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- 1 - VAXXITEK™ is a registered trademark of Merial in the United States of America and elsewhere. - 1 - Editorial This VAXXITEK® NEWS n°4 will provide scientific information on how to build a solid vaccination program based on hatchery vaccination with VAXXITEK HVT+IBD. Over 60 papers dealing with VAXXITEK HVT+IBD hatchery vaccination have been published or presented since the beginning of research on vectored HVT-IBD vaccines in the nineties. This issue also provides information from several papers submitted to the XVIII th  Congress of the World Veterinary Poultry Association to be held in Nantes, France in August 2013. This issue emphasizes the need of building an immune foundation to enable prevention of post-vaccine reactions, as well as to enhance vaccine take. Vaccination against the main viral immunosuppressive diseases of the chicken, infectious bursal disease and Marek’s disease, lay the ground level of the immune foundation. Visible effects on bursa health immediately show the benefit of such vaccination. A hatchery vaccination program includes live vaccines to be sprayed onto the day-old chicks to protect against the common respiratory viral diseases, Newcastle disease and infectious bronchitis. In many countries, day old programs include inactivated vaccines in oil adjuvant for Newcastle disease or Fowl Pox vaccines, plain or vectored expressing avian influenza protective antigen. A hatchery vaccination program has to be tailored according to the country and operation epidemiological conditions that may differ from one continent to another. Areas of the world will need protection against avian influenza when in other countries this may be not needed. Velogenic Newcastle disease is a threat in many countries, but not the case in North America and Western Europe. We hope that you enjoy reading VAXXITEK NEWS n°4 and invite you to discover and read our approach on establishing a solid immune foundation by using VAXXITEK HVT+IBD. Dr. Stephane LEMIERE Avian Global Technical Director VAXXITEK™ is a registered trademark of Merial in the United States of America and elsewhere. MERIAL TECHNICAL NEWSLETTER Number 4

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Page 1: MERIAL TECHNICAL NEWSLETTERavian.merial.com/sites/merial.avian/files/vaxxiteknews-4...occur most commonly E. coli (2), that require antibiotic treatment. 1. Introduction The objective

- 1 -VAXXITEK™ is a registered trademark of Merial in the United States of America and elsewhere.

- 1 -

EditorialThis VAXXITEK® NEWS n°4 will provide scientifi c information on how to build a solid vaccination program based on hatchery vaccination with VAXXITEK HVT+IBD. Over 60 papers dealing with VAXXITEK HVT+IBD hatchery vaccination have been published or presented since the beginning of research on vectored HVT-IBD vaccines in the nineties. This issue also provides information from several papers submitted to the XVIIIth Congress of the World Veterinary Poultry Association to be held in Nantes, France in August 2013.

This issue emphasizes the need of building an immune foundation to enable prevention of post-vaccine reactions, as well as to enhance vaccine take. Vaccination against the main viral immunosuppressive diseases of the chicken, infectious bursal disease and Marek’s disease, lay the ground level of the immune foundation. Visible eff ects on bursa health immediately show the benefi t of such vaccination. A hatchery vaccination program includes live vaccines to be sprayed onto the day-old chicks to protect against the common respiratory viral diseases, Newcastle disease and infectious bronchitis. In many countries, day old programs include inactivated vaccines in oil adjuvant for Newcastle disease or Fowl Pox vaccines, plain or vectored expressing avian infl uenza protective antigen.

A hatchery vaccination program has to be tailored according to the country and operation epidemiological conditions that may diff er from one continent to another. Areas of

the world will need protection against avian infl uenza when in other countries this may be not needed. Velogenic Newcastle disease is a threat in many countries, but not the case in North America and Western Europe.

We hope that you enjoy reading VAXXITEK NEWS n°4 and invite you to discover and read our approach on establishing a solid immune foundation by using

VAXXITEK HVT+IBD.

Dr. Stephane LEMIERE

Avian Global Technical Director

VAXXITEK™ is a registered trademark of Merial in the United States of America and elsewhere.

