A PRELIMINARY SURVEY ON THE PARASITES OF FREE RANGE CHICKEN IN ABEOKUTA, OGUN STATE, NIGERIA

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ISSN - 2277-0593 UNAAB 2010 Journal of Natural Sciences, Engineering and Technology A PRELIMINARY SURVEY ON THE PARASITES OF FREE RANGE CHICKEN IN ABEOKUTA, OGUN STATE, NIGERIA 1*U.F. EKPO, 1 A.A. OGBOOYE, 1 A.S. OLUWOLE AND 2 M. TAKEET 1Department of Biological Sciences, University of Agriculture, Abeokuta, Nigeria 2Department of Veterinary Microbiology and Parasitology, University of Agriculture, Abeokuta, Nigeria. *Corresponding author: ekpouf:unaab.edu.ng Tel: +234802755689 ABSTRACT A preliminary study was carried out to assess the parasitic burden of domesticated and free range chicken in Abeokuta, Ogun State, Nigeria. A total of twenty birds where purchased from five popular markets in Abeokuta namely, Itoku, Kuto, Lafenwa and Osiele and examined for presence of parasites. The skin and feathers of the birds were also combed to check for ectoparasites. Afterward, the birds were slaughtered and the intact gastro-intestinal tract were then separated and opened to check for endoparasites. All parasites found were collected into petri-dishes and examined under microscope for identification. Two species of ectoparasites Menacanthus stramineus with a prevalence of 90.0% and Lipeurus caponis with a prevalence of 60.0% were recovered. Three species of endoparasites found consisted of two nematodes (Ascaridia galli and Heterakis gallinarum) and one cestode (Raillietina echinobothridia). Ascaridia galli and Raillietina echinobothridia were seen in the small intestine and Heterakis gallinarum in the caecum. Raillietina echinobothridia had the highest prevalence of 80.0% followed by Ascaridia galli and Heterakis gallinarum each with 60.0% prevalence. The results show that free-range chickens in Abeokuta carry high parasitic burden which could be a big constraint to their productivity and commercial value. Key words: Endoparasite, s, Free range, chickens, Abeokuta, Nigeria INTRODUCTION The poultry industry has an important position in the provision of animal protein (meat and egg) to man and plays a vital role in the national economy as a source of revenue. Poultry is one of the most intensively reared of the domesticated species and one of the most developed and profitable animal production enterprises (Obiora, 1992). In Nigeria, backyard poultry represents about 60.0% of the 140 million poultry population, thus, the most important form of poultry production (Ikpi and Akin- wunmi, 1981). It is estimated that this provide 12kg of poultry needs per inhabitants per year whereas cattle provides 5.3kg (Forsido, 1986). This means that by comparison, poultry meat is more available to the people than beef. Parasitism has been identified as one of the major factors that threatens village freerange chicken production (Adene and Dipeolu, 1975). Reports have shown that mortality due to parasitic diseases is higher than those attributed to Newcastle disease, J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 123

1U.F. EKPO, 1 A.A. OGBOOYE, 1 A.S. OLUWOLE AND 2 M. TAKEET and other viral infection of poultries. Common poultry parasites range from lice, mites, fleas, ticks, and helminths to gnats and coccidia (Nnadi and George, 2010). Parasitic infection or their concurrent infections has been known to result in immunosuppression, especially in response to vaccines against some poultry diseases (Horning et al., 2003). Helminths infestations are known to cause interference with host metabolism resulting in poor feed utilization and reduced growth rate as well as size and age at maturity (Nnadi et al., 2007). Studies in other countries had shown that the prevalence of parasitic infestations in village chicken flocks is close to 100.0%, and in most cases individual birds harbour more than one parasite type (Permin et al., 1997). It is believed that, understanding of parasitic diseases of birds will help in devising the measures to improve health and utility of these birds (Msoffe et al., 2010). The present study is therefore a preliminary survey to determine the prevalence of ecto and endo parasites of local chicken in Abeokuta. MATERIALS AND METHODS Study animals Twenty adult free range chickens were bought from Osiele, Itoku, Lafenwa and Kuto markets. Five chickens were bought from each market. They were of indigenous breed of both sexes of which 40.0% of the birds were brown, 30.0% were black, 20.0% were grey and 10.0% were white. Examination of chicken for ectooparasites The body of the chickens, including the head, cloacal, bronchial, ventral and femoral areas were combed for ectoparasites. The parasites were removed with camel hair brush, transferred and preserved in 10% formol saline. J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 124 Examination of chicken for endoparasites The chickens were then slaughtered and the intact gastro-intestinal tracts were then separated into oesophagus, crop, proventiculus, gizzard, intestine and caecum. Each part was opened and its content was emptied separately into labelled beakers. Contents were washed into petri-dishes and examined under a stereo microscope. Parasites found were counted and stored in bottles containing formalin. Identification of parasites Identification of parasites was carried out at the Department of Veterinary Microbiology and Parasitology, College of Veterinary Medicine, University of Agriculture, Ogun State. Nigeria. All parasites were identified under light microscope with 40x - 100x magnification, using identification keys of Walker et al., (2003). Data Analysis The data collected from the study were entered and analysed with SPSS version 11. Chi square analysis was used to compare differences in prevalence of parasites. RESULTS Of the 20 chickens examined, nine (45%) were males while 11(55%) were females. The prevalence of ecto and endo parasite in the chicken population by sex is shown in Table1. Statistical analysis at (p>0.05) shows no significant difference in infection status among the sexes for both ecto and endoparasite. All (100%) the chickens examined were with endoparasites. Three species of endoparasites were identified and these consist of two nematodes (Ascaridia galli and Heterakis gallinarum) one cestode (Raillietina echinobothridia). There was no trematode infection. The prevalence of the spe-

