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Genotype diet interaction in Fayoumi and Rhode Island
Red layers and their crosses. Note.
M. Abou-El-Kassem Abd-El-Latif, A. Bordas
To cite this version:
Note
Genotype
diet
interaction
in
Fayoumi
and
Rhode Island Red
layers
and their
crosses M. ABOU-EL-KASSEM ABD-EL-LATIFA. BORDAS,
P.MÉRAT
1.N.R.A., Centre de Recherches de
Jouy-en-Josas,
Laboratoire deGénétique
factorielle,
F 78350Jouy-en-Josas
Summary
Fayoumi
and Rhode Island Red(R.I.R.)
layers
and their tworeciprocal
crosses were distributed into 2 groups which received different diets in thelaying period.
The diets had thesame calculated energy level and their total
protein
content differedby
less than 1 p. 100, but oneof them contained 40 p. 100
barley
and the other contained none. With thebarley-containing
diet,feed
consumption,
egg mass, egg number and mean eggweight
per hen were reduced, but the effects were more marked in the R.LR. line and one of thereciprocal
crosses, with asignificant
genotype x diet interaction for egg mass, average clutch
length,
total feed intake and its residualcomponent.
Key
words : Hen,Fayoumi,
Rhode Island Red, eggproduction,
feed, barley.
Résumé
Interaction
génotype-régime
alimentaire chez despondeuses Fayoumi,
Rhode Island et leurs croisements
Des
poules Fayoumi
et Rhode Island(R.LR.)
et leurs 2 croisementsréciproques
ont étérépartis
en 2 groupes recevant unrégime
alimentaire différent enpériode
de ponte. Les 2régimes
avaient la même teneurénergétique
et un tauxprotéique différant
de moins de 1 p. 100 mais l’un contenait 40 p. 100d’orge,
l’autre n’en contenait pas. Enprésence
de la ration à based’orge,
la consommation alimentaire et la masse d’oeufsproduite
parpoule,
ainsi que le nombre et lepoids
moyen des oeufs, étaient abaissés, mais les effets étaient
plus marqués
dans lalignée
R.LR. etdans l’un des croisements
réciproques,
avec une interactionrégime
x typegénétique
significative
pour la masse d’oeufs, lalongueur
moyenne des séries de ponte, la consommation alimentaire totale et sa composante « résiduelle ».Mots clés : Poule,
Fayoumi,
Rhode Island, ponte,régime
alimentaire, orge.( *
I. Introduction
Interactions between
genotype
and feedcomposition
havegenerally
been recordedin the
growth period.
Hutnrr & PROUDFOOT(1981)
observed interactions between lines andprotein
level of theration ;
S!RENSEN
(1980),
with 2 lines selected forgrowth
ratewith a different
protein
level,
similarly
noticed an interaction between lines andprotein
content of the feed. On the other
hand,
HUGHES(1979)
reviewed data onappetite
forspecific
nutrients but did not mentionpossible genetic
or environmental variations for it. Thepresent
paper describes an observationpossibly
related to thisfield,
with agenotype
x feed interaction inFayoumi
and Rhode Island Red hens and their Fl crosses.The initial purpose was to compare these
genotypes
at 2protein
levels. The actualdifference in this
respect
was lower thanexpected according
to the available compo-nents in the rations. On the otherhand,
the nature of thesecomponents
differedmarkedly
between the 2 rations. Thiscomplicates
theinterpretation
of the results and makes thepresent
work a verypreliminary
one.II. Material and methods
A. Birds and
experimental
conditionsOn March 14th and 29 th
1983,
twopedigree
hatches,
from eggs collected over a 3 weekperiod,
tookplace,
from 9Fayoumi
and 9 Rhode Island Red(R.LR.)
sires. Each sire was mated to 3Fayoumi
and 3 R.I.R. hens. The R.LR. line had been bred for alow « residual » feed
consumption during
thelaying period
(B
ORDAS
&MT
RAT
,
1984)
for 7
generations.
