ArticlePDF Available

Effect of Antibiotic and Prebiotic On Immunity and Reproductivity of Broiler Breeder Flock

Authors:

Abstract

This study was carried out to explore effects of antibiotics (Tylosin, Colestin) and prebiotic (enzymes) on immune status and reproduction of commercial Ross broilers breeder flock of 6000 females and 700 males to use viral vaccines (ND,AI, IB, IBD and CIA) as well as MG and MS infection by ELISA-test. Results revealed that mean ELISA titers against MS was 685±120.7, 1200.4±322.7, 924.6±99.9, 1373±168.5 and 925.7 ±133.4 at 6, 27 ,35, 44 and 61 weeks, respectively; while CV% still is below 30%. Mean ELISA titer against MG was 2891.8±146.64, 608.5±208.5, 2961±1319.5, 3199.2±1331.2 at 6th, 27th, 35th and 44th week, respectively. While CV% was 5.1 at 6 th week and increased gradually to be 48.4 %. The fluctuation in MS and MS ELISA titers might indicate active infection and/or low challenge frequency that was suppressed by the use of drugs. ELISA for viral vaccines including ND was 7594±4810, 18906±3562, 17543±5478 and 16232±2718 at 6th, 15 th , 35th and 61 st week, respectively. CV% was higher with 63.3 at 6th week (week) and after that was good and excellent. ELISA titer for AI was 6214.6±1571.3 at 6 th week and gradually increased to 14805.8 ±2260.7 at 35 th week with CV% less than 30%. Titers against IBD virus was 3716±1188 at 6 th week, increased to 9476±4578 by 35 th weeks, then decreased to 3232 ±1780 at 61 st weeks. ELISA titer against IB virus started with 3642 ±1048 and increased to 11192 ±3458 at 53 rd week. CIA titers started with 1188±410, 7848±1923 and 6056±1385 at 6 th , 27 th and 53 rd week. Interpretation of the recorded ELISA titers with CV% indicating uneven immunity at 6 th week followed by varied increase from good to excellent. This indicates good uniform flock immune by repeated vaccination, medication and good management; while the decreased titers in last weeks were due to normal decaying of antibody. Cumulative mortality rate in the flock was 2.5 % lower than farm stander. Regarding flock productivity as compared with flock stander resulted in high egg production percent in the first 10 weeks. Decreased egg production and hatched eggs at the last weeks (16, 64) can be attributed to big sized eggs. An increase was seen in both average fertility with 1.35% and average hatchability 0.66% as well as cumulative produced chicks/ hen by 5 chicks/hen than farm stander. Conclusion: Based on serological mortality and reproduction results, this study pointed out that the applied vaccination program and preventive medication (Tylosin, Colestin and enzyme prebiotic) in ration or water to broiler breeders resulted in a higher immunity and reproductive performance.
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
18
Effect of Antibiotic and Prebiotic On
Immunity and Reproductivity of Broiler Breeder
Flock
Mohamed M. Amer1, Ghazi .A. M. Zohair2, A. EL-shemy3, Hoda M. Mekky4, Dalia M.
Sedeek4
1 Department of Poultry Diseases, Faculty Veterinary Medicine, Cairo University, P.O. Code 12211 Giza, Egypt.
2 Department of animal production, Faculty of Agriculture, Sana`a University, Republic of Yemen.
3 Department of Parasitology and Animal Diseases, Veterinary Research Division, National Research Centre, P.O. Code
12311Dokki, Giza, Egypt.
4 Department of Poultry Diseases, Veterinary Research Division, National Research Centre, P.O. Code 12311 Dokki, Giza,
Egypt.
ABSTRACT
This study was carried out to explore effects of antibiotics (Tylosin, Colestin) and prebiotic (enzymes) on immune status and
reproduction of commercial Ross broilers breeder flock of 6000 females and 700 males to use viral vaccines (ND,AI, IB, IBD
and CIA) as well as MG and MS infection by ELISA-
test. Results revealed that mean ELISA titers against MS was 685±120.7,
1200.4±322.7, 924.6±99.9, 1373±168.5 and 925.7 ±133.4 at 6, 27 ,35, 44 and 61 weeks, respectively; while CV% still is
below 30%. Mean ELISA titer against MG was 2891.8±146.64, 608.5±208.5, 2961±1319.5, 3199.2±1331.2 at 6th, 27th, 35th
and 44th week, respectively. While CV% was 5.1 at 6th week and increased gradually to be 48.4 %. The fluctuation in MS and
MS ELISA titers might indicate active infection and/or low challenge frequency that was suppressed by the use of drugs.
ELISA for viral vaccines including ND was 7594±4810, 18906±3562, 17543±5478 and 16232±2718 at 6th, 15th, 35th and 61st
week, respectively. CV% was higher with 63.3 at 6th week (week) and after that was good and excellent. ELISA titer for AI
was 6214.6±1571.3 at 6th week and gradually increased to 14805.8 ±2260.7 at 35th week with CV% less than 30%. Titers
against IBD virus was 3716±1188 at 6th week, increased to 9476±4578 by 35th weeks, then decreased to 3232 ±1780 at 61st
weeks. ELISA titer against IB virus started with 3642 ±1048 and increased to 11192 ±3458 at 53rd week. CIA titers started
with 1188±410, 7848±1923 and 6056±1385 at 6th, 27th and 53rd week.
Interpretation of the recorded ELISA titers with CV% indicating uneven immunity at 6th week followed by varied increase
from good to excellent. This indicates goo
d uniform flock immune by repeated vaccination, medication and good
management; while the decreased titers in last weeks were due to normal decaying of antibody.
Cumulative mortality rate in the flock was 2.5 % lower than farm stander. Regarding flock productivity as compared with
flock stander resulted in high egg production percent in the first 10 weeks. Decreased egg production and hatched eggs at the
last weeks (16, 64) can be attributed to big sized eggs. An increase was seen in both average fertility with 1.35% and average
hatchability 0.66% as well as cumulative produced chicks/ hen by 5 chicks/hen than farm stander.
Conclusion: Based on serological mortality and reproduction results, this study pointed out that the applied vaccination
program and preventive medication (Tylosin, Colestin and enzyme prebiotic) in ration or water to broiler breeders resulted
in a higher immunity and reproductive performance.
Key Words: Broiler breeder chicken, ELISA test, Antibiotic, prebiotic, reproduction, immune response.
eIJPPR 2017; 7(4):18-25
HOW TO CITE THIS ARTICLE: Mohamed M. Amer, Ghazi .A. M. Zohair, A. EL-shemy, Hoda M. Mekky, Dalia M. Sedeek. (2017). Immune
status and reproduction of medication vaccinated broiler breeder chickens”
, International
Journal of Pharmaceutical and
Phytopharmacological Research, 7(4), pp.18-25.
INTRODUCTION
Vaccination of breeder flocks providing 1 day old chicks
with MDA, protect chicks from infection in the 1st 3rd
week [1;5]. Vaccine strategies are based on the prevention
of vertical and horizont
al transmission of virus to very young chicks by
immunization of breeder flocks and have been successful
in reducing the incidence of chicken infectious anemia
Corresponding author:
Mohamed M. Amer
Address:
Department of Poultry Diseases, Faculty Veterinary Medicine, Cairo University, P.O. Code 12211 Giza, Egypt.
e-mail profdramer@yahoo.com
Relevant conflicts of interest/financial disclosures: The authors declare that the research was conducted in the absence of any
commercial or financial relationships that could be construed as a potential conflict of interest.
Received:
14 November 2016;
Revised:
02 June 2017;
Accepted:
24 June 2017
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
19
(CIA) in young chicks [6]. Antibodies reduced virus
shedding from infected chickens [1,7,8] and keep birds in
high productivity [9] . The success of passive immunity
depends upon antibody titer of the breeder hen, the higher
titer (measure of circulating antibodies) in the hen, the
greater transfer to the chick. For Newcastle disease (ND),
Avian influenza (AI) and Infectious bursal disease (IBD),
there is about 50% transfer of titer from the breeder hen to
the chick [1, 10, 11]. High uniform titers in breeders are
usually obtained with vaccination programs that involve
initial administration of a live virus (primer) followed by
a killed virus at some older age.
