IP Library › Granted Patent US 12,449,424
Granted Patent B2
US 12,449,424 · App. 17/413,548 · Granted Oct 21, 2025

In vitro method for detecting avian intestinal dysbiosis

Inventors: Stefan Pelzer (Gütersloh, DE); Monika Flügel (Steinhagen, DE); Sarah Hark (Gütersloh, DE); Evy Goossens (Wachtebeke, BE); Filip Van Immerseel (Eke, BE); Richard Ducatelle (Wortegem-Petegem, BE); Lieven Van Meulebroek (Zottegem, BE); Lynn Vanhaecke (Balegem, BE)
Assignee: Evonik Operations GmbH
G01N33/6848G01N30/7233G01N33/6893G01N2800/06G01N2800/52
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Quick Facts
Patent No.
US 12,449,424
App. No.
17/413,548
Granted
Oct 21, 2025
Kind
B2
Abstract

The invention pertains to an in vitro method for detecting avian intestinal dysbiosis, the method comprising determining the presence and/or level of isoleucyl-arginine (C 12 H 25 O 3 N 5 ) or isomers thereof in avian sample material wherein the presence and/or an increased level of isoleucyl-arginine (C 12 H 25 O 3 N 5 ) or isomers thereof in comparison to a non-affected control is indicative for avian intestinal dysbiosis.

Claims (19)

1. An in vitro method for detecting avian intestinal dysbiosis, comprising:

a) determining the presence or level of isoleucyl-arginine or isomers thereof in avian sample material, wherein the presence or an increased level of isoleucyl-arginine or isomers thereof in comparison to a non-affected control animal is indicative for avian intestinal dysbiosis, wherein the presence or level of isoleucyl-arginine or isomers thereof are detected or quantified via LC-MS, an enzyme assay, or LC combined with pre- or post-column derivatization and fluorescence or UV detection; and

b) administering probiotic agents, prebiotic agents, botanicals, organic/fatty acids, zeolites, bacteriophages or bacteriolytic enzymes or a combination thereof to animals exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof in comparison to a control animal.

2. The method of claim 1 , wherein the avian sample material is, of comprises, avian excremental material.

3. The method of claim 1 , wherein the avian sample material is, of comprises, avian feces.

4. The method of claim 1 , wherein the avian sample material is, of comprises, pooled avian feces deriving from an avian flock.

5. The method of claim 1 , wherein the isoleucyl-arginine or isomers thereof are detected or quantified via LC-MS.

6. The method of claim 1 , wherein the isoleucyl-arginine or isomers thereof are detected or quantified via an enzyme assay.

7. The method of claim 1 , wherein the isoleucyl-arginine or isomers thereof are detected or quantified via LC combined with pre- or post-column derivatization and fluorescence or UV detection.

8. The method of claim 4 , wherein the isoleucyl-arginine or isomers thereof are detected or quantified via LC-MS.

9. The method of claim 4 , wherein the isoleucyl-arginine or isomers thereof are detected or quantified via an enzyme assay.

10. The method of claim 4 , wherein the isoleucyl-arginine or isomers thereof are detected or quantified via LC combined with pre- or post-column derivatization and fluorescence or UV detection.

11. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is administered a probiotic agent in its feed or water.

12. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is administered a prebiotic in its feed or water.

13. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is administered a botanical in its feed or water.

14. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is administered organic acid in its feed or water.

15. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is treated by administering a fatty acid to the animal in its feed or water.

16. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is administered a zeolite in its feed or water.