A PRELIMINARY SURVEY ON THE PARASITES OF FREE RANGE CHICKEN IN... cies of endoparasite is significantly different Menacanthus stramineus was significantly higher (p=0.025) among parasite species. The most (p=0.028) than infestation with Lipeurus caponis with prevalence of 18 (90%) and 12 common infection observed in the chicken population is with the cestode; Raillietina (60%) respectively. Also the number of echinobothridia 16 (80%) and the least common were nematodes Ascaridia galli 12 nificantly (p=0.0000) more than Lipeurus ca- Menacanthus stramineus (71) collected was sig- (60%) and Heterakis gallinarum 12(60%). ponis (21). Out of two nematodes identified one was found in the small intestine and the other in the caecum and the only cestode parasite was found in the small intestine (Table 2). There was no parasite in the gizzard and trachea. The prevalence of nematode parasites was significantly higher than that of cestode parasite (p= 0.0000). Also all the chickens examined were with one or two species of ectoparasites. These were lice. Infestation with The pattern of infection with ecto and endo parasite is shown in Table 3.Mixed infections with endoparasites were found in 75% of the chickens, while 25% had single infections. Among the mixed infections, 25% had triple infection 50% had double infection. Mixed infections with ectoparasites occurred as double infections in 50% of the chickens while 50% had single infections. There was no significant difference in the pattern of infection in both ecto (p=0.653) and endo (p= 0.413) parasites. Table 1: Prevalence of infection by sex of free range chicken examined in Abeokuta Parasites MALE FEMALE Endoparasite examined % examined % P value Ascaridia galli 9 3 33.33 11 9 81.82 0.081 Raillietina echinobothridia 9 Heterakis gallinarum 9 7 77.78 11 9 81.82 0.736 6 66.67 11 6 54.55 0.927 Menacanthus 9 8 88.89 11 10 90.91 stramineus Lipeurus 9 5 55.56 11 7 63.64 0.927 Caponis J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 125

1U.F. EKPO, 1 A.A. OGBOOYE, 1 A.S. OLUWOLE AND 2 M. TAKEET Table 2: Prevalence of infection by location in the chicken s body in Abeokuta n (Endoparasite) =122, n ()=98 Parasite Endoparasite Location of parasite in the body Parasite count of Infected chickens % prevalence of parasite in chicken population Ascaridia galli Small intestine 51 12 60 41.80 Raillietina echinobothridia Small intestine 40 16 80 32.79 Heterakis gallinarum Caecum 31 12 60 25.41 P value 0.3012 0.025 Menacanthus stramineus Skin 71 18 90 72.45 Lipeurus caponis Feather 27 12 60 27.55 P value 0.028 0.000 % prevalence of parasite spp Table 3: Pattern of infection with Ecto and Endo parasites of free range chicken in Abeokuta Endoparasite Male Female Total (%) Single Infection 3 2 5 ( 25) Double infection 5 5 10 (50) Triple infection 1 4 5 (25) P value 0.413 Single Infection 5 5 10(45) Double infection 4 6 1050 P value 0.653 The mean parasite burden with endo and ecto parasite in chicken population sampled is shown in Table 4. There was no significant difference in mean parasite burden for all parasite species between sexes of chicken. All the chicken irrespective of type of plumage were with both ecto and endo parasite (Table 5). A comparison between endo and ecto - parasites collected from the chicken population revealed that infection with endoparasite is significantly higher (p=0.02) than infestation with ectoparasite. J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 126

