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Alpha-1-Acid Glycoprotein Quantification Via Spatial Proximity Analyte Reagent Capture Luminescence Assay: Application As Diagnostic and Prognostic Marker in Serum and Effusions of Cats with Feline Infectious Peritonitis Undergoing GS-441524 Therapy

Abstract

Until recently, the diagnosis of feline infectious peritonitis (FIP) in cats usually led to euthanasia, but recent research has revealed that antiviral drugs, including the nucleoside analog GS-441524, have the potential to effectively cure FIP. Alpha-1-acid glycoprotein (AGP) has been suggested as a diagnostic marker for FIP. However, AGP quantification methods are not easily accessible. This study aimed to establish a Spatial Proximity Analyte Reagent Capture Luminescence (SPARCL) assay on the VetBio-1 analyzer to determine the AGP concentrations in feline serum and effusion samples. Linearity was found in serial dilutions between 1:2000 and 1:32,000; the intra-run and inter-run precision was <5% and <15%, respectively; and AGP was stable in serum stored for at least 8 days at room temperature, at 4 °C and at -20 °C. Cats with confirmed FIP had significantly higher serum AGP concentrations (median: 2954 µg/mL (range: 200-5861 µg/mL)) than those with other inflammatory diseases (median: 1734 µg/mL (305-3449 µg/mL)) and clinically healthy cats (median 235 µg/mL (range: 78-616 µg/mL); < 0.0001). The AGP concentrations were significantly higher in the effusions from cats with FIP than in those from diseased cats without FIP ( < 0.0001). The AGP concentrations in the serum of cats with FIP undergoing GS-441524 treatment showed a significant drop within the first seven days of treatment and reached normal levels after ~14 days. In conclusion, the VetBio-1 SPARCL assay offers a precise, fast and cost-effective method to measure the AGP concentrations in serum and effusion samples of feline patients. The monitoring of the AGP concentration throughout FIP treatment provides a valuable marker to evaluate the treatment's effectiveness and identify potential relapses at an early stage.

Citing Articles

Short Treatment of 42 Days with Oral GS-441524 Results in Equal Efficacy as the Recommended 84-Day Treatment in Cats Suffering from Feline Infectious Peritonitis with Effusion-A Prospective Randomized Controlled Study.

Zuzzi-Krebitz A, Buchta K, Bergmann M, Krentz D, Zwicklbauer K, Dorsch R Viruses. 2024; 16(7).

PMID: 39066306 PMC: 11281457. DOI: 10.3390/v16071144.

References
1.
Murphy B, Perron M, Murakami E, Bauer K, Park Y, Eckstrand C . The nucleoside analog GS-441524 strongly inhibits feline infectious peritonitis (FIP) virus in tissue culture and experimental cat infection studies. Vet Microbiol. 2018; 219:226-233. PMC: 7117434. DOI: 10.1016/j.vetmic.2018.04.026. View

2.
Akhavan-Tafti H, Binger D, Blackwood J, Chen Y, Creager R, de Silva R . A homogeneous chemiluminescent immunoassay method. J Am Chem Soc. 2013; 135(11):4191-4. DOI: 10.1021/ja312039k. View

3.
Ceron J, Eckersall P, Martynez-Subiela S . Acute phase proteins in dogs and cats: current knowledge and future perspectives. Vet Clin Pathol. 2005; 34(2):85-99. DOI: 10.1111/j.1939-165x.2005.tb00019.x. View

4.
Gut M, Leutenegger C, Huder J, Pedersen N, Lutz H . One-tube fluorogenic reverse transcription-polymerase chain reaction for the quantitation of feline coronaviruses. J Virol Methods. 1999; 77(1):37-46. PMC: 7185542. DOI: 10.1016/s0166-0934(98)00129-3. View

5.
Stoddart C, Scott F . Intrinsic resistance of feline peritoneal macrophages to coronavirus infection correlates with in vivo virulence. J Virol. 1989; 63(1):436-40. PMC: 247703. DOI: 10.1128/JVI.63.1.436-440.1989. View