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Int. J. Agron. Agri. R.
Brou et al. Page 17
RESEARCH PAPER OPEN ACCESS
Analysis of ectoparasites and gastrointestinal parasites of
chickens in modern farms of the City of Korhogo
Gatien Konan Gboko Brou*1
, Guillaume Biégo Gragnon2
, Nicolas Bosson Aboly1
1
Laboratory of Biology, Production and Animal Health, Institute of Agropastoral Management (IGA),
Peleforo Gon Coulibaly University (UPGC) of Korhogo, Côte d'Ivoire
2
National Laboratory for Agricultural Development Support (LANADA), Côte d'Ivoire
Article published on February 28, 2021
Key words: Parasites, Modern breeding, Broilers, Laying hens, Korhogo
Abstract
A study was carried out in the commune of Korhogo to assess gastrointestinal parasites and ectoparasites in
modern poultry farms. To achieve this, 214 droppings samples, including 129 broilers and 85 laying hens from 40
broiler farms and 12 laying chicken farms were collected and analyzed using the flotation method. The results
highlighted two (2) species of mallophagous lice namely Menopon gallinae (50%) and Menacanthus stramineus
(33%) and a species of bug namely Cimex lectularius (17%) for ectoparasites. As for the gastro-parasites, two (2)
species and four (4) genera namely Trichostrongylus tenuis (17%), Syngamus trachea (19%); Heterakis sp (10%),
Ascaridia sp (17%), Raillietina sp (8%) and Eimeria sp (29%) have been identified. Coccidiosis (Eimeria) was the
most important pathology in broiler farms with 67% and less important in laying hens (33%). Helminth eggs have
been observed more in laying hens. Ultimately laying hens are more infested than broilers.
* Corresponding Author: GKG Brou  gatienbrou@gmail.com
International Journal of Agronomy and Agricultural Research (IJAAR)
ISSN: 2223-7054 (Print) 2225-3610 (Online)
http://www.innspub.net
Vol. 18, No. 2, p. 17-24, 2021
Int. J. Agron. Agri. R.
Brou et al. Page 18
Introduction
Ectoparasites are small organisms that mainly
affect the skin. These organisms feed either by
eating the dead cells of the skin and feathers, or by
piercing the seed coat and sucking blood or
secretions from tissues including the lymph
(Baud'huin, 2003). The proliferation leads to
extreme discomfort, itching that disturbs food
intake. Severe irritation may be observed and
results in damage to the plumage. The symptoms
developed are therefore a disturbance in the birds'
rest, stunted growth in young birds and weight loss
in adult subjects (Wangrawa, 2010). The presence
of parasites on poultry leads to slower laying and
deteriorates the quality of the eggs. The numerous
bites caused by these parasites can cause severe
anemia in the hen which can die from exhaustion
(Algom, 1994). Gastrointestinal parasites are small
living organisms that live inside their host. Their
bodies are segmented at least in the adult stage.
They are compulsory parasites with a heteroxene
cycle (Amoussou, 2007; Baker, 2007). Their
presence translates on the one hand to significant
losses due to mortalities and reduced performance,
and on the other hand to the high costs of
medication (Bon, 2006). In addition, the
epidemiological situation of external and internal
parasitism of chickens from modern farms in the
commune of Korhogo is poorly understood. The
overall objective of this study is to help improve the
health status of poultry raised on modern farms.
Material and methods
Study site
The study was carried out on 52 farms in the
commune of Korhogo distributed in seven (7) districts
(Nagnenefou, Oshenin, Teguere, Residentiel,
Residentiel 1, Delafosse and Nouveau-quartier) and
four (4) villages (Bafime, Lakpolo, Waraniene and
Natiokobadara) as shown in Fig. 1.
Fig. 1. Survey site ; Source : RGPH, 2014.
Biological material
The biological material used in this study consists of
broilers and laying hens raised in the commune of
Korhogo. On each subject it was collected and
identified ectoparasites (fleas, scabies, lice and ticks)
and collected droppings for analysis in the laboratory.
Collection of ectoparasites
The collection was done after restraining each animal,
then body inspection of the head on the legs. The
feathers have been raised to make the poultry skin
visible. The ectoparasites present on the body were
then torn off using the fingers and put in Eppendorf
Int. J. Agron. Agri. R.
Brou et al. Page 19
tubes containing 70° alcohol to ensure their
conservation and facilitate their transport to the
laboratory for analysis.
Droppings
The droppings were also collected on the subjects in
the farms surveyed and put in a cooler for the
conservation of the eggs of the parasites.
Identification of ectoparasites
The identification of ectoparasites was done using a
binocular magnifier. Ectoparasites were identified
according to their morphological characteristics,
using the entomological diagnosis of Borror and
White (1970) and Klein (1979).
