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Resistance to chicken amyloid arthropathy is associated with a dysfunctional mutation in serum amyloid A

Falker-Gieske, Clemens (författare)
Department of Animal Sciences, Georg-August-University, Göttingen, Germany
Paul, Nora-Fabienne (författare)
Department of Animal Sciences, Georg-August-University, Göttingen, Germany
Spourita, Maria (författare)
Department of Animal Sciences, Georg-August-University, Göttingen, Germany
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Gilthorpe, Jonathan D. (författare)
Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB)
Gustmann, Karolin (författare)
Department of Animal Sciences, Georg-August-University, Göttingen, Germany
Tetens, Jens (författare)
Department of Animal Sciences, Georg-August-University, Göttingen, Germany; Center for Integrated Breeding Research, Georg-August-University, Göttingen, Germany
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 (creator_code:org_t)
John Wiley & Sons, 2023
2023
Engelska.
Ingår i: The FASEB Journal. - : John Wiley & Sons. - 0892-6638 .- 1530-6860. ; 37:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Chicken amyloid arthropathy is a debilitating disease with a major impact on animal welfare. Since the disease is triggered by bacterial infection, preventative treatment also contributes to the widespread overuse of antibiotics. Bacterial infection initiates an acute phase response including increased serum amyloid A (SAA) production by the liver. SAA accumulates at sites of infection and in particular in large joints of affected birds. Interestingly, white egg-laying chickens (WL) are resistant to the disease whilst brown egg-laying chickens (BL) are most affected. Disease susceptibility has an immunological basis but the possible contribution of underlying genetic risk factors is not understood. Using a whole genome sequencing approach, we discovered a novel variant in the SAA gene in WL, which is predicted to result in an arginine to serine substitution at position 90 (SAA.R90S). Surprisingly, when overexpressed in chicken hepatocellular carcinoma cells, SAA.R90S was expressed at a higher rate and secreted to a greater degree than the wild-type SAA protein. Moreover, RNASeq analysis showed that the R90S mutant exerted a differential effect on the expression of core transcription factors linked to cell fate determination and cell differentiation. Comparative analysis of gene expression in murine CD4 T-cells stimulated with IL-6/SAA, suggests that SAA.R90S might block an induced cell fate change toward pro-inflammatory T helper 17 cells, which are required for immunological protection against pathogenic bacteria during an acute phase response. Our results provide first mechanistic insights into the genetic resistance of WL to amyloid arthropathy and could be applied to commercial layer breeding programs to improve animal welfare and reduce the negative effects of the overuse of antibiotics.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Nyckelord

amyloidosis
avian amyloid arthropathy
genomics
next generation sequencing
protein aggregation
serum amyloid A
transcriptomics

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