IP Library Granted Patent US 11,529,412
Granted Patent B2
US 11,529,412 · App. 17/185,618 · Granted Dec 20, 2022

Method and system for protecting honey bees from pesticides

Inventor: Joseph E. Kovarik (Englewood, CO)
Assignee: Seed Health, Inc.
A61K39/35A61K9/007A61K9/0034A61K9/0043A61K35/74A61K35/741A61K35/742A61K35/745A61K35/747A61K39/0008A61K39/39A61K39/395A61K45/06C07K16/00A61K2039/505A61K2039/541A61K2039/544A61K2039/55A61K2039/55583A61K2039/577A61K2039/58A61K2039/70
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,529,412
App. No.
17/185,618
Granted
Dec 20, 2022
Kind
B2
Abstract

A method and system for the treatment of honey bees ( Apis mellifera ), bats, and butterflies protects them from various life threatening conditions, including Colony Collapse Disorder and in particular, provides honey bees with the ability to assimilate and degrade pesticides such as neonicotinoids and fipronil.

Claims (19)

1. A method for providing a honey bee with the ability to assimilate pesticides, comprising, inoculating a honey bee with a culture of pesticide degrading bacteria, wherein the pesticide degrading bacteria include genes whose expression by the pesticide degrading bacteria results in the degradation of the pesticide, said pesticide degrading bacteria being modified to include said genes using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or using a clustered regularly interspaced short palindromic repeats (CRISPR) from Prevotella and Francisella 1 (Cpf1) nuclease, said pesticide degrading bacteria selected from the group consisting of L. rhamnosus and L. plantarum.

2. The method as set forth in claim 1 , wherein said genes express cytochrome P450 enzymes.

3. The method as set forth in claim 1 , wherein said genes comprise P450 genes of the CYP6 and CYP3 Glade.

4. The method as set forth in claim 1 , wherein said inoculating comprises spraying a honey bee with said pesticide degrading bacteria.

5. The method as set forth in claim 1 , wherein said inoculating comprises providing the pesticide degrading bacteria in a sweetened solution.

6. The method as set forth in claim 1 , wherein the pesticide comprises a neonicotinoid insecticide.

7. The method as set forth in claim 1 , further comprising employing a different CRISPR-Cas9/CRISPR-Cpf1 to ameliorate pathogens in the honey bee gut.

8. The method as set forth in claim 1 , wherein said inoculating comprises providing the pesticide degrading bacteria in a sweetened solution or spraying a honey bee with said pesticide degrading bacteria.

9. The method as set forth in claim 6 , wherein said genes express cytochrome P450 enzymes.

10. The method as set forth in claim 1 , further comprising employing CRISPR-Cas9/CRISPR-Cpf1 to delete antibiotic resistance genes transferred to pathogenic bacteria in the honey bee gut.

11. The method as set forth in claim 2 , further comprising employing a different CRISPR-Cas9/CRISPR-Cpf1 to ameliorate pathogens in the honey bee gut.

12. A method for providing a honey bee with the ability to assimilate pesticides, comprising, providing a honey bee with a culture of pesticide degrading bacteria, wherein the pesticide degrading bacteria include genes whose expression by the pesticide degrading bacteria results in the degradation of the pesticide, wherein said step of providing comprises using bacteriophage as a delivery vehicle for said genes, and wherein said pesticide degrading bacteria comprises L. rhamnosus.

13. The method as set forth in claim 12 , wherein said genes express cytochrome P450 enzymes.

14. The method as set forth in claim 12 , wherein said genes comprise P450 genes of one of the CYP6 and CYP3 clades.

15. The method as set forth in claim 12 , wherein said genes are selected from the group consisting of a CYP353D1v2 gene and a SCL3-10 nitrile hydratase beta subunit gene.

16. The method as set forth in claim 12 , further comprising employing CRISPR-Cas9/CRISPR-Cpf1 to delete antibiotic resistance genes transferred to pathogenic bacteria in the honey bee gut.

17. The method as set forth in claim 12 , further comprising improving honey bee fitness by modifying the honey bee microbiome by using CRISPR-Cas9/CRISPR-Cpf1 to select and modify microbial communities to positively affect honey bee fitness.

18. The method as set forth in claim 12 , wherein the pesticide degrading bacteria further comprises bacteria selected from the group consisting of: Lactobacillus spp, Bifidobacterium sp., Gilliamella apicola and Snodgrassella alvi.

19. The method as set forth in claim 16 , further comprising employing a different CRISPR-Cas9/CRISPR-Cpf1 to ameliorate pathogens in the honey bee gut.

Assignments (2)
SECURITY INTEREST Recorded Jul 21, 2026
From: SEED HEALTH, INC.
To: JPMORGAN CHASE BANK, N.A., AS LENDER
Reel/Frame 076028/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2022
From: KOVARIK, JOE
To: SEED HEALTH, INC.
Reel/Frame 059690/0210 →
Continuity (9)
Continuation In Part 16892623 · Jun 4, 2020
Continuation In Part 16246652 · Jan 14, 2019
Continuation In Part 16139232 · Sep 24, 2018
Continuation In Part 15379579 · Dec 15, 2016
Continuation In Part 15270034 · Sep 20, 2016
Continuation 14954074 · Nov 30, 2015
Provisional Application 62277571 · Jan 12, 2016
Provisional Application 62278046 · Jan 13, 2016
Related Publication 20210177963A1 · Jun 17, 2021
Cited By (1)
US 12,239,706