The broiler breeder hen usually starts egg production at
the age of 23-24 weeks and produces around 183
hatchable eggs out of 199 total hens housed eggs
produced in 65 weeks of its laying cycle [12]. Farooq et
al. [13] reported smaller per hen-housed egg production
(188 ±0.56 eggs) representing 88 ± 0.23% hatchable and
14± 0.18%, unhatchable eggs than that reported by North
[12]. Probable reason for that could be shorter egg laying
cycle and poor rearing environment in former than in later
case. Higher mortality rate adversely affect production
performance of broiler breeders. Mortality and its
negative association with net profit was reported [13,14].
Moreover, North [12] and Ali [15] reported poor
economic performance of breeders at mortality level of
above 10% and maximum level of mortality 13.11%,
respectively.
Serologic monitoring will establish a baseline of
antibody titers that are the result of both vaccination and
field challenge. Changes in the regular observed antibody
titers may indicate a decrease in the efficacy of vaccine
administration or an increased field challenge by a
particular pathogen. A regular serologic monitoring
program is also helpful to determine whether a flock is
exposed to a new pathogen [16]. Evolution and diagnostic
advantages of the graphic presentation of ELISA are
based on flock-profiling data in combination with gross
and microscopic pathology data [17].
Prebiotics are non-digestibility and selected ferments
capability by some bacterial groups. Most prebiotics are
carbohydrates. Moreover, ingredients are often made of
several compounds. These molecules not only differ in
the polymerization degree but also in the production
technology (as, fractions can be obtained either by
enzymatic hydrolysis or by extraction); these two
manufacturing processes lead up to different mixtures of
final products. Intestinal bacteria metabolize these
compounds in different ways [18, 19, and 20].
Respiratory disease of poultry cause severe
economic losses specially AI, ND, Infectious bronchitis
(IB) and Mycoplasma gallisepticum (MG). These
affections could be prevented by vaccination that plays an
important role in the health management of the poultry
flock by triggering or boosting the bird’s immune system
to produce antibodies that in turn fight the invading
causal organisms using live and inactivated vaccine
against usage of antibiotics. IBD and CIA cause to a
variable degree of immunosuppression in the affected
birds [16]. Infection of chicks in the early age displays a
severe and prolonged immunosuppression [21].
Talebi and Ghasemi-lak [22] compared ELISA titers of
MG and MS infected broiler breeders at 35 weeks-old
before and after treatment with tylosin for 5 days and
concluded that the antibiotics affect the outcome of the
MG and MS infections in broiler breeders and reduce
serological titres of MG and MS in infected birds but do
not completely cure the birds from the
infections. Antibiotic antibacterial medications are still
used in poultry industry in several indications including
therapeutic treatment, prevention or as traditional growth
promoters [23, 24]. However, using such antibiotics
during vaccination has not been established well yet and
few data are available in such indication. Both MG and
MS are reported as spread chicken pathogens among
Egyptian chicken flocks by either serological and /or
isolation and identification methods [25, 26]. The
eradication of mycoplasma infection can be achieved
through improvements in hygiene and management
practices, therapeutic treatment of breeder layers and/or
hatching eggs and better monitoring procedures.
Antimycoplasma drugs are used intensively to improve
productivity and reproduction of laying [16, 27, 28].
Stipkovits and Kempf [29] stated that antibiotics could be
used for therapeutic treatment or prophylactic medication.
Fewer MG and fewer positive reactors was recovered
from infected medicated chicks [30]. Administration of
very low levels of tylosin in feeding MG infected layers
in multiple-age complexes was found to lessen egg
production losses [31].
The CV is a measure of variation of antibodies within a
group of serum samples. Lower CV indicates the more
uniform antibody response and typically associated with
good vaccination procedures or with a recent antibody
response after field exposure to a given pathogen.
Because an ELISA titer or an ELISA titer range reflects
simply a quantitative response, such titers should be used
as follows: 1) as a reference for possible trends in
seroconversion in a poultry company upon field
challenges; 2) for identification of rapid seroconversion in
paired acute and convalescent samples in a diagnostic
situation; 3) for evaluations of vaccines and vaccine
application procedures; or 4) to document the absence of
antibodies against pathogens such as AIV, MG, or MS
(IDEXX manual).
Both colistin (polymexins), Tylosin (macroloids)
antibiotics and prebiotic used in this study showed
positive impacts in controlling MG and E.coli and
bacterial complication with such bacteria together with
enhancement immune response of broiler chickens to use
viral vaccines [32,33,34,35].
The objective of present study was to evaluate immune
status of commercial broiler breeder chicken flock raised
with antibiotic and/ or prebiotic medicated to some used
viral vaccines by ELISA- test against ND,AI, IB, IBD and
CIA as well as antibody against MG and MS infection in
relation to flock reproductively.
MATERIAL AND METHODS
1- Experimental Chicken flock:
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
20
A total number of 6700 Ross broilers breeder flock of
6000 females and 700 males were housed in
semiautomatic deep litter house.
2. Ration:
Commercial breeder chicken ration were given according
to Ross breeding manual and [36]. The used commercial
balanced ration was based on yellow corn or soya bean
that met with [37] broiler breeder chicken requirements.
3- Vaccine Strains and vaccination:
The used viral vaccines, time and route of vaccination are
shown in table (1).
Table (1): Vaccination Program for breeder chickens
no
Vaccine
Method
Manufacturer
1
THV
sc
merial
2
coccivac
feed spray
shering plough
3
ND CLONE
D.W
INTERVET
4
AI(H5)+ND and REO LIVE
im/sc
merial/intervet
5
Gumboro D78
D.W
INTERVET
6
Clone HB
D.W
IZO
7
Gumboro D78 intermediate
D.W
INTERVET
8
ILT
E.D
INTERVET
9
REO,IB,IBD,ND
S,C
INTERVET
10
Vectorrmune (pox)
W.W
Biomune
11
Colone HB
D.W
IZO
12
AI(H5) + ND+IB
sc
Lohhman/Merial
13
ILT
E.D
INTERVET
14 13 ws
CAV
D.W
Lohhman
TRT Live
D.W
INTERVET
15
Clone ND
D.W
INTERVET
16
EDS and AI(H5)+ND
im/sc
Biomune/Lohhman
17
IBH120
D.W
INTERVET
18
ND La Sota
D.W
INTERVET
19
TRT inac+Reo+IB+ND+IBD
im/sc
INTERVET/Biomune
20
AI(H5) +ND La Sota
s.c/ D.W
INTERVET
34 week &
Every 5 ws
ND La Sota D.W INTERVET
4- Natuzyme® Prebiotic:
It is a multienzyme poultry feed supplements commercial
product, Novartis Limited, India contains: Cellulase,
xylanase, beta-lucanase, alpha-amylase and pectinases. It
also contains phytase, protease, hemicelluse,
amyloglycosidase, pentosanase and phyton activities.
Dosage: 500 gm/ton of feed. Prebiotic was given in
ration in the first 28 days, then 3 days before vaccination.
5- Antibiotics:
a- Colistin sulphate 6 MIU®: each gm contains 6000.000
IU colistin sulphate. Lot No. 150415 . Jordan Vet. and
Agr. Med. Ind. Co Amman Jordan.
b- Tylox® : tylosin water soluble powder 100gm - Lot.
No. 150118. Jordan Vet. and Agr. Med. Ind. Co
Amman Jordan. Both Tylosin and colestin were at first
3 days and 28-30 days followed by every 45 days dose of
tylosin + colistin 2 days in water.
6- Samples:
Blood samples for serum were collected for ELISA test at
the end of the week 6, 15, 24, 35, 44, 53 and 61 of life to
detect ELISA antibody titers against ND, AI, IB, IBD,
CIA , MG and MS. Results are shown in tables (1 - 3).
