Trichostrongylus

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Ian Beveridge - One of the best experts on this subject based on the ideXlab platform.

  • a comparison of the first internal transcribed spacer of ribosomal dna in seven species of Trichostrongylus nematoda trichostrongylidae
    International Journal for Parasitology, 1998
    Co-Authors: H Hoste, Neil B Chilton, Ian Beveridge, Robin B Gasser
    Abstract:

    Abstract The first internal transcribed spacer (ITS-1) of the ribosomal DNA of seven species of Trichostrongylus was sequenced. The length of ITS-1 in the different species varied from 387 to 390 bases. The G+C content of the ITS-1 sequences were approximately 42%. Little or no intraspecific variation was detected in the three species, Trichostrongylus axei, Trichostrongylus colubriformis and Trichostrongylus vitrinus, for which multiple isolates from different geographical regions were sequenced. In contrast, the level of ITS-1 sequence differences between species ranged from 1.3% to 5.7%. The greatest sequence differences were detected between T. tenuis, the parasite species which infects birds and the six species found in mammals. Some of the nucleotide differences occurred at sites corresponding to recognition sites for restriction endonucleases. These results are compared with previous data obtained for the second internal transcribed spacer (ITS-2). The ITS-1 data indicate that this region of rDNA may also be useful for systematic studies in trichostrongylid nematodes.

  • Abnormal spicule development in a laboratory strain of Trichostrongylus vitrinus
    Journal of Helminthology, 1997
    Co-Authors: Ian Beveridge
    Abstract:

    The occurrence of specimens in a laboratory strain of Trichostrongylus vitrinus exhibiting unusual spicules resembling those of T. minor and T. angistris is reported and the abnormal spicules described. The specimens include individuals with one spicule typical of T. vitrinus and the other spicule of the abnormal type. Possible reasons for the occurrence of such abnormalities are discussed.

  • differences in the second internal transcribed spacer ribosomal dna between five species of Trichostrongylus nematoda trichostrongylidae
    International Journal for Parasitology, 1995
    Co-Authors: H Hoste, Neil B Chilton, Robin B Gasser, Ian Beveridge
    Abstract:

    Abstract The second internal transcribed spacer (ITS-2) of the ribosomal DNA of 5 species of Trichostrongylus has been sequenced. The ITS-2 of the 5 species was 237 or 238 bases in length, and had a GC content of approximately 30%. No evidence of intraspecific variation was detected in the ITS-2 sequence of T. colubriformis, T. vitrinus or T. retortaeformis, irrespective of the life cycle stage examined. There was evidence, however, of variation at five positions in the ITS-2 sequence of T. vitrinus samples and at one position in T. axei, indicating intra-individual variation in the sequence of different copies of the ribosomal DNA. Nonetheless, there were consistent sequence differences between the five Trichostrongylus species examined. The level of interspecific differences in nucleotide sequence was low (1.3–7.6%), with the species infecting birds (T. tenuis) being genetically more different to the four species found in mammals. Some of the nucleotide differences between species occurred at the recognition sites of endonucleases, which makes them of important diagnostic value for species identification. Also of significance are the recognition sites for several enzymes located within the regions of sequence homology for the five species of Trichostrongylus. These may prove useful in distinguishing between genera of trichotrongyle nematodes.

  • lack of intraspecific variation in the second internal transcribed spacer its 2 of Trichostrongylus colubriformis ribosomal dna
    International Journal for Parasitology, 1993
    Co-Authors: H Hoste, Neil B Chilton, Robin B Gasser, S Mallet, Ian Beveridge
    Abstract:

    Abstract The nucleotide sequence of the second internal transcribed spacer (ITS-2) was determined for three populations of the parasitic nematode Trichostrongylus colubriformis which differed in their susceptibility to benzimidazole anthelmintics and/or in their geographical origin. No intraspecific variation was found in the ITS-2 sequence, indicating that this region of rDNA is inadequate to discriminate between resistant and susceptible populations of T. colubriformis , but it may prove useful for distinguishing between species of Trichostrongylus .

Peter J Hudson - One of the best experts on this subject based on the ideXlab platform.

Andrew P Dobson - One of the best experts on this subject based on the ideXlab platform.

Robin B Gasser - One of the best experts on this subject based on the ideXlab platform.

  • in silico analysis of expressed sequence tags from Trichostrongylus vitrinus nematoda comparison of the automated estexplorer workflow platform with conventional database searches
    International Conference on Bioinformatics, 2008
    Co-Authors: Shivashankar H Nagaraj, Robin B Gasser, Alasdair J Nisbet, Shoba Ranganathan
    Abstract:

    Background The analysis of expressed sequence tags (EST) offers a rapid and cost effective approach to elucidate the transcriptome of an organism, but requires several computational methods for assembly and annotation. Researchers frequently analyse each step manually, which is laborious and time consuming. We have recently developed ESTExplorer, a semi-automated computational workflow system, in order to achieve the rapid analysis of EST datasets. In this study, we evaluated EST data analysis for the parasitic nematode Trichostrongylus vitrinus (order Strongylida) using ESTExplorer, compared with database matching alone.

