Key result
RNAscope with digital image analysis correlates with qRT-PCR for quantifying porcine lung viral burden.
Why the study?
PRRS is a significant disease causing major economic losses in the swine industry, prompting the development of a novel RNA-based in situ hybridization technique to detect PRRSV RNA in lung tissues.
Does RNAscope combined with digital image analysis correlate with qRT-PCR for detecting PRRSV-1 in lung tissues of infected piglets?
Does RNAscope combined with digital image analysis correlate with qRT-PCR for detecting PRRSV-1 in lung tissues of infected piglets?
RNAscope combined with digital image analysis provides a reliable semi-quantitative method for detecting PRRSV-1 in pig lung tissues, correlating significantly with qRT-PCR.
Answers are grounded in this paper and cite their sources.
May support RNAscope-digital analysis in porcine PRRSV models; leaves open prospective validation before broader adoption.
Betaarterivirus suid 1 and 2 are the causative agents of porcine reproductive and respiratory syndrome (PRRS), which is one of the most significant diseases of the swine industry, causing significant economic losses in the main pig producing countries. Here, we report the development of a novel, RNA-based in situ hybridization technique (RNAscope) to detect PRRS virus (PRRSV) RNA in lung tissues of experimentally infected animals. The technique was applied to lung tissues of 20 piglets, which had been inoculated with a wild-type, highly pathogenic PRRSV-1 strain. To determine the RNAscope’s applicability as a semi-quantitative method, we analysed the association between the proportion of the virus-infected cells measured with an image analysis software (QuPath) and the outcome of the real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) tests performed in parallel. The results of the quantitative approach of these two molecular biological methods show significant association (pseudo R2 = 0.3894, p = 0.004). This is the first time RNAscope assay has been implemented for the detection of PRRSV-1 in experimental animals.
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Dénes et al. (2021) studied Porcine reproductive and respiratory syndrome (PRRS) (n=25). RNAscope in situ hybridization vs. qRT-PCR was evaluated on Association between proportion of infected cells (RNAscope) and log10 genome copy numbers (qRT-PCR) (pseudo R2 = 0.3894, p=0.004). RNAscope in situ hybridization combined with digital image analysis demonstrated a significant association with qRT-PCR for quantifying PRRSV-1 viral burden in porcine lung tissues (pseudo R2 = 0.3894, p = 0.004).
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