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.
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http://dx.doi.org/10.1016/j.saa.2025.125863 | DOI Listing |
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 PDFAnimals (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 PDFVet 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 PDFPLoS Pathog
June 2024
College of Veterinary Medicine, Northwest A&F University, Yangling, China.
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 PDFFront 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).
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