(Source: 31st
Annual
Poultry Health Conference. Poultry Industry
Council, Ontario)
Control of Coccidiosis in Turkeys
- Global Review -
Peter Gazdzinski DVM, PhD. Dip.Path. Dip. ACPV.
Cuddy Farms Inc, Strathroy, Ontario
Coccidiosis
is among the most common diseases in turkeys. Coccidia are
species specific enteric parasites, and in turkeys seven Eimeria
species have been described although only four are of major concern to
the turkey industry: E.adenoides, E. meleagrimitis, E.gallopavonis and
E. dispersa. Of these, the first two are the most significant and most
common pathogens.
Transmission of coccidiosis is by fecal material and there are no
intermediate hosts.
The clinical signs are not very specific and they are the same as we
see with many other diseases: lethargy, anorexia, diarrhea, ruffled
feathers and huddling. It is considerably more difficult to diagnose
subclinical coccidiosis in turkeys than in chickens, since there is a
lack of discrete lesions in turkeys. The peak of shedding of oocysts
occurs between 3-6 weeks. Fortunately, coccidia are very immunogenic
and most treatment programs and vaccines rely on the immune response to
control the disease. There is probably no age resistance as described
by some authors but rather immunity as a result of some exposure.
Current approaches to coccidiosis prevention in turkeys include:
- Chemotherapy with anticoccidials.
- Vaccination with live oocysts.
At
the present time, anticoccidials are still the main measure of
prophylaxis in Europe and North America. However, vaccination is used
more and more often. In Ontario, approximately 35% of all produced
turkeys are vaccinated.
Chemotherapy
The number of anticoccidials available for turkeys is very limited.
Some anticoccidials used in chickens can create severe toxicity in
turkeys (f.e.salinomycin). Intoxication with salinomycin leads to high
mortality on the order of 28%- 46%. Narasin is also toxic for turkeys.
There are also reports that monensin can lead, in certain
circumstances, to toxic effects and this is so called "knock-down"
syndrome. The frequency of occurrence of "knock-down" is higher in the
summer and early fall. Other aspects of anticoccidials are
incompatibilities between therapeutics and coccidiostats such as
sulfonamides and ionophores.
The list of commonly used anticoccidials is enclosed in the table
below. They can be divided into two groups:
Ionophores and Chemicals. All drugs used for coccidiosis control are
unique in the mode of action. A drug may be efficacious against one or
several species and very few are equally efficacious against all. The
ionophores which include Monensin, Lasalocid and Maduramicine cause
upset of the osmotic balance of the protozoan cell by changing the
permeability of cell membranes for some cations.
The ionophore anticoccidials seem to be more efficacious for long term
application than chemicals. There may be two reasons responsible for
this. It has been reported that ionophores, unlike chemical drugs,
allow the development of certain number of coccidia, therefore allowing
a higher degree of immune response to be induced. Another reason could
be that since ionophores cause massive disruption to cell membranes of
coccidia, affecting all enzyme systems, it may take much longer for
mutations to render the coccidia resistant to disruption to their
various systems.
The majority of drugs in North America are used up to 9 or 10 weeks of
age. In Europe they are used longer till 12-16 weeks. However, the
oocyst excretion can even be up to 20 weeks. There are very little data
on resistance of coccidia to the anticoccidials in turkeys. In order to
minimize the induction of resistance the rules of thumb are:
- Do not use products continuously on the same farm,
- Give the various products a sufficient rest period
after
each use
- Rotate between products of different chemical classes
- Respect the advised concentration in the turkey feed
because some can be very toxic to turkeys.
| Chemical Group |
Active Substance |
Brand Name |
Minimum Concentration in PPM |
Maximum Concentration in PPM |
Withdrawal Time in days |
| Ionophores |
Monensin
Lasalocid
Maduramicin |
Coban
Avatec
Cygro |
90
90
5 |
100
125
5 |
0
0
5
|
| Benzenacetonitril |
Diclazuril |
Clinacox |
1 |
1 |
5 |
| Quinazoline derivative |
Halofuginone |
Stenrol |
2 |
3 |
5 |
| Guanidine |
Robenidine |
Cycostat |
30 |
36 |
6 |
| Pyridine derivatives |
Clopidol |
Lerbek |
110 |
110 |
5 |
| Thiamine analogues |
Amprolium |
Amprol |
66.5 |
133 |
0 |
Vaccination
The use of vaccination for the control of coccidiosis became more
common in the last 7 years. There are only 8 anticoccidial drugs
effective in turkeys and more than 25 in chickens. The emergence of
coccidia resistance to the limited anticoccidials, the susceptibility
of turkeys to ionophores toxicity, and public opinion against the use
of chemicals and drugs has made the use of vaccines more attractive.
The principle of immunization by exposure to a small number of
pathogenic oocysts of important species of coccidia was developed with
chickens first and then in turkeys.
In North America there are two vaccines available for turkeys: Immucox
made by Vetech Laboratories, Guelph Ontario and Coccivac T made by
Shering Plough, Animal Health.
In spite of the big demand for vaccination in Europe, there is only one
vaccine for turkeys Livacox T made in Chech Republic. In some countries
like Poland and Denmark Immucox has been registered and used in the
last few years.
Immucox vaccine has been successfully used in North America in the last
7 years. The majority of this vaccine is used in a gel pack form for
poult consumption up to 3 days of life. The gel delivery system
replaced the liquid application via drinking water which is more labor
intensive. Immucox vaccine contains the species of E.adenoides and
E.meleagrimitis.
Coccivac T vaccine has been introduced last year in the USA and Canada.
It is administered in the hatchery by spray cabinet. The vaccine
contains four species: coccidia E. adenoids, E.meleagrimitis,
E.gallopavonis and E.dispersa.
Vaccination is a controlled exposure of poults to defined numbers of
oocysts. All poults must receive an adequate number of oocysts of each
of pathogenic species to provide protective immunity to the oocysts
that will be picked up from the litter. Birds develop immunity after
two or three cycles of coccidia. The first cycle is from the vaccine
and the second and third from a lifter. It is important that they don't
pick up excessive numbers of oocysts from the litter when immunity is
not fully developed. Practically, after 2 or 3 weeks the immunity
should be fully developed. The immunity after vaccination is based on
cellular immunity.
Performance of vaccinated birds will be discussed. In general in many
trials performance of turkeys vaccinated with Immucox was the same or
better compared to anticoccidials.
Viewing the trends of limited use of anticoccidial drugs, vaccination
against coccidiosis seems to have a good future. New methods of their
administration may improve efficacy and eliminate side effects.
Disclaimer
Copyright © 2007, Vetech Laboratories Inc.