Coprological examinations
The coprological examination consisted of looking for
eggs in the faeces. Its purpose is the qualitative
diagnosis of infestations and the assessment of the
degree of these infestations. It therefore includes both
qualitative and quantitative methods. As part of our
study, the flotation enrichment method (qualitative
method) was used. Briefly, in a porcelain mortar, 2g
of droppings were suitably crushed in 30 ml of a
saturated solution of sodium chloride which
constitutes the enrichment liquid. The mixture was
then poured into a test tube through a tea strainer to
remove organic debris. After allowing it to stand for a
few minutes, an object slide was brought into contact
with the solution supernatant. After 5 min, the slide
covered with a coverslip was observed under an
optical microscope at 10X magnification.
Epidemiological measures
Two (2) epidemiological measures were studied,
namely prevalence and frequency.
Prevalence
Prevalence (P) is the ratio of the number of parasitized
subjects to the total number of subjects present in the
population studied at the same given time.
It was calculated using the following formula:
P (%) = Number of disease cases/Total population
exposed ∗ 100
Frequencies
The frequency (f) of a parasite is represented by the
ratio of the total number of this parasite to the total
number of parasites in the study. It was determined
by the following formula:
f (%) = number of cases of the disease/total number
of sick individuals ∗ 100
Data analysis
Quantitative and qualitative data were collected
during the survey. A descriptive analysis was made
using computer tools. SPHINX software version
4.5.0.19 was used to develop the sample card, collect
data, and determine averages, frequencies. The
Microsoft Office EXCEL 2007 spreadsheet made it
possible to create tables and graphs
Results
Frequency of gastrointestinal parasites
Fig. 2 shows the frequency of gastrointestinal
parasites in the study chickens. Out of the 214
droppings samples analyzed, 103 samples harbored
gastrointestinal parasites, an overall prevalence of
48.13% with the following decreasing prevalences
such as 30 eimeria carrier chickens (29%); 20 carriers
Sygamus trachea (19%); 17 Ascaridia sp carriers
(17%); 17 carriers Trichostrongylus tenuis (17%); 10
Heterakis sp carriers (10%) and 8 Raillietina carriers
(8%).
Fig. 2. Frequency of gastrointestinal parasites in the
farms studied.
Frequency of parasites by type of farming
Table 1 shows the frequency of chickens carrying
gastrointestinal parasites by type of farm. Coccidiosis
(Eimeria sp) was the most common disease in meat
farming with a prevalence of 67% and less in laying
hens (33%).
Int. J. Agron. Agri. R.
Brou et al. Page 20
Table 1. Frequency of gastrointestinal parasites by
type of farming.
Gastrointestinal
parasites
Types of
chickens
Proportion
(%)
Eimeria sp
Broilers 67
Laying hens 33
Trichostrongylus tenuis
Broilers 56
Laying hens 44
Heterakis sp
Broilers 40
Laying hens 60
Sygamus trachea
Broilers 50
Laying hens 50
Ascaridia sp
Broilers 59
Laying hens 41
Raillietina
Broilers 63
Laying hens 37
Frequency of ectoparasites
Fig. 3 shows the overall frequency of chickens
carrying ectoparasites. Analysis of the data collected
revealed that 120 chickens out of the 214 individuals
sampled carried at least one species of ectoparasites,
thus translating an overall prevalence of 56% in the
commune of which 60 chickens were carrying
Menopon gallinae (50%), 40 were carriers of
Menacanthus stramineus (33%) and 20 were carriers
of Cimex lectularius (17%).
Fig. 3. Frequency of ectoparasites.
Frequency of ectoparasites by type of farming
Table 2 shows the frequency of chickens carrying
ectoparasite by type of farm. Irrespective of the type
of parasite, the parasites were more common in the
breeding of laying hens and were more infested than
that of broilers.
Table 2. Frequency of ectoparasite by type of farm.
Ectoparasites Types of chickens
Proportion
(%)
Menacanthus
stramineus
Broilers 38
Laying hens 62
Menopon gallinae
Broilers 33
Laying hens 67
Cimex lectularius
Broilers 25
Laying hens 75
Overall prevalence of ectoparasites and
gastrointestinal parasites
Table 3 shows the overall prevalence of ectoparasites
and gastrointestinal parasites. Out of the 214
droppings samples analyzed, 103 harbored
gastrointestinal parasites and 120 harbored
ectoparasites, giving an overall prevalence of 48% and
56% respectively.
Table 3. Prevalence of ectoparasites and
gastrointestinal parasites.
Parasites
Health status of
chickens
Proportio
n (%)
Gastrointestinal
parasites
Infested chickens 48
Uninfested
chickens
52
Ectoparasites
Infested chickens 56
Uninfested
chickens
44
Prevalence by species of gastrointestinal parasite
Fig. 4 shows the overall prevalence of gastrointestinal
parasites. During the study, six species of
gastrointestinal parasite were identified. These are in
decreasing numerical order of importance, Eimeria
(14%), Sygamus trachea (9%); Trichostrongylus
tenuis (8%), Ascaridia sp (8%), Heterakis sp (5%),
Raillietina (4%). The most frequent parasite was
Eimeria with 42%.
Fig. 4. Prevalence by species of gastrointestinal
parasite.
Prevalence of gastrointestinal parasites by type of
farming
Table 4 presents the prevalence of gastrointestinal
parasites by type of farming. The study showed that
laying hens (51.8%) were more infested than broilers
(47.73%).