A PRELIMINARY SURVEY ON THE PARASITES OF FREE RANGE CHICKEN IN... Table 4: Mean Parasite, standard deviation and range of parasites in Male and Female chickens Parasites MALE FEMALE Endoparasite Mean SD Range Mean SD Range P value Ascaridia galli 1.2222 1.9221 3-5 3.6363 2.2482 2-6 0.1841 Raillietina echinobothridia 1.6667 1.1180 1-3 2.2727 1.4894 1-4 0.324 Heterakis gallinarum 1.8028 1-5 1.4545 1.6949 1-5 0.7891 1.6667 Menacanthus 3.7778 1.7159 3-6 3.3636 1.6293 2-6 0.5863 stramineus Lipeurus caponis 1.3333 1.3229 2-3 1.3636 1.2060 1-3 0.9578 Table 5: Prevalence of ecto and endo parasites by Plumage of free range chicken in Abeokuta Endoparasite Plumage examined % examined % Black 6 6 100 6 6 100 White 2 2 100 2 2 100 Brown 8 8 100 8 8 100 Grey 4 4 100 4 4 100 J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 127 DISCUSSION The result of this study showed the presence of parasitic infestations among free range chickens in Abeokuta. The high prevalence of endoparasitism (100%) in the present study might be a result of open range conditions that facilitate infection of birds. Local chickens satisfy their nutrient requirement by roaming from place to place and they usually seek their food in the superficial layers of the soil which is often contaminated with parasites eggs and larva of all kinds, including various insects or earthworm that serve as paratenic or intermediate hosts for endoparasites that infest poultry (Muhairwa et al., 2007 Puttalakshmamma et al., 2008). The prevalence reported here is similar to those of (Hove et al., 2002; Sam- Wobo and Mafiana, 2003) who reported 100 and 98% respectively of endoparasite infec-

1U.F. EKPO, 1 A.A.OGBOOYE, 1 A.S.OLUWOLE AND 2 M. TAKEET tion. The presence of multiple endoparasitic infections shows the serious risk of infection in local chickens kept in Africa (Kimani, et al., 1999; Ashenafi and Eshutu, 2004). Studies have also shown that almost 100% of local chickens are with helminths parasites (Permin et al., 1997; Horning et al., 2003). The total numbers of intestinal helminths observed in this study are lower than those reported by Sam- Wobo and Mafiana (2003) in Abeokuta, Nigeria and Permin et al., (2002) in Zimbabwe and Ashenafi and Eshutu (2004) in Ethiopia, this may be due to the small number of chicken examined in this study. The three species of intestinal helminths identified in this study are most prevalent intestinal helminths of birds reported (Horning et al., 2003). The percentage prevalence of Raillietina echinobothridia observed from this study is higher than the observations of Sam-Wobo and Mafiana (2003) and Ashenafi and Eshutu (2004) with prevalence of 35.9 and 65.3% respectively. The percentage prevalence of Ascaridia galli, 60% was lower compared to similar observations by Permin et al., (2002) and Sam-Wobo and Mafiana (2003) which had 69 and 73.4% respectively but was higher than the studies done by Kimani et al. (1999) and Ashenafi and Eshutu (2004) with prevalence of 10.03 and 55.3% respectively. The prevalence of Heterakis gallinarum was 60% which was found to be higher than those done by Kimani et al. (1999) and Ashenafi and Eshutu (2004) with a prevalence of 21.33 and 32.6% respectively. However in the present study none of the birds harboured trematode parasites, (this might be due to non accessibility of snails. (Puttalakshmamma et al., 2008). All the chickens examined for ectoparasites were (100%). This result is similar J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 128 to those of Hove et al. (2002), Njunga (2003) and Salam et al. (2006), which had prevalence of 100 and 97.69% respectively. The two species of ectoparasite identified from the study were lice out of which Menacanthus stramineus was more prevalent. Earlier reports of similar studies have indicated lice infestation as the most outstanding infestation among ectoparasite of chickens (Benbrook, 1965 and Fabiyi, 1988) Menacanthus stramineus had a prevalence of 90% which was higher than the observations of Mungube et al. (2005) in Kenya and Belihu (2009) in Ethiopia with prevalence of 79.4 and 65.5% respectively but was similar to the reports of Hove et al. (2002) with a prevalence of 88%. Lipeurus caponis had a prevalence of 60% which was higher than the percentages reported by (Salam et al. 2006) in India with, (Lalitha et al., 2008) and (Eneanya et al., 2008) in South East Nigeria with a prevalence of 39.66, 29.1 and 41.61% respectively. There was no observations of infestation with fleas in this study this is similar to the findings of (Adene and Dipeolu, 1975). However, Nnadozie and George (1996) reported fleas as the dominant ectoparasites in domestic chickens in their survey of blood and ecto-parasites of domestic fowls in Ibadan, Western Nigeria while Salfina (1990) reported fleas as the least occurring of ectoparasites of birds. The result of this study shows that there was no significant difference in infection status for sex and plumage of the chickens. It means that chickens of all sexes and colours are vulnerable to parasite infection. CONCLUSION This study clearly indicated that free range chickens in Abeokuta, Nigeria carry high burden of parasitic infections. This is associated with their indiscriminate scavenging behaviour. Despite the absence of any veteri-

