Wen‐Wei Zhang

ORCID: 0000-0003-1996-876X
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About
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Research Areas
  • Research on Leishmaniasis Studies
  • Trypanosoma species research and implications
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Parasites and Host Interactions
  • Atrial Fibrillation Management and Outcomes
  • Virus-based gene therapy research
  • CRISPR and Genetic Engineering
  • Ferroptosis and cancer prognosis
  • Probiotics and Fermented Foods
  • Amoebic Infections and Treatments
  • Innovation and Socioeconomic Development
  • Animal Genetics and Reproduction
  • Cancer Research and Treatments
  • Adipose Tissue and Metabolism
  • Antimicrobial Peptides and Activities
  • Pediatric Hepatobiliary Diseases and Treatments
  • Cardiac electrophysiology and arrhythmias
  • Viral Infectious Diseases and Gene Expression in Insects
  • Pancreatitis Pathology and Treatment
  • Thyroid Cancer Diagnosis and Treatment
  • Conducting polymers and applications
  • Genetic Mapping and Diversity in Plants and Animals
  • Protein Hydrolysis and Bioactive Peptides
  • Protein Tyrosine Phosphatases

McGill University
2014-2025

Gansu Agricultural University
2018-2025

Zhejiang Chinese Medical University
2023-2025

Hangzhou First People's Hospital
2025

Chinese People's Liberation Army
2023-2024

Nanjing Agricultural University
2005-2024

Northwestern University
2019-2024

Zhongshan Hospital
2024

Renal Research Institute
2019-2020

Qingdao University
2015-2018

Recombinant adenoviruses containing the canine factor IX (FIX) cDNA were directly introduced in hind leg muscle of mice. We show that (i) nude mice, high expression (1-5 micrograms/ml plasma) FIX protein can be detected for > 300 days; (ii) contrast, was transient (7-10 days) normal mice; (iii) CD8+ lymphocytes could within 3 days infected tissue; (iv) use beta 2-microglobulin and immunoglobulin M heavy chain "knockout" mice showed lack sustained is due to cell-mediated humoral immune...

10.1073/pnas.92.5.1401 article EN Proceedings of the National Academy of Sciences 1995-02-28

ABSTRACT The prokaryotic CRISPR (clustered regularly interspaced short palindromic repeat)-Cas9, an RNA-guided endonuclease, has been shown to mediate efficient genome editing in a wide variety of organisms. In the present study, CRISPR-Cas9 system adapted Leishmania donovani , protozoan parasite that causes fatal human visceral leishmaniasis. We introduced Cas9 nuclease into L. and generated guide RNA (gRNA) expression vectors by using rRNA promoter hepatitis delta virus (HDV) ribozyme. It...

10.1128/mbio.00861-15 article EN cc-by-nc-sa mBio 2015-07-22

Leishmaniasis is a neglected tropical disease caused by Leishmania protozoa transmitted infected sand flies. Vaccination through leishmanization with live major has been used successfully but no longer practiced because it resulted in occasional skin lesions. A second generation described here using CRISPR genome edited L. strain (LmCen-/-). Notably, LmCen-/- genetically engineered centrin gene knock-out mutant that antibiotic resistant marker free and does not have detectable off-target...

10.1038/s41467-020-17154-z article EN cc-by Nature Communications 2020-07-10

A central question in Leishmania research is why most species cause cutaneous infections but others fatal visceral disease. Interestingly, L. donovani causes both and leishmaniasis Sri Lanka. clinical isolates were therefore obtained from (CL-SL) (VL-SL) patients The CL-SL isolate was severely attenuated compared to the VL-SL for survival organs BALB/c mice. Genomic transcriptomic analysis argue that gene deletions or pseudogenes specific are not responsible difference disease tropism single...

