Nested PCR effective to detect low viral loads of SARS-CoV-2 in animal samples

• Published in: Preventive veterinary medicine 2024-10, Vol.231, p.106303, Article 106303
• Main Authors: Panei, Carlos Javier, Fuentealba, Nadia Analía, Bravi, María Emilia, Moré, Gastón, Brasso, Natalia
• Format: Article
• Language: English
• Subjects: Animals; Cat Diseases - diagnosis; Cat Diseases - virology; Cats; COVID-19 - diagnosis; COVID-19 - veterinary; COVID-19 - virology; COVID-19 Nucleic Acid Testing - methods; Dog Diseases - diagnosis; Dog Diseases - virology; Dogs; Humans; Limit of detection; Nested PCR; Polymerase Chain Reaction - methods; Polymerase Chain Reaction - veterinary; Real-Time Polymerase Chain Reaction - methods; Real-Time Polymerase Chain Reaction - veterinary; SARS-CoV-2; SARS-CoV-2 - isolation & purification; Sensitivity and Specificity; Viral Load
• ISSN: 0167-5877; 1873-1716; 1873-1716
• DOI: 10.1016/j.prevetmed.2024.106303

SARS-CoV-2 emerged from an animal source and was then transmitted to humans, causing the COVID-19 pandemic. Since a wide range of animals are susceptible to SARS-CoV-2 infection, the zoonotic potential of SARS-CoV-2 increases with every new animal infected. The molecular gold standard assay for SARS-CoV-2 detection is real-time RT-PCR, where the Ct obtained is proportional to the amount of nucleic acid and can be a semi-quantitative measure of the viral load. However, since the use of real-time RT-PCR assays in animal samples is low due to the high costs, the use of validated nested PCR assays will help to monitor large-scale animal samplings, by reducing the costs of detection. In the present study, 140 samples from dogs and cats (15 SARS-CoV-2-positive samples with Ct values from 27 to 33, and 125 negative samples), previously analyzed by real-time RT-PCR, were analyzed by nested PCR. To increase the number of positive samples to determine the sensitivity of the assay, 40 human samples obtained during COVID-19 diagnosis in 2020 were included. The specificity of the primers was analyzed against samples positive to canine coronavirus (CCV) and feline infectious peritonitis virus (FIPV). To calculate the limit of detection (LoD) of the nested PCR, the viral load was estimated extrapolating the Ct value obtained by real-time RT-PCR. The Ct values obtained were considered as semi-quantitative and were able to distinguish between high, moderate and low viral loads. The Kappa value or “agreement” between assays and reliability of the nested PCR were also determined. Eleven of the animal samples analyzed by nested PCR targeting the N gene were detected as positive, while 129 were detected as negative to the virus, with Ct values ranging between17 and 31.5. All the samples from humans analyzed by nested PCR were positive. These results indicate that the assay has a sensitivity of near 95 % and a specificity of 100 %. No unspecific reactions analyzed by nested PCR were observed with the samples positive to CCV and FIPV. The samples detected as positive to SARS-CoV-2 by nested PCR were those that presented a Ct between17 and 31.5. The LoD of the nested PCR was estimated close to 50 copies/µL of viral load, corresponding with a Ct of 31.5. The Kappa value between assays was excellent (k = 0.829). The results obtained demonstrate that nested PCR is useful to detect SARS-CoV-2 low viral loads at a lower cost than with real-time RT-PCR. •Nested PCR is effective to ampl