Core-shell Au@Ag NPs-based SERS-LFIA for the simultaneous quantitation of PEDV and PoRVA on site.

Spectrochim Acta A Mol Biomol Spectrosc

College of Animal Science and Technology, Guangxi Key Laboratory of Animal Breeding, Disease Control and Prevention, Guangxi University, Nanning 530004 Guangxi, China. Electronic address:

Published: May 2025

Porcine epidemic diarrhea virus (PEDV) and porcine group A rotavirus (PoRVA) are predominant pathogens responsible for infectious diarrhea in porcine. Co-infections of PEDV and PoRVA have become a common situation in porcine farms in recent years, which increases the severity of the diarrhea disease and makes the accurate diagnosis more difficult. Rapid quantitation of PEDV and PoRVA is of great significance for the guarantee of disease control. In this study, a 4-mercaptobenzoic acid (MBA) modified core-shell Au@Ag nanoparticles (Au@MBA@Ag NPs) based lateral flow immunochromatography (LFIA) with dual-signal modes of visual observation and surface-enhanced Raman scattering (SERS) signal analysis was developed for the rapid and sensitive detection of PEDV and PoRVA. The established SERS-LFIA was capable of simultaneous quantitation of PEDV and PoRVA in porcine fecal samples within 20 min, with visual limits of detection (LODs) of 6.25 × 10 TCID/mL and 7.42 × 10 copies/μL for PEDV and PoRVA, respectively. The LODs based on Raman signals were as low as 8.01 × 10 TCID/mL and 3.19 × 10 copies/μL for PEDV and PoRVA, respectively, which were more than two orders of magnitude lower than the conventional colloidal gold (AuNPs) based colorimetric immunochromatography. Additionally, the SERS-LFIA exhibited no cross-reactivity with other prevalent pathogens and was highly repeatability, with a coefficient of variation (CV) of less than 15 %. When detecting clinical samples, the overall compliance of the SERS-LFIA with RT-PCR results was 93.3 %. Thus, the developed SERS-LFIA showed great potential for field applications on the rapid diagnosis of PEDV and PoRVA infection.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.saa.2025.125863DOI Listing

Publication Analysis

Top Keywords

pedv porva
32
quantitation pedv
12
pedv
9
porva
9
core-shell au@ag
8
simultaneous quantitation
8
copies/μl pedv
8
sers-lfia
5
porcine
5
au@ag nps-based
4

Similar Publications

Core-shell Au@Ag NPs-based SERS-LFIA for the simultaneous quantitation of PEDV and PoRVA on site.

Spectrochim Acta A Mol Biomol Spectrosc

May 2025

College of Animal Science and Technology, Guangxi Key Laboratory of Animal Breeding, Disease Control and Prevention, Guangxi University, Nanning 530004 Guangxi, China. Electronic address:

Porcine epidemic diarrhea virus (PEDV) and porcine group A rotavirus (PoRVA) are predominant pathogens responsible for infectious diarrhea in porcine. Co-infections of PEDV and PoRVA have become a common situation in porcine farms in recent years, which increases the severity of the diarrhea disease and makes the accurate diagnosis more difficult. Rapid quantitation of PEDV and PoRVA is of great significance for the guarantee of disease control.

View Article and Find Full Text PDF

Genome Characterization of Mammalian Orthoreovirus and Porcine Epidemic Diarrhea Virus Isolated from the Same Fattening Pig.

Animals (Basel)

January 2025

Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China.

In 2020, severe diarrhea occurred in four-month-old fattening pigs from nine farms in Shandong Province, China. Fecal samples were collected from diseased pigs and tested by PCR for the presence of mammalian orthoreovirus (MRV), porcine epidemic diarrhea virus (PEDV), porcine deltacoronavirus (PDCoV), porcine rotavirus A (PoRVA), transmissible gastroenteritis virus (TGEV), porcine kobuvirus (PKV), and pseudorabies virus (PRV). The viral RNA of MRV and PEDV was detected in the fecal samples.

View Article and Find Full Text PDF

Development and Clinical Application of a Molecular Assay for Four Common Porcine Enteroviruses.

Vet Sci

July 2024

Key Laboratory of Poultry Disease Diagnosis and Immunity in Shandong Province, Poultry Research Institute, Shandong Academy of Agricultural Sciences, Jinan 250100, China.

Porcine epidemic diarrhea virus (PEDV), porcine transmissible gastroenteritis virus (TGEV), porcine deltacoronavirus (PDCoV), and porcine rotavirus-A (PoRVA) are the four main pathogens that cause viral diarrhea in pigs, and they often occur in mixed infections, which are difficult to distinguish only according to clinical symptoms. Here, we developed a multiplex TaqMan-probe-based real-time RT-PCR method for the simultaneous detection of PEDV, TGEV, PDCoV, and PoRVA for the first time. The specific primers and probes were designed for the M protein gene of PEDV, N protein gene of TGEV, N protein gene of PDCoV, and VP7 protein gene of PoRVA, and corresponding recombinant plasmids were constructed.

View Article and Find Full Text PDF

PoRVA and PEDV coinfections are extremely common in clinical practice. Although coinfections of PoRVA and PEDV are known to result in increased mortality, the underlying mechanism remains unknown. Here, we found that PoRVA infection promoted PEDV infection in vivo and in vitro and that PoRVA G9P[23] (RVA-HNNY strain) enhanced PEDV replication more significantly than did PoRVA G5P[7] (RVA-SXXA strain).

View Article and Find Full Text PDF

Development of a triplex quantitative reverse transcription-polymerase chain reaction for the detection of porcine epidemic diarrhea virus, porcine transmissible gastroenteritis virus, and porcine rotavirus A.

Front Microbiol

May 2024

State Key Laboratory for Animal Disease Control and Prevention, Heilongjiang Provincial Key Laboratory of Laboratory Animal and Comparative Medicine, National Poultry Laboratory Animal Resource Center, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.

Porcine viral diarrhea is caused by many pathogens and can result in watery diarrhea, dehydration and death. Various detection methods, such as polymerase chain reaction (PCR) and real-time quantitative PCR (qPCR), have been widely used for molecular diagnosis. We developed a triplex real-time quantitative reverse transcription PCR (qRT-PCR) for the simultaneous detection of three RNA viruses potentially associated with porcine viral diarrhea: porcine epidemic diarrhea virus (PEDV), porcine transmissible gastroenteritis virus (TGEV), and porcine rotavirus A (PoRVA).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!