Int. J. Agron. Agri. R.
Brou et al. Page 21
Table 4. Prevalence of gastrointestinal parasites by
type of farming.
Prevalences
Broilers (129) 47.73%(n=62)
Laying hens (85) 51.8%(n=44)
Prevalence by species of parasites by type of farming
Table 5 presents the prevalence by species of parasite by
type of farm. Coccidiosis (Eimeria) was the most prevalent
pathology in the two types of farming with respective
prevalence of15.5% for broilers and 11.76%for layinghens.
Table 5. Prevalence by species of parasites by type of farming.
Eimeria sp
Trichostrongylus
tenuis
Heterakis sp Sygamus trachea Ascaridia sp Raillietina
Broilers (129) 15.5% (20) 7.75%(10) 3.1%(4) 7.75%(10) 7.75%(10) 3.88%(5)
Laying hens (85) 11.76%(10) 9.41%(8) 5.1%(4) 11.76%(10) 8.24%(7) 5.53%(4)
Prevalence by species of ectoparasites
Fig. 5 shows the overall prevalence of ectoparasites.
The results show that the mallophagous lice
represented by the two species Menacanthus
stramineus and Menopon gallinae had the highest
prevalence with 33% and 50% respectively against
17% for Cimex lectularius.
Fig. 5. Prevalence of ectoparasite species.
Prevalence of ectoparasites by type of farming
Table 6 presents the prevalence of ectoparasites by
type of farming. Laboratory analysis has shown that
laying hens are more infested than broiler chickens
with the prevalence 94% and 31% respectively.
Table 6. Prévalence des ectoparasites selon le type
d’élevage.
Prévalences
Broilers (129) 31% (n=40)
Laying hens (85) 94% (n=80)
Prevalence by ectoparasite species by type of farming
Table 7 presents the prevalence by species of
ectoparasites by type of farming. Whatever the type of
parasite, laying hens were more infested than broiler
chickens. Broilers were more infested with Menopon
gallinae 15.5%.
Table 7. Prevalence by ectoparasite species by type of
farming.
Menacanthus
stramineus
Menopon
gallinae
Cimex
lectularius
Broilers (129) 11.62% (n=15) 15.5% (n=20) 3.87% (n=5)
Laying hens (85) 29.41% (n=25) 47% (n=40) 17.64% (n=15)
Table 8. Prevalences of gastrointestinal parasite associations.
Types of
parasitism
Associated Parasites Broilers (n=129) Laying hens (n=85)
Numbers Prevalence Numbers Prevalence
Diparasitism Eimeria+Heterakis 3 2,32% 3 3,52%
Eimeria+Trichostrongylus 2 1,55% 4 4,70%
Eimeria+Ascaridia 2 1,55% 2 2,35%
Eimeria+Sygamus trachea 3 2,32% - -
Trichostrongylus+Heterakis 1 0,77% - -
Trichostrongylus+Ascaridia 1 0,77% 1 1,17%
Heterakis+Ascaridia - - 2 2,35%
Diparasitism total 10 9,28% 12 14,09%
Triparasitism E+A+H - - 1 1,17%
E+A+T - - 2 2,23%
Triparasitism - - 3 3,23%
Tetraparasitism E+A+T+R - - 2 2,23%
E=Eimeria ; A=Ascaridia ; H=Heterakis ; T=Trichostrongylus tenuis ; R=Raillietina
Int. J. Agron. Agri. R.
Brou et al. Page 22
Prevalences of gastrointestinal parasite associations
Table 8 below presents the different prevalence of
parasite associations observed in modern chicken
farming. Gastrointestinal parasite associations were
more common in laying hens with 14.09%
diparasitism compared to 9.28% in broiler chickens.
No case of triparasitism or tetraparasitism has been
detected in broiler chickens.
Prevalences of ectoparasite associations
Table 9 presents the prevalence of ectoparasite
associations. Associations of ectoparasites were more
common in layers than in flesh.
Table 9. Prevalences of ectoparasites associations.
Types of
parasitism
Associated Parasites
Broilers (n=129) Laying hens (n=85)
Numbers Prevalence Numbers Prevalence
Diparasitism
Menacanthus
stramineus+Menopon gallinae
10 7.75% 16 18.82%
Menacanthus
stramineus+Cimex lectularius
8 6.20% 12 14.11%
Menoon gallinae+Cimex
lectularius
5 3.87% 14 16.47%
Diparasitism total 23 17.82% 42 49.4%
Triparasitism M.stramineus+M.gallinae+C 4 3.10% 6 7%
Triparasitism total 4 3.10% 6 7%
Discussion
Three species of ectoparasites have been identified in
modern poultry farms visited. These include two (2)
species of Mallophagous lice, Menacanthus
stramineus and Menopon gallinae, as well as one
species of bed bug: Cimex lectularius. These results
are contrary to those of Djelil (2012), who found only
Mallophagous lice and several species of mites on
farm chicken in Algeria. This difference may be due to
the divergence of agro-ecological zones and the
farming method. Indeed, the author worked in a
temperate zone on animals in extensive system.
