Journal
PLOS PATHOGENS
Volume 13, Issue 2, Pages -Publisher
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.1006206
Keywords
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Categories
Funding
- BBSRC Animal Health Research Club [BB/L004143/1]
- Genus plc
- BBSRC Institute Strategic Programme grant [BBS/E/D/20241866]
- BBSRC [BB/N015339/1, BB/L007371/1, BBS/E/D/20241866, BB/M018385/1, BBS/E/D/20241863, BB/M028313/1, BBS/E/D/20221658, BB/L004143/1, BBS/E/R/00001608, BBS/E/D/20241864, BB/M018342/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BBS/E/D/20221658, BBS/E/D/20241863, BB/N015339/1, BBS/E/D/20002172, BBS/E/D/20241866, BB/M028313/1, 1309079, BBS/E/D/20241864, BBS/E/R/00001608, BBS/OS/NW/000015, BB/L004143/1, BB/L007371/1, BB/M018385/1, BB/M018342/1] Funding Source: researchfish
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Porcine Reproductive and Respiratory Syndrome (PRRS) is a panzootic infectious disease of pigs, causing major economic losses to the world-wide pig industry. PRRS manifests differently in pigs of all ages but primarily causes late-term abortions and stillbirths in sows and respiratory disease in piglets. The causative agent of the disease is the positive-strand RNA PRRS virus (PRRSV). PRRSV has a narrow host cell tropism, limited to cells of the monocyte/macrophage lineage. CD163 has been described as a fusion receptor for PRRSV, whereby the scavenger receptor cysteine-rich domain 5 (SRCR5) region was shown to be an interaction site for the virus in vitro. CD163 is expressed at high levels on the surface of macrophages, particularly in the respiratory system. Here we describe the application of CRISPR/Cas9 to pig zygotes, resulting in the generation of pigs with a deletion of Exon 7 of the CD163 gene, encoding SRCR5. Deletion of SRCR5 showed no adverse effects in pigs maintained under standard husbandry conditions with normal growth rates and complete blood counts observed. Pulmonary alveolar macrophages (PAMs) and peripheral blood monocytes (PBMCs) were isolated from the animals and assessed in vitro. Both PAMs and macrophages obtained from PBMCs by CSF1 stimulation (PMMs) show the characteristic differentiation and cell surface marker expression of macrophages of the respective origin. Expression and correct folding of the SRCR5 deletion CD163 on the surface of macrophages and biological activity of the protein as hemoglobin-haptoglobin scavenger was confirmed. Challenge of both PAMs and PMMs with PRRSV genotype 1, subtypes 1, 2, and 3 and PMMs with PRRSV genotype 2 showed complete resistance to viral infections assessed by replication. Confocal microscopy revealed the absence of replication structures in the SRCR5 CD163 deletion macrophages, indicating an inhibition of infection prior to gene expression, i.e. at entry/fusion or unpacking stages.
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