10.1371/journal.ppat.1004244 article EN cc-by PLoS Pathogens 2014-07-03

Due to the strong stress resistance, causing food spoilage and toxin production of spore‐forming Bacillus species, their presence will be detrimental quality assurance dairy products. Impacts five strains ( licheniformis H1, B. H2, subtilis Z2, cereus Z6‐1 Z6‐2) originated from products on pasteurised yoghurt were investigated. Physiological characteristics strains, including growth, acid production, proteolysis, amylase extracellular polysaccharide biofilm formation, analysed. Additionally,...

10.1111/1471-0307.13169 article EN International Journal of Dairy Technology 2025-02-01

Emerging evidence documents a key function for the forkhead transcription factor FoxO1 in cellular metabolism. Here, we investigate role of regulation fatty acid (FA) metabolism muscle cells. C2C12 cells expressing an inducible construct with either wild type or mutant form (FoxO1/TSS) refractory to protein kinase B inhibitory effects were generated. activation after myotube formation altered expression several genes FA Acyl-CoA oxidase and peroxisome proliferator-activated receptor δ mRNA...

10.1074/jbc.m413625200 article EN cc-by Journal of Biological Chemistry 2005-02-04

Leishmania donovani is the etiologic agent of fatal visceral leishmaniasis in man. During their life cycle, exist as flagellated promastigotes within sandfly vector and nonflagellated amastigotes macrophage phagolysosomal compartment mammalian host. The transformation from to a critical step for establishment infection, molecular basis this poorly understood. To define amastigote survival host, we previously identified an stage-specific gene family termed “A2.” In present study, have...

10.1073/pnas.94.16.8807 article EN Proceedings of the National Academy of Sciences 1997-08-05

Leishmania donovani is a protozoan parasite that exists as free-living promastigote in the sandfly insect vector and an amastigote inside mammalian host macrophage phagolysosome compartment. The L. A2 genes have been described previously developmentally expressed amastigotes but can be induced experimentally promastigotes by combination of pH temperature shifts, conditions mimic phagolysosomal compartment cell. Considering importance stage human infections, we examined molecular basis for...

10.1074/jbc.271.29.17081 article EN cc-by Journal of Biological Chemistry 1996-07-01

Activation of Toll-like receptors (TLRs) on antigen-presenting cells the innate immune system initiates, amplifies, and directs antigen-specific acquired response. Ligands that stimulate TLRs therefore represent potential vaccine adjuvants. In present study, we determined whether imiquimod its related compound R848, which are TLR7 and/or TLR8 agonists, adjuvants when delivered topically, subcutaneously, or intramuscularly. Using Leishmania major infection model in BALB/c mice, vaccination...

10.1128/iai.01527-07 article EN Infection and Immunity 2008-05-13

CRISPR-Cas9-mediated genome editing has recently been adapted for Leishmania spp. parasites, the causative agents of human leishmaniasis. We have optimized this genome-editing tool by selecting cells with CRISPR-Cas9 activity through cotargeting miltefosine transporter gene; mutation gene leads to resistance. This strategy integrated into a triple guide RNA (gRNA) expression vector was used delete all 11 copies A2 multigene family; not previously possible traditional gene-targeting method....

10.1128/msphere.00340-16 article EN cc-by mSphere 2017-01-19

Abstract Visceral Leishmaniasis (VL), a potentially fatal disease is caused by Leishmania donovani parasites with no vaccine available. Here we produced dermotropic live attenuated centrin gene deleted major ( LmCen −/− ) under Good Laboratory Practices and demonstrated that single intradermal injection confers robust durable protection against lethal VL transmitted naturally via bites of L. -infected sand flies prevents mortality. Surprisingly, immunogenicity characteristics revealed...

10.1038/s42003-021-02446-x article EN cc-by Communications Biology 2021-07-30

Leishmaniasis is a neglected protozoan disease affecting over 12 million people globally with no approved vaccines for human use. New World cutaneous leishmaniasis (CL) caused by L. mexicana characterized the development of chronic non-healing skin lesions. Using CRISPR/Cas9 technique, we have generated live attenuated centrin knockout (LmexCen-/-) parasites. Centrin cytoskeletal protein important cellular division in eukaryotes and, Leishmania, required only intracellular amastigote...

