Absence of population genetic structure in Heterakis gallinarum of chicken from Sichuan, inferred from mitochondrial cytochrome c oxidase subunit I gene

References

• Allendorf FW. (1983). Isolation, gene flow, and genetic differentiation among populations. Genet Conserv 18:51–65
   Google Scholar
• Bazh EK. (2013). Molecular identification and phylogenetic analysis of Heterakis gallinae from native chickens in Egypt. Parasitol Res 112:3557–60
   PubMed Web of Science ®Google Scholar
• Boucher AC, Mimee B, Montarry J, Bardou-Valette S, Bélair G, Moffett P, Grenier E. (2013). Genetic diversity of the golden potato cyst nematode Globodera rostochiensis and determination of the origin of populations in Quebec, Canada. Mol Phylogenet Evol 69:75–82
   PubMed Web of Science ®Google Scholar
• Campbell G, Garcia HH, Nakao M, Ito A, Craig PS. (2006). Genetic variation in Taenia solium. Parasitol Int 55:S121–6
   PubMed Web of Science ®Google Scholar
• Clement M, Posada D, Crandall KA. (2000). TCS: A computer program to estimate gene genealogies. Mol Ecol 9:1657–9
   PubMed Web of Science ®Google Scholar
• Daş G, Abel H, Savaş T, Sohnrey B, Gauly M. (2014). Egg production dynamics and fecundity of Heterakis gallinarum residing in different caecal environments of chickens induced by fibre-rich diets. Vet Parasitol 205:606–18
   PubMed Web of Science ®Google Scholar
• Elliott T, Muller A, Brockwell Y, Murphy N, Grillo V, Toet H, Anderson G, et al. (2014). Evidence for high genetic diversity of NAD1 and COX1 mitochondrial haplotypes among triclabendazole resistant and susceptible populations and field isolates of Fasciola hepatica (liver fluke) in Australia. Vet Parasitol 200:90–6
   PubMed Web of Science ®Google Scholar
• Excoffier L, Lischer HE. (2010). Arlequin suite ver 3.5: A new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour 10:564–7
   PubMed Web of Science ®Google Scholar
• Fu YX. (1997). Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics 147:915–25
   PubMed Web of Science ®Google Scholar
• Grant W, Bowen B. (1998). Shallow population histories in deep evolutionary lineages of marine fishes: Insights from sardines and anchovies and lessons for conservation. J Hered 89:415–26
   Web of Science ®Google Scholar
• Holsinger KE, Weir BS. (2009). Genetics in geographically structured populations: Defining, estimating and interpreting FST. Nat Rev Genet 10:639–50
   PubMed Web of Science ®Google Scholar
• Larkin MA, Blackshields G, Brown N, Chenna R, McGettigan PA, McWilliam H, Valentin F, et al (2007). Clustal W and Clustal X version 2.0. Bioinformatics 23:2947–8
   PubMed Web of Science ®Google Scholar
• Lavery S, Moritz C, Fielder D. (1996). Indo-Pacific population structure and evolutionary history of the coconut crab Birgus latro. Mol Ecol 5:557–70
   Web of Science ®Google Scholar
• Librado P, Rozas J. (2009). DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25:1451–2
   PubMed Web of Science ®Google Scholar
• Liu YZ, Li SR, Wang RQ, Yang M, Li LJ. (2006). The case of Chrysolophus pictus infected by Heterakis gallinae. Chin J Zool 41:121–3
   Web of Science ®Google Scholar
• Lv ZH, Xu GT, Lin RQ, Song Hq, Zhu XQ. (2005). PCR amplification, cloning and sequencing of ITS-1 rDNA from Heterakis gallinarum. Chin J Husbandry Vet Med 32:41–4
   Google Scholar
• McDougald L. (2005). Blackhead disease (histomoniasis) in poultry: A critical review. Avian Dis 49:462–76
   PubMed Web of Science ®Google Scholar
• Nei M. (1987). Molecular evolutionary genetics. New York: Columbia University Press
   Google Scholar
• Neigel JE, Avise JC. (1993). Application of a random walk model to geographic distributions of animal mitochondrial DNA variation. Genetics 135:1209–20