These ectoparasites were found in 56% of modern
farms visited in the Municipality of Korhogo.
Whatever the type of parasite, laying hen farms were
more infested than broiler chickens. Broilers were
38% more infested with Menacanthus stramineus.
The strong presence of these mallophagous lice can be
explained by the fact that these insects complete their
entire life cycle on the body of the poultry, which
translates their permanence on the bird according to
Wangrawa (2010).
The lower infestation level of broilers (25%)
compared to laying hens (75%) is due to their short
duration of breeding (35-45 days). According to Seguy
(2007), the development cycle (from the egg stage to
the adult stage) of Mallophagous lice, ranging from
two to three weeks, would limit their proliferation on
the flesh. In addition, Salifou et al. (2008) indicate
that the prevalence of parasitism increases
significantly with the age of the animals.
Unlike Capinera (2008) who found a 100% prevalence
of Dermanyssus gallinae in the laying hen in France,
our study did not show any case of infestation by "red
lice". This could be explained by the absence of optimal
humidity conditions necessary for their development.
In addition, the intermittent life cycle of these mites
makes them difficult to see on animals.
As for gastrointestinal parasites, our results
highlighted eggs of Coccidia of the genus Eimeria and
of helminths composed of nematodes of the genera
Ascaridia, Trichostrongylus, Heterakis and
Syngamus and of cestodes only of the genus
Raillietina, identified in the droppings. In addition to
Trichostrongylus tenuis, identical observations were
made by Amoussou (2007) on local chicken in Benin.
The prevalence for the most numerous coccidia is
67%. This high rate makes coccidiosis the major
parasitosis. It was frequent in the 2 types of farms.
These results are similar to those of Domenech et al,
(1991). Indeed, these authors report that coccidiosis is
Int. J. Agron. Agri. R.
Brou et al. Page 23
at the top of avian pathologies in industrial farms in
Côte d'Ivoire. Furthermore, the prevalence of
coccidiosis is higher in the flesh and increases with
age. In laying hens, the low prevalence observed is
probably explained by an age-related resistance
phenomenon which would develop in them due to
their duration in breeding. In this regard, Fournier
(2005) indicates that after an infestation, the chicks
gradually develop their own immunity to new
infestations. This immunity is linked to white blood
cells. Its development depends on the frequency and
duration of infestation of animals by the parasite
(Aboghe, 2001). During the study, the helminths
identified belonged to several species.
The digestive helminthoses encountered like
ascariasis are linked to the length of the poultry
production cycle (Buldgen et al., 1996). They relate
more to laying hens (more than 12 months of
breeding) than broilers (45 days of breeding or less).
This can also be understood by the fact that in the
laying of laying hens, the litter is generally not
renewed or treated on a regular basis to prevent the
perpetuation of host-parasite contact (Habyarimana,
1998). Parasite associations, although more diverse in
the laying of laying hens, had low prevalence. These
results could be the fact that inside the same host,
some parasites may not find the ideal environmental
conditions. Interspecific competition is observed for
the resources available (Dayon and Arbelot, 1997).
Conclusion
The present study has made it possible to highlight the
major external and internal parasitoses which prevail
in modern poultry farms in the commune of Korhogo.
It made it possible to know the prevalence of these
parasitoses in these farms. Three (3) species of
ectoparasites were found on 120 animals among the
214 sampled, representing a prevalence of 56%. The
study also revealed the presence of gastrointestinal
parasites identified in 103 out of 214 animals, a
prevalence of 48%. Ultimately, parasitosis is one of the
major constraints to the productivity of chickens from
modern farms. Other complementary studies could be
carried out in other localities of the commune of
Korhogo in order to confirm the results obtained.
Conflict of interest
No conflict of interest exists between the different
authors.
Acknowledgement
Our thanks go to the University authorities of
Peleforo Gon Coulibaly University and especially the
Management of the Agropastoral Management
Institute for the supervision of this work. Thank you
to the IGA Research Teachers for their contribution in
writing, not for getting the Master 2 Zootechnics
students who spent days and nights in the villages
collecting the data.
References
Aboghe EG. 2001. Contribution to the evaluation of
the quality of operation of the Senegalese Network for
Avian Surveillance Epidemic (RESESAV), doctoral
thesis, EISMV, Dakar 86p.
Algom BO. 1994. Contribution to the study of the
dominant pathologies in semi-industrial poultry
farms in the Dakar Region: anatomo-pathological
surveys. . Doctoral thesis, EISMV, Dakar 97p.
Amoussou KB. 2007. Ectoparasitism and
helminthic parasitism of local chicken in southern
Benin (the Departments of the Atlantic, the littoral,
the Ouéme and the Plateau). Thesis, EISMV 78p.
Baker DG. 2007. Flynn’s parasits of Laboratory
Animals. Second edition. Blackwell publishing, USA
p.255-259; 263-274.
Baud’huin B. 2003. Parasites of the quail (Coturnix
coturnix). Doctoral thesis, University of Toulouse,
France 122p.