  • a comparison of the first internal transcribed spacer of ribosomal dna in seven species of Trichostrongylus nematoda trichostrongylidae
    International Journal for Parasitology, 1998
    Co-Authors: H Hoste, Neil B Chilton, Ian Beveridge, Robin B Gasser
    Abstract:

    Abstract The first internal transcribed spacer (ITS-1) of the ribosomal DNA of seven species of Trichostrongylus was sequenced. The length of ITS-1 in the different species varied from 387 to 390 bases. The G+C content of the ITS-1 sequences were approximately 42%. Little or no intraspecific variation was detected in the three species, Trichostrongylus axei, Trichostrongylus colubriformis and Trichostrongylus vitrinus, for which multiple isolates from different geographical regions were sequenced. In contrast, the level of ITS-1 sequence differences between species ranged from 1.3% to 5.7%. The greatest sequence differences were detected between T. tenuis, the parasite species which infects birds and the six species found in mammals. Some of the nucleotide differences occurred at sites corresponding to recognition sites for restriction endonucleases. These results are compared with previous data obtained for the second internal transcribed spacer (ITS-2). The ITS-1 data indicate that this region of rDNA may also be useful for systematic studies in trichostrongylid nematodes.

  • differences in the second internal transcribed spacer ribosomal dna between five species of Trichostrongylus nematoda trichostrongylidae
    International Journal for Parasitology, 1995
    Co-Authors: H Hoste, Neil B Chilton, Robin B Gasser, Ian Beveridge
    Abstract:

    Abstract The second internal transcribed spacer (ITS-2) of the ribosomal DNA of 5 species of Trichostrongylus has been sequenced. The ITS-2 of the 5 species was 237 or 238 bases in length, and had a GC content of approximately 30%. No evidence of intraspecific variation was detected in the ITS-2 sequence of T. colubriformis, T. vitrinus or T. retortaeformis, irrespective of the life cycle stage examined. There was evidence, however, of variation at five positions in the ITS-2 sequence of T. vitrinus samples and at one position in T. axei, indicating intra-individual variation in the sequence of different copies of the ribosomal DNA. Nonetheless, there were consistent sequence differences between the five Trichostrongylus species examined. The level of interspecific differences in nucleotide sequence was low (1.3–7.6%), with the species infecting birds (T. tenuis) being genetically more different to the four species found in mammals. Some of the nucleotide differences between species occurred at the recognition sites of endonucleases, which makes them of important diagnostic value for species identification. Also of significance are the recognition sites for several enzymes located within the regions of sequence homology for the five species of Trichostrongylus. These may prove useful in distinguishing between genera of trichotrongyle nematodes.

  • lack of intraspecific variation in the second internal transcribed spacer its 2 of Trichostrongylus colubriformis ribosomal dna
    International Journal for Parasitology, 1993
    Co-Authors: H Hoste, Neil B Chilton, Robin B Gasser, S Mallet, Ian Beveridge
    Abstract:

    Abstract The nucleotide sequence of the second internal transcribed spacer (ITS-2) was determined for three populations of the parasitic nematode Trichostrongylus colubriformis which differed in their susceptibility to benzimidazole anthelmintics and/or in their geographical origin. No intraspecific variation was found in the ITS-2 sequence, indicating that this region of rDNA is inadequate to discriminate between resistant and susceptible populations of T. colubriformis , but it may prove useful for distinguishing between species of Trichostrongylus .

Lukas F Keller - One of the best experts on this subject based on the ideXlab platform.

  • bayesian paternity analysis and mating patterns in a parasitic nematode Trichostrongylus tenuis
    Heredity, 2010
    Co-Authors: Paul C D Johnson, Jarrod D Hadfield, Lucy M I Webster, Aileen Adam, Barbara K Mable, Lukas F Keller
    Abstract:

    Bayesian paternity analysis and mating patterns in a parasitic nematode, Trichostrongylus tenuis

  • abundant variation in microsatellites of the parasitic nematode Trichostrongylus tenuis and linkage to a tandem repeat
    Molecular and Biochemical Parasitology, 2006
    Co-Authors: Paul C D Johnson, Lucy M I Webster, Aileen Adam, Lukas F Keller, Robert J Buckland, Deborah A Dawson
    Abstract:

    An understanding of how genes move between and within populations of parasitic nematodes is important in combating the evolution and spread of anthelmintic resistance. Much has been learned by studying mitochondrial DNA markers, but autosomal markers such as microsatellites have been applied to only a few nematode species, despite their many advantages for studying gene flow in eukaryotes. Here, we describe the isolation of 307 microsatellites from Trichostrongylus tenuis, an intestinal nematode of red grouse. High levels of variation were revealed at sixteen microsatellite loci (including three sex-lined loci) in 111 male T. tenuis nematodes collected from four hosts at a single grouse estate in Scotland (average He = 0.708; mean number of alleles = 12.2). A population genetic analysis detected no deviation from panmixia either between (F(ST) = 0.00) or within hosts (F(IS) = 0.015). We discuss the feasibility of developing microsatellites in parasitic nematodes and the problem of null alleles. We also describe a novel 146-bp repeat element, TteREP1, which is linked to two-thirds of the microsatellites sequenced and is associated with marker development failure. The sequence of TteREP1 is related to the TcREP-class of repeats found in several other trichostrongyloid species including Trichostrongylus colubriformis and Haemonchus contortus.