2021
DOI: 10.1016/j.crpvbd.2021.100037
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Illuminating the bacterial microbiome of Australian ticks with 16S and Rickettsia-specific next-generation sequencing

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Cited by 11 publications
(10 citation statements)
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“…and Rickettsia sp. endosymbionts comprising a MRA of 31.27% and 13.73%, respectively, in H. bancrofti samples (Figures 3 , S4 , S6 ) (Beninati et al., 2009 ; Greay et al., 2021 ). No dominant bacterial endosymbiont was identified in the single I. trichosuri pool, although Mycobacteriaceae were highly abundant (MRA: 17.2%).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…and Rickettsia sp. endosymbionts comprising a MRA of 31.27% and 13.73%, respectively, in H. bancrofti samples (Figures 3 , S4 , S6 ) (Beninati et al., 2009 ; Greay et al., 2021 ). No dominant bacterial endosymbiont was identified in the single I. trichosuri pool, although Mycobacteriaceae were highly abundant (MRA: 17.2%).…”
Section: Resultsmentioning
confidence: 99%
“…Conversely, P. nasuta samples formed a distinct cluster separate from other wildlife samples, indicating a unique microbial community profile (Figure 2). (Beninati et al, 2009;Greay et al, 2021).…”
Section: Metatranscriptomic Analysismentioning
confidence: 99%
“…This was clearly demonstrated via the results achieved when testing our nanopore sequencing method on VBB-positive controls ( Table 2 ). Here, closely related Rickettsia species were distinguishable via the use of the full-length 16S rRNA gene, a feat that would not have been achievable using one or a few hypervariable regions given the highly conserved nature of this gene across many pathogenic members of the genus ( 42 , 43 ). Furthermore, through our method, reads were obtainable from a range of different sample types, including from minute quantities, such as dots of culture on slides, with genomic DNA concentrations as low as 0.05 ng/μL still detectable for Anaplasma phagocytophilum and Ehrlichia chaffeensis .…”
Section: Discussionmentioning
confidence: 99%
“…This method is among the most accurate for diagnosing Rickettsia infection since, according to the data analysed in previous investigations using the real-time PCR method, its detection in the blood is problematic because it is a bacterium that multiplies within the endothelial cells [ 54 ]. Nevertheless, the future of confirmation is focused on genome sequencing and metagenomics [ 55 , 56 ]. Reports on the use of next-generation sequencing (NGS) and metagenomics to diagnose Rickettsia spp.…”
Section: Discussionmentioning
confidence: 99%