- Research article
- Open Access
Gene diversity, agroecological structure and introgression patterns among village chicken populations across North, West and Central Africa
© Leroy et al.; licensee BioMed Central Ltd. 2012
- Received: 4 November 2011
- Accepted: 7 May 2012
- Published: 7 May 2012
Chickens represent an important animal genetic resource for improving farmers’ income in Africa. The present study provides a comparative analysis of the genetic diversity of village chickens across a subset of African countries. Four hundred seventy-two chickens were sampled in 23 administrative provinces across Cameroon, Benin, Ghana, Côte d’Ivoire, and Morocco. Geographical coordinates were recorded to analyze the relationships between geographic distribution and genetic diversity. Molecular characterization was performed with a set of 22 microsatellite markers. Five commercial lines, broilers and layers, were also genotyped to investigate potential gene flow. A genetic diversity analysis was conducted both within and between populations.
High heterozygosity levels, ranging from 0.51 to 0.67, were reported for all local populations, corresponding to the values usually found in scavenging populations worldwide. Allelic richness varied from 2.04 for a commercial line to 4.84 for one population from Côte d’Ivoire. Evidence of gene flow between commercial and local populations was observed in Morocco and in Cameroon, which could be related to long-term improvement programs with the distribution of crossbred chicks. The impact of such introgressions seemed rather limited, probably because of poor adaptation of exotic birds to village conditions, and because of the consumers’ preference for local chickens. No such gene flow was observed in Benin, Ghana, and Côte d’Ivoire, where improvement programs are also less developed. The clustering approach revealed an interesting similarity between local populations found in regions sharing high levels of precipitation, from Cameroon to Côte d’Ivoire. Restricting the study to Benin, Ghana, and Côte d’Ivoire, did not result in a typical breed structure but a south-west to north-east gradient was observed. Three genetically differentiated areas (P < 0.01) were identified, matching with Major Farming Systems (namely Tree Crop, Cereal-Root Crop, and Root Crop) described by the FAO.
Local chickens form a highly variable gene pool constituting a valuable resource for human populations. Climatic conditions, farming systems, and cultural practices may influence the genetic diversity of village chickens in Africa. A higher density of markers would be needed to identify more precisely the relative importance of these factors.
- Allelic Richness
- Genetic Introgression
- Membership Coefficient
- Chicken Population
- Commercial Line
Knowledge-based management of animal genetic resources (AnGR) is critical to answer the current agricultural, socio-economic, and environmental challenges. Consequently, characterization of AnGR constitutes one of the priorities of the FAO global plan of action for AnGR , in particular in developing countries, where there is a lack of information regarding what and how to conserve, develop, and select among local breeds.
Village poultry make a significant contribution to poverty alleviation and household food security in many developing countries . About 1.5 billion chickens are raised in Africa, 80% of them belonging to local chicken populations . Indigenous chickens are considered to make a significant contribution to food security and the economical sustainability of rural households [4–6]. However, little is known about their genetic diversity. A recent FAO survey has shown that economic drivers and poor livestock sector policies are the main threats to AnGR: intensification of agriculture, importation of exotic breeds, and indiscriminate cross-breeding . In the case of poultry, poor conservation strategies represent a relatively important threat, and incentives for a continued and sustainable use of local populations are lacking. Conservation strategies require a good knowledge of the genetic structure of these local populations, within or between countries, as well as an assessment of their diversity at the molecular level, to provide recommendations regarding their future management. Several studies of the genetic diversity and structure of local chicken populations in Africa have been done separately for different countries [8–15], and very few have considered a larger region such as East Africa . More specifically, possible relationships between genetic diversity and environmental conditions have been investigated for chicken populations with contrasted results depending on the country of study [9, 11, 16]. Thus, an integrated study encompassing several African countries is still lacking but is undoubtedly required in order to give a more complete analysis of the current diversity of local chickens on this continent, where domestic chickens arrived from various origins such as India and the Mediterranean area [17, 18].
The aim of the present study was to provide a large-scale analysis of the genetic diversity of local chickens in several countries from the central, western and northern parts of the African continent, in order to address questions important for further conservation strategies. These questions deal with (i) the amount of genetic diversity found within these populations, (ii) the search for a possible correlation between the genetic structure and agroecological distribution, and (iii) the detection of a possible gene flow between local populations and commercial lines.
Sample collection and genotypes
Origin and sample size of the 28 chicken populations
White egg layer-A
Brown egg layer-C
Genomic DNA was extracted from blood using the Qiagen® Kit (Qiagen, Valencia, CA, USA) at the biotechnology laboratory of the University of Ghana (samples from Benin, Côte d’Ivoire, Ghana, and Cameroon) or using the NaOH extraction protocol at the IAV (Moroccan samples). A total of 601 individuals, including 472 local African chickens and 129 individuals from commercial lines, were genotyped for 22 microsatellite loci from the AvianDiv panel . PCR amplification and genotyping were performed by the same laboratory (Labogena, France), using a capillary sequencer (ABI PRISM 3100 Genetic Analyzer; Applied Biosystems). Genotypes are available upon request.
