RECOMBINANT CHICKEN INTERLEUKIN-1 BETA PROTEIN FOR PRODUCING ANTIBODY EARLY AND RETAINING FOR A LONGER PERIOD OF TIME AND APPLICATION THEREOF

Abstract

The present invention provides a recombinant chicken interleukin-1β protein for producing antibody early and retaining for a longer period of time, which has a sequence of SEQ ID NO:2 or SEQ ID NO:3. The recombinant chicken interleukin-1β protein is created by using point mutation in a genetic engineering method; it can significantly improve the original vaccine efficacy to enhance antibody responses, produce antibody one week earlier and extend the protective effect until chickens sold off. Therefore, the recombinant chicken interleukin-1β protein of the present invention can produce significant higher antibody responses than the with-type chicken interleukin-1β protein, it helps to develop avian interleikin-1β vaccine adjuvant and uses in medical application and livestock production.

Claims

1. A recombinant chicken interleukin-1β protein for producing antibody early and retaining for a longer period of time, which has a sequence containing a point mutation.

2. The recombinant chicken interleukin-1β protein according to claim 1, wherein the sequence containing a point mutation is SEQ ID NO:2 or SEQ ID NO:3.

3. The recombinant chicken interleukin-1β protein according to claim 1, wherein a time for producing antibody is one week earlier.

4. The recombinant chicken interleukin-1β protein according to claim 1, wherein the longer period of time is at least four weeks to extend the protective effect, and a booster is not given.

5. The recombinant chicken interleukin-1β protein according to claim 1, which is supplemented with a vaccine.

6. The recombinant chicken interleukin-1β protein according to claim 5, wherein the vaccine an inactivated vaccine or an attenuated vaccine.

7. The recombinant chicken interleukin-1β protein according to claim 5, wherein the vaccine is administered via eye drop, nose drop or intravenous injection.

8. The recombinant chicken interleukin-1β protein according to claim 1, which is supplemented with a vaccine adjuvant.

9. A method of producing antibody early and retaining for a longer period of time by using the recombinant chicken interleukin-1β protein according to claim 1.

10. The method according to claim 9, wherein a time for producing antibody is one week earlier.

11. The method according to claim 9, wherein the longer period of time is at least four weeks to extend the protective effect, and a booster is not given.

12. A method of producing antibody early and retaining for a longer period of time by using a vaccine supplemented with the recombinant chicken interleukin-1β protein according to claim 1.

13. The method according to claim 12, wherein a time for producing antibody is one week earlier.

14. The method according to claim 12, wherein the longer period of time is at least four weeks to extend the protective effect, and a booster is not given.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0019] The present invention will be apparent to those skilled in the art by reading the following detailed description of a preferred embodiment thereof, with reference to the attached drawings, in which:

[0020] FIG. 1 is a flow chart of constructing the recombinant chicken interleukin-1β (IL-1β) protein of the present invention;

[0021] FIG. 2 is 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS PAGE) of the recombinant chicken interleukin-1β (IL-1β) protein of the present invention after clone, recombinant protein expression and purification, ChIL-1β mutant 1 is indicated the recombinant chicken interleukin-1β protein having the first mutation and ChIL-1β mutant 2 is indicated the recombinant chicken interleukin-1β protein having the second mutation;

[0022] FIG. 3 shows that the plasma cortisol levels in chickens administrated the recombinant chicken interleukin-1β protein, PBS is indicated phosphate-buffered saline; HmIL-1β is indicated human interleukin-1β, ChIL-1β is indicated wild-type chicken interleukin-1β, ChIL-1β mutant 1 is indicated the recombinant chicken interleukin-1β protein having the first mutation and ChIL-1β mutant 2 is indicated the recombinant chicken interleukin-1β protein having the second mutation;

[0023] FIG. 4 shows HI antibody titers of the chickens administrated Newcastle disease live attenuated vaccine supplemented with the recombinant chicken interleukin-1β protein via eye drop using hemagglutination inhibition test, ChIL-1β is indicated wild-type chicken interleukin-1β, ChIL-1β MU1 is indicated the recombinant chicken interleukin-1β protein having the first mutation, ChIL-1β MU2 is indicated the recombinant chicken interleukin-1β protein having the second mutation, control is indicated PBS; pre is indicated before eye drop vaccination, PRI is indicated a primary dose, a booster is indicated a second dose;

