98%
921
2 minutes
20
The current study is the first comprehensive report on the expression of fibrinogen binding protein (FIB) antigen in the genetically engineered switchgrass. Mammary tissue inflammation is one of the major infectious diseases caused by in the dairy animals. The aim of the present study is to develop an efficient and economical bioengineered immunogen for controlling mastitis in developing countries. Plant parts are served as bio-factories to produce antigens against infectious diseases. In this research, mastitis antigenic target (FIB) of was expressed in switchgrass via Ag-nanoparticle mediated nuclear gene transformation to ease oral delivery of FIB antigen. FIB gene was cloned in expression vector through TOPO and Gateway cloning method. Transformation and integration of transgene was confirmed through PCR. The maximum concentration of total soluble fraction of FIB was calculated, and total soluble protein accumulated up to 0.5%. The recombinant FIB protein was purified and extract was prepared. FIB protein induced humoral immune response in mice and immunized orally. To administration oral immunogens against mastitis, FIB from was commercially synthesized and PCR purified, the purified FIB gene was cloned into expression vector. Ag-NPs were encapsulated with pFIB and used as nanocarrier to target delivery of gene in forage grass. Forage seeds were successfully transformed through nuclear delivery and presence of transgene was confirmed through polymerase chain reaction. Transgenic lines of forage grass expressing FIB antigen is successfully developed. The transgenic lines expressing FIB gene were used for mouse study and in-vivo trials showed that switchgrass as transgenic immunogen developed antibodies in blood of animals upon orally delivering the FIB antigen. The expression of mastitis antigen in edible plants could contribute significantly to the development of cost effective and orally administered antigen-based subunit immunogen against dairy mastitis.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11646247 | PMC |
http://dx.doi.org/10.1007/s12298-024-01528-4 | DOI Listing |
Discov Nano
September 2025
Department of Rehabilitation Medicine, Rehabilitation Medical Center, Key Laboratory of Rehabilitation Medicine in Sichuan Province, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Immunoelectron Microscopy (IEM) is a technique that combines specific immunolabeling with high-resolution electron microscopic imaging to achieve precise spatial localization of biomolecules at the subcellular scale (< 10 nm) by using high-electron-density markers such as colloidal gold and quantum dots. As a core tool for analyzing the distribution of proteins, organelle interactions, and localization of disease pathology markers, it has irreplaceable value, especially in synapse research, pathogen-host interaction mechanism, and tumor microenvironment analysis. According to the differences in labeling sequence and sample processing, the IEM technology system can be divided into two categories: the first is pre-embedding labeling, which optimizes the labeling efficiency through the pre-exposure of antigenic epitopes and is especially suitable for the detection of low-abundance and sensitive antigens; the second is post-embedding labeling, which relies on the low-temperature resin embedding (e.
View Article and Find Full Text PDFViruses
August 2025
Institution of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.
In the modern era of HIV treatment, people co-infected with HIV and HBV still face poor liver outcomes, including liver fibrosis, liver cirrhosis, and hepatocellular carcinoma. We investigated baseline characteristics and long-term liver function outcomes in 435 people living with HIV and HBV co-infection, focusing on HCC-associated point mutations (PMs) and PreS region deletion mutations. PMs were present in 72.
View Article and Find Full Text PDFJ Infect
August 2025
The Francis Crick Institute, 1 Midland Road, London, UK; Department of Infectious Diseases, University College London Hospitals, Euston Road, London, UK; Division of Infection and Immunity, University College London, Gower Street, London, UK. Electronic address:
Objectives: We set out to evaluate Hepatitis B core-related antigen (HBcrAg) as a proxy for hepatitis B (HBV) viral load (VL) and liver disease in two different population settings.
Methods: We undertook a cross-sectional retrospective observational study using samples and data from adults living with chronic HBV infection from the United Kingdom (UK, n=142) and South Africa (SA, n=211). We assessed HBcrAg distribution, relationship with other biomarkers, and risk stratification performance, applying point of care test (POCT) thresholds.
Virol J
August 2025
Department of Epidemiology and Biostatistics, Indiana University Bloomington, Bloomington, IN, USA.
Background: Evaluation of liver fibrosis appears to be easily overlooked in the clinic for the chronic Hepatitis D. Herein, we determine the Clinical Impact of liver fibrosis among HBsAg-positive/Anti-HDV positive US general adults.
Methods: Data were obtained from the National Health and Nutrition Examination Survey (NHANES) 1999-2020.
Eur J Pediatr
August 2025
Pediatrics Department, Faculty of Medicine, Benha University, Benha, Egypt.
Unlabelled: Children with chronic liver diseases (CLD) face more significant clinical problems. The most reliable technique for detecting liver fibrosis is still liver biopsy (LB). Our investigation assessed Von-Willebrand Factor Antigen (VWF Ag) plasma titer as a probable non-invasive predictor for grading liver fibrosis in children with CLD.
View Article and Find Full Text PDF