Findings indicate that while Mp co-detections with other pathogens are frequent, they generally do not alter the clinical presentation or severity of the illness.
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Objectives: Pertussis is a highly transmissible acute respiratory infection caused by the bacterial pathogen Bordetella pertussis. The purpose of this study was to develop a rapid, simple and sensitive diagnostic test for detecting this pathogen.

Methods: Here we present a recombinase aided amplification (RAA) assay incorporating competitive internal amplification control (IAC) to detect Bordetella pertussis using the DNA obtained by boiling.

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Based on excitation emission matrix spectroscopy (EEMs) technology combined with parallel factor analysis (PARAFAC) and UV-Vis spectra, we analyzed the spectral characteristics and sources of dissolved organic matter (DOM) in rainwater with different DOC molecular weight in summer and autumn in the Zhoucun Reservoir. The results show that the UV-Vis absorption spectrum of DOM have no notably characteristic peak and the variation coefficient of the absorption coefficient ranges between 75% and 469%, which shows the properties of DOM with different molecular weight. The changes of and E3/E4 show that the relative concentration of DOM and the proportion of fulvic acid in DOM both increase from summer to autumn, respectively; Two humic-like substances (C1, C2), one fulvic-like substance (C3), and one protein-like substance (C4) were identified with the PARAFAC model, with a significant correlation coefficient (<0.

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Article Synopsis
  • RSV, HRV, and HMPV are key viruses that cause respiratory infections in hospitalized patients, making accurate detection crucial for treatment.
  • A new test called mOTNRT-PCR was developed, which can simultaneously detect these viruses with high sensitivity (5 copies/reaction) and no cross-reactivity with other viruses.
  • The mOTNRT-PCR outperformed traditional RT-qPCR methods, identifying more positive cases and confirming 33 samples that were missed by RT-qPCR through sequencing.
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  • Respiratory syncytial virus (RSV) is a major cause of respiratory infections, particularly challenging to detect in vulnerable populations due to its low viral load.
  • Researchers developed a highly sensitive assay called OTNRT-PCR that is easier to use and reduces contamination risks compared to traditional methods.
  • The study found that OTNRT-PCR detects RSV more accurately than conventional qRT-PCR, confirming 143 samples that were previously considered negative.
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Some serotypes of enterovirus (EV) may lead to transient and symptomatic gastrointestinal infections while others are commensal residents of the human gut. To determine whether certain EV types are more often associated with diarrhea, we conducted a preliminary study on the prevalence of EV serotypes and common diarrhea viruses in fecal samples of diarrhea children and healthy controls. EV was tested with one step nest polymerase chain reaction and typed by direct sequencing while common causative diarrhea viruses rotavirus (RV), norovirus (NoV), adenovirus (AdV), bocavirus (HBoV), and astrovirus (AstV) were screened with multiplex PCR assays.

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Background: Diarrhea is a major source of morbidity and mortality among young children in low-income and middle-income countries. Human adenoviruses (HAdV), particular HAdV species F (40, 41) has been recognized as important causal pathogens, however limited data exist on molecular epidemiology of other HAdV associated with acute gastroenteritis.

Methods: In the present preliminary study, we performed a case-control study involving 273 children who presented diarrheal disease and 361 healthy children matched control in Children's hospital of Hebei Province (China) to investigate the relationship between non-enteric HAdV and diarrhea.

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Background: Human adenovirus (HAdV) serotypes 2, 3 and 7 are more prevalent than other serotypes and have been associated with severe pneumonia in pediatric children. Molecular typing of HAdV is not routinely performed in clinical diagnostic laboratories as it is time-consuming and labor-intensive.

Methods: In the present study, we developed a triplex quantitative real-time PCR assay (tq-PCR) in a single closed tube for differential detection and quantitative analysis of HAdV serotypes 2, 3 and 7.

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The sensitivity of qRT-PCR assay is not adequate for the detection of the samples with lower viral load, particularly in the cerebrospinal fluid (CSF) of patients. Here, we present the development of a highly sensitive real-time nested RT-PCR (RTN RT-PCR) assay in a single closed tube for detection of human enterovirus (HEV). The clinical performance of both RTN RT-PCR and qRT-PCR was also tested and compared using 140 CSF and fecal specimens.

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Article Synopsis
  • A rapid reverse-transcription recombinase aided amplification (RT-RAA) assay was developed to quickly detect RSV subgroups A and B at 39°C within 30 minutes.
  • The assay demonstrated high sensitivity with 38 and 35 copies per reaction for RSVA and RSVB respectively, and showed no cross-reactivity with other respiratory viruses.
  • In testing 306 clinical specimens, the assay identified 79 positive RSV cases, aligning closely with results from the standard RSV RT-qPCR test, indicating it as a reliable and efficient detection method.
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Article Synopsis
  • The Respiratory Pathogen 13 Detection Kit (13× kit) detects 11 respiratory viruses along with Mycoplasma pneumoniae and Chlamydia in one reaction.
  • In a study of 572 nasopharyngeal samples from hospitalized children, the 13× kit demonstrated a high accuracy rate of 95.98% when compared to a standard 2-tube multiplex PCR assay.
  • The kit's effectiveness in diagnosing MP and Chlamydia can assist doctors in making informed treatment decisions, potentially reducing unnecessary antibiotic prescriptions.
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Antitumor-analgesic peptide (AGAP) is a novel recombinant polypeptide. The primary study showed that AGAP 1.0 mg/kg exhibited strong analgesic and antitumor effects.

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Background: Cognitive behavioral therapy for insomnia (CBT-I) is well-validated in the western countries. However, it has not been widely adopted or disseminated in China. One possibility is that therapeutic approaches drawn from traditional Chinese medicine (TCM) will be more widely accepted.

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Objective: To investigate the effect of Angelica polysaccharide (APS), platelet-derived growth factor (PDGF) and thrombopoietin (TPO) on the proliferation and apoptosis of human megakaryocytic cell line M-07e.

Methods: Cell count and the viability testing of M-07e cells (trypan blue exclusion assay) were performed at 24 hours, 48 hours and 72 hours after treatment with APS, PDGF or TPO. Three apoptosis related flow cytometric assays including Annexin V, Caspase-3 and JC-1 were performed to determine apoptotic rate of each group at 72 hours after the treatment.

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