Bon G. 2006. Red lice of poultry Dermanyssus
gallinae in laying hen farms in the South East of
France: Epidemiological and experimental study for
application in organic farming. Thesis, National
Veterinary School of Lyon. France. N ° 35, 61p.
Buldgen A, Parent R, Steyaert P, Legrand D.
1996. Semi-industrial poultry farming in tropical
climate. Practical Guide. GEMBLOUX: Gembloux
agricultural presses: AGCD 122p.
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Capinera JL. 2008. Encyclopedia of entomolgy.
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Dayon J, Arbelot B. 1997. Guide to poultry farming
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Analysis of ectoparasites and gastrointestinal parasites of chickens in modern farms of the City of Korhogo

  • 1. Int. J. Agron. Agri. R. Brou et al. Page 17 RESEARCH PAPER OPEN ACCESS Analysis of ectoparasites and gastrointestinal parasites of chickens in modern farms of the City of Korhogo Gatien Konan Gboko Brou*1 , Guillaume Biégo Gragnon2 , Nicolas Bosson Aboly1 1 Laboratory of Biology, Production and Animal Health, Institute of Agropastoral Management (IGA), Peleforo Gon Coulibaly University (UPGC) of Korhogo, Côte d'Ivoire 2 National Laboratory for Agricultural Development Support (LANADA), Côte d'Ivoire Article published on February 28, 2021 Key words: Parasites, Modern breeding, Broilers, Laying hens, Korhogo Abstract A study was carried out in the commune of Korhogo to assess gastrointestinal parasites and ectoparasites in modern poultry farms. To achieve this, 214 droppings samples, including 129 broilers and 85 laying hens from 40 broiler farms and 12 laying chicken farms were collected and analyzed using the flotation method. The results highlighted two (2) species of mallophagous lice namely Menopon gallinae (50%) and Menacanthus stramineus (33%) and a species of bug namely Cimex lectularius (17%) for ectoparasites. As for the gastro-parasites, two (2) species and four (4) genera namely Trichostrongylus tenuis (17%), Syngamus trachea (19%); Heterakis sp (10%), Ascaridia sp (17%), Raillietina sp (8%) and Eimeria sp (29%) have been identified. Coccidiosis (Eimeria) was the most important pathology in broiler farms with 67% and less important in laying hens (33%). Helminth eggs have been observed more in laying hens. Ultimately laying hens are more infested than broilers. * Corresponding Author: GKG Brou  gatienbrou@gmail.com International Journal of Agronomy and Agricultural Research (IJAAR) ISSN: 2223-7054 (Print) 2225-3610 (Online) http://www.innspub.net Vol. 18, No. 2, p. 17-24, 2021
  • 2. Int. J. Agron. Agri. R. Brou et al. Page 18 Introduction Ectoparasites are small organisms that mainly affect the skin. These organisms feed either by eating the dead cells of the skin and feathers, or by piercing the seed coat and sucking blood or secretions from tissues including the lymph (Baud'huin, 2003). The proliferation leads to extreme discomfort, itching that disturbs food intake. Severe irritation may be observed and results in damage to the plumage. The symptoms developed are therefore a disturbance in the birds' rest, stunted growth in young birds and weight loss in adult subjects (Wangrawa, 2010). The presence of parasites on poultry leads to slower laying and deteriorates the quality of the eggs. The numerous bites caused by these parasites can cause severe anemia in the hen which can die from exhaustion (Algom, 1994). Gastrointestinal parasites are small living organisms that live inside their host. Their bodies are segmented at least in the adult stage. They are compulsory parasites with a heteroxene cycle (Amoussou, 2007; Baker, 2007). Their presence translates on the one hand to significant losses due to mortalities and reduced performance, and on the other hand to the high costs of medication (Bon, 2006). In addition, the epidemiological situation of external and internal parasitism of chickens from modern farms in the commune of Korhogo is poorly understood. The overall objective of this study is to help improve the health status of poultry raised on modern farms. Material and methods Study site The study was carried out on 52 farms in the commune of Korhogo distributed in seven (7) districts (Nagnenefou, Oshenin, Teguere, Residentiel, Residentiel 1, Delafosse and Nouveau-quartier) and four (4) villages (Bafime, Lakpolo, Waraniene and Natiokobadara) as shown in Fig. 1. Fig. 1. Survey site ; Source : RGPH, 2014. Biological material The biological material used in this study consists of broilers and laying hens raised in the commune of Korhogo. On each subject it was collected and identified ectoparasites (fleas, scabies, lice and ticks) and collected droppings for analysis in the laboratory. Collection of ectoparasites The collection was done after restraining each animal, then body inspection of the head on the legs. The feathers have been raised to make the poultry skin visible. The ectoparasites present on the body were then torn off using the fingers and put in Eppendorf