10.1038/s41541-022-00449-1 article EN cc-by npj Vaccines 2022-03-02

The A2 gene family is present in Leishmania donovani, which causes fatal visceral leishmaniasis human patients, but not major, cutaneous infections. genes L. donovani are stage specific and expressed at high levels the amastigote mammalian host, promastigote insect sandfly vector. tandem repeated with a distinct termed A2rel genes. In order to characterize structure function of A2-A2rel clusters, 5' 3' DNA sequences flanking cluster were isolated, sequenced used generate mutants through...

10.1046/j.1365-2958.2001.02286.x article EN Molecular Microbiology 2001-02-01

In Old World Leishmania infections, donovani is responsible for fatal visceral leishmaniasis, and L. major non-fatal cutaneous leishmaniasis in humans. The genetic differences between these species which govern the pathology or site of infection are not known. We have therefore carried out detailed analysis A2 loci because expressed but major, required survival organs by donovani. demonstrate that although contains gene regulatory sequences, multiple repeats exist protein coding regions...

10.1074/jbc.m305030200 article EN cc-by Journal of Biological Chemistry 2003-09-01

Leishmania donovani is responsible for visceral leishmaniasis, a neglected and lethal parasitic disease with limited treatment options no vaccine. The study of L. has been hindered by the lack high-quality reference genome this can impact experimental outcomes including identification virulence genes, drug targets vaccine development. We therefore generated complete assembly deep sequencing using combination second generation (Illumina) third (PacBio) technologies. Compared to current...

10.1038/s41598-018-34812-x article EN cc-by Scientific Reports 2018-11-02

The antibody response against an amastigote-specific protein (A2) from Leishmania donovani was investigated. Sera patients with trypanosomiasis and various forms of leishmaniasis were screened for anti-A2 antibodies. infected only L. or mexicana specifically recognized the A2 recombinant protein. These results consistent karyotype analyses which revealed that gene is conserved in strains. potential this antigen diagnosis further explored by screening a series sera obtained regions Sudan...

10.1128/cdli.4.5.530-535.1997 article EN Clinical and Diagnostic Laboratory Immunology 1997-09-01

In this study, crucial genes and microRNAs (miRNAs) associated with the progression, staging, prognosis of papillary thyroid cancer (PTC) were identified.Four PTC datasets, including our own mRNA-sequencing (mRNA-seq) dataset three public datasets downloaded from Gene Expression Omnibus The Cancer Genome Atlas, used to analyze differentially expressed (DEGs) miRNAs (DEMs) between tumor tissues paired normal (control). ontology (GO) terms pathways these DEGs identified, protein-protein...

10.1186/s40659-018-0188-1 article EN cc-by Biological Research 2018-11-10

Due to differences in double-strand DNA break (DSB) repair mechanisms, CRISPR-Cas9 gene editing efficiency can vary greatly different organisms. In contrast mammalian cells, the protozoan parasite Leishmania uses microhomology-mediated end joining (MMEJ) and, occasionally, homology-directed (HDR) DSBs but lacks nonhomologous end-joining pathway. Here, we show that predominantly single-strand annealing (SSA) instead of MMEJ for DSB repairs (DSBR), resulting large deletions include multiple...

10.1128/msphere.00408-19 article EN cc-by mSphere 2019-08-20

Dogs are the main reservoir host of Leishmania infantum, etiological agent zoonotic visceral leishmaniasis (ZVL). An effective vaccine against Canine Visceral Leishmaniasis (CVL) will help control and elimination ZVL. In this study, we evaluated in dogs safety, immunogenicity, efficacy a live attenuated major Centrin gene-deleted (LmCen−/−) as vaccine. Two doses (106 or 107) LmCen−/− were administered intradermally prime-boost regimen. Both induced equally high level IgG anti-Leishmania...

10.1038/s41541-025-01070-8 article EN cc-by-nc-nd npj Vaccines 2025-02-14
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