17. The method of claim 1 , wherein, in step b), said animal exhibiting the presence of, or an increased level of, isoleucyl-arginine or isomers thereof is administered a bacteriophage or a bacteriolytic enzyme in its feed or water.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2021
From: PELZER, STEFAN; FLÜGEL, MONIKA; HARK, SARAH; GOOSSENS, EVY; VAN IMMERSEEL, FILIP; DUCATELLE, RICHARD; VAN MEULEBROEK, LIEVEN; VANHAECKE, LYNN
To: EVONIK OPERATIONS GMBH
Reel/Frame 056956/0708 →
Priority Claims (1)
EP 18212599 · Dec 14, 2018 · regional
Continuity (1)
Related Publication 20220050115A1 · Feb 17, 2022
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“Clostridium perfringens strain NE_10 plasmid pNetB-NE10, complete sequence,” XP-002761708, Database accession No. JQ655731 (Dec. 2012). [cited by applicant]
Database WPI, Thomson Scientific, London, GB; XP-002744039; CN 102 697 812 A (Univ. Shandong Agric.), abstract (Oct. 2012). [cited by applicant]
Database accession No. BDE57256; [cited by applicant]
Database accession No. EA946288; Sequence 166055 from U.S. Pat. No. 7,374,927; (Aug. 2008). [cited by applicant]
Database accession No. EA876028; Sequence 95795 from U.S. Pat. No. 7,374,927; (Aug. 2008). [cited by applicant]
Database accession No. BCL09680; Avena sativa BAD specific multiplex PCR primer; (Mar. 2016). [cited by applicant]
Database accession No. BCL16835; Avena sativa BAD specific multiplex PCR primer; (Mar. 2016). [cited by applicant]
Database accession No. HJ900945; Sequence 97404 from U.S. Pat. No. 8,673,560; (Feb. 2015). [cited by applicant]
Database accession No. AWZ90261; [cited by applicant]
Database accession No. AFB71766; [cited by applicant]
Database accession No. HW832967; A method for simultaneous detection and/or quantification of multiple bacteria; (Oct. 2015). [cited by applicant]
Database accession No. GS_NUC_ALERT:WO2016201272.163953; standard, peptide; (Jun. 2015). [cited by applicant]
Aade, et al., “Haematological parameters change in [cited by applicant]
Abeyrathne, et al.. “Sequential separation of lysozyme, ovomucin, ovotransferrin, and ovalbumin from egg white,” [cited by applicant]
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Benjamini, et al., “Controlling the False Discovery Rate: a Practical and Powerful Approach to Multiple Testing,” [cited by applicant]
Bischoff, et al., “Intestinal permeability—a new target for disease prevention and therapy,” [cited by applicant]
Chapman, “Milestones in avian coccidiosis research: A review,” [cited by applicant]
Chen, et al., “Identification of potential biomarkers for gut barrier failure in broiler chickens,” [cited by applicant]
Chen, et al., “Microfluidic isolation and transcriptome analysis of serum microvesicles,” [cited by applicant]
Cheruvanky, et al., “Rapid isolation of urinary exosomal biomarkers using a nanomembrane ultrafiltration concentrator,” [cited by applicant]
Chuka, et al., “A Comparison of the haematological and biochemical indices of broiler and red jungle (Hamburgh) fowl ( [cited by applicant]
Clayton, et al., “Analysis of antigen presenting cell derived exosomes, based on immuno-magnetic isolation and flow cytometry,” [cited by applicant]
Cooper, et al., “Diagnosing clostridial enteric disease in poultry,” [cited by applicant]
Dalloul, et al., “Poultry coccidiosis: recent advancements in control measures and vaccine development,” [cited by applicant]
Ding, et al., “Transport of Antihypertensive Peptide RVPSL, Ovotransferrin 328-332, in Human Intestinal Caco-2 Cell Monolayers,” [cited by applicant]
Dinh, et al., “Modulation of microRNAs in two genetically disparate chicken lines showing different necrotic enteritis disease susceptibility,” [cited by applicant]
Fukui, et al., “Changes of Intestinal Functions in Liver Cirrhosis,” [cited by applicant]
Garcia, et al., “Experimental infection of commercial layers using a [cited by applicant]
Gholamiandehkordi, et al., “Quantification of gut lesions in a subclinical necrotic enteritis model,” [cited by applicant]
Gilani, et al., “New biomarkers for increased intestinal permeability induced by dextran sodium sulphate and fasting in chickens,” [cited by applicant]
Gohari, et al., “A Novel Pore-Forming Toxin in Type A [cited by applicant]
Goossens, et al., “ [cited by applicant]
Goossens, et al., “Elevated faecal ovotransferrin concentrations are indicative for intestinal barrier failure in broiler chickens,” [cited by applicant]
Guerrant, et al., “Biomarkers of Environmental Enteropathy, Inflammation, Stunting and Impaired Growth in Children in Northeast Brazil,” [cited by applicant]
Johnson, et al., “Anticoccidial drugs: lesion scoring techniques in battery and floor-pen experiments with chickens,” [cited by applicant]
Kogut, et al., “Editorial: Gut Health: The New Paradigm in Food Animal Production,” [cited by applicant]
Lee, et al., “Therapeutic potential of hen egg white peptides for the treatment of intestinal inflammation,” [cited by applicant]
Moore, et al., “Necrotic enteritis predisposing factors in broiler chickens,” [cited by applicant]
M'Sadeq, et al., “Towards the control of necrotic enteritis in broiler chickens with in-feed antibiotics phasing-out worldwide,” [cited by applicant]
O'Reilly, et al., “Acute phase proteins: a review of their function, behaviour and measurement in chickens,” [cited by applicant]
O'Reilly, Emily “Acute phase proteins and biomarkers for health in chickens,” PHD thesis, University of Glasgow, Scotland, pp. 1-137 (Jan. 2016). [cited by applicant]
O'Reilly, Emily “Acute phase proteins and biomarkers for health in chickens,” PHD thesis, University of Glasgow, Scotland, pp. 138-316 (Jan. 2016). [cited by applicant]
Pavia, et al., “Necrotic enteritis: Applications for the poultry industry,” [cited by applicant]
Vicuña, et al., “Dose titration of FITC-D for optimal measurement of enteric inflammation in broiler chicks,” [cited by applicant]
Williams, “Intercurrent coccidiosis and necrotic enteritis of chickens: rational, integrated disease management by maintenance of gut integrity,” [cited by applicant]
Xie, et al., “Changes in Serum Ovotransferrin Levels in Chickens with Experimentally Induced Inflammation and Diseases,” [cited by applicant]