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

Abstract

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.

Keywords: SARS-CoV-2; canine infectious respiratory disease complex (CIRDC); canine respiratory pathogens; influenza virus A; multiplex reverse-transcriptase qPCR (RT-qPCR).

Figure 1

Comparison of analytical sensitivity of each singleplex and multiplex qPCR and RT-qPCR assays for the detection of pathogens associated with CIRDC and SARS-CoV-2. Ct: cycle threshold; IVT RNA: in vitro transcribed RNA; R²: linearity; E: efficiency.

Figure 2

UpSet plot summarizing the number of CIRDC pathogens and SARS-CoV-2 detected in dogs using the newly developed panel. The number samples with single infection or co-infection are shown as vertical bars. The bottom left horizontal bar graph labeled Set Size shows the total number of positive samples for each specific CIRDC pathogens and SARS-CoV-2.