Administrative provinces were considered as sampling units for performing preliminary estimations of genetic polymorphism. The presence of null alleles was tested using FreeNA : loci with estimated frequencies of null alleles r ≥ 0.2 could be considered to be potentially problematic for calculations. The allele frequencies, number of alleles, observed (H o ), non-biased expected (H e ) heterozygosity, and F-Statistics  were estimated using GENETIX 4.05.2. GENEPOP 4.07 was used to evaluate departure from Hardy-Weinberg equilibrium and pairwise genic differentiation among breeds . Allelic richness (Ar) was computed with the rarefaction method using FSTAT 126.96.36.199. Test significance was corrected with sequential Bonferroni correction on loci.
Clustering approaches were performed, in a first step, on the 27 populations using a Bayesian clustering procedure implemented in STRUCTURE , considering a number of K clusters ranging from 1 to 16. For each K, 100 runs were performed with 100 000 iterations following a burn-in period of 100 000, under admixture and correlated allele frequency model. As consistency across runs seems to be an informative method for assessing species structure across breeds [33, 34], we used CLUMPP  to estimate the similarity function G’ over runs for the different values of K, using LARGEKGREEDY algorithm. We selected a subset of runs that included the run with the highest number of similar runs (symmetric similarity coefficients SSC higher than 0.95) and the corresponding runs. We used this subset to compute a mean Q-matrix. In a second step, analysis was reduced to the 326 individuals with exact coordinates from Benin, Côte d’Ivoire, and Ghana. A clustering approach was also conducted under the same conditions for K = 1 to 6. On the basis of membership coefficients for K = 2, the genetic structure of the set was interpolated spatially with the Kriging approach, using the R procedure described by François . Membership values, according to agroecological zones, were tested using t-test procedures.
Potential genetic introgression from commercial lines to local populations was investigated by computing the individual allele shared distance (DAS)  matrix for each country, including all individuals from commercial lines. Matrices and dendrograms were obtained using POPULATION 1.2.28 and TREEPLOT 0.7 respectively.
Amongst the 22 markers, 188 alleles were identified, with the number of alleles per marker ranging from 2 to 23 ( Additional file 1). When grouped by country or commercial lines altogether, total number of alleles ranged from 117 (commercial lines) to 156 (Côte d’Ivoire), number of private alleles ranged from 2 (Cameroon and Morocco) to 7 (Côte d’Ivoire), while allelic richness ranged from 4.85 (commercial lines) to 5.96 (Côte d’Ivoire).
Summary of genetic diversity measures across African and commercial populations
Ar (N > 10)
Population relationships and clustering
Individual dendrograms (Additional files 7, 8, 9, 10 and 11) established for the different countries showed that some local chickens were intermingled with chickens from commercial lines. If no individuals from Benin were classified with commercial chickens, this was the case for a few individuals from Côte d’Ivoire and Ghana (1 and 3 respectively), all of them being found at the periphery of commercial clusters. A much larger number of individuals from Cameroon were misclassified, while chickens from Morocco were separated into different clusters distributed across commercial lines. When compared with individual membership results from the STRUCTURE approach (for K = 6), chickens with qi > 0.2 for clusters specific to commercial lines were in general clustered in small groups (Additional files 10 and 11), even if they were not always assigned close to commercial clusters. Note also that the BEL cluster, if always clearly defined, plotted with the other selected in three cases (Benin, Ghana, and Morocco, Additional files 7, 9 and 11 respectively) but was positioned within the local population for the two other cases (Côte d’Ivoire and Cameroon, Additional files 8 and 10 respectively).
Gene diversity and gene flow
Several studies have been published which include a large collection of chicken populations genotyped with microsatellite markers [8, 10, 20, 21, 43, 44]. Heterozygosity levels reported here, for the 23 local African chicken populations, were similar to the values found in other scavenging populations, in Africa or in Asia, ranging from 0.53 to 0.7 [8, 9, 11, 15, 16, 44–46] and being larger than those found in standardized (fancy) breeds (0.28–0.63) or commercial lines (0.34–0.63) [10, 21, 47]. Such levels can be expected for domestic populations which are not selected and have not been submitted to any bottlenecks in a recent past.