  • 3. Int. J. Agron. Agri. R. Brou et al. Page 19 tubes containing 70° alcohol to ensure their conservation and facilitate their transport to the laboratory for analysis. Droppings The droppings were also collected on the subjects in the farms surveyed and put in a cooler for the conservation of the eggs of the parasites. Identification of ectoparasites The identification of ectoparasites was done using a binocular magnifier. Ectoparasites were identified according to their morphological characteristics, using the entomological diagnosis of Borror and White (1970) and Klein (1979). Coprological examinations The coprological examination consisted of looking for eggs in the faeces. Its purpose is the qualitative diagnosis of infestations and the assessment of the degree of these infestations. It therefore includes both qualitative and quantitative methods. As part of our study, the flotation enrichment method (qualitative method) was used. Briefly, in a porcelain mortar, 2g of droppings were suitably crushed in 30 ml of a saturated solution of sodium chloride which constitutes the enrichment liquid. The mixture was then poured into a test tube through a tea strainer to remove organic debris. After allowing it to stand for a few minutes, an object slide was brought into contact with the solution supernatant. After 5 min, the slide covered with a coverslip was observed under an optical microscope at 10X magnification. Epidemiological measures Two (2) epidemiological measures were studied, namely prevalence and frequency. Prevalence Prevalence (P) is the ratio of the number of parasitized subjects to the total number of subjects present in the population studied at the same given time. It was calculated using the following formula: P (%) = Number of disease cases/Total population exposed ∗ 100 Frequencies The frequency (f) of a parasite is represented by the ratio of the total number of this parasite to the total number of parasites in the study. It was determined by the following formula: f (%) = number of cases of the disease/total number of sick individuals ∗ 100 Data analysis Quantitative and qualitative data were collected during the survey. A descriptive analysis was made using computer tools. SPHINX software version 4.5.0.19 was used to develop the sample card, collect data, and determine averages, frequencies. The Microsoft Office EXCEL 2007 spreadsheet made it possible to create tables and graphs Results Frequency of gastrointestinal parasites Fig. 2 shows the frequency of gastrointestinal parasites in the study chickens. Out of the 214 droppings samples analyzed, 103 samples harbored gastrointestinal parasites, an overall prevalence of 48.13% with the following decreasing prevalences such as 30 eimeria carrier chickens (29%); 20 carriers Sygamus trachea (19%); 17 Ascaridia sp carriers (17%); 17 carriers Trichostrongylus tenuis (17%); 10 Heterakis sp carriers (10%) and 8 Raillietina carriers (8%). Fig. 2. Frequency of gastrointestinal parasites in the farms studied. Frequency of parasites by type of farming Table 1 shows the frequency of chickens carrying gastrointestinal parasites by type of farm. Coccidiosis (Eimeria sp) was the most common disease in meat farming with a prevalence of 67% and less in laying hens (33%).
  • 4. Int. J. Agron. Agri. R. Brou et al. Page 20 Table 1. Frequency of gastrointestinal parasites by type of farming. Gastrointestinal parasites Types of chickens Proportion (%) Eimeria sp Broilers 67 Laying hens 33 Trichostrongylus tenuis Broilers 56 Laying hens 44 Heterakis sp Broilers 40 Laying hens 60 Sygamus trachea Broilers 50 Laying hens 50 Ascaridia sp Broilers 59 Laying hens 41 Raillietina Broilers 63 Laying hens 37 Frequency of ectoparasites Fig. 3 shows the overall frequency of chickens carrying ectoparasites. Analysis of the data collected revealed that 120 chickens out of the 214 individuals sampled carried at least one species of ectoparasites, thus translating an overall prevalence of 56% in the commune of which 60 chickens were carrying Menopon gallinae (50%), 40 were carriers of Menacanthus stramineus (33%) and 20 were carriers of Cimex lectularius (17%). Fig. 3. Frequency of ectoparasites. Frequency of ectoparasites by type of farming Table 2 shows the frequency of chickens carrying ectoparasite by type of farm. Irrespective of the type of parasite, the parasites were more common in the breeding of laying hens and were more infested than that of broilers. Table 2. Frequency of ectoparasite by type of farm. Ectoparasites Types of chickens Proportion (%) Menacanthus stramineus Broilers 38 Laying hens 62 Menopon gallinae Broilers 33 Laying hens 67 Cimex lectularius Broilers 25 Laying hens 75 Overall prevalence of ectoparasites and gastrointestinal parasites Table 3 shows the overall prevalence of ectoparasites and gastrointestinal parasites. Out of the 214 droppings samples analyzed, 103 harbored gastrointestinal parasites and 120 harbored ectoparasites, giving an overall prevalence of 48% and 56% respectively. Table 3. Prevalence of ectoparasites and gastrointestinal parasites. Parasites Health status of chickens Proportio n (%) Gastrointestinal parasites Infested chickens 48 Uninfested chickens 52 Ectoparasites Infested chickens 56 Uninfested chickens 44 Prevalence by species of gastrointestinal parasite Fig. 4 shows the overall prevalence of gastrointestinal parasites. During the study, six species of gastrointestinal parasite were identified. These are in decreasing numerical order of importance, Eimeria (14%), Sygamus trachea (9%); Trichostrongylus tenuis (8%), Ascaridia sp (8%), Heterakis sp (5%), Raillietina (4%). The most frequent parasite was Eimeria with 42%. Fig. 4. Prevalence by species of gastrointestinal parasite. Prevalence of gastrointestinal parasites by type of farming Table 4 presents the prevalence of gastrointestinal parasites by type of farming. The study showed that laying hens (51.8%) were more infested than broilers (47.73%).
