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  • Baneth, Gad  (2)
  • Biology  (2)
  • 1
    Online Resource
    Online Resource
    American Society for Microbiology ; 2009
    In:  Applied and Environmental Microbiology Vol. 75, No. 19 ( 2009-10), p. 6393-6398
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 75, No. 19 ( 2009-10), p. 6393-6398
    Abstract: To overcome the problem of nonspecific by-products in quantitative PCR (qPCR) assays, we constructed DNA-RNA chimeric primers and evaluated their use in the detection and quantification of the Ehrlichia canis 16S rRNA, Babesia canis Hsp70, and canine β-actin genes. Several RNA bases were incorporated into specific positions in the DNA primers, while no RNA stretches were allowed. qPCR reactions were carried out without preamplification steps. This resulted in decreased formation of undesirable by-products and a 10-fold increase in assay sensitivity.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2009
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
    Location Call Number Limitation Availability
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  • 2
    In: Molecular Ecology, Wiley, Vol. 24, No. 6 ( 2015-03), p. 1364-1373
    Abstract: Fleas are acknowledged vectors and reservoirs of various bacteria that present a wide range of pathogenicity. In this study, fleas collected from wild rodents from the Negev desert in southern Israel were tested for Rickettsia DNA by targeting the 16S rRNA ( rrs) gene. Thirty‐eight Xenopsylla ramesis , 91 Synosternus cleopatrae and 15 Leptopsylla flea pools (a total of 568 fleas) were screened. Rickettsia DNA was detected in 100% of the X. ramesis and in one S. cleopatrae flea pools. None of L. algira flea pools was found positive. All positive flea pools were further characterized by sequencing of five additional genetic loci ( gltA , ompB , ompA , htrA and fusA ). The molecular identification of the positive samples showed all sequences to be closely related to the ‘ Rickettsia felis ‐like’ organisms (99–100% similarities in the six loci). To further investigate the association between ‘ R. felis ‐like’ and X. ramesis fleas, ten additional single X. ramesis adult fleas collected from the wild and five laboratory‐maintained X. ramesis imago, five larva pools (2–18 larvae per pool) and two egg pools (18 eggs per pool) were tested for the presence of ‘ R. felis ‐like’ DNA . All samples were found positive by a specific ompA PCR assay, confirming the close association of this Rickettsia species with X. ramesis in all its life stages. These results suggest a symbiotic association between ‘ Rickettsia felis ‐like’ and X. ramesis fleas.
    Type of Medium: Online Resource
    ISSN: 0962-1083 , 1365-294X
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2015
    detail.hit.zdb_id: 2020749-9
    detail.hit.zdb_id: 1126687-9
    SSG: 12
    Location Call Number Limitation Availability
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