Development and Validation of a Panel of One-Step Four-Plex qPCR/RT-qPCR Assays for Simultaneous Detection of SARS-CoV-2 and Other Pathogens Associated with Canine Infectious Respiratory Disease Complex

被引:8
|
作者
Thieulent, Come J. [1 ,2 ]
Carossino, Mariano [1 ,2 ]
Peak, Laura [1 ]
Strother, Keith [1 ]
Wolfson, Wendy [3 ]
Balasuriya, Udeni B. R. [1 ,2 ]
机构
[1] Louisiana State Univ, Sch Vet Med, Louisiana Anim Dis Diag Lab, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
[3] Louisiana State Univ, Sch Vet Med, Dept Vet Clin Sci, Baton Rouge, LA 70803 USA
来源
VIRUSES-BASEL | 2023年 / 15卷 / 09期
关键词
multiplex reverse-transcriptase qPCR (RT-qPCR); canine respiratory pathogens; canine infectious respiratory disease complex (CIRDC); SARS-CoV-2; influenza virus A; REAL-TIME PCR; INFLUENZA-VIRUS; EMERGING PATHOGENS; PARAINFLUENZA VIRUS; DOGS; DIFFERENTIATION; ZOOEPIDEMICUS; SURVEILLANCE; TRANSMISSION; PNEUMOVIRUS;
D O I
10.3390/v15091881
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Canine infectious respiratory disease complex (CIRDC) is the primary cause of respiratory disease in the canine population and is caused by a wide array of viruses and bacterial pathogens with coinfections being common. Since its recognition in late 2019, Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has been reported to cause respiratory disease in dogs. Therefore, the rapid detection and differentiation of SARS-CoV-2 from other common viral and bacterial agents is critical from a public health standpoint. Here, we developed and validated a panel of four one-step multiplex qPCR/RT-qPCR assays for the detection and identification of twelve pathogens associated with CIRDC (canine adenovirus-2, canine distemper virus, canine herpesvirus-1, canine influenza A virus, canine parainfluenza virus, canine pneumovirus, canine respiratory coronavirus, SARS-CoV-2, Bordetella bronchiseptica, Streptococcus equi subsp. zooepidemicus, Mycoplasma cynos, and M. canis), as well as the identification of three main CIV subtypes (i.e., H3N2, H3N8, and H1N1). All developed assays demonstrated high specificity and analytical sensitivity. This panel was used to test clinical specimens (n = 76) from CIRDC-suspected dogs. M. canis, M. cynos, and CRCoV were the most frequently identified pathogens (30.3%, 25.0%, and 19.7% of samples, respectively). The newly emerging pathogens CPnV and SARS-CoV-2 were detected in 5.3% of samples and coinfections were identified in 30.3%. This new multiplex qPCR/RT-qPCR panel is the most comprehensive panel developed thus far for identifying CIRDC pathogens, along with SARS-CoV-2.
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页数:16
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