  • 5. Int. J. Agron. Agri. R. Brou et al. Page 21 Table 4. Prevalence of gastrointestinal parasites by type of farming. Prevalences Broilers (129) 47.73%(n=62) Laying hens (85) 51.8%(n=44) Prevalence by species of parasites by type of farming Table 5 presents the prevalence by species of parasite by type of farm. Coccidiosis (Eimeria) was the most prevalent pathology in the two types of farming with respective prevalence of15.5% for broilers and 11.76%for layinghens. Table 5. Prevalence by species of parasites by type of farming. Eimeria sp Trichostrongylus tenuis Heterakis sp Sygamus trachea Ascaridia sp Raillietina Broilers (129) 15.5% (20) 7.75%(10) 3.1%(4) 7.75%(10) 7.75%(10) 3.88%(5) Laying hens (85) 11.76%(10) 9.41%(8) 5.1%(4) 11.76%(10) 8.24%(7) 5.53%(4) Prevalence by species of ectoparasites Fig. 5 shows the overall prevalence of ectoparasites. The results show that the mallophagous lice represented by the two species Menacanthus stramineus and Menopon gallinae had the highest prevalence with 33% and 50% respectively against 17% for Cimex lectularius. Fig. 5. Prevalence of ectoparasite species. Prevalence of ectoparasites by type of farming Table 6 presents the prevalence of ectoparasites by type of farming. Laboratory analysis has shown that laying hens are more infested than broiler chickens with the prevalence 94% and 31% respectively. Table 6. Prévalence des ectoparasites selon le type d’élevage. Prévalences Broilers (129) 31% (n=40) Laying hens (85) 94% (n=80) Prevalence by ectoparasite species by type of farming Table 7 presents the prevalence by species of ectoparasites by type of farming. Whatever the type of parasite, laying hens were more infested than broiler chickens. Broilers were more infested with Menopon gallinae 15.5%. Table 7. Prevalence by ectoparasite species by type of farming. Menacanthus stramineus Menopon gallinae Cimex lectularius Broilers (129) 11.62% (n=15) 15.5% (n=20) 3.87% (n=5) Laying hens (85) 29.41% (n=25) 47% (n=40) 17.64% (n=15) Table 8. Prevalences of gastrointestinal parasite associations. Types of parasitism Associated Parasites Broilers (n=129) Laying hens (n=85) Numbers Prevalence Numbers Prevalence Diparasitism Eimeria+Heterakis 3 2,32% 3 3,52% Eimeria+Trichostrongylus 2 1,55% 4 4,70% Eimeria+Ascaridia 2 1,55% 2 2,35% Eimeria+Sygamus trachea 3 2,32% - - Trichostrongylus+Heterakis 1 0,77% - - Trichostrongylus+Ascaridia 1 0,77% 1 1,17% Heterakis+Ascaridia - - 2 2,35% Diparasitism total 10 9,28% 12 14,09% Triparasitism E+A+H - - 1 1,17% E+A+T - - 2 2,23% Triparasitism - - 3 3,23% Tetraparasitism E+A+T+R - - 2 2,23% E=Eimeria ; A=Ascaridia ; H=Heterakis ; T=Trichostrongylus tenuis ; R=Raillietina
  • 6. Int. J. Agron. Agri. R. Brou et al. Page 22 Prevalences of gastrointestinal parasite associations Table 8 below presents the different prevalence of parasite associations observed in modern chicken farming. Gastrointestinal parasite associations were more common in laying hens with 14.09% diparasitism compared to 9.28% in broiler chickens. No case of triparasitism or tetraparasitism has been detected in broiler chickens. Prevalences of ectoparasite associations Table 9 presents the prevalence of ectoparasite associations. Associations of ectoparasites were more common in layers than in flesh. Table 9. Prevalences of ectoparasites associations. Types of parasitism Associated Parasites Broilers (n=129) Laying hens (n=85) Numbers Prevalence Numbers Prevalence Diparasitism Menacanthus stramineus+Menopon gallinae 10 7.75% 16 18.82% Menacanthus stramineus+Cimex lectularius 8 6.20% 12 14.11% Menoon gallinae+Cimex lectularius 5 3.87% 14 16.47% Diparasitism total 23 17.82% 42 49.4% Triparasitism M.stramineus+M.gallinae+C 4 3.10% 6 7% Triparasitism total 4 3.10% 6 7% Discussion Three species of ectoparasites have been identified in modern poultry farms visited. These include two (2) species of Mallophagous lice, Menacanthus stramineus and Menopon gallinae, as well as one species of bed bug: Cimex lectularius. These results are contrary to those of Djelil (2012), who found only Mallophagous lice and several species of mites on farm chicken in Algeria. This difference may be due to the divergence of agro-ecological zones and the farming method. Indeed, the author worked in a temperate zone on animals in extensive system. These ectoparasites were found in 56% of modern farms visited in the Municipality of Korhogo. Whatever the type of parasite, laying hen farms were more infested than broiler chickens. Broilers were 38% more infested with Menacanthus stramineus. The strong presence of these mallophagous lice can be explained by the fact that these insects complete their entire life cycle on the body of the poultry, which translates their permanence on the bird according to Wangrawa (2010). The lower infestation level of broilers (25%) compared to laying hens (75%) is due to their short duration of breeding (35-45 days). According to Seguy (2007), the development cycle (from the egg stage to the adult stage) of Mallophagous lice, ranging from two to three weeks, would limit their proliferation on the flesh. In addition, Salifou