The number of sires pergeneration
was8,
then 9. This limitednumber,
causing
a moderate increase of theinbreeding
level,
added to the fact that the basepopulation
had beenkept
without selection for 10generations
before the startof
the selection
experiment, explains
why
thelaying performance
was not of ahigh
standard. On the other
hand,
theFayoumi
line came frompedigree
eggs of a lineselected for egg number in Cairo
University,
sent in December 1978. From this timethe line was
pedigree
reproduced
in ourlaboratory
withoutselection,
from 8 sires pergeneration
(MÉ
RAT
etal.,
1983).
Female
chicks,
afterculling
of the smallestfamilies,
were raised in floor pens tillthe age of 17
weeks,
thenthey
wereput
into individual cages in 2 houses(one
for eachhatch).
At the start each house contained 40pullets
of eachgenetic
type
(Fayoumi,
Fayoumi
xR.I.R.,
7!. 7.!!. xFayoumi,
R.I.R.).
Pullets from each hatch wererandomly
distributed into two groups
receiving
a different feed(1,
2)
from 17 weeks to the end of therecording period
(39
weeks ofage).
The two feeds differed in certain compo-nents and(to
a limitedextent)
in their totalprotein
content. Theircomposition
isgiven
in table 1.B. Measuremercts
Egg
number was recorded from first egg till the age of 39 weeks.Laying intensity
first egg laid until the age of 39
weeks).
A clutch includes eggs laid on successivedays.
Pauses are defined as
periods
of at least 2 successivedays
without an egg ; their totalduration is
expressed
as apercentage
of the number ofrecording
days.
Mean eggweight
was measured between 36 and 38 weeks of age.Finally,
over 28days
betweenthe ages of 34 and 38
weeks,
4 traits were measured to estimate feedefficiency :
v mean
body weight (W),
. body weight
variationduring
theperiod (0 W),
. total egg massproduced
(E),
. feed
consumption (0).
The « residual » feed intake
R,
is the deviation of the observed feed intake(0)
from that
expected
from amultiple regression
equation
onW,
0 W and E(B
YERLY
,
1941 ;
Gous etal., 1978 ;
McD
ONALD
,
1978 andothers).
Feedefficiency
is the ratio O/E.C. Statistical
analyses
Hatch,
feed andgenotype
effects and their interactions were testedby 3-way
variance
analyses taking
account ofunequal
numbers in thesubclasses,
according
toIII. Results and discussion
Table 2 shows the means for each variable per
genotype
and feed and the overall means for each feed. Table 3gives
thecorresponding
varianceanalyses.
The hatch effects are not relevant here.
Moreover,
interactions between hatch andgenotype
have no clearinterpretation. However,
apossible
reason for this is the shortness of therecording period (till
39 weeks ofage)
with breedsthat
have aconsiderable difference of age at the first egg
laid ;
the difference exceeded 8 weeks between the R.LR. and one of the Fl crosses. The overallgenotype
effectcorresponds
to the
large
and well-known differences inbody
and eggssize,
laying
rate and egg shellstrength
between theFayoumi
and R.I.R. breeds.Table 2 shows that the crosses were intermediate between the
parental
breeds for adultbody weight
andweight
gain,
mean eggweight,
feedconsumption.
There existedheterosis
(the
crossesbeing superior
to themidparent),
more marked for theFayoumi
x R.l. R. cross than for thereciprocal,
for 17 wkbody weight,
age at first egg, eggnumber,
laying
intensity,
mean clutchlength,
per cent pauses and per cent cracked eggs. For an unknown reason, thelaying
rate of the R.LR. line was poorer thanexpected,
even with the control feed. However nosign
of disease was recorded.These results are
comparable
with those obtained on the same crossesby
MÉRAT etal.
(1983), showing
heterosis forlaying
rate, egg number and feedefficiency,
theFayoumi
x R.LR. crossbeing
superior
to thereciprocal
for egg number. On the otherhand,
the heterosis in thepresent
comparison
on 17 weekbody weight
may becompared
with that obtained on earliergrowth
rateby
ABOU-EL-KASSEM et al.(1986)
on the same
parental
lines and crosses.Overall,
feed 1significantly
lowered egg mass,laying
rate(by
5.6 p.100)
and feed intake(by
4.4 p.100)
and increased theproportion
of « pause» days (by
12.9 p.100).