[0024] FIG. 5 shows the antibody level of the chickens administrated ND vaccine supplemented with the recombinant chicken interleukin-1β protein, PBS is indicated phosphate-buffered saline, ChIL-1β is indicated wild-type chicken interleukin-1β, ChIL-1β mutant 1 is indicated the recombinant chicken interleukin-1β protein having the first mutation and ChIL-1β mutant 2 is indicated the recombinant chicken interleukin-1β protein having the second mutation;

[0025] FIG. 6 shows immunohistochemistry staining of the chickens administrated ND vaccine supplemented with the recombinant chicken interleukin-1β protein, A is indicated to administrate PBS, B is indicated to administrate vaccine, C is indicated to administrate vaccine supplemented with wild-type interleukin-1β protein (ChIL-1β), D is indicated to administrate vaccine supplemented with the recombinant chicken interleukin-1β protein having the first mutation (ChIL-1β mutant 1) and E is indicated to administrate vaccine supplemented with the recombinant chicken interleukin-1β protein having the second mutation (ChIL-1β mutant 2);

[0026] FIG. 7 shows HI antibody titers of the chickens administrated one dose of live attenuated Newcastle disease vaccine supplemented with the recombinant chicken interleukin-1β protein using hemagglutination inhibition test, ChIL-1β is indicated wild-type chicken interleukin-1β, ChIL-1β MU2 is indicated the recombinant chicken interleukin-1β protein having the second mutation, control is indicated PBS; pre is indicated before eye drop vaccination, PRI is indicated a primary dose, 14 is indicated after administrating 2 weeks, 28 is indicated after administrating 4 weeks.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0027] The accompanying drawings are included to provide a further understanding of the invention, and are incorporated in and constitute a part of this specification. The drawings illustrate embodiments of the invention and, together with the description, serve to explain the principles of the invention.

[0028] The present invention provides a recombinant chicken interleukin-1β protein for producing antibody early and retaining for a longer period of time, which can stimulate cytokine secretion and enhance antibody production. The recombinant chicken interleukin-1β protein is an effective and low cost vaccine adjuvant for outbreaks of avian disease.

[0029] Therefore, the present invention constructs two new recombinant chicken interleukin-1β protein from an improved design of the amino acid sequence of wild-type chicken interleukin-1β (IL-1β), which are respectively named as the recombinant chicken interleukin-1β protein having first mutation (ChIL-1β mutant 1) and the recombinant chicken interleukin-1β protein having second mutation (ChIL-1β mutant 2). The present invention uses the recombinant chicken interleukin-1β proteins with a common vaccine in Taiwan and global poultry industry, Newcastle disease (ND), to conduct animal clinical trials. The results show that the recombinant chicken interleukin-1β protein of the present invention can stimulate the immune system to produce antibody for ND vaccine, and the chicken can only receive one dose to continue producing antibodies and to extend the protective effect. The local tissue administrated vaccine or vaccine adjuvant comprising the recombinant chicken interleukin-1β protein not only can produce secretory immunoglobulin A (IgA) but also maintain a high level of immunoglobulin G (IgG) in the blood. In addition, the vaccine comprising the recombinant chicken interleukin-1β protein can have positive synergistic effect on high IgG antibody production rates to extend the protective effect until chickens sold off. Therefore, the recombinant chicken interleukin-1β protein of the present invention helps to develop avian vaccine adjuvant and uses in medical application and livestock production.

EXAMPLE 1

Construct the Recombinant Chicken Interleukin-1B Protein

[0030] The flow chart of constructing the circular permutation interleukin-1β (CP IL-1β) in one embodiment of the present invention as shown in FIG. 1. The present invention designs a wild-type chicken interleukin-1β sequence (SEQ ID NO:1) to have a point mutation, which is obtained from predicting an amino acid position that may affect biological activity by using a 3D structure of wild-type chicken interleukin-1β and its receptors, the point mutations are respectively Q19A and R140A. Therefore, the present mutation constructs the first mutation of the recombinant chicken interleukin-1β sequence having Q19A (SEQ ID NO:2) and the second mutation of the recombinant chicken interleukin-1β sequence having R140A (SEQ ID NO:3).