Since introgression from commercial lines may constitute a major issue for conservation and management of local chicken populations [6, 11], we tried to assess the evidence and impact of such gene flows. Two contrasted situations were observed. In the first case, involving populations from Benin, Ghana, and Côte d’Ivoire, introgression can be considered as negligible or limited, although introduction of commercial lines in these countries has taken place (see [48, 49] for some examples in Côte d’Ivoire). In the second case, observed in Cameroon and Morocco, clustering results and individuals’ dendrograms suggest that such gene flows have impacted the population structure to some extent. Observations on phenotypic variability may be used to confirm this suggestion because some traits are quite typical of commercial lines. This is the case of the yellow shank phenotype due to a recessive autosomal mutation at the W locus  found in all commercial layers, either white-egg or brown-egg, and in several broiler lines, whereas the wild type is a grey-blue shank colour. Previous surveys showed that the yellow shank phenotype is quite rare in Benin (5% ) and Côte d’Ivoire (15% ) or in other African countries such as Senegal (4% ), while it is much more common either in Cameroon (31 to 38% [53, 54]) or Morocco (60% in the studied sample; Benabdeljelil, personal observation). Furthermore, the presence of the W mutation was found to be correlated with an improvement of anatomical traits in Cameroon . In Cameroon also, the dwarf phenotype (allele DW) found in low frequency in some regions, may also indicate commercial introgression from broiler lines .
As in other places in Africa, several cooperating programs (FAO, bilateral cooperation, NGO…) were set up in these countries in order to improve poultry production, some of these involving the introduction of exotic cockerels for genetic improvement. Differences in the temporal framework of these programs could be, at least partially, responsible for the contrasting patterns of genetic introgression observed in our study. On the one hand, long-term operations took place in Morocco and Cameroon. In Morocco , the first poultry station was built in 1920 at Meknes. More recently, commercial hatcheries could supply traditional farmers with either male chicks of commercial layer lines or crossbred chicks obtained from Rhode Island and slow-growing meat type lines, such as French label and Barred Plymouth Rock. In Cameroon , supply of chicks to farmers was conducted by three pilot stations from 1960 to 1984. In these cases, introduction of exotic chickens within the local livestock was more or less continuous for a long time. On the other hand, Ghana , Benin , or Côte d’Ivoire  operations were characterized by short-term actions: some programs for poultry development, with the introduction of limited numbers of cockerels, have been registered and, according to our results, had a very limited genetic impact on the local chicken gene pool.
Yet, taking into account the duration of exotic cocks introduction, genetic introgression appears finally relatively low even in Morocco and Cameroon. Limited impact of introductions may be explained by a poor adaptation of the genotypes introduced to local conditions or by the consumer’s preference. Indeed, commercial lines have been counter-selected against broodiness, and then females have lost the ability to incubate their eggs naturally, whereas this ability is particularly important for self propagation of village chickens in harsh environments. Although the genetic determinism of broodiness is still under study , it is expected that F1 females from exotic cocks are not as successful as the local hens in natural reproduction and chick rearing. Furthermore, commercial chicks have been selected with an optimum feeding system, and may not satisfy their nutritional needs in scavenging conditions. According to some authors [3, 61], there is a consumer preference for local chickens, both for meat and eggs. Such preference has the effect that the sale price of local chickens (and eggs) is higher than that of products from commercial lines in African countries, including those studied here [49, 56–59, 62, 63]. We also observed that phenotypic variability is very important due to the diversified social uses of local chickens [51, 54, 64] such as religious rituals or indigenous pharmacopeia. Some traits may be retained from industrial birds when they have a relative advantage, particularly the white color, as described by  who observed that a white plumage color was a peace symbol in Benin. Plumage color is determined by major genes which may interact with each other. Some of these genes may have been introgressed from commercial lines into local chickens, as in the case of the yellow shank due to an autosomal recessive mutation .
Chicken population structure
Usually, scavenging chicken populations do not exhibit a typical breed structure [11, 15, 45, 65] even if some more or less marked differentiation could eventually be found [9, 46], in particular for large geographical data sets involving several African countries . When considering our data globally, we found the same result. Yet, some relations with climatic conditions may be observed: local chickens from regions with high precipitations (>1400 mm/year ), i.e. south-eastern Côte d’Ivoire, southern Ghana, and Cameroon, seemed to share a similar genetic background according to Structure results (Figure 2) in contrast to chickens of the other regions with lower precipitations. The fact that a similar diversity pattern was found both in Cameroon and in southern Ghana/Côte d’Ivoire seems to indicate that such an observation could not result from genetic drift only. Restricting the analysis to Côte d’Ivoire, Ghana, and Benin, made it possible to identify a north-east/south-west cline illustrated in Figure 3. According to the FAO , this area may be divided into three Major Farming Systems (MFS). Considering our genetic differentiation results (Figure 3), the Tree Crop Farming System (TCFS) corresponds to the south-west side of the cline, involving Côte d’Ivoire and southern Ghana, while the Cereal-Root Crop Farming System (C-RCFS) lies on the north-east side (northern part of Ghana and Benin). An intermediate area corresponding to the Root Crop Farming System (RCFS) and including middle Ghana and southern Benin exhibited a more similar pattern to C-RCFS, both for genetic data and farming system. On the basis of Structure results, the three zones showed significantly different membership values (P < 0.01 for RCFS/C-RCFS comparison and P < 0.001 for the two other ones). Within the RCFS, according to surveys conducted in Benin , the weight and body measures of Savannah chickens (north of Benin) were found to be significantly higher than those of Forest chickens (south of Benin). Experimental comparisons  showed the same difference, suggesting that it could correspond, to some extent, to genetic effects, although no significant difference (P = 0.059) was observed between animals of northern and southern part of Benin, according to the Structure analysis restricted to Benin, Ghana, and Côte d’Ivoire (based on the individuals q i ). The number of markers used may be too limited to ensure detection of a genetic differentiation on a quantitative trait such as growth.
