Amino acid compositions for the treatment of porcine epidemic diarrhea
The subject invention provides therapeutic compositions, and uses thereof for the treatment or amelioration of symptoms of a disease selected from the group consisting of: Ebola virus infection, HIV infection, ataxia, environmental enteropathy, cancer, hangover, inflammatory disease, and porcine epidemic diarrhea. In preferred embodiments, the composition includes a combination of one or more amino acids selected from the group comprising lysine, aspartic acid, glycine, isoleucine, threonine, tyrosine, valine, tryptophan, asparagine and/or serine.
1. A method for treating porcine epidemic diarrhea in a porcine subject in need thereof comprising:
administering to the porcine subject in need thereof, wherein the porcine subject in need thereof is infected with porcine epidemic diarrhea virus (PEDV), an effective amount of a formulation consisting essentially of:
free amino acids of aspartic acid, valine, serine, threonine, tyrosine, lysine, glycine, and isoleucine;
optionally tryptophan; and
optionally electrolytes, vitamins, minerals, or any combination thereof;
wherein the formulation does not comprise:
free amino acid glutamine;
a glutamine-containing dipeptide; or
any combination thereof;
or, when free amino acid glutamine, a glutamine-containing dipeptide, or any combination thereof is present, the free amino acid glutamine, the glutamine-containing dipeptide, or any combination thereof is present at a concentration less than 300 mg/l;
wherein the formulation does not comprise glucose;
or, when glucose is present, glucose is present at a concentration of less than 1 g/l; and
wherein the formulation does not comprise:
free amino acid methionine;
a methionine-containing dipeptide; or
any combination thereof;
or, when free amino acid methionine, a methionine-containing dipeptide, or any combination thereof is present, the free amino acid methionine, the methionine-containing dipeptide, or any combination thereof is present at a concentration less than 300 mg/l; and
wherein the effective amount of the formulation is sufficient to treat the porcine subject infected with PEDV.
2. The method of claim 1 , wherein the formulation is formulated for oral administration.
3. The method of claim 1 , wherein the formulation is administered through enteral feeding.
4. The method of claim 1 , wherein the formulation is administered parenterally.
5. The method of claim 1 , wherein the formulation is administered in pill form.
6. The method of claim 1 , wherein aspartic acid is at a concentration of between 532 to 4792 mg/l, valine is at a concentration of between 469 to 4217 mg/l, serine is at a concentration of between 420 to 3784 mg/l, threonine is at a concentration of between 476 to 4288 mg/l, tyrosine is at a concentration of between 725 to 6523 mg/l, lysine is at a concentration of about 730 to 6575 mg/l, glycine is at a concentration of about 300 to 2703 mg/l, and isoleucine is at a concentration of about 525 to 4722 mg/l.
7. The method of claim 1 , wherein the porcine subject infected with PEDV is a piglet.
8. A method for reducing symptoms of porcine epidemic diarrhea in a porcine subject in need thereof comprising:
administering to the porcine subject in need thereof, wherein the porcine subject in need thereof is infected with porcine epidemic diarrhea virus (PEDV), an effective amount of a formulation consisting essentially of:
free amino acids of aspartic acid, valine, serine, threonine, tyrosine, lysine, glycine, and isoleucine;
optionally tryptophan; and
optionally electrolytes, vitamins, minerals, or any combination thereof
wherein the formulation does not comprise:
free amino acid glutamine;
a glutamine-containing dipeptide; or
any combination thereof;
or, when free amino acid glutamine, a glutamine-containing dipeptide, or any combination thereof is present, the free amino acid glutamine, the glutamine-containing dipeptide, or any combination thereof is present at a concentration less than 300 mg/l;
wherein the composition does not comprise glucose;
or, when glucose is present, glucose is present at a concentration of less than 1 g/l; and
wherein the formulation does not comprise:
free amino acid methionine;
a methionine-containing dipeptide; or
any combination thereof;
or, when free amino acid methionine, a methionine-containing dipeptide, or any combination thereof is present, the free amino acid methionine, the methionine-containing dipeptide, or any combination thereof is present at a concentration less than 300 mg/l; and
wherein the effective amount of the formulation is sufficient to reduce symptoms of PEDV in the porcine subject.
9. The method of claim 8 , wherein reduction of the symptoms of porcine epidemic diarrhea virus infection comprises reduction in at least one of severe diarrhea or dehydration.
10. The method of claim 8 , wherein the formulation is formulated for oral administration.
11. The method of claim 8 , wherein the formulation is administered through enteral feeding.
12. The method of claim 8 , wherein the formulation is administered parenterally.
13. The method of claim 8 , wherein the formulation is administered in pill form.
14. The method of claim 8 , wherein aspartic acid is at a concentration of between 532 to 4792 mg/l, valine is at a concentration of between 469 to 4217 mg/l, serine is at a concentration of between 420 to 3784 mg/l, threonine is at a concentration of between 476 to 4288 mg/l, tyrosine is at a concentration of between 725 to 6523 mg/l, lysine is at a concentration of about 730 to 6575 mg/l, glycine is at a concentration of about 300 to 2703 mg/l, and isoleucine is at a concentration of about 525 to 4722 mg/l.
15. The method of claim 8 , wherein the porcine subject infected with PEDV is a piglet.
16. The method of claim 1 , wherein the formulation consists of free amino acids of aspartic acid, valine, serine, threonine, tyrosine, lysine, glycine, and isoleucine.
17. The method of claim 1 , wherein the formulation consists of free amino acids of aspartic acid, valine, serine, threonine, tyrosine, lysine, glycine, isoleucine, and tryptophan.
18. The method of claim 8 , wherein the formulation consists of free amino acids of aspartic acid, valine, serine, threonine, tyrosine, lysine, glycine, and isoleucine.
19. The method of claim 8 , wherein the formulation consists of free amino acids of aspartic acid, valine, serine, threonine, tyrosine, lysine, glycine, isoleucine, and tryptophan.