[0031] First, designing the forward and reverse primers comprising the point mutation for the two point mutation sequences of chicken interleukin-1β protein (SEQ ID NO:2 and SEQ ID NO: 3), wherein Q19A forward and reverse primers of the first mutation sequence (SEQ ID NO:2) respectively are SEQ ID NO: 4 and SEQ ID NO: 5; R140A forward and reverse primers of the second mutation sequence (SEQ ID NO:3) respectively are SEQ ID NO:6 and SEQ ID NO:7. And, using polymerase chain reaction to amplify wild-type chicken interleukin-1β sequence (SEQ ID NO:1) for the mutation site, wherein wild-type chicken interleukin-1β sequence is as a template (SEQ ID NO:1), the forward primer of wild-type chicken interleukin-1β (SEQ ID NO:8) and Q19A reverse primer (SEQ ID NO: 5) amplify Q19A mutation site to obtain the first fragment of the first mutation sequence (SEQ ID NO: 10), Q19A forward primer (SEQ ID NO:4) and the reverse primer of wild-type chicken interleukin-1β (SEQ ID NO: 9) amplify Q19A mutation site to obtain the second fragment of the first mutation sequence (SEQ ID NO: 11); and the forward primer of wild-type chicken interleukin-1β (SEQ ID NO:8) and R140A reverse primer (SEQ ID NO: 7) amplify R140A mutation site to obtain the first fragment of the second mutation sequence (SEQ ID NO: 12), R140A forward primer (SEQ ID NO:6) and the reverse primer of wild-type chicken interleukin-1β (SEQ ID NO: 9) amplify R140A mutation site to obtain the second fragment of the second mutation sequence (SEQ ID NO: 13). Then, the first (SEQ ID NO: 10) and second (SEQ ID NO: 11) fragments of the first mutation sequence serve as templates and primers for extension to obtain the first mutation of the recombinant chicken interleukin-1β sequence having Q19A mutation site (SEQ ID NO:2); and the first (SEQ ID NO: 12) and second (SEQ ID NO: 13) fragments of the second mutation sequence serve as templates and primers for extension to obtain the second mutation of the recombinant chicken interleukin-1β sequence having R140A mutation site (SEQ ID NO:3).

[0032] Furthermore, amplifying the first mutation of the recombinant chicken interleukin-1β sequence having Q19A (SEQ ID NO:2) as template using the forward (SEQ ID NO:8) and reverse (SEQ ID NO:9) primers of wild-type chicken interleukin-1β; and amplifying the second mutation of the recombinant chicken interleukin-1β sequence having R140A mutation site (SEQ ID NO:3) as template using the forward (SEQ ID NO:8) and reverse (SEQ ID NO:9) primers of wild-type chicken interleukin-1β.

[0033] Finally, cloning, expressing and purifying wild-type chicken interleukin-1β sequence (SEQ ID NO: 1), the first mutation of the recombinant chicken interleukin-1β sequence (SEQ ID NO: 2), and the second mutation of the recombinant chicken interleukin-1β sequence (SEQ ID NO: 3). As shown in FIG. 2, the molecular weight of wild-type chicken IL-1β (ChIL-1β), the recombinant chicken interleukin-1β protein having the first mutation (ChIL-1β mutant 1) and the recombinant chicken interleukin-1β protein having the second mutation (ChIL-1β mutant 2) is 23.6 kDa by 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS PAGE).

EXAMPLE 2

Bioactivity Assay of the Recombinant Chicken Interleukin-1β

[0034] To determine the in vivo activity of the recombinant chicken interleukin-1β, the present invention detects the plasma cortisol level after the recombinant chicken interleukin-1β proteins having the first (ChIL-1β mutant 1) and the second (ChIL-1β mutant 2) mutation are respectively injected into the wing vein of specific pathogen free (SPF) chicken. As shown in FIG. 3, the plasma cortisol levels in chickens are significantly enhanced by intravenous injections of the recombinant chicken interleukin-1β protein having the first (ChIL-1β mutant 1) or the second (ChIL-1β mutant 2) mutation, but the same result is not found in the chicken injected phosphate-buffered saline (PBS). Therefore, the recombinant chicken interleukin-1β protein of the present invention has more bioactivity than wild-type chicken interleukin-1β protein. The result indicates that the recombinant chicken interleukin-1β protein has great benefit for vaccine adjuvant.