7- Serological ELISA test:
The collected sera were tested to evaluate the antibodies
titer against ND, AI, IB, IBD MG, CIA and MS
antibodies procedure performed using commercial ELISA
kits according to the manufacturer's recommendations:
a. AI: Indirect ELISA methods, including ProFLOCK
plus AIV Ab test kit (Synbiotics, USA), indirect ELISA
methods were performed.
b. ND: Chicken serum samples were examined for NDV
antibodies by indirect ELISA, using a commercial ELISA
test kit ProFLOK® NDV Plus (Synbiotics, San Diego,
CA), run in 96-well micro-titer plates containing NDV
antigen.
c. IBD: The sera obtained from blood of experimental
chicks at various time points were tested for IBD
antibodies using the PROFLOK® plus IBD Ab test kit
(Symbiotics, San Diego, CA).
d. IB: The PROFLOK® IBV ELISA Kit (Synbiotics,
USA), which is a rapid serologic test used for the
detection of IBV antibody in chicken serum samples.
e. CIA: All samples were analyzed by Elisa kit (Synbiotic
Corp., USA) in the same condition. According to the kit’s
instruction, the serum samples with the S/P ratio equal or
less than 0.349 were considered zero titer and S/P ratio
equal or greater than 0.350 (≥1472) were considered
positive serum.
f. MG: The procedure used in this test was performed
using commercial ELISA kits for the presence of anti-MG
antibodies ProFLOK® MG Antibody Test Kit, Synbiotics
Corp. - USA].
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
21
g. MS: commercial ELISA kit (Synbiotics Corp.,
ProFlock, USA) to detect specific antibodies against MS
were used according to the manufacturer’s instructions.
8- Coefficient of variation (CV%) values:
The CV% is the standard deviation divided by the mean,
multiplied by 100, whether we are relating to antibody
titers. Interpretation of CV values in vaccinated birds can
be done as: > 30% : Excellent; 30-50%: Good; 51-80%:
Fair and >80%: poor.
9. Reproduction:
Reproduction of the flock under study was calculated at
27th, 35th , 44th, 53rd and 61st week of life according to
North [12] as compared with breed stander as well as the
farm stander [36], which is the average of reproduction of
last 3 successive flocks from starting of egg laying at 24th
64th week (40 production weeks). The obtained results
are seen in table (4-6).
RESULTS AND DISCUSSION
Good management, vaccination program and preventive
medication are required to obtain high performance and
production as well as hatchery parameters in poultry
farms. Results of table (2) revealed that mean ELISA
titers against MS was 685±120.7 and increased to
1200.4±322.7 till 27th week, then slightly decreased to
924.6±99.9 at 35th week, then increased again at 44th
week to 1373±168.5 and decreased at 61st week to
925.67±133.4 , ELISA titers reduction at 35th week might
be due to using antibiotic at this time and susceptibility of
infected strain to such antibiotic [39,40] resulting in
decreased bacterial population while such titer rose at
Table ( 2 ): Main ELISA titers against MS and MG in vaccinated and medicated breeder flock.
Age/
weeks No of
samples
MS MG
mean SD CV% mean SD CV%
6
31
685
120.7
17.6
2891.8
146.64
5.1
15
45
1924.6
50.4
2.6
1446.2
176.8
12.2
27
30
1200.4
322.7
26.9
608.5
208.5
34.3
35
30
924.6
99.9
10.8
2961
1319.5
44.6
44
35
1373.3
168.5
12.3
3199.2
1331.2
41.6
53
20
1099
313.5
28.5
668.3
281.5
42.1
61 48 925.67 133.4 14.4 364.9 176.6 48.4
44th week indicating activation of latent infection again,
which gradually decreased at 53rd and 61st week, which
indicate normal decaying of antibody [41], while CV%
still is below 30% all observation time indicate persistent
infection in spite of antibiotic treatment, which indicates
resistance to used antibiotic or persistence on material in
poultry environment [42]. Moreover, other researchers
stated that antibiotic treatment against MS could decrease
symptoms of the disease but did not eliminate infection
[43]. While mean ELISA titer against MG was
2891.8±146.64 at 6th week of life, gradually decreased
till 27th week of life and become 608.5±208.5, then
sharply increase again at 35th and 44th week of life to
2961±1319.5 and 3199.2±1331.2, respectively, which
indicates active infection [44] . Then, again decreased
gradually in next 53 and 61 weeks of life which indicates
possible normal decaying of antibody [41], while CV%
was 5.1 at week 6 and increased gradually to 48.4 %
indicate uneven immunity due to challenge frequency.
Table ( 3 ): Main ELISA titers against ND and AI in vaccinated and medicated breeder flock
Age/
week
No of
samples
ND
AI
Mean
SD
CV%
Mean
SD
CV%
6
31
7594
4810
63.3
6214.6
1571.3
25
15
45
18906
3562
18.8
10113.8
1372.1
14
27
30
12083
3239
26.8
12547.5
1908.5
15
35
30
17543
5478
31.2
14805.8
2260.7
15
44
35
14762
3217
21.8
6366.4
2260.2
36
53
20
15682
3458
22.1
4986.5
2310.5
46
61
48
16232
2718
16.7
4121.7
2260.2
55
Results of mean ELISA for ND at 6 weeks of age was
7594±4810 , which increased by 15 weeks of age to
18906±3562 indicating good vaccination immune
response [45] by 27 weeks of age. This titer become
12083±3239, which indicate field challenge [46], then
increased by 35 weeks of age to 17543±5478 good
immune response due to vaccination , then decreased by
44 weeks of age to 14762±3217 indicating field
challenge due to indemicity of such disease and increase
again and still was high at 53 and 61 weeks of age to be
15682±3458 and 16232±2718, respectively, which maybe
indicate good immune response due to vaccination and
absence of field challenge, while CV% was higher with
63.3 at 6 weeks of age and decreased very good flock
immune uniformity [47]. ELISA titer for AI (Table 3)
was 6214.6±1571.3 at 6 week-old, which gradually
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
22
increased weekly to 14805.8±2260.7 at 35 week-old with
CV% less than 30, which indicate good vaccination
immune response with no challenge [48] , then decreased
by week 44 to 6366.4±2260.2, which indicate maybe field
challenge [49].
Mean ELISA titers against IBD virus at 6 week-old was
3716±1188, started to increase 9476±4578 by 35th week.
This indicates good immune response due to vaccination
without any field challenge [50, 51], then decreased
gradually to 3232±1780 at 61st weeks indicating normal
decaying of antibody [41]. While mean antibody titer
against IB virus starts with 3642±1048 and increases
gradually to 21170±13329 at 27th weeks due to
vaccination with no evidence of field challenge then
decrease gradually to 11192±3458 at 53rd week [52] .
Concerning CIA mean antibody titers start with 1188±410
and increase gradually to 7848±1923 at 27th week
indicating good antibody response due to vaccination [53]
and decreased by 35 and 44 weeks of age then increase
again to 6056±1385 at 53rd week.
Table ( 4 ): Main ELISA titers against IBD, IB and CIA in vaccinated and medicated breeder flock
Age/
week
No of
samples
IBD
IB
CIA
Mean
SD
CV%
Mean
SD
CV%
Mean
SD
CV%
6
31
3716
1188
32.0
3642
1048
28.8
1188
410
34.5
15
45
2088
1356
64.9
15501
3256
21.0
7078
1536
21.7
27
30
4083
929
22.8
21170
13329
63.0
7848
1923
24.5
35
30
9476
4578
48.3
18006
14325
79.6
4008
2847
71.0
44
35
7119
2137
30.0
16377
17321
105.8
2780
732
26.3
53
20
5574
2158
38.7
11192
3458
30.9
6056
1385
22.9
61
48
3232
1780
55.1
15176
12718
83.8
5394
1278
23.7
Interpretation of the recorded ELISA titres to CV%,
indicates uneven immunity at 6 weeks and followed by
increased titres and to be varied from good to excellent.