Human settlements and migrations may constitute another driving factor for the genetic structure of chicken populations. Although not well documented, there is a lot of movement of chickens between these countries as a result of long history of trade and migration. In particular, a large part of the human groups living in the south-east part of Côte d’Ivoire and south-west part of Ghana belong to the same ethnic group, namely the Akan, originating from Ghana [68, 69]. Among others, these groups share most of the same cultural practices  implying similar uses of chicken resources  as part of this cultural background. Nevertheless, the admixture pattern could be related to commercial exchanges amplified by the high mobility of the people and the fact that chickens can be easily freighted , limiting the extent of genetic differentiation among areas.
These agroecological, cultural and demographic factors could result in genetic drift, gene flows or adaptation phenomena, and therefore explain the genetic structure pattern found across these countries. On the basis of the present data, it is, however, difficult to assess to what extent each of these factors has impacted genetic differentiation of these chicken populations.
African local chickens form a highly variable gene pool which constitutes a valuable resource for human populations. There is a large number of driving forces playing either for or against population differentiation of local chickens. Molecular studies bring complementary information to social surveys and phenotypic data, and allows to set up an integrated program of characterization and conservation of indigenous populations, as recommended by the FAO [1, 71]. In this study, we were able to prove that such differentiation may exist among chicken populations, nevertheless, the relative importance of climatic influences and social practices are difficult to disentangle. Further analysis with a higher density of markers is necessary to ascertain the genetic structure of local chicken populations with a higher accuracy, and landscape genomics approaches would be useful to connect genetic differentiation with environmental conditions .
We would like to thank farmers from Ghana, Benin, Côte d’Ivoire, Cameroon and Morocco for their cooperation in obtaining samples. We also thank Jean-Luc Coville, Nicolas Bruneau (INRA), Aurélie Thomas (LABOGENA) and Ahmed Nabich (IAV) for their laboratory assistance. We thank Mrs Tatiana Zerjal and Wendy Brand-Williams for linguistic revision. This study was financially supported by the Duras Project DCG1-08, IRAD-Cameroon, AgroParisTech and INRA.
- FAO: The Global Plan of Action for Animal Genetic Resources and the Interlaken Declaration on Animal Genetic Resources. 2007, FAO, Rome, ItalyGoogle Scholar
- Alders RG, Pym RAE: Village poultry: still important to millions eight thousand years after domestication. World Poultry Sci J. 2009, 65: 181-190. 10.1017/S0043933909000117.View ArticleGoogle Scholar
- Gueye EF: Village egg and fowl meat production in Africa. World Poultry Sci J. 1998, 54: 73-86. 10.1079/WPS19980007.View ArticleGoogle Scholar
- Gueye EF: Employment and income generation through family poultry in low-income food-deficit countries. World Poultry Sci J. 2002, 58: 541-557. 10.1079/WPS20020039.View ArticleGoogle Scholar
- Aboe P, Boa-Amponsem K, Okantah S, Dorward P, Bryant M: Free-range village chickens on the Accra Plains, Ghana: Their contribution to households. Trop Anim Health Prod. 2006, 38: 223-234. 10.1007/s11250-006-4357-9.View ArticlePubMedGoogle Scholar
- Faustin V, Adégbidi VF, Garnett ST, Koudandé DO, Agbo V, Zander KK: Peace, health or fortune? Preferences for chicken traits in rural Benin. Ecol Econ. 2010, 69: 1848-1857. 10.1016/j.ecolecon.2010.04.027.View ArticleGoogle Scholar
