US2015024385A1PendingUtilityA1

Prediction of fertility in males

Assignee: WISCONSIN ALUMNI RES FOUNDPriority: Jul 22, 2013Filed: Jul 22, 2014Published: Jan 22, 2015
Est. expiryJul 22, 2033(~7 yrs left)· nominal 20-yr term from priority
Inventors:John Parrish
G01N 2800/367G01N 2015/1472G01N 33/5091G01N 2015/1006G01N 15/147C12N 5/061G01N 2015/1497G01N 15/1475G01N 15/1433
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Claims

Abstract

A method for evaluating sperm fertility. The method includes the steps of obtaining a sample of sperm from an animal of a species; staining the sample with a fluorescent DNA-binding dye; collecting at least one image of the stained sample; determining an edge of a nucleus of at least one sperm within the stained sample in the at least one image; measuring an intensity of the DNA-binding dye within an area defined by the edge of the nucleus of the at least one sperm; determining an average intensity per unit area of the area defined by the edge of the nucleus of the at least one sperm; comparing the average intensity per unit area to an average intensity per unit area for high-fertility sperm and low-fertility sperm of the same species to determine if the sample has high or low fertility.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for evaluating sperm fertility, comprising the steps of:
 obtaining a sample of sperm from an animal of a species;   staining the sample with a fluorescent DNA-binding dye;   collecting at least one image of the stained sample;   determining an edge of a nucleus of at least one sperm within the stained sample in the at least one image;   measuring an intensity of the DNA-binding dye within an area defined by the edge of the nucleus of the at least one sperm;   determining an average intensity per unit area of the area defined by the edge of the nucleus of the at least one sperm; and   comparing the average intensity per unit area to average intensities per unit area for high-fertility sperm and low-fertility sperm of the same species to determine if the sample has high or low fertility.   
     
     
         2 . The method of  claim 1 , wherein staining the sample with a fluorescent DNA-binding dye comprises staining the sample with Hoechst 33342. 
     
     
         3 . The method of  claim 1 , wherein staining the sample with a fluorescent DNA-binding dye further comprises applying the stained sample to a substrate. 
     
     
         4 . The method of  claim 3 , wherein the nucleus of the at least one sperm within the stained sample comprises a flattened oval and wherein the flattened portion is adjacent to the substrate. 
     
     
         5 . The method of  claim 1 , wherein obtaining a sample of sperm from an animal of a species comprises obtaining a sample of sperm from a bull, a boar, a human, a horse, a ram, or a dog. 
     
     
         6 . The method of  claim 1 , wherein collecting at least one image of the stained sample comprises deconvolving the at least one image to remove out of focus information. 
     
     
         7 . The method of  claim 1 , wherein the high-fertility sperm has a lower intensity per unit area than the low-fertility sperm. 
     
     
         8 . A method for evaluating sperm fertility, comprising the steps of:
 obtaining a sample of sperm from an animal of a species;   staining the sample with a fluorescent DNA-binding dye;   obtaining fluorescent intensity measurements from a plurality of sperm in the stained sample;   determining an average intensity of the fluorescent intensity measurements obtained from the plurality of sperm in the stained sample; and   comparing the average intensity to average intensities for high-fertility sperm and low-fertility sperm of the same species to determine if the sample has high or low fertility.   
     
     
         9 . The method of  claim 8 , wherein obtaining fluorescent intensity measurements from a plurality of sperm in the stained sample further comprises collecting at least one image of the stained sample. 
     
     
         10 . The method of  claim 9 , wherein determining an average intensity of the fluorescent intensity measurements obtained from the plurality of sperm in the stained sample further comprises
 determining an edge of a nucleus of at least one sperm within the stained sample in the at least one image,   measuring an intensity of the DNA-binding dye within an area defined by the edge of the nucleus of the at least one sperm, and   determining an average intensity per unit area of the area defined by the edge of the nucleus of the at least one sperm.   
     
     
         11 . The method of  claim 10 , wherein collecting at least one image of the stained sample comprises deconvolving the at least one image to remove out of focus information. 
     
     
         12 . The method of  claim 11 , wherein staining the sample with a fluorescent DNA-binding dye further comprises applying the stained sample to a substrate. 
     
     
         13 . The method of  claim 12 , wherein the nucleus of the at least one sperm within the stained sample comprises a flattened oval and wherein the flattened portion is adjacent to the substrate. 
     
     
         14 . The method of  claim 8 , wherein obtaining fluorescent intensity measurements from a plurality of sperm in a sample comprises obtaining fluorescent intensity measurements using flow cytometry. 
     
     
         15 . The method of  claim 14 , wherein obtaining fluorescent intensity measurements using flow cytometry comprises obtaining fluorescent intensity measurements using flow cytometry with an orienting nozzle. 
     
     
         16 . The method of  claim 8 , wherein obtaining a sample of sperm from an animal of a species comprises obtaining a sample of sperm from a bull, a boar, a human, a horse, a ram, or a dog. 
     
     
         17 . The method of  claim 8 , wherein staining the sample with a fluorescent DNA-binding dye comprises staining the sample with Hoechst 33342. 
     
     
         18 . The method of  claim 8 , wherein the high-fertility sperm has a lower average intensity than the low-fertility sperm.

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