However,
these effects of thefeeding regime
wereunequal
for the differentgenetic
types.
Food intake and egg mass showed asignificant
genotype
x feedtype
interaction. For these 2traits,
table 4 shows the means obtained with feed 1 in per cent of those obtained with feed 2 for eachgenotype.
Although
feed intake wasrelatively
less affected than egg mass, thetendency
wassimilar for these 2 variables. Feed 1 reduced them most in the Rhode Island
line,
then in the 7?./.7!. xFayoumi
cross, and the reduction was lower for theFayoumi
and theFayoumi
x R.LR. cross. This may be demonstrated in another wayby
testing
thedifference between feeds within each
genetic
type :
the t-values aresignificant
only
in the R.I.R. line : t = 2.23(P
<0.05)
and t = 2.71(P
<0.01)
for egg mass and feed intakerespectively.
No feed x hatch nor second order interaction
appeared,
suggesting
that the effect of feed on the differentgenotypes
did not differmarkedly
in the 2 hatches. Inaddition,
one sees noreason why
differences in age at first egg such as that between the R.LR. breed and the othergroups
could causeby
themselves a different response to a dietgiven
after 17 weeks ofage.
On the otherhand,
the 2reciprocal
crosses showed aOur data cannot
explain unequivocally
the unfavorable effects of theexperimental
feed. The difference between feeds in totalprotein
is rather small. ForM.E.,
the estimated value isidentical,
and even a moderate difference would not beexpected
tohave
large
effects onperformance. Unfortunately experimental
determinations of M.E. were not available. Differences in morespecific
components
like aminoacids cannot be ruled out butthey
were not determined.Finally,
favorable substancesmight
belacking
or substances
depressing appetite
and/orlaying performance might
be contained incomponents
specific
to theexperimental
feed. This feed lacked thesoybean
and alfalfa meal and included less wheat andmaize ;
suchchanges theoretically
should not causeany imbalance. On the other
hand,
the mostimportant quantitative
difference in thecomposition
of the rations is the presence of 40 p. 100barley
in feed1 ;
certain adverse effects associated with thiscereal,
possibly
due to soluble fibercomponents,
have been identified for chicks(Anonymous,
1984).
These effects seem to have been found lessfrequently
forlaying
hens but KARUNAJEEWA & BAGOT(1977)
observed adrop
of egg number without decrease of feedconsumption
with 57 p. 100barley.
GOHLet al.
(1978)
indicate that in Sweden the use ofbarley
is limited to 250 to 350g/kg
inlayer
diets and showed that the addition onp-glucanase
inbarley-containing
feeds suppresses the appearance ofsticky droppings
and poorperformance,
theseproblems
being
due to a viscousfactor
which ishydrolyzed by p-glucanase.
These studiessuggest
a
possible
mechanismthrough
whichbarley
may have had a deleterious effect in feed 1 of thepresent
work.Our data show that when our
Fayoumi
and R. L R. lines arecompared
the former is lesssusceptible
to the unfavorablefactor(s)
contained in feed 1. Wepointed
that therate of
lay
for the R.1. R. breed was rather lower than usual. Thismight
suggest
thatsome disease
agent
rendered the R.LR. birds moresusceptible
to a less favorable diet : this would be an interaction between breed and a combination of environmental factorsrather than the feed alone.
However,
it hasalready
been mentioned that no diseasecondition was observed.
Although
theproportionate
reduction wasgreater
for eggproduction
than for feedintake,
it is difficult to determine whether thedepressing
effect on eggproduction
caused the
drop
in feedconsumption,
or if the former was a consequence of a loweredappetite
for this feed.Possibly
the fact that the Rhode Island line has been selected forlow consumers of a « normal » feed may be more
susceptible
to arelatively
«unpalata-ble » feed.
Finally,
the difference in the response of the 2reciprocal
crosses isinteresting.
It maysuggest
a sex-linkedeffect,
with one of the crossesbeing
closer to itspaternal
breed. Received March4,
1986.Accepted
November5,
1986. References A BOU -E L -KASSEM ABD-EL-LATIF M., ORDASB A., MÉRAT P., 1986. Croissance, indice de
consom-mation et
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