EXAMPLE 3

Hemagglutination Inhibition Test (HI Test) of the Recombinant Chicken Interleukin-1β

[0035] To determine vaccine adjuvant effect of the recombinant chicken interleukin-1β protein, the present invention administrates Newcastle disease (ND) live attenuated vaccine or which supplemented with the recombinant chicken interleukin-1β protein to specific pathogen free (SPF) chickens via eye drop, the chickens at one week of age is administrated primary (PRI) dose, the chickens at three weeks of age is administrated booster dose. The present invention draws blood samples from the wing vein of the chickens at two and four weeks of age to evaluate the immune response to Newcastle disease vaccine by measuring HI antibody titers using hemagglutination inhibition test.

[0036] As shown in FIG. 4, the chickens only administrated Newcastle disease vaccine (vaccine-PRI) cannot produce enough antibody against Newcastle disease at two weeks of age. Only a few of the chickens administrated Newcastle disease vaccine supplemented with wild-type chicken interleukin-1β protein (vaccine+IL-1β) can produce enough antibodies against Newcastle disease at two weeks of age. All the chickens administrated Newcastle disease vaccine supplemented with the recombinant chicken interleukin-1β protein having the first (vaccine+ChIL-1β MU 1-PRI) or the second mutation (vaccine+ChIL-1β MU2-PRI) can produce enough antibodies against Newcastle disease at two weeks of age. These results show that the recombinant chicken interleukin-1β protein can be a vaccine adjuvant to promote the host producing antibody earlier and extending the protective titers.

EXAMPLE 4

Antibody Levels Produced by the Recombinant Chicken Interleukin-1β

[0037] To evaluate the humoral immunity response produced by the host administrated the recombinant chicken interleukin-1β as vaccine adjuvant, the present invention performs a 1:100 dilution of the serum obtained from EXAMPLE 3 to measure the quantity of avian IgG using enzyme-linked immunosorbent assay (ELISA).

[0038] As shown in FIG. 5 and Table 1, the IgG level in each sample is larger than the maximum of standard curve, and the serum is made dilution of 1:5000 and 1:10000. These results show that the IgG level of the host administrated ND vaccine supplemented with the recombinant chicken interleukin-1β is more than the host only administrated a ND vaccine or a ND vaccine supplement with wild-type chicken interleukin-1β, and the host only administrated PBS via eye drop is no IgG level in the blood. Therefore, these results validate that the recombinant chicken interleukin-1β can be a vaccine adjuvant to help ND vaccine elevating IgG level in the serum, it can generate immune responses against ND disease virus and other microorganisms that cause disease can be bacteria or virus.

TABLE-US-00001 TABLE 1 the serum IgG level of the host administrated ND live attenuated vaccine and/or the recombinant chicken interleukin- 1β of the present invention via eye drop Dilution Range, ng/ml Sample 1/100 1/5000 1/10000 Mock 200.399 48.285 25.015 Vaccine 201.578 59.678 26.371 Vaccine + chIL-1β 203.123 62.276 35.772 Vaccine + chIL-1β mutant 1 202.690 77.835 39.521 Vaccine + chIL-1β mutant 2 201.446 95.087 48.417

EXAMPLE 5

The Immunohistochemistry Staining of the Recombinant Chicken Interleukin-1β

[0039] To confirm the IgA distribution secreted by mucosal immune system in the nasal cavity of the host after administrating ND live attenuated vaccine supplemented with the recombinant chicken interleukin-1β protein via nose drop. The nasal cavity tissues are cut into slices three weeks after vaccination and stained using immunohistochemistry.