This indicates good flock immune uniformity by repeated
vaccination field challenge; while the decreased titres in
last weeks were due to normal decaying of antibody.
The recorded cumulative mortality (Table 5) rate (
12.5%) in the flock was 1.5 % lower than farm stander
(14%). This result indicates improvement and higher
production performance and immunity of broiler breeders
[12,13,14,15].
Table (5): Average weekly Egg production % , egg produced and hatching eggs / hen housed / week of farm stander
and treated flocks.
Age/weeks
Egg production %
Egg/Housed hen/week
Hatch Egg/Housed hen/week
Farm Stander
Treated
Farm
Standard
Treated
Farm
Standard
Treated
27
55.0
56.5
3.85
3.66
3.96
3.81
35
84.0
86.9
5.88
5.57
6.08
5.40
44
75.0
79.5
5.15
4. 82
5.57
4.90
53
66.5
67.5
4.66
4.40
4.73
4.43
61
56.0
45.5
3.92
3.75
3.18
3.10
64
48
46.3
3.36
3.23
3.24
3.08
Average egg production %
63.01
65.13
Cumulative egg
178.56
164.73
180.32
173.50
Cumulative Mortality%
14
12.5
* Hen-week (%) is based on the assumption that mortality in lay is 8% with 0.2% mortality per week.
** A hatching egg is considered to be an egg which is 50- 70 g.
Regarding effect of Treatment of flock productivity as
compared with flock stander (Table 5), resulted in
increased egg production percent in the first 10 weeks.
This was matched with Torki et al. [54] who found that
enzymes improves productive performance and egg
quality of laying hens, moreover use of both tylosin and
colistin could improve egg production percent due to
controlling infectious agents such as Mycoplasma spp.
and /or complicating agents such as avian pathogenic
E.coli and Mycoplasma [32,38,34] affected both quantity
and quality of produced egg [55,56]. Decreased egg
production and hatched eggs at the last weeks (61 and 64)
can be attributed to big sized eggs.
Results of reproduction (Table 6) increased average
fertility with 1.35% and average hatchability 0.66% with
improvement of shell characters. This may be due to that
controlling infectious agents such as MG, MS, E.coli and
Salmonella by antibiotic used resulting in improving
fertility and hatchability [22,32,57,58].
Table (6): Weekly Hatchability and hick Production, average Fertility and Hatchability as well as cumulative chick/hen
and total culls percentage in treated and farm stander of breeder chickens.
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
23
Age/weeks
Farm Standard
Treated
Hatchability
(%)
Chicks/Week
Hen-Housed
Hatchability
(%)
Chicks/week
Hen-Housed
27
80.6
2. 35
81.8
2.47
35
90.5
5. 60
92.3
5.63
44
86.5
4. 62
86.8
4.78
53
79.9
3.62
77.6
3.68
61
73.6
2. 35
75.6
3.18
64
70.2
2.45
71.8
2. 62
Average
Fertility %
93.60
94.95
Average hatchability
82.0
82.66
Cumulative
168.5
173.5
Culled chick%
1.71
1.55
NOTES: * Hatchability is based on an average egg age of 3 days. Hatchability will drop by 0.5% per day of storage
between 7 and 11 days.
Cumulative produced chicks per hen was increased due to
treatment by 5 chicks/hen than farm stander. This may be
due to controlling poultry pathogens leading to embryonic
death in hatcheries, such as avian pathogenic mycoplasma
[16], E.coli [59], and Salmonella spp. [60] as both
pathogens affect fertility and hatchability.
From both serological results and productivity, we can
notice that flock under test had good immune response
and production parameters.
In conclusion, our field study pointed out that the applied
vaccination program and preventive medication (Tylosin,
Colestin and enzyme prebiotic) in ration or water to
broiler breeders resulted in a higher immunity and
reproductive performance as compared with farm stander
as control.
REFERENCES
[1] Allan W H, Lancaster J E, Toth B. 1978.
Newcastle disease vaccinesTheir production
and use. FAO Animal Production and Health
Series No. 10. FAO: Rome, Italy. 2. Lucio B,
Hitchner SB .1979. Infectious bursal disease
emulsified vaccine: Effect upon neutralizing-
antibody levels in the dam and subsequent
protection of the progeny. Avian Dis 23:466-
478.
[2] Klieve, A. V. and R. B. Cumming(1988):
Infectious bronchitis: Safety and protection in
chickens with maternal antibody. Aust. Vet. J.
65: 396397.
[3] Naylor C J, Worthington K J , Jones RC. 1997.
Failure of maternal antibodies to protect young
turkey poults against challenge with turkey
Rhinotracheitis virus. Avian Dis 41:968- 971.
[4] Yuasa, N., T. Noguchi, K. Furuta, and I.
Yoshida. (1980): Maternal antibody and its
effect on the susceptibility of chicks to chicken
anemia agent. Avian Dis., 24:197–201.
[5] Engström B E. 1999. Prevalence of antibody to
chicken anaemia virus (CAV) in Swedish
chicken breeding flocks correlated to outbreaks
of blue wing disease (BWD) in their progeny.
Acta Veterinaria Scandinavia 40 :97107.
[6] Parede L, Young P L.1990. The pathogenesis of
velogenic Newcastle disease virus infection of
chickens of different ages and different levels of
immunity. Avian Dis., 34:803–808.
[7] Ladman B S, Pope C R, Ziegler A F,
Swieczkowski T, Callahan C J, Davison S ,
Gelb J Jr. 2002. Protection of chickens after live
and inactivated virus vaccination against
challenge with nephropathogenic infectious
bronchitis virus PA/Wolgemuth/98. Avian Dis
46:938–944.
[8] Miller J Patti, Claudio L Afonso, John El
Attrache , Kristi M Dorsey , Sean C Courtney ,
Zijing Guo , Darrell R Kapczynski .2013. Effects
of Newcastle disease virus vaccine antibodies on
the shedding and transmission of challenge
viruses. Developmental and Comparative
Immunol 41 (4); 505-513.
[9] Skeeles J K, Lukert PD, Fletcher O J , Leonard J
D . 1979. Immunization studies with a cell-
culture-adapted infectious bursal disease virus.
Avian Dis 23:456- 465.
[10] Amer M M, Hamouda A S , EL-Bayomi K M.
2010. Studies on maternal antibodies to avian
influenza H9N2 vaccine. In procc. of the 6th sci.
Conf., Facult. Vet. Med., Beni- Suef Uni., 24-27,
April 2010.
[11] North M O. 1984. Breeder Management. In
commercial chicken production manual. The
Avi. Publishing Co.Inc. Westport, Connecticut.
240-243 and 298-321.
[12] Farooq M, Mian M A, Faisal S , Durrani F R,
Arshad M, Khurshid A . 2001. Status of broiler
breeder stocks in Abbotabad and Mansehra.
Sarhad J Agri 17: 489-495.
[13] Asghar A , Farooq M, Mian M A, Perveez ,
Khurshid A .2000. Economics of broiler
production in Mardan Division. J. Rural
Development and Administration, Vol. XXXII:
56-64.
[14] Ali M ,Farooq M, Durrani F R, Chand N,
Sarbiland K, Riaz A. 2003. Egg Production
Performance and Prediction of Standard Limits
for Traits of Economic Importance in Broiler
Breeders. Int J of Poult Sci 2 (4): 275-279.
[15] Saif, Y M, Barnes H J, Fadly A M, Glisson J
R, Swayne D E .2003. In Poultry diseases. ,11th
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
24
Ed., Iowa State Press, Iowa. A Blackwell
Publishing Co. p 3- 45.
[16] Mallinson E T, Snyder D B, Marquardt W W,
Gorham S. 1988. In Principles of Disease
Prevention: Diagnosis and Control by Alex J.
Bermudez and Bruce Stewart-Brown in poultry
diseases.
[17] Roberfroid M B, Van Loo J A, Gibson G R
.1998. The bifidogenic nature of chicory inulin
and its hydrolysis products. J. Nutr 128: 11-19.