A PRELIMINARY SURVEY ON THE PARASITES OF FREE RANGE CHICKEN IN... farms in Awka, Anambra, Nigeria. International Journal of Zoonoses, 13(2):93-97. nary care for free range village birds, their contribution to supply of eggs, meat for household consumption and income generation cannot be mistreated. It is therefore; necessary that control and preventive measures with better management system should be provided for keepers of local chickens so as to boost the poultry production sector of agriculture. ACKNOWLEDGEMENTS The authors wish to thank the Technologist of Department of Veterinary Microbiology and Parasitology, College of Veterinary Medicine, University of Agriculture, Abeokuta for his assistance in the identification of the parasites. REFERENCES Adene, D.F., Dipeolu, O.O. 1975. Survey of blood and ectoparasites of domestic fowls in Ibadan, Western State of Nigeria. Bulletin Animal. Health and Production in Africa, 23: 333- Ashenafi, H., Eshutu, Y. 2004. Study on Gastro-intestinal Helminthes of local chickens in Central Ethiopia. Revue de Medecine Veterinaire. 155(10):504-507. Belihu, K. 2009. Prevalence of ectoparasites in backyard local chickens in three agroecologic zones of East Shoa, Ethiopia. Revue de Medecine Veterinaire. 160(11):537-541. Benbrook, E.A. 1965. External parasites of poultry. In Biester, H. E and Schwart L.H. 482 edn. Diseases of poultry. 5th edn.iowa State University Press, USA. Pp 925-962. Eneanya, C.I., Amagba I.C., Ikpeze, O.O. 2008. Ectoparasitic fauna of poultry Fabiyi, J.P. 1988. Lice infestation in domestic chicken in Nigeria. Bulletin Of Animal of Health. Prod. Africa, 36:390-394. Forsido, T. 1986. Studies on the meat production potential of some local strains of chickens in Ethiopia. Justus Liebig University, Giessen, Germany, PhD Thesis. Horning G, Rasmussen S., Permin A., M. Bisgaard, 2003. Investigation on the influence of Helminths parasites on vaccination of chicken s against Newcastle diseases Virus under village conditions. Tropical Animal health and Production, 35: 415-424 Hove,T., Permin, A., Esmann, J.B., Hoj, C.H., Mukaratirwa, S. 2002. Ecto, endo and haemoparasites in free range chickens in the Goromonzi District in Zimbabwe. Preventive Veterinary Medicine, 54(3):213-224. Ikpi, A, Akiniwumi J. 1981. The future of the poultry industry in Nigeria, World Poultry Sciences Journal, 37(1): 39-43. Kimani, R.N., Irungu, L.W., Kisia. S.M. 1999. Intestinal parasites of chickens in Kenya. Kenyan Journal of Agricultural Science, 13:67-74. Lalitha, J., Rani, N., Basith, S. 2008. Prevalence of ectoparasites of chicken reared under different systems of management. Journal of Veterinary Parasitology, 22(2):45-50. Msoffe P.L.M., Muhairwa A.P., Chiwanga, G.H., Kassuku A.A. 2010. A study of ecto and endo-parasites of domestic pigeons in Morogoro Municipality, Tanzania. African Journal of Agricultural Research, 5(3):264 J. Nat. Sci. Engr. Tech. 2010, 9(2):123-130 129

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