MERIAL TECHNICAL NEWSLET TER

Number 4

Page 2: MERIAL TECHNICAL NEWSLETTERavian.merial.com/sites/merial.avian/files/vaxxiteknews-4...occur most commonly E. coli (2), that require antibiotic treatment. 1. Introduction The objective

Number 4

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2.3. Prevention

of immunosuppression

Preventing economic losses is linked to control of immunosuppression in poultry production, especially broiler production (3). It may decrease mortality, increase performance, and positively impact the industry by processing birds with less health problems.

3. An Immune Foundation

A solid immune foundation not only enhances the immune system, it also establishes barriers along the most common routes of infection for avian pathogens. Breeder vaccination pro-grams to passively protect progeny are the fi rst approach. The second approach is to protect the growing chickens against immunosup-pressive diseases and their economic consequences (3). The immune foundation is best induced by early vaccination in presence of maternally-derived antibodies, against Marek’s and IBD, both of which are main viral causes of immunosuppression. To accomplish this principal, a unique concept of vaccination was introduced worldwide in 2006: the injection, either in ovo, or at day-old, of a vector vaccine based on the HVT strain, the HVT-IBD vector vaccine, VAXXITEK HVT+IBD.

2. Immunosuppression

Immunosuppression occurs in the poultry production environment due to exposure to stressors and infectious diseases that impair immunity, as well as reduce general health, welfare, and potential for effi cient production  (1). Multiple stressors in the poultry house environment can insult the immune system, including viral diseases. The main consequences are significant economic losses.

2.1. Causes of immunosuppression

Among the causes of immunosuppres-sion in poultry, the main recognized and implicated viruses are IBD, Marek’s and chicken infectious anemia  (CIA) viruses (1). These viruses are known to have direct negative eff ects on the immune system, thereby increasing susceptibility to other diseases and interfering with vaccinal immunity (1).

2.2. Consequences

of immunosuppression

In immunosuppressed birds, either the vaccine take can be decreased or the post-vaccine reaction can be excessive, following administration of live respiratory disease vaccines. Secondary bacterial infections often occur most commonly E.  coli  (2), that require antibiotic treatment.

1. Introduction

The objective of this newsletter is to review how to establish vaccination programs of chickens, in both short-lived birds, i.e.  broilers, or long-lived birds, i.e. layers and breeders.One current trend is to move many of the vaccinations being performed in the fi eld into the hatchery. Vaccinations in the hatchery can be administered as early as in ovo at 18  days of embryonation and also at day-old in newly hatched birds. Novel vector vaccines are steadily increasing in use in hatchery programs. Especially, the HVT-based vaccines that protect against Marek’s disease  (MD), as well as another viral diseases, such as infectious bursal disease  (IBD), Newcastle disease  (ND), or infectious laryngotracheitis (ILT).Hatchery vaccination programs are based on the equipment technologies available to administer the vaccines in ovo or using more conventional routes, such as spray, eye drop, or sub-cutaneous injections, as well as the product’s portfolio. Not all vaccines are not suitable for hatchery vaccination. The trend is to get more hatchery vaccines licensed in order to respond to the demand for more vaccines to be used in that context.

VAXXITEK™ is registered trademark of Merial in the United States of America and elsewhere.

How to build a hatchery vaccination program based on immune foundation?The immunosuppression that is commonly observed in poultry production is due to many factors, including, but not only, viral diseases. Signifi cant economic losses are attributed to immunosuppression in the poultry industry worldwide. Establishing a solid immune foundation not only enhances the immune system, but it also establishes barriers along the most common routes of infection by avian pathogens.

In building a day-old vaccination program, the compatibilities between the vaccines must be studied in order to make educated decisions on vaccine associations. Using VAXXITEK HVT+IBD as the center of a hatchery vaccination program prepares the immune system to be stimulated by concomitant and additional vaccinations. The art of combining vaccines to build a hatchery vaccination program must be according to the history of the disease challenge in the given area and the estimation of the current epidemiological risks.

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3.1. Protection

of the immune function

The bursa of Fabricius is the cornerstone of immunity of the chicken, where B  lymphocytes and antibody-producing plasmocytes originate. Damage to the bursa leads to immune depression. Lesions in the bursa are usually attributed to IBD virus. Marek’s disease virus can also damage the bursa and cause immunosuppression  (1). Early IBD viral infection lesions appear similar to early MD viral infection lesions. The use of VAXXITEK HVT+IBD signifi cantly protects bursal health with measurable results on the humoral immune system as well as circulating and intra-bursal B cells. Indirect measurements, such as monitoring ND vaccination, also clearly show the benefi t of VAXXITEK HVT+IBD (4).