[18] Perrin S, Fougnies C, Grill J, Jacobs H,
Schneider F. 2002. Fermentation of chicory
fructooligosaccharides in mixtures of different
degrees of polymerization by three strains of
bifidobacteria. Can J Microbiol. 48: 759- 763.
[19] Kaplan H, Hutkins R. 2003. Metabolism of
fructooligosaccharides by Lactobacillus
paracasei 1195. Appl Environ Microbiol 69,
2217-2222.
[20] Lukert P D, Saif Y M. 1991. Infectious bursal
disease. Diseases of poultry, 9th Ed. Lowa State.
University press. Ames, Lowa USA. 1060-1085.
[21] Talebi A, Ghasemi-lak M . 2004. Investigation
of antibiotic effects on serological titers of
infected Ross broiler breeders with Mg and Ms.
J. of the Facult. of Vet. Med., University of
Tehran 59 (3) : 271-275.
[22] Miles R D, Butcher G D , Henry P R. Littell R
C .2006. Effect of antibiotic growth promoters
on broiler performance, intestinal growth
parameters, and quantitative morphology. Poult
Sci 85(3): 476-85.
[23] 24. Diarra S Moussa, Francois Malouin .2014.
Antibiotics in Canadian poultry productions and
anticipated alternatives. Front Microbiol.; 5:282
doi:10.3389/fmicb.2014.00282.
[24] 25. El-Shater S A A, Khair El Din A M W,
Oraby F. 1990. Incidence of mycoplasma in
gallinaceous birds. Procc 4th Science. Congress,
Facult. of Vet. Med., Assiut University, 1003-
1010.
[25] 26. Abou El Makarem M M. 2003. Evaluation of
serological tests for the diagnosis of M.
gallisepticum in comparison with the frequency
of isolation. Assiut Vet Med J 49: 220-227.
[26] 27. Carpenter T E, Mallinson E T, Miller K F,
Gentry R F, Schwartz L D.1981. Vaccination
with F-Strain Mycoplasma gallisepticum to
reduce production losses in layer chickens.
Avian Dis 25: 404- 409.
[27] 28. Levisohn, S. and S. H. Kleven (2000):
Avian mycoplasmosis (Mycoplasma
gallisepticum). Rev Scientific Technology,
19:425-442.
[28] 29. Stipkovits L, Kempf I. 1996.
Mycoplasmoses in poultry. Rev Sci
Tech15(4):1495-525.
[29] 30. Jordan FT, Forrester CA, Ripley PH, Burch
DG. 1998. In vitro and in vivo comparisons of
valnemulin, tiamulin, tylosin, enrofloxacin, and
lincomycin / spectinomycin against Mycoplasma
gallisepticum. Avian Dis 42(4):738- 745.
[30] 30. Ose E E, Wellenreiter R H, Tonkinson L V.
1979. Effects of feeding tylosin to layers
exposed to Mycoplasma gallisepitcum. Poult Sci
58:4249.
[31] 32. Amer M M, Zohair G A, EL-Bayomi Kh
M, Zenab M S Gera . 2012 . Effect of tilmicosin
in control of mycoplasmosis in broiler chickens
from infected breeders using ELISA test for
evaluation. J of Amer Sci 8 (3): 696-700.
[32] 33. Amer M M, Elbayoumi Kh. M, Zeinab M
S Amin Girh, Eman R Hassan, Bosila M A.
2016. Studies on effect of prebiotic on immune
response of broiler chicken to ND -AI combined
inactivated vaccine. Int J of Chem Tech Res 9
(12) 182- 190. CODEN (USA) : IJCRGG, ISSN:
0974-4290, IS SN(Online): 2455-9555
[33] 34. Amer M M, Elbayoumi Kh M , Zeinab M S
Amin Girh, Eman R Hassan, Bosila M A , Hoda
M Mekky. 2016. Effect of prebiotic and/ or
antibacterial drug on performance of broiler
infected with E.coli. Int J of Pharm Tech Res 9
(12): 58-69.
[34] 35. Elbayoumi Kh M, Zeinab M S Amin Girh,
Eman R Hassan, Aziza . Amer, Ghazi A M
Zohair, Amer M M. 2016. Enhancement of
immune response against IBD and IB in
antibiotic treated Mycoplasma gallisepticum
serologically positive broiler chickens. Int J of
Chem Tech Res 9 (12) 934-942.
[35] 36. Amer M M, EL-Bayomi Kh M ,Zeinab, M
S Amin. Girh . 2011. Field studies on effect of
probiotic on reproductivity of 51 weeks old
broiler breeder chickens fed on mycotoxins
contaminated ration. J of Amer Sci 7(4) 840 -
844.
[36] 36. Leeson S, Summers J D. 2000. Broiler
breeder production. Published by Nottingham
University Press Manor Farm, Church Lane
Thrumpton, Nottingham NG11 0AX, England.
[37] 37. NRC (National Research Council).1984.
National requirement for poultry. 9th Ed.,
Washington DC, National Academy Press.
[38] 39. Feizi Adel, Soroosh Babakhani , Hossein
Nikpiran 2013. Comparative survey of tiamulin
and tylosin in control of Mycoplasma
gallisepticum in broiler chickens. Eur J of
Experimental Biol 3 (1):536 -539.
[39] 40. Messaï C R, Aït-Oudhia, K, Khelef D,
Hamdi T M, Chenouf N S, Messaï M R . 2015.
Serogroups and antibiotics susceptibility pattern
of avian pathogenic Escherichia coli strains
responsible for Colibacillosis in broiler breeding
farms in the east of Algeria. African J of
Microbiol Res 9 (49): 2358-2363.
[40] 41. Gharaibeh S , Mahmoud K .2013. Decay of
maternal antibodies in broiler chickens. Poult
Sci. 2013 Sep;92(9):2333-6. doi:
10.3382/ps.2013-03249.
[41] 42. Stipkovits L T .2000. Current questions of
the control of Mycoplasma synoviae infection.
Magyar Allatorvosok Lapja. 122 (3) :165-167.
International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR) | Augst 2017 | Volume 7 | Issue 4 | Page 18-25
Mohamed M. Amer., Immune status and reproduction of medication vaccinated broiler breeder chickens
ISSN (Online) 2249-6084 (Print) 2250-1029 www.eijppr.com
25
[42] 43. Kleven S H. 2003. Mycoplasma synoviae
infection, in: Barnes H.J., Glisson J.R., Fadly
A.M., McDougald L.R., Saif Y.M. (Eds.),
Diseases of Poultry, 11th ed., Iowa State
University Press, Ames, Iowa, pp. 756-766.
[43] 44. Luciano R L , Cardoso A L S P, Stoppa G
F Z, Kanashiro A M I, de Castro A G M,
Tessari E N C.2011. Comparative study of
serological tests for Mycoplasma
synoviae diagnosis in commercial poultry
breeders. Vet. Med. International Volume 2011,
Article ID 304349, 5 pages
http://dx.doi.org/10.4061/2011/304349
[44] 45. Banu N A, Islam M S, Chowdhury M M H,.
Islam M A. 2009. Determination of immune
response of Newcastle disease virus vaccines in
layer chickens. J Bangladesh Agril Univ 7(2) :
329- 334.
[45] 46. Perozo F , Marcano R , Afonso CL. 2012.
Biological and phylogenetic characterization of a
genotype VII Newcastle disease virus from
Venezuela: efficacy of field vaccination. J Clin
Microbiol 50(4):1204-8. doi:
10.1128/JCM.06506-11.
[46] 47. Dimitrova M. Kiril, Claudio L. Afonsoa ,
Qingzhong Yub , Patti J. Miller (2016):
Newcastle disease vaccines-A solved problem or
a continuous challenge. VETMIC 7477 Pages
11.
[47] 48. Khalili Iraj, Rahim Ghadimipour, Saeed
Sadigh Eteghad, Mohsen Fathi Najafi,
Mohammad Majid Ebrahimi, Naser Godsian,
Yousef Sefidi Heris, Mohammad Taghi Khalili .