et al. (2008) indicate that the prevalence of parasitism increases significantly with the age of the animals. Unlike Capinera (2008) who found a 100% prevalence of Dermanyssus gallinae in the laying hen in France, our study did not show any case of infestation by "red lice". This could be explained by the absence of optimal humidity conditions necessary for their development. In addition, the intermittent life cycle of these mites makes them difficult to see on animals. As for gastrointestinal parasites, our results highlighted eggs of Coccidia of the genus Eimeria and of helminths composed of nematodes of the genera Ascaridia, Trichostrongylus, Heterakis and Syngamus and of cestodes only of the genus Raillietina, identified in the droppings. In addition to Trichostrongylus tenuis, identical observations were made by Amoussou (2007) on local chicken in Benin. The prevalence for the most numerous coccidia is 67%. This high rate makes coccidiosis the major parasitosis. It was frequent in the 2 types of farms. These results are similar to those of Domenech et al, (1991). Indeed, these authors report that coccidiosis is
  • 7. Int. J. Agron. Agri. R. Brou et al. Page 23 at the top of avian pathologies in industrial farms in Côte d'Ivoire. Furthermore, the prevalence of coccidiosis is higher in the flesh and increases with age. In laying hens, the low prevalence observed is probably explained by an age-related resistance phenomenon which would develop in them due to their duration in breeding. In this regard, Fournier (2005) indicates that after an infestation, the chicks gradually develop their own immunity to new infestations. This immunity is linked to white blood cells. Its development depends on the frequency and duration of infestation of animals by the parasite (Aboghe, 2001). During the study, the helminths identified belonged to several species. The digestive helminthoses encountered like ascariasis are linked to the length of the poultry production cycle (Buldgen et al., 1996). They relate more to laying hens (more than 12 months of breeding) than broilers (45 days of breeding or less). This can also be understood by the fact that in the laying of laying hens, the litter is generally not renewed or treated on a regular basis to prevent the perpetuation of host-parasite contact (Habyarimana, 1998). Parasite associations, although more diverse in the laying of laying hens, had low prevalence. These results could be the fact that inside the same host, some parasites may not find the ideal environmental conditions. Interspecific competition is observed for the resources available (Dayon and Arbelot, 1997). Conclusion The present study has made it possible to highlight the major external and internal parasitoses which prevail in modern poultry farms in the commune of Korhogo. It made it possible to know the prevalence of these parasitoses in these farms. Three (3) species of ectoparasites were found on 120 animals among the 214 sampled, representing a prevalence of 56%. The study also revealed the presence of gastrointestinal parasites identified in 103 out of 214 animals, a prevalence of 48%. Ultimately, parasitosis is one of the major constraints to the productivity of chickens from modern farms. Other complementary studies could be carried out in other localities of the commune of Korhogo in order to confirm the results obtained. Conflict of interest No conflict of interest exists between the different authors. Acknowledgement Our thanks go to the University authorities of Peleforo Gon Coulibaly University and especially the Management of the Agropastoral Management Institute for the supervision of this work. Thank you to the IGA Research Teachers for their contribution in writing, not for getting the Master 2 Zootechnics students who spent days and nights in the villages collecting the data. References Aboghe EG. 2001. Contribution to the evaluation of the quality of operation of the Senegalese Network for Avian Surveillance Epidemic (RESESAV), doctoral thesis, EISMV, Dakar 86p. Algom BO. 1994. Contribution to the study of the dominant pathologies in semi-industrial poultry farms in the Dakar Region: anatomo-pathological surveys. . Doctoral thesis, EISMV, Dakar 97p. Amoussou KB. 2007. Ectoparasitism and helminthic parasitism of local chicken in southern Benin (the Departments of the Atlantic, the littoral, the Ouéme and the Plateau). Thesis, EISMV 78p. Baker DG. 2007. Flynn’s parasits of Laboratory Animals. Second edition. Blackwell publishing, USA p.255-259; 263-274. Baud’huin B. 2003. Parasites of the quail (Coturnix coturnix). Doctoral thesis, University of Toulouse, France 122p. Bon G. 2006. Red lice of poultry Dermanyssus gallinae in laying hen farms in the South East of France: Epidemiological and experimental study for application in organic farming. Thesis, National Veterinary School of Lyon. France. N ° 35, 61p. Buldgen A, Parent R, Steyaert P, Legrand D. 1996. Semi-industrial poultry farming in tropical climate. Practical Guide. GEMBLOUX: Gembloux agricultural presses: AGCD 122p.
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