- FAO: Threats to animal genetic resources –their relevance, importance and opportunities to decrease their impact. 2009, FAO, Rome ItalyGoogle Scholar
- Wimmers K, Ponsuksili S, Hardge T, Valle-Zarate A, Mathur PK, Horst P: Genetic distinctness of African, Asian and South American local chickens. Anim Genet. 2000, 31: 159-165. 10.1046/j.1365-2052.2000.00605.x.View ArticlePubMedGoogle Scholar
- Msoffe PLM, Mtambo MMA, Minga UM, Juul-Madsen HR, Gwakisa PS: Genetic structure among the local chicken ecotypes of Tanzania based on microsatellite DNA typing. Afr J Biotechnol. 2005, 4: 768-771.Google Scholar
- Granevitze Z, Hillel J, Chen GH, Cuc NTK, Feldman M, Eding H, Weigend S: Genetic diversity within chicken populations from different continents and management histories. Anim Genet. 2007, 38: 576-583. 10.1111/j.1365-2052.2007.01650.x.View ArticlePubMedGoogle Scholar
- Muchadeyi FC, Eding H, Wollny CBA, Groeneveld E, Makuza SM, Shamseldin R, Simianer H, Weigend S: Absence of population substructuring in Zimbabwe chicken ecotypes inferred using microsatellite analysis. Anim Genet. 2007, 38: 332-339. 10.1111/j.1365-2052.2007.01606.x.View ArticlePubMedGoogle Scholar
- Loukou NE, Yapi-Gnaoré CV, Gnénékita T, Coulibaly Y, Rognon X, Kayang BB, Youssao IAK, Tixier-Boichard M, N’guetta ASP: Evaluation de la diversité des poulets traditionnels de deux zones agroecologiques de Côte d’Ivoire à l’aide de marqueurs microsatellites. J Anim Plant Sci. 2009, 5: 425-436.Google Scholar
- Osei-Amponsah R, Kayang BB, Naazie A, Osei YD, Youssao IAK, Yapi-Gnaoré VC, Tixier-Boichard M, Rognon X: Genetic diversity of Forest and Savannah chicken populations of Ghana as estimated by microsatellite markers. Anim Sci Journal. 2010, 81: 297-303. 10.1111/j.1740-0929.2010.00749.x.View ArticleGoogle Scholar
- Youssao IAK, Tobada PC, Koutinhouin BG, Dahouda M, Idrissou ND, Bonou GA, Tougan UP, Ahounou S, Yapi-Gnaoré V, Kayang B, Rognon X, Tixier-Boichard M: Phenotypic characterisation and molecular polymorphism of indigenous poultry populations of the species Gallus gallus of Savannah and Forest ecotypes of Benin. Afr J Biotechnol. 2010, 9: 369-381.Google Scholar
- Mtileni BJ, Muchadeyi FC, Maiwashe A, Groeneveld E, Groeneveld LF, Dzama K, Weigend S: Genetic diversity and conservation of South African indigenous chicken populations. J Anim Breed Genet. 2011, early view: http://dx.doi.org/10.1111/j.1439-0388.2010.00891.xGoogle Scholar
- Mwacharo JM, Nomura K, Hanada H, Jianlin H, Hanotte O, Amano T: Genetic relationships among Kenyan and other East African indigenous chickens. Anim Genet. 2007, 38: 485-490. 10.1111/j.1365-2052.2007.01641.x.View ArticlePubMedGoogle Scholar
- Williamson K: Did chickens go west?. The origins and development of African livestock. Edited by: Blenck RM, MacDonald KC. 2000, UCL Press, London, New-York, 368-448.Google Scholar
- MacDonald KC: The domestic chicken (Gallus gallus) in sub-saharan Africa: a background to its introduction and its osteological differentiation from indigenous fowls (Numidinae and Francolinus sp.). J Archeaol Sci. 1992, 19: 303-318. 10.1016/0305-4403(92)90019-Y.View ArticleGoogle Scholar
- Fotsa JC, Poné Kamdem D, Rognon X, Tixier-Boichard M, Meffeja , Tchoumboué J, Manjeli Y, Bordas A: Etudes comparées des caractéristiques de ponte de la poule camerounaise (Gallus gallus) et d’un label. Bull Anim Hlth Prod Afr. 2011, 59: 239-251.Google Scholar
- Hillel J, Groenen MAM, Tixier-Boichard M, Korol AB, David L, Kirzhner VM, Burke T, Barre-Dirie A, Crooijmans RPMA, Elo K, Feldman MW, Freidlin PJ, Mäki-Tanila A, Oortwijn M, Thomson P, Vignal A, Wimmers K, Weigend S: Biodiversity of 52 chicken populations assessed by microsatellite typing of DNA pools. Genet Sel Evol. 2003, 35: 533-557. 10.1186/1297-9686-35-6-533.PubMed CentralView ArticlePubMedGoogle Scholar