2015. Evaluation of immune response against
inactivated avian influenza (H9N2) vaccine, by
using chitosan nanoparticles. Jundishapur J
Microbiol 8 (12): e27035.
[48] 49. Swayne E David , David L Suarez, Erica
Spackman, Samadhan Jadhao, Gwenaelle
Dauphin, Mia Kim-Torchetti, James McGrane,
John Weaver, Peter Daniels, Frank Wong, Paul
Selleck, Agus Wiyono, Risa Indriani, Yuni
Yupiana, Elly Sawitri Siregar, Teguh Prajitno,
Derek Smith, Ron Fouchier .2015. Antibody titer
has positive predictive value for vaccine
protection against challenge with natural
antigenic-drift variants of H5N1 high-
pathogenicity Avian Influenza viruses from
Indonesia. J of Virol 1; 89(7): 37463762.
[49] 50. Jakka P, , Reddy Y K, Kirubaharan J
J, Chandran N D J. 2014. Evaluation of immune
responses by live infectious bursal disease
vaccines to avoid vaccination failures. Eur J
Microbiol Immunol (Bp). 2014 Jun; 4(2): 123
127.
[50] 51. Parker Daniel , de Wit Sjaak .2014.
Assessment of impact of a novel infectious
bursal disease (IBD) vaccination programme in
breeders on IBD humoral antibody levels
through the laying period. Vet Rec Open ;
1:e000016. doi:10.1136/vropen-2013-000016.
[51] 52. Jordan Brian . 2017. Vaccination against
infectious bronchitis virus: A continuous
challenge.
https://doi.org/10.1016/j.vetmic.2017.01.002.
[52] 53. Zhang X, Wu B, Liu Y, Chen W, Dai Z, Bi
Y, Xie Q (2015): Assessing the efficacy of an
inactivated chicken anemia virus vaccine.
Vaccine. 15;33 (16):1916-1922.
[53] 54. Torki M, Zangiabadi H , Ghasemi HA 2014.
Effects of enzyme supplementation on
productive performance and egg quality of
laying hens fed diets containing graded levels of
whole date waste. Poult Sci J l, 2 (2): 139-151.
[54] 55. Ley D H .2003. Mycoplasmosis-
Mycoplasma gallisepticum infection. Pages 722
744 in Diseases of Poultry. 11 th ed. Y. M. Saif,
H. J. Barnes, J. R. Glisson, A. M. Fadly, L. R.
McDougald, and D. E. Swayne, ed. Iowa State
Press, Ames.
[55] 56. Jordan FTW, Williams NJ, Wattret A, Jones
T. 2005. Observations on salpingitis, peritonitis
and salpingoperitonitis in a layer breeder flock.
The Vet Rec 157, 573577.
[56] 57. Vandekerchove D, De Herdt P, Laevens H ,
Pasmans F .2004. Colibacillosis in caged layer
hens: characteristics of the disease and the
aetiological agent. Avian Pathol. 33, 117-125.
[57] 58. Lutful Kabir S M . 2010. Avian
Colibacillosis and Salmonellosis: A Closer look
at epidemiology, pathogenesis, diagnosis, control
and public health concerns. Int J Environ Res
Public Health 7(1): 89114.
[58] 59. Mellata M .2013. Human and Avian
Extraintestinal Pathogenic Escherichia coli:
Infections, Zoonotic Risks, and Antibiotic
Resistance Trends. Food borne Pathog Dis
10(11): 916932. doi: 10.1089/fpd.2013.1533.
[59] 60. Hameed Umair, Waseem Akram ,
Muhammad Safdar Anjum .2014. Effect of
salmonella on hatchability and fertility in laying
hen, an Assessment. Veterinaria 1 (2): 22-26.
... Additionally, air easily contributes to the transmission of bacterial pathogens to the tracheal region faster than to the lower part of the body [33]. Therefore, conscious efforts should be made to ensure strict adherence to biosecurity measures and early detection in commercial chicken farm Also, selection of chicken breeds with higher humoral responses to mycoplasma, use of essential oils [26], use of herbal extracts [35], use of phytogenic products [36], use of prebiotics and antibiotics [37], use of probiotics [14], use of synbiotics [38], use of biologically sensitized nanoparticles [39] and possibly chickens with high levels of mannose-binding lectin [40] in chicken production should be encouraged. ...
Article
Full-text available
Background The impact of chickens on maintaining the economy and livelihood of rural communities cannot be overemphasized. In recent years, mycoplasmosis has become one of the diseases that affect the success of South African chicken production. Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) are the most prevalent strains of Mycoplasma in South Africa. MG and MS are significant respiratory pathogens affecting the productivity of chickens. The present study aimed to molecularly detect using qPCR and characterize the presence of MG and MS using phylogenetic analysis. The phylogenetic analysis was utilized to clarify general evolutionary relationships between related taxa of different MG and MS observed in tracheal swabs from South African chicken breeds. Methods Forty-five tracheal swabs of the Lohmann Brown (n = 9), Rhode Island Red (n = 9), Ovambo (n = 9), Venda (n = 9), and Potchefstroom Koekoek (n = 9) breeds were collected from symptomatic chickens present in the commercial farm. To detect MG and MS, DNA was extracted from tracheal swabs and faecal samples, and qPCR was performed with a 16 s rRNA (310 bp) and vlhA (400 bp) gene fragment. Following the sequencing of all the amplicons, MG, and MS dendrograms showing the evolutionary relationships among the five South African chicken breeds and the GeneBank reference population were constructed. Results The qPCR revealed the presence of MG and MS in 22% (2/9) of the tracheal swab samples tested for MS only in Rhode Island Red breeds; 66.6% (6/9) and 33% (3/9) of the tested samples in Ovambo breeds; and 11.1% (1/9) and 44.4% (4/9) of the tested samples in Venda breeds. No MG or MS were detected in the Lohmann Brown or Potchefstroom Koekoek breed. Furthermore, qPCR revealed the presence of MG in pooled faecal samples from Lohmann Brown and Ovambo breeds. Eight different bacterial isolates were recognized from both samples. Four isolates were of the 16 s ribosomal ribonucleic acid (rRNA) gene (named PT/MG51/ck/00, PT/MG48/ck/00, PT/MG41/ck/00 and PT/MG71/ck/00) gene of Mycoplasma gallisepticum, and the other was Mycoplasma Synoviae variable lipoprotein hemagglutinin A (vlhA) gene (named PT/MSA22/ck/01, PT/MS41/ck/01, PT/MS74/ck/01 and PT/MS46/ck/01) which were available in GenBank. These isolates were successfully sequenced with 95–100% similarity to the isolates from the gene bank. Conclusion The study revealed the presence of both MG and MS in the chicken breeds sampled. Furthermore, the different breeds of chicken were found to be susceptible to infection under the intensive or commercial management system. Therefore, continuous surveillance is encouraged to prevent the spread and outbreak of MG and MS in the poultry industry in South Africa.