[0040] As show in FIG. 6, the vaccine supplemented with the recombinant chicken interleukin-1β protein having the first (ChIL-1β mutant 1) or the second mutation (ChIL-1β mutant 2) can stimulate lymphatic tissue, nasal epithelial cells and around glandular cells to produce a large amount of IgA distribution (FIGS. 6D and 6E), the vaccine supplemented with wild-type chicken interleukin-1β protein can stimulate nasal epithelial cells and glandular cells to produce a moderate amount of IgA distribution (FIG. 6C). However, only the vaccine administrated via nose drop can stimulate nasal epithelial cells and glandular cells to produce a few of IgA distribution (FIG. 6B), only PBS administrated via nose drop cannot stimulate glandular cells and lymphatic tissue in nasal cavity to produce any IgA (FIG. 6A). Therefore, these results validate that the recombinant chicken interleukin-1β can be a vaccine adjuvant to stimulate mucosal immune system producing a large amount of secretory IgA antibodies.

EXAMPLE 6

The Recombinant Chicken Interleukin-1β has the Capability of Producing Antibody Earlier and Extending the Protective Effect

[0041] To test the protective effect of only administrating host one dose of ND live attenuated vaccine supplemented with the recombinant chicken interleukin-1β protein. The present invention follows EXAMPLE 3 protocol to administrate host at one week of age one dose of ND vaccine supplemented with the vaccine adjuvant of the recombinant chicken interleukin-1β protein having the second mutation (ChIL-1β mutant 2), and draws blood samples of host at two and four weeks of age to evaluate the immune response by measuring HI antibody titers using hemagglutination inhibition test.

[0042] As shown in FIG. 7, the host administrated the ND vaccine adjuvant of the recombinant chicken interleukin-1β protein having the second mutation (ChIL-1β mutant 2) can produce enough antibodies against ND virus at two weeks of age and extend the protective effect at four weeks of age. But the host administrated one dose of the ND vaccine supplemented with wild-type chicken interleukin-1β protein cannot produce enough antibodies against ND virus until the host at four weeks of age. Therefore, the recombinant chicken interleukin-1β protein of the present invention as a vaccine adjuvant supplementing with a vaccine is only administrated a host one dose to extend the protective effect and not to be weakened over time. The recombinant chicken interleukin-1β protein can save booster cost.

[0043] The present invention is to create two kinds of the recombinant chicken interleukin-1β protein as vaccine adjuvant using point mutation in a genetic engineering method, it can significantly enhance the capability of producing antibody, produce antibody one week earlier, and extend the protective effect until chicken sold off. Furthermore, the present invention has validated that the recombinant chicken interleukin-1β protein as a vaccine adjuvant using with Newcastle disease (ND) has significant effects on immune response. Also, the cost of the recombinant chicken interleukin-1β protein as a vaccine adjuvant is 0.1 Taiwan Dollar (TWD) for each chicken, it can be more lower cost resulted from mass production to produce market competition. The recombinant chicken interleukin-1β protein has a biological decomposition, and it can store at a room temperature or in the freezer to maintain activity for 4 to 10 days (not precipitation), and store at −20° C. to maintain activity for 6 months (not precipitation). Therefore, the recombinant chicken interleukin-1β protein has good quality, stability, safety and including no side effects.

[0044] Accordingly, the recombinant chicken interleukin-1β protein of the present invention as a biological adjuvant directly uses with an inactivated or activated avian vaccine used in the veterinary vaccines market, it can significantly improve the original vaccine efficacy to enhance antibody responses, produce neutralizing antibody against virus earlier. The recombinant chicken interleukin-1β protein of the present invention helps to develop avian interleikin-1β vaccine adjuvant and uses in medical application and livestock production. Nowadays, all countries in the world including Taiwan have faced the problems of drug-resistance updates and new mutant recombinant virus including avian influenza; therefore, the recombinant chicken interleukin-1β protein of the present invention as a vaccine adjuvant can significantly enhance the effect of vaccine to protect livestock and poultry from disease threats.

[0045] Although the present invention has been described with reference to the preferred embodiments thereof, it is apparent to those skilled in the art that a variety of modifications and changes may be made without departing from the scope of the present invention which is intended to be defined by the appended claims.