3.2. Positive interactions

with other vaccinations

Examining the clearance of live IB vaccines also indicates the protective advantage of VAXXITEK HVT+IBD. Birds vaccinated with VAXXITEK HVT+IBD displayed intact bursas with signifi cantly less IB vaccine virus detection in the IB virus target organs. The other vaccinates had regressed bursas and more re-isolation of IB vaccine viruses. This refl ects the importance of bursa integrity in the clearance of the vaccine viruses hence avoiding or reducing respiratory diseases in chicks (5).

- 3 -

4. Compatibilities with VAXXITEK HVT+IBD

To build a vaccination program the compatibilities between the vaccines must be examined. Reviewing those studies enable making educated decisions on vaccine associations.

4.1. Marek’s disease

vaccination program

Full compatibility between VAXXITEK HVT+IBD and Rispens Marek’s disease vaccines has been demonstrated  (6) (Table 1).

4.2. Fowl Pox vaccines, vector or plain

Full compatibility between VAXXITEK HVT+IBD vector vaccine and Fowl Pox vectored avian infl uenza H5 has been demonstrated (7) (Table 1).

4.3. Live respiratory disease vaccines

Full compatibility in vivo between VAXXITEK HVT+IBD and live sprayed ND and IB live vaccines at the hatchery has been demonstrated (8) (Table 2).

4.4. Inactivated

in oil adjuvant vaccines

Full compatibility between VAXXITEK HVT+IBD vector vaccine and inactivated ND vaccines in oil adjuvant has been demonstrated (9) (Table 2).

5. Incompatibilities with VAXXITEK HVT+IBD

Other HVT vector vaccines may be used for hatchery vaccination, but the main problem is that they are not compatible with each other.

5.1. HVT vaccines

A HVT-IBD vector vaccine cannot be mixed with currently registered native HVT vaccines, as both vaccine strains will compete against each other in vivo and will lead to decreased vaccine take  (Merial internal study reports). This is also true for combined vaccines of HVT and Rispens, as well as HVT+SB-1 (Table3).

5.2. HVT vector vaccines

A HVT-IBD vector vaccine cannot be mixed with other currently registered HVT vector vaccines, vector of Newcastle disease with a F  protein coding gene insert (Merial internal study reports) or any vector vaccine of infectious laryngotracheitis viral glycoprotein coding gene insert (Table 3).

Live respiratory vaccinesNewcastle disease vaccinesIB vaccines, etc.SPRAY CABINET

Inactivated in oil adjuvant vaccinesNewcastle diseaseAvian infl uenza, etc.NON-MISCIBLE VACCINE INJECTIONS

Table 2: Poultry hatchery vaccine most commonly recommended associations – non miscible vaccines with VAXXITEK HVT+IBD.

Fowlpox vaccinesSAME MAREKS DILUENT

Fowlpox vector vaccines,FP AIV-H5, etc.SAME MAREKS DILUENT

Serotype 1 Mareks vaccines,Rispens strainsSAME MAREKS DILUENT

Serotype 2 Mareks vaccines,SB-1 strainsSAME MAREKS DILUENT

Table 1: Poultry hatchery vaccine most commonly recommended associations – miscible vaccines with VAXXITEK HVT+IBD.

VAXXITEK™ is registered trademark of Merial in the United States of America and elsewhere.

HVT serotype 3 vaccines

HVT + Rispens vaccines

HVT + SB-1 vaccines

HVT-ILT vector vaccines

HVT-ND vector vaccines

VAXXITEK HVT+IBD Immune foundation

Table 3: Poultry hatchery vaccine forbidden associations.

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Number 4

6. A la carte vaccination programs with VAXXITEK HVT+IBD

- 4 -

Using VAXXITEK  HVT+IBD as the base for the hatchery vaccination program will prepare the immune system to be stimulated by concomitant and additional vaccinations. The art of combining vaccines to build a hatchery vaccination program has to be in accordance to the history of the disease challenge in the given area and the estimation of the current epidemiological risks.