Preprint
Full-text available
Background The impact of chickens onmaintaining the economy and livelihood of rural communities cannot be overemphasized. In recent years, one of the diseases affecting its success has been Mycoplasma spp. Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) are significant respiratory pathogens that affect chickens. The presentstudy aimed to molecularly detect and characterize the presence of MG and MS intracheal swabsand fecalsamples fromSouth African chicken breeds. Methods: Forty-five tracheal swabs from the Lohmann Brown (n=9), Rhode Island (n=9), Ovambo (n=9), Venda (n=9), and Potchefstroom Koekoek (n=9) breeds were collected.To detect MG and MS, DNA was extracted from tracheal swabsand faecal samples,and qPCR was performed with a 16S rRNA (185 bp) and vlhA (392 bp) gene fragment. Following the sequencing of all the amplicons, MG, and MS dendrograms showing the evolutionary relationships among the five South African chicken breeds and the reference population from the GenBankwere constructed. Results: The qPCR revealed the presence of MG and MS in 22% (2/9) of the tested tracheal swab samples for MS only in Rhode Island breeds;66.6% (6/9) and 33% (3/9) of the tested samples in Ovambo breeds;and 11.1% (1/9) and 44.4% (4/9) of the tested samples in Venda breeds. No MG orMS were detected in the Lohmann Brown orPotchefstroom Koekoek breed. Furthermore, qPCR revealed the presence of MG in pooled faecal samples from Lohmann Brown and Ovambo breeds. Eight different bacterial isolates were recognized from both samples. Four isolates were of the Mycoplasma gallisepticum 16sribosomal ribonucleic acid (rRNA) gene (named PT/MG51/ck/00, PT/MG48/ck/00, PT/MG41/ck/00 and PT/MG71/ck/00),and one was of the Mycoplasma Synoviae variable lipoprotein hemagglutinin A (vlhA) gene (named PT/MSA22/ck/01, PT/MS41/ck/01, PT/MS74/ck/01 and PT/MS46/ck/01). These isolateswere successfully sequenced with 95–100percentage similarity with isolates from the gene bank. Conclusion: The study revealedgreat variation in susceptibility to MG and MS amongthe chicken breeds sampled. This, therefore, poses a threat to South Africa poultry production becausethere is a need for strict biosecurity measures and constant detection of the presence of MG and MS to prevent their spread.
Article
Full-text available
This study was carried out to study effect of antibiotics and or prebiotics on immune response of Mycoplasma gallisepticum (MG) serologically positive broiler chickens to IBD and IB live vaccine. A total number of 210, 1 day old broiler chickens were used. Chicks were divided into seven equal groups and treated as follows: betaine, macroloids (tylosin), polymyxins (colistin), tylosin and betaine, colistin and betaine was given to group 1, 2 , 3, 4and 5; respectively. While group 6 and 7 was kept nontreated vaccinated and non vaccinated non treated (negative) control ; respectively. Chickens groups 1-6 were vaccinated with vector IBD and IB commercial vaccines simulating commercial field. Evaluating antibody titers against used vaccines was done using ELISA kits on sera collected at 0 day of life and every 10 days till the end of the experiments. Results revealed that the best means ELISA titer results against IBD vaccine by the end of the experiments was 7950 in both colistin group (3) and colistin and betaine group (5), followed by group (4) received tylosin and betaine which was 7800 , followed by group (2) received tylosin which was 7750 followed by group (1) received betaine only which was 7700 , followed by 7400 in group 6 (vaccinated non treated). The mean ELISA titers against IB live vaccine the highest was in group (5) received colistin and betain which was 1540, followed by group (3) received colistin only which was 1490, followed by group (4) received tylosin and betaine which was 1345, followed by group (1) received betaine only which was 1395, followed by group (2) which received tylosin which was 1300,while non treated vaccinated group 6 gives 1212. The recorded mean ELISA titers of MG, IBD and IB in sera of chicks at 1 day of life 5269,11000 and 5790; respectively are due to maternal derived antibodies. Maternal derived antibodies to IBD and IB was gradually decreased in non vaccinated non treated group 7 to reach 2800 and 111 at the 30th day of life. While MG antibodies was markedly increased after live vaccine application, on the other hand non observed lesions was detected in antibiotic medicated group. It could be concluded that both polymexins (colistin) and macroloids (tylosin) antibiotics used in this study has positive impacts in controlling of Mycoplasma galisepticum and on immune response of broiler chickens to IB and IBD vaccines. Prebiotic (betaine) enhanced positively immune system to produce humoral immune response. A combination between antibiotic and prebiotic can be used to minimize the possible adverse effects of excessive use of antibiotic on vital organs.
Article
Full-text available
Newcastle disease (ND) has been defined by the World Organisation for Animal Health as infection of poultry with virulent strains of Newcastle disease virus (NDV). Lesions affecting the neurological, gastrointestinal, respiratory, and reproductive systems are most often observed. The control of ND must include strict biosecurity that prevents virulent NDV from contacting poultry, and also proper administration of efficacious vaccines. When administered correctly to healthy birds, ND vaccines formulated with NDV of low virulence or viral-vectored vaccines that express the NDV fusion protein are able to prevent clinical disease and mortality in chickens upon infection with virulent NDV. Live and inactivated vaccines have been widely used since the 1950's. Recombinant and antigenically matched vaccines have been adopted recently in some countries, and many other vaccine approaches have been only evaluated experimentally. Despite decades of research and development towards formulation of an optimal ND vaccine, improvements are still needed. Impediments to prevent outbreaks include uneven vaccine application when using mass administration techniques in larger commercial settings, the difficulties associated with vaccinating free-roaming, multi-age birds of village flocks, and difficulties maintaining the cold chain to preserve the thermo-labile antigens in the vaccines. Incomplete or improper immunization often results in the disease and death of poultry after infection with virulent NDV. Another cause of decreased vaccine efficacy is the existence of antibodies (including maternal) in birds, which can neutralize the vaccine and thereby reduce the effectiveness of ND vaccines. In this review, a historical perspective, summary of the current situation for ND and NDV strains, and a review of traditional and experimental ND vaccines are presented.
Article
Full-text available
Effect of prebiotic on immune response to companied inactivated ND-AI vaccine in presence of bacterial infection were studied, 160 day old Cobb broiler chicks were divided into 4 equal groups; 40 chicks in each. Group 1 negative control non vaccinated while group 2 received lysozyme while groups 3 received Betaine, finally group 4 were kept as positive vaccinated control positive group. Chickens group were vaccinated subcutaneously with the recommended dose of inactivated ND-AI combined vaccine. E.coli O78 K80 H11 strains in phosphate buffered saline)PBS) was used as a bacterial challenge strain and was used by oral infection each chick was given 0.5ml containing 1 x 10 4 viable microorganism/ml. Blood samples were collected weekly for haemagllutination inhibition (HI) test , bursa and liver were collected for histopathological examination. Results of HI test against ND revealed that best mean antibody titer was 6.14±0.69 in birds received Betaine (gr 3), followed by 6.00 ±0.95 in those received lysozyme (gr 2) , followed by that of group 4 (positive vaccinated) which showed 4.00±1.89 , then finally 4.00 ±0.58 in negative control group. Results of HI test for AI haemagllutination inhibition antibodies was the best in group 2 that betaine which (4.86±0.69) followed by 4.71± 0.95 in lysozyme (gr. 2) , followed by group (4) positive vaccinated group which was 4.43± 0.54 and finally 3.43±0.79 in the negative control group1. Also it was noticed that group (4) vaccinated infected with E.coli control positive showing clinical signs of E.coli infection in the form of diarrhea and subcutaneous inflammation (cellulitis) mortality rate was 30%. Concerning histopathological findings the examined bursa, thymus and liver stained sections of control negative group show no detectable pathological lesions until the end of the experiment, on the other hand it was found that Bursa of Fibricus of group (3) which received Betain showing moderate hyperplasic activity of the lymphoid follicle which later on become more obvious by the end of the experiment, concerning liver sections group (4) infected vaccinated non treated group showed severe hydropic degeneration other field showed severe congestion of the central vein while groups (2) and (3) were less affected as they showed mild congestion of portal vein. In conclusion building immune foundation against respiratory virus is crucial and can be fulfilled by proper vaccination programme and can be supported by prebiotics which could improve antibody titers of inactivated respiratory vaccine , unfortunately this need further investigations specially of studding aspects of celluler and humeral immune response with used prebiotics.