- Berthouly C, Bed’Hom B, Tixier-Boichard M, Chen CF, Lee YP, Laloë D, Legros H, Verrier E, Rognon X: Using molecular markers and multivariate methods to study the genetic diversity of local European and Asian chicken breeds. Anim Genet. 2008, 39: 121-129. 10.1111/j.1365-2052.2008.01703.x.View ArticlePubMedGoogle Scholar
- Chapuis MP, Estoup A: Microsatellites null alleles and estimation of population differentiation. Mol Biol Evol. 2007, 24: 621-631.View ArticlePubMedGoogle Scholar
- Weir BS, Cockerham CC: Estimating F-statistics for the analysis of population structure. Evolution. 1984, 38: 1358-1370. 10.2307/2408641.View ArticleGoogle Scholar
- Belkhir K, Borsa P, Goudet J, Chikhi L, Bonhomme F: GENETIX, logiciel sous Windows TM pour la génétique des populations. Laboratoire Génome, Populations, Interactions: CNRS.UPR. 9060. 2004, Université Montpellier II, Montpellier, France, version 4.0.3Google Scholar
- Rousset F: Genepop’007: a complete re-implementation of the genepop software for Windows and Linux. Mol Ecol Res. 2008, 8: 103-106. 10.1111/j.1471-8286.2007.01931.x.View ArticleGoogle Scholar
- Goudet J, Raymond M, de-Meeus T, Rousset F: Testing Differentiation in Diploid Populations. Genetics. 1996, 144: 1933-1940.PubMed CentralPubMedGoogle Scholar
- Goudet J: FSTAT, a program to estimate and test gene diversities and fixation indices. J Hered. 1995, 86: 485-486. [version 2.9.3: available from http://www.unil.ch/izea/softwares/fstat.html]Google Scholar
- Reynolds J, Weir BS, Cockerham CC: Estimation of the coancestry coefficient: basis for a short-term genetic distance. Genetics. 1983, 105: 767-779.PubMed CentralPubMedGoogle Scholar
- Felsenstein J: PHYLIP - Phylogeny Inference Package (Version 3.2). Cladistics. 1989, 5: 164-166.Google Scholar
- Bryant D, Moulton V: Neighbor-Net: An Agglomerative Method for the Construction of Phylogenetic Networks. Mol Biol Evol. 2004, 21: 255-265.View ArticlePubMedGoogle Scholar
- Huson DH, Bryant D: Application of Phylogenetic Networks in Evolutionary Studies. Mol Biol Evol. 2006, 23: 254-267.View ArticlePubMedGoogle Scholar
- Pritchard JK, Stephens M, Donnelly P: Inference of Population Structure Using Multilocus Genotype Data. Genetics. 2000, 155: 945-959.PubMed CentralPubMedGoogle Scholar
- Wang S, Lewis CM, Jakobsson M, Ramachandran S, Ray N, Bedoya G, Rojas W, Parra MV, Molina JA, Gallo C, et al: Genetic Variation and Population Structure in Native Americans. PLoS Genet. 2007, 3 (11): e185-10.1371/journal.pgen.0030185.PubMed CentralView ArticlePubMedGoogle Scholar
- Leroy G, Verrier E, Meriaux JC, Rognon X: Genetic diversity of dog breeds: within-breed diversity comparing genealogical and molecular data. Anim Genet. 2009, 40: 323-332. 10.1111/j.1365-2052.2008.01842.x.View ArticlePubMedGoogle Scholar
- Jakobsson M, Rosenberg NA: CLUMPP: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure. Bioinformatics. 2007, 23: 1801-1806. 10.1093/bioinformatics/btm233.View ArticlePubMedGoogle Scholar
- François O: How to display admixture coefficients (Q matrix) spatially?. [http://membres-timc.imag.fr/Olivier.Francois/admix_display.html]
- Jin L, Chakraborty R: Estimation of genetic distance and coefficient of gene diversity from single-probe multilocus DNA fingerprinting data. Mol Biol Evol. 1994, 11: 120-127.PubMedGoogle Scholar
- Langella O: Populations version 1.2.28. [http://www.bioinformatics.org/project/?group_id=84]
- Langella O: Treeplot version 0.7. [https://sourcesup.cru.fr/projects/treeplot/]
- Evanno G, Regnaut S, Goudet J: Detecting the number of clusters of individuals using the software structure: a simulation study. Molecular Ecology. 2005, 14: 2611-2620. 10.1111/j.1365-294X.2005.02553.x.View ArticlePubMedGoogle Scholar
- Pritchard JK, Wen X, Falush D: Documentation for structure software: Version 2.3. . 2010, [http://pritch.bsd.uchicago.edu/structure.html]