   PubMed Web of Science ®Google Scholar
• Posada D, Crandall KA. (2001). Intraspecific gene genealogies: Trees grafting into networks. Trends Ecol Evol 16:37–45
   PubMed Web of Science ®Google Scholar
• Ribas A, de Bellocq JG, Ros A, Ndiaye PI, Miquel J. (2013). Morphometrical and genetic comparison of two nematode species: H. spumosa and H. dahomensis (Nematoda, Heterakidae). Acta Parasitol 58:389–98
   PubMed Web of Science ®Google Scholar
• Rogers AR, Harpending H. (1992). Population growth makes waves in the distribution of pairwise genetic differences. Mol Biol Evol 9:552–69
   PubMed Web of Science ®Google Scholar
• Ruan ZX, Wang Q, Zeng ZM, Yang AS, He H, Gou ZP, Yang TJ, et al. (2004). A survey of parasitic of beasts and poultry in Bijie region of Guizhou province and the benefit of control and prevention. Chin J Vet Parasitol 9:43–4
   Google Scholar
• Schwarz A, Gauly M, Abel H, Daş G, Humburg J, Weiss ATA, Breves G, Rautenschlein S. (2011). Pathobiology of Heterakis gallinarum mono-infection and co-infection with Histomonas meleagridis in layer chickens. Avian Pathol 40:277–87
   PubMed Web of Science ®Google Scholar
• Seddiek SA, Ali MM, Khater HF, El-Shorbagy MM. (2011). Anthelmintic activity of the white wormwood, Artemisia herba-alba against Heterakis gallinarum infecting turkey poults. J Med Plants Res 5:3946–57
   Web of Science ®Google Scholar
• Sharma M, Devi KR, Sehgal R, Narain K, Mahanta J, Malla N. (2014). Genetic similarity between Taenia solium cysticerci collected from the two distant endemic areas in North and North East India. Infect Genet Evol 21:436–9
   PubMed Web of Science ®Google Scholar
• Shi MQ, Zhang L, Zhang LP. (2010). Study on some species of the genus Heterakis (Nematoda: Heterakidae) from birds in Shanxi and Shaanxi, China. Sichuan J Zool 29:527–35
   Google Scholar
• Tajima F. (1989). Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123:585–95
   PubMed Web of Science ®Google Scholar
• Tam N, Duy V, Duc N, Giap V, Xuan B. (2014). Genetic variation in and spatial structure of natural populations of Dipterocarpus alatus (Dipterocarpaceae) determined using single sequence repeat markers. Genet Mol Res 13:5378–86
   PubMed Web of Science ®Google Scholar
• Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. (2011). MEGA5: Molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–9
   PubMed Web of Science ®Google Scholar
• Wang PQ. (1962). A survey of parasitic nematode of poultry in Fujian. Chin J Vet Med 10:7–8
   Google Scholar
• Wang SY, Lian JH, Lian AL. (2003). History and future development in chick industry of China. Shandong Poultry 1:8–13
   Google Scholar
• Wright S. (1978). Vol. 4: Variability within and among natural populations. Chicago, IL: University of Chicago Press
   Google Scholar
• Xie Y, Zhou X, Zhang Z, Wang C, Sun Y, Liu T, Gu X, et al. (2014). Absence of genetic structure in Baylisascaris schroederi populations, a giant panda parasite, determined by mitochondrial sequencing. Parasite Vector 7:606–17
   PubMed Web of Science ®Google Scholar
• Yin F, Gasser RB, Li F, Bao M, Huang W, Zou F, Zhao G, et al. (2013). Genetic variability within and among Haemonchus contortus isolates from goats and sheep in China. Parasite Vector 6:279–87
   PubMed Web of Science ®Google Scholar
• Zhou X, Xie Y, Zhang ZH, Wang CD, Sun Y, Gu XB, Wang SX, et al. (2013). Analysis of the genetic diversity of the nematode parasite Baylisascaris schroederi from wild giant pandas in different mountain ranges in China. Parasite Vector 6:233–41
   PubMed Web of Science ®Google Scholar