Article
Full-text available
This study was conducted in order to investigate the beneficial effect induced by lysozyme , betain tylosine and/or colistine on performance of broiler chickens in presence of infection with avian pathogenic E.coli (APEC) treated with tylosine and or colistine.360 one old day broiler chick divided into 9 equal groups; 40 chicks in each. Groups 2-8 experimentally infected with E.coli groups 2, 3, 4 and 6 treated with tylosine, gr 2 and 8 treated with colistine sulphate , groups 4 and 5 received lysozymes while groups 6 and 7 were given Betain. Birds of groups 1 and 9 were kept as negative and positive control; respectively. Average body weight (ABW), organ body weight (liver, intestine, Gizzard and Bursa) as well as organ body weight ratio (BWR) at 3 rd , 7 th and 10 th dpi were calculated together with feed conversion rate (FCR) and average feed intake. Samples from liver and intestine were collected for histopathological examination. The best FCR was in group (6) that received tylosine and betain (1.44) followed by (1.46) group (7) which received betain then followed 1.49 of gr (5) received lysozyme then followed by group (2) which received tylosine and colistine and group (4) which received tylosine and lysozme those showed similar result 1.50 followed by group (3) received tylosine which was 1.51 then control negative group (1) which was 1.53 then the lowest 1.72 in E.coli infected nontreated. Organ BWR in the 10 th days post challenge the highest is spleen of group 7 received betaine which was 0.15, followed similar results (0.13) of group 6 and group 5 , followed by group 4 which was 0.12 , then groups 8, control positive group group 9 and gr2 has similar results which was 0. group 7 which was 0.21, followed by g 6 which was 0.20, followed by group 4 and group 8 which show similar results 0.18, followed by group 3 and group 5 which also show similar results 0.17, then groups 2 and group 9 are showing similar results which was 0.16, finally group 1 which was 0.15. Histopatholgical finding of liver are varied from group to another as group one shows no changes while gr 2,6,7 and 8 showed mild changes after challenge in form of mild congestion of portal vein on the other hand control positive gr 9 showed severe congestion of the portal vein and sinusoids the hepatocytes suffering from vacuolar degeneration in the cytoplasm with disorganization of the hepatic cord, groups 3,4 and 5almost showed the same lesion in the form of mild congestion of the portal vein, congestion of the central vein and vacuolar degeneration of hepatocyte which considered a reversible condition. Concerning histopathological finding of intestine, group (1) control negative group showing no lesions and normal histopathological section as shown in fig.(6), while gr (9) control positive showing severe congestion of the blood vessels in the sub mucosa accompanied with mild edema with inflammatory cells inflation in both the mucosa and the sub mucosa, while chickens groups 2,4,5 and 8 showing mild inflammatory cell infiltration as shown in fig (8), while groups 3,6 and 7 showing inflammation with inflammatory cell infiltration in mucosa and submucosal layer as shown in fig (9).this results revealed that antibiotic colistine and lysozymes control E.coli and prevent destructive effect on intestinal mucosa. It could be concluded that antibiotics used against avian pathogenic E.coli still of value in control of infection by improving performance either single or in combination. The used prebiotic showed to play an important role in improving productivity of infected chickens. The used combinations are safe and effective. Therefore, we can advice to use of combination between antibacterial and prebiotic for prevention and control of infection in high risk facing poultry industry.
Article
Full-text available
Abstract: Studying the effect of Tilmicosin (Pulmotil Ac) in the treatment and prevention of chorionic respiratory disease (CRD) in broiler was the purpose of this study. In this study, 10.000, 1 day old commercial broiler chicks from both Cobb and Ross reared in 4 houses; 2 Cobb and 2 Ross (5000 chicks each). The breeder and their chicks were positive to MG and MS. Tilmicosin was used as 75 mg/ liter at 35 weeks of age for 2 days with repletion at 20 day of age. Cobb breeder sera tested with serum plate agglutination (SPA) test were positive Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) (20 % and 26.7%), while Ross breeder was negative for MG and 23.33% positive results for MS. Furthermore, the 1 day old chicks tested sera were positive to MG in 10%, 15% 27.5 % and 27.5 and for MS in 30%, 25% , 37% and 30% ; respectively. Tilmicosin completely eliminate the serum positive titers for MG and partially eliminate it for MS as measured by Enzyme linked immunoassay (ELISA) titres and SPA test. In treated Cobb chicks MS ELISA titres still positive at the 17 days of age, while it was negative for MG. The recorded results of SPA test in treated flocks were generally lower than non treated ones. At PM examination the prevalence of marked air sac gross lesions in non treated control group indicated the development of CRD, the lesions increased in severity with age in non treated. The treated groups showed milder lesions varied from normal to slight turbidity without marked difference between medicated flocks. Generally; the livability taken in inconsideration the growth and mortality rates of treated flock was better than those of same non treated frocks. It can be concluded that usage of Tilmicosin can be essential in the treatment and prevention of CRD in broilers derived from positive breeders. In the other hand, the usage of such drug must be controlled to keep sensitivity of the organism [
Article
Full-text available
In East Algeria, 100 Escherichia coli strains were isolated from livers and spleens of 120 broiler carcasses that presented colibacillosis lesions at autopsy. Serogrouping of these strains demonstrated that 83% of their serogroups belong to the most pathogenic serogroups of Avian Pathogenic Escherichia coli (APEC): O1 (14%), O2 (53%) and O78 (16%). In vitro susceptibility to antimicrobials of veterinary significance was determined by disc diffusion test. Antibiogram demonstrated a high level of resistance to enrofloxacin (82%), trimethoprim-sulfmethoxazole (82%), ampicillin (89%) and amoxicillin/ Ac clavulanic (90%), nalidixic acid (99%) and tetracycline (100%). There were moderate levels of resistance to neomycin (49%) and nitrofurantoin (53%). There were low levels of resistance to gentamicin (2%), chloramphenicol (13%) and no resistance to colistin sulfate (0%). All strains were multi-drug resistant and more than half (58%) of the isolates were resistant to seven antibiotics at least. Thus, thirty one antibiotic resistant patterns of E. coli strains were detected, of which 11 were present significantly. Co-resistance was found in eight of the eleven most common multidrug resistant patterns, 62% of the strains expressed this co-resistance. E. coli strains isolated expressed resistances to molecules that are routinely used in the field. It is clear that these are less effective against colibacillosis. It is more than ever necessary to perform antibiotic susceptibility testing prior to treatment in order to prescribe the molecule of choice, and set up a monitoring program in Algeria to monitor antimicrobial resistance in pathogenic bacteria that could be potentially transmitted to humans from animal food. Key words: Algeria, antibiotic resistance, colibacillosis, Escherichia coli, serogroups.
Article
Infectious bronchitis virus (IBV) is a significant respiratory pathogen of commercial poultry that causes millions of dollars in lost revenue worldwide each year. Even though the poultry industry extensively vaccinates against IBV, emergence of new serotypes and variants continually occur, making control of the disease difficult. Current mass application strategies for IBV vaccines are inefficient and frequently result in vaccination failures. Novel vaccine technology development has been slow, and is hindered by the constraints of large-scale poultry production. Further complicating the situation is the lack of knowledge of IBV protein and host cell interactions, making targeted vaccine intervention strategies near impossible. Taken together, it is easy to see why this disease remains significant in poultry production. This review outlines the current situation as it relates to IBV control, including vaccination, vaccines, and development of immunity, and recent developments in vaccine technology that may provide better protection in the future.
Article
Mycoplasma synoviae infection is widepread both abroad and in Hungary because of the variability of strains in this Mycoplasma species. Some strains have decreased virulence in layers. For this reason breeding companies do not lay stress on eradication of M. synoviae infection from their breeding stocks. On the other hand variant strains show a significant virulence for broiler chickens and broiler breeders, especially in combination with some virus infections (e. g. infectious bronchitis). Organotropism of variant strains has changed also in the last few years; M. synoviae infection causes no synovitis but respiratory disease. Variant strains have different antigen structure, they induce a weak and late serological response making serological detection of the infection difficult. It is more difficult Co culture the variant strains and to perform more modern methods, such as ELISA, DNA probes, PCR, Western blot. M synoviae strains have higher antibiotic resistance than other avian mycoplasmas, therefore it is more difficult to treat infected flocks successfully. To decrease the economical losses caused by M. synoviae it is important to diagnose the infection as soon as possible. Infected flocks should be treated in the framework of a systematic program to prevent decrease of egg production and spread of infection to their offspring. Broiler chicken flocks originating from infected parent flocks should be also treated with adequate antibiotics. Every effort should be made to import M. synoviae free flocks and to raise them free of Mycoplasma infection.