- Dixon J, Gulliver A, Gibbon D: Farming Systems and Poverty: Improving Farmers’ Livelihoods in a Changing World. 2001, FAO, RomeGoogle Scholar
- Rosenberg NA, Burke T, Elo K, Feldman MW, Freidlin PJ, Groenen MAM, Hillel J, Maki-Tanila A, Tixier-Boichard M, Vignal A, et al: Empirical Evaluation of Genetic Clustering Methods Using Multilocus Genotypes From 20 Chicken Breeds. Genetics. 2001, 159: 699-713.PubMed CentralPubMedGoogle Scholar
- Qu L, Li X, Xu G, Chen K, Yang H, Zhang L, Wu G, Hou Z, Xu G, Yang N: Evaluation of genetic diversity Chinese indigenous chicken breeds using microsatellite markers. Sci China C Life Sci. 2006, 49: 332-341. 10.1007/s11427-006-2001-6.View ArticlePubMedGoogle Scholar
- Berthouly C, Leroy G, Nhu Van email T, Hoang Thanh H, Bed’hom B, Trong Nguyen B, Vu Chi C, Monicat F, Tixier-Boichard M, Verrier E, Maillard JC, Rognon X: Genetic analysis of local Vietnamese chickens provides evidence of gene flow between domestic and wild populations. BMC Genet. 2009, 10: 1-PubMed CentralView ArticlePubMedGoogle Scholar
- Cuc NTK, Simianer H, Eding H, Tieu HV, Cuong VC, Wollny CBA, Groeneveld LF, Weigend S: Assessing genetic diversity of Vietnamese local chicken breeds using microsatellites. Anim Genet. 2010, 41: 545-547. 10.1111/j.1365-2052.2010.02039.x.View ArticlePubMedGoogle Scholar
- Tadano R, Sekino M, Nishibori M, Tsudzuki M: Microsatellite marker analysis for the genetic relationships among Japanese long-tailed chicken breeds. Poultry Sci. 2007, 86: 460-469.View ArticleGoogle Scholar
- Zana O, Aman N, Kouassi NF, Zoumana C: Enquête sur la production avicole traditionnelle en milieu rural an nord de la Côte d’Ivoire : cas de la zone dense de Korhogo. Agron Afr. 1999, 11: 49-56.Google Scholar
- Kone S, Danho T: Etude du secteur avicole en Côte d’Ivoire, structure, importance et perspective. Cas de l’aviculture semi-industrielle. Revue du Secteur Avicole. 2008, Animal Production and Health Division, , [available at http://www.fao-ectad-bamako.org/fr/IMG/pdf/Cote_d_Ivoire_FR_.pdf]Google Scholar
- Eriksson J, Larson G, Gunnarsson U, Bed’hom B, Tixier-Boichard M, Strömstedt L, Wright D, Jungerius A, Vereijken A, Randi E, et al: Identification of the Yellow Skin Gene Reveals a Hybrid Origin of the Domestic Chicken. PLoS Genet. 2008, 4 (2): e1000010-10.1371/journal.pgen.1000010. doi:10.1001371/journal.pgen.1000010PubMed CentralView ArticlePubMedGoogle Scholar
- Yapi-Gnaoré V, Loukou NGE, N’guetta ASP, Kayang B, Rognon X, Tixier-Boichard M, Touré G, Coulibaly Y, Youssao IAK: Diversités phénotypique et morphométrique des poulets locaux (Gallus gallus) de deux zones agroécologiques de Côte d’Ivoire. Cah Agric. 2010, 19: 439-445.Google Scholar
- Missohou A, Sow RS, Ngwe-Assoumou C: Caractéristique morphologique des poulets du Sénégal. Anim Genet Res. 1998, 24: 63-69.View ArticleGoogle Scholar
- Keambou TC, Boukila B, Moussounda G, Manjely Y, Téguia A: Performances zootechniques et caractéristiques morphométriques de la poule locale des zones urbaine et rurale de l’Ouest Cameroun. Livest Res Rural Dev. 2007, 19: 107-[Retrieved July 1, 2011, from http://www.lrrd.org/lrrd19/8/keam19107.htm]Google Scholar
- Fotsa J-C, Rognon X, Tixier-Boichard M, Coquerelle G, Poné Kamdem D, Ngou Ngoupayou JD, Manjeli Y, Bordas A: Caractérisation phénotypique des populations de poules locales (Gallus Gallus) de la zone forestière dense humide à pluviométrie bimodale du Cameroun. Anim Genet Res. 2010, 46: 49-59.View ArticleGoogle Scholar
- Fotsa J-C, Poné Kamdem D, Rognon X, Tixier-Boichard M, Manjeli Y, Bordas A: Influence de certaines mutations à effets visibles sur les performances pondérales et les mensurations corporelles chez la poule locale de la zone forestière dense humide du Cameroun. Bull Anim Hlth Prod Afr. 2009, 57: 276-284.Google Scholar