6.1. Broiler breeders

A broiler breeder vaccination program based on VAXXITEK HVT+IBD is fully vali-dated by wide use in many operations worldwide. Day-old or in ovo application of the vaccine is combined with other Marek’s vaccine serotypes, such as SB-1 and/or Rispens. VAXXITEK  HVT+IBD is used as a primer to immunize the chickens with re-vaccination recommended prior to the point of lay with inactivated IBD vaccines. Two primary objectives are accomplished: protection against IBD during the high risk period of pullet growth and priming in order to optimize the IBD antibody production and transmission to the progeny for passive immunity against IBD (10). Broiler breeder management and feeding procedures are key success factors; the impact of feeding systems and vaccination programs on Salmonella Enteritidis colonization and clearance of E.  coli are minimal in VAXXITEK HVT+IBD + SB-1 vaccinates (11).

6.2. Broilers

Broiler vaccination programs based on VAXXITEK  HVT+IBD aim at immunizing against the detrimental immunosup-pressive eff ects of both diseases, IBD and Marek’s disease. Production type and local disease challenge may neces-sitate an additional vaccine strain, such as SB-1, for Marek’s disease prevention. Vaccination with VAXXITEK  HVT+IBD provides early onset of protection against IBD, consequently early protection of the functional immune system in short-lived chickens, and protection of the bursa of Fabricius. The overall benefi t is then demonstrated by an improved control of the common secondary bacterial infections in broiler production environments, as shown by decreased condemns at the slaughterhouse (12) or by decreased antibiotic use (13).

6.3. Layer Pullets

Layer pullet vaccination programs based on VAXXITEK  HVT+IBD aim at immunizing at day old or in ovo against IBD and against Marek’s disease, as long as it is complemented by another serotype Marek’s vaccine  (i.e., SB-1 and/or Rispens). The main benefi t in layer type pullets is to allow protection of the functional immune system and to induce signifi cantly increased antibody response to the crucial vaccine components of the vaccination program to protect egg production (i.e., Newcastle disease, egg drop syndrome, infectious bronchitis) (14).

References1. Hoerr FJ. Clinical Aspects of Immunosuppression in Poul-try. Avian Dis., 2010; 54:2-15.

2. Fussell LW. Poultry Industry Strategies for Control of Immunosuppressive Diseases. Poult. Sci., 1998; 77:1193-1196.

3. Naqi S, Thompson G, Bauman B, Mohammed H. The Exac-erbating Eff ect of Infectious Bronchitis Virus Infection on the Infectious Bursal Disease Virus-Induced Suppression of Opso-nization by Escherichia coli Antibody in Chickens. Avian Dis., 2001; 45:52-60.

4. Rautenschlein S, Lemiere S, Simon B, Prandini F. A comparison of the eff ects on the humoral and cell-mediated immunity between an HVT-IBD vector vaccine and an IBDV immune complex vaccine after in ovo vaccination of commercial broilers. Article. XVIIth Congress of the World Veterinary Poultry Association, Cancun, Mexico, 2011; p830-843.

5. Ganapathy K, Wilkins M, Forrester A, Lemiere S, Jones R. The infl uence of bursa of Fabricius on infectious bronchitis vaccination in commercial broiler chicks. Article. 7th International Symposium on Avian Corona-

and Metapneumoviruses and Complicating Pathogens. Rauischholzhausen, Germany, 2012; p151-154.

6. Lemiere S, Wong YS, Saint-Gerand AL, Goutebroze S, le Gros FX. Compatibility of Turkey Herpesvirus–Infectious Bursal Disease Vector Vaccine with Marek’s Disease Rispens Vaccine Injected into Day-Old Pullets. Avian Dis., 2011; 55:113-118.

7. Richard-Mazet A, Goutebroze S, Duboeuf M, Le Gros FX, Lemiere S, Bublot M. Compatibility of fowlpox-avian infl u-enza and herpesvirus of turkey-infectious bursal disease vector vaccines injected in ovo to embryonated chicken eggs. Article. XVIIth Congress of the World Veterinary Poul-try Association, Cancun, Mexico, 2011; p852-857.

