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      Cryptic Eimeria genotypes are common across the southern but not northern hemisphere

      research-article
      a , 1 , a , b , c , c , c , d , a , 2 , e , f , a , c , d , e , g , h , i , j , k , l , m , n , o , p , c , c , q , b , a , a , *
      International Journal for Parasitology
      Elsevier Science
      Eimeria, Chicken, Genetic diversity, Operational taxonomic units, Vaccine

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          Graphical abstract

          Highlights

          • The seven Eimeria spp. recognised to infect chickens are present globally.

          • Cryptic Eimeria operational taxonomic units (OTUs) are common in the southern but not northern hemisphere.

          • Parasite population structure appears to vary between Eimeria spp.

          Abstract

          The phylum Apicomplexa includes parasites of medical, zoonotic and veterinary significance. Understanding the global distribution and genetic diversity of these protozoa is of fundamental importance for efficient, robust and long-lasting methods of control. Eimeria spp. cause intestinal coccidiosis in all major livestock animals and are the most important parasites of domestic chickens in terms of both economic impact and animal welfare. Despite having significant negative impacts on the efficiency of food production, many fundamental questions relating to the global distribution and genetic variation of Eimeria spp. remain largely unanswered. Here, we provide the broadest map yet of Eimeria occurrence for domestic chickens, confirming that all the known species ( Eimeria acervulina, Eimeria brunetti, Eimeria maxima, Eimeria mitis, Eimeria necatrix, Eimeria praecox, Eimeria tenella) are present in all six continents where chickens are found (including 21 countries). Analysis of 248 internal transcribed spacer sequences derived from 17 countries provided evidence of possible allopatric diversity for species such as E. tenella (F ST values ⩽0.34) but not E. acervulina and E. mitis, and highlighted a trend towards widespread genetic variance. We found that three genetic variants described previously only in Australia and southern Africa (operational taxonomic units x, y and z) have a wide distribution across the southern, but not the northern hemisphere. While the drivers for such a polarised distribution of these operational taxonomic unit genotypes remains unclear, the occurrence of genetically variant Eimeria may pose a risk to food security and animal welfare in Europe and North America should these parasites spread to the northern hemisphere.

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          Most cited references37

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          TreeView: an application to display phylogenetic trees on personal computers.

          R D Page (1996)
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            Bellerophon: a program to detect chimeric sequences in multiple sequence alignments.

            Bellerophon is a program for detecting chimeric sequences in multiple sequence datasets by an adaption of partial treeing analysis. Bellerophon was specifically developed to detect 16S rRNA gene chimeras in PCR-clone libraries of environmental samples but can be applied to other nucleotide sequence alignments. Bellerophon is available as an interactive web server at http://foo.maths.uq.edu.au/~huber/bellerophon.pl
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              Analysis of Plasmodium falciparum diversity in natural infections by deep sequencing

              Malaria elimination strategies require surveillance of the parasite population for genetic changes that demand a public health response, such as new forms of drug resistance. 1,2 Here we describe methods for large-scale analysis of genetic variation in Plasmodium falciparum by deep sequencing of parasite DNA obtained from the blood of patients with malaria, either directly or after short term culture. Analysis of 86,158 exonic SNPs that passed genotyping quality control in 227 samples from Africa, Asia and Oceania provides genome-wide estimates of allele frequency distribution, population structure and linkage disequilibrium. By comparing the genetic diversity of individual infections with that of the local parasite population, we derive a metric of within-host diversity that is related to the level of inbreeding in the population. An open-access web application has been established for exploration of regional differences in allele frequency and of highly differentiated loci in the P. falciparum genome.
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                Author and article information

                Contributors
                Journal
                Int J Parasitol
                Int. J. Parasitol
                International Journal for Parasitology
                Elsevier Science
                0020-7519
                1879-0135
                1 August 2016
                August 2016
                : 46
                : 9
                : 537-544
                Affiliations
                [a ]Department of Pathology and Pathogen Biology, Royal Veterinary College, North Mymms, Hertfordshire, UK
                [b ]Department of Veterinary Parasitology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, India
                [c ]Division of Parasitology, Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh, India
                [d ]Department of Animal Breeding and Genetics, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria
                [e ]Department of Parasitology and Entomology, Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria
                [f ]School of Agriculture, Food and Rural Development, Newcastle University, Newcastle upon Tyne, UK
                [g ]Universidad Central de Venezuela, Facultad de Agronomía Instituto de Producción Animal, Av. Universidad via El Limón, Maracay, Venezuela
                [h ]Accra Veterinary Laboratory, Accra, Ghana
                [i ]Department of Poultry Science, University of Arkansas, Fayetteville, AR, USA
                [j ]Southern African Centre for Infectious Disease Surveillance, Morogoro, Tanzania
                [k ]Department of Biotechnical and Diagnostic sciences College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, Kampala, Uganda
                [l ]Department of Paraclinical Studies, University of Zambia, Faculty of Veterinary Medicine, Lusaka, Zambia
                [m ]Production and Population Health, Royal Veterinary College, North Mymms, Hertfordshire, UK
                [n ]National Animal Protozoa Laboratory & College of Veterinary Medicine, China Agricultural University, Beijing, China
                [o ]CSIR-Centre for Cellular and Molecular Biology, Hyderabad, India
                [p ]Augusta University, Augusta, GA, USA
                [q ]Department of Animal Biotechnology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, India
                Author notes
                [* ]Corresponding author. dblake@ 123456rvc.ac.uk
                [1]

                Current address: The Roslin Institute, The University of Edinburgh, Midlothian, UK.

                [2]

                Current address: London School of Hygiene and Tropical Medicine, London, UK.

                Article
                S0020-7519(16)30120-5
                10.1016/j.ijpara.2016.05.006
                4978698
                27368611
                eca248d7-b453-40af-beb7-8dc98a63b895
                © 2016 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 8 March 2016
                : 20 May 2016
                : 24 May 2016
                Categories
                Article

                Parasitology
                eimeria,chicken,genetic diversity,operational taxonomic units,vaccine
                Parasitology
                eimeria, chicken, genetic diversity, operational taxonomic units, vaccine

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