- Barbok A: Structure et importance des secteurs avicoles commercial et traditionnel au Maroc. Revue du Secteur Avicole. 2008, Animal Production and Health Division, , [available at ftp://ftp.fao.org/docrep/fao/011/ai377f/ai377f00.pdf]Google Scholar
- Ngatchou A, Teleu Ngandeu E: Première évaluation du secteur avicole au Cameroun. Revue du Secteur Avicole. 2008, Animal Production and Health Division, , [available at http://www.fao-ectad-bamako.org/fr/IMG/pdf/Cameroon_FR_.pdf]Google Scholar
- Aning KG: The structure and importance of commercial and village based poultry in Ghana. Revue du Secteur Avicole. 2008, Animal Production and Health Division, , [available at http://www.fao-ectad-bamako.org/fr/IMG/pdf/Ghana_EN_.pdf]Google Scholar
- Fanou U: Première évaluation de la structure et de l’importance du secteur avicole commercial et familial en Afrique de l’Ouest. Cas du Bénin. Revue du Secteur Avicole. 2008, Animal Production and Health Division, , [available at http://www.fao-ectad-bamako.org/fr/IMG/pdf/Benin_FR_.pdf]Google Scholar
- Basheer A, Wilson PW, Talbot RJ, Sharp PJ, Law A, Windsor D, Haley C, Dunn I: Detection of genetic loci for incubation behavior in chickens. Brit Poult Abstr. 2010, 6: 43-44.Google Scholar
- Obioha FC, Nwosu CC, Gowen F, Etim DB, Obanu Z, Ihemelandu E, Onuora GI: Comparative meat yield and anthropometric indices of the Nigerian native chicken and an exotic strain. World Rev Anim Prod. 1983, 19 (1): 59-64.Google Scholar
- Rodriguez LC, Herrero M, Baltenweck I: Community-based interventions for the use and conservation of animal genetic resources: the case of indigenous scavenger chicken production in Benin. Trop Anim Health Prod. 2011, 43: 961-966. 10.1007/s11250-011-9790-8.View ArticlePubMedGoogle Scholar
- Fotsa JC, Poné Kamdem D, Manjeli Y, Ngou Ngoupayou JD: The state of Cameroon rural chickens: Production and development perspectives for poverty alleviation. Ghanaian J Anim Sci. 2007, 2–3: 175-180.Google Scholar
- Ekue NF, Poné Kamdem D, Mafeni JM, Nfi AN, Njoya J: Survey of the traditional poultry production system in Bamenda area, Cameroon. Characteristics parameters of family poultry production in Africa. Results of a FAO/IAEA Co-ordinated Research programme IAEA. 2002, Backhuys Publishers, Leiden, 15-25.Google Scholar
- Cuc NTK, Muchadeyi FC, Baulain U, Eding H, Weigend S, Wollny CBA: An Assessment of Genetic Diversity of Vietnamese H’mong Chickens. Int J Poult Sci. 2006, 5: 912-920.View ArticleGoogle Scholar
- Water resources and irrigation in Africa. [http://www.fao.org/nr/water/aquastat/watresafrica/index3.stm]
- Youssao IAK, Senou M, Dahouda M, Kpodékon MT, Djenontin J, Idrissou N-D, Bonou GA, Tougan UP, Ahounou S, Assogba HM, et al: Genetic Improvement of Local Chickens by Crossing with the Label Rouge (T55XSA51): Growth Performances and Heterosis Effects. Int J Poult Sci. 2009, 8: 536-544.View ArticleGoogle Scholar
- Ki-Zerbo J: Histoire de l’Afrique noire. 1972, Hatier, ParisGoogle Scholar
- Baba Kaké I: La dislocation des grands empires. L’Afrique occidentale du XVIe au XVIIIe siècle. 1977, ACCT/Présence Africaine, Paris/DakarGoogle Scholar
- Kipre P: Des lagunes ivoiriennes à la Volta. Histoire générale de l’Afrique - IV. L’Afrique du XIIe au XVIe siècle. Edited by: Ki-Zerbo J, Niane DT. 1991, Présence Africaine/Edicef/Unesco, Paris, 209-218.Google Scholar
- Tixier-Boichard M, Bordas A, Rognon X: Characterisation and monitoring of poultry genetic resources. World Poultry Sci J. 2009, 65: 272-285. 10.1017/S0043933909000233.View ArticleGoogle Scholar
- Pariset L, Joost S, Marsan PA, Valentini A: Landscape genomics and biased FST approaches reveal single nucleotide polymorphisms under selection in goat breeds of North-East Mediterranean. BMC Genet. 2009, 10: 7-PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.