8. Jay ML, Bizzini S, Duboeuf M, Goutebroze S, Le-Gros FX. Compatibility of a novel vector vaccine HVT-Gumboro with Newcastle and infectious bronchitis vaccination at one day of age. Abstract. 16th congress of the World Veterinary Poul-try Association, Marrakesh, Morocco, 2009; p341.

9. Lemiere S, Fernandez R, Pritchard N, Cruz-Coy J, Rojo F, Wong SY, Saint-Gerand AL, Gauthier JC, Perozo F. Concomitant Turkey

Herpesvirus–Infectious Bursal Disease Vector Vaccine and Oil-Adjuvanted Inactivated Newcastle Disease Vaccine Administra-tion: Consequences Compatibility of Turkey Herpesvirus–Infec-tious Bursal Disease. Avian Dis., 2011; 55:642-649.

10. Lemiere S, Gauthier J.C., Kodjo A., Vinit L., Delvecchio A., Prandini F. Evaluation of the Protection against Infectious Bursal Disease (IBD) Challenge in Progeny Born to Parents Having Received a Vaccination Program Using a Herpesvirus of Turkey-Infectious Bursal Disease (HVT-IBD) Vector Vac-cine. World J. Vaccines, 2013; 3:46-51.

11. Montiel ER, Buhr RJ, Cox NA, Hofacre CL, Davis AJ, McLen-don BL, Lemiere S, Wilson JL. Impact of feeding systems and vaccination programs on Salmonella enteritidis colonization and clearance of E. coli in broiler breeder pullets. Abstract. XVIIIth Congress of the World Veterinary Poultry Association, Nantes, France, 2013; in-press.

12. Alonso Castro M, Merino Cabria D, Fernandez Garcia D, Torru-bia Diaz J, Herreras Viejo R, Fernandez Revuelta J, Mateo Oyague J, Carvajal Uruena A. Evaluation of the eff ects of vaccination with a HVT-IBD vector vaccine on bursa Fabricii, production

parameters and meat properties in broilers. Abstract. XVIIIth

Congress of the World Veterinary Poultry Association, Nantes,

France, 2013; in-press.

13. Lemiere S, Rojo R, He S, Tang S, Li W, Herrmann A, Pran-

dini F. Benefi ts of the Herpesvirus of Turkey vector vaccine of

Infectious Bursal Disease in control of immune-depression

in broilers and decrease of use of antibiotic medication.

Abstract. XVIIIth Congress of the World Veterinary Poultry

Association, Nantes, France, 2013; in-press.

14. Rautenschlein S, Lemiere S, Prandini F. Evaluation of the

eff ects of an HVT-IBD vector vaccine on the immune system

of layer pullets in comparison with two commercial live IBD

vaccines. Abstract. XVIIIth Congress of the World Veterinary

Poultry Association, Nantes, France, 2013; in-press.

15. Devaud I, Herin JB, Trotel A, Pagot E, Voisin F. A fi eld study in

commercial layers to evaluate the eff ects of an HVT-IBD vector

vaccine on production performances in comparison with a live

IBD vaccine. Abstract. XVIIIth Congress of the World Veterinary

Poultry Association, Nantes, France, 2013; in-press.

The overall benefi t is then demonstrated by signifi cantly increased numbers of laid eggs and improvement of egg shell quality parameters, as compared to vaccination programs based on classical modifi ed live IBD vaccines (15).

6.4. Special emphasis on

Newcastle disease prevention

Premium vaccination programs in countries in which the velogenic form of Newcastle disease is endemic requires two injectable vaccines, VAXXITEK  HVT+IBD and an oil adjuvanted ND vaccine. Both vaccines are not miscible but can be injected at the same time at day old in the hatchery. Full compatibility between both types of vaccines, cell-associated aqueous phase and oil adjuvanted phase, was demonstrated regardless of the injection system used, double needle, single needle with alternate vaccine fl ows, or joint vaccine fl ows (9). The main benefi t of the use of such a combination at the hatchery is the enhanced Newcastle disease vaccine take as the result of VAXXITEK HVT+IBD vaccination (14).

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VAXXITEK™ is registered trademark of Merial in the United States of America and elsewhere.