2007
DOI: 10.1016/j.meegid.2007.01.002
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Molecular identity and heterogeneity of trichomonad parasites in a closed avian population

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Cited by 41 publications
(28 citation statements)
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“…DNA was extracted from trichomonad cultures using the same technique. PCR was used to amplify the ITS1/5.8S/ITS2 ribosomal region using published TFR1 and TFR2 primers [30] with an adapted protocol. Briefly, PCR reactions were run with 3 µL of 10X PCR buffer (Qiagen), 3 µL of 25 mM MgCl 2 (Qiagen), 0.5 µL of 5 U/µL HotStar Taq Plus DNA Polymerase (Qiagen), 2 µL template DNA, 0.4 µL of 100 mM dNTP mix (Bioline, UK), 3 µL of 10 µM forward and reverse primer and molecular grade water to complete the 50 µL per reaction.…”
Section: Methodsmentioning
confidence: 99%
“…DNA was extracted from trichomonad cultures using the same technique. PCR was used to amplify the ITS1/5.8S/ITS2 ribosomal region using published TFR1 and TFR2 primers [30] with an adapted protocol. Briefly, PCR reactions were run with 3 µL of 10X PCR buffer (Qiagen), 3 µL of 25 mM MgCl 2 (Qiagen), 0.5 µL of 5 U/µL HotStar Taq Plus DNA Polymerase (Qiagen), 2 µL template DNA, 0.4 µL of 100 mM dNTP mix (Bioline, UK), 3 µL of 10 µM forward and reverse primer and molecular grade water to complete the 50 µL per reaction.…”
Section: Methodsmentioning
confidence: 99%
“…Dientamoeba fragilis causes human gastrointestinal disease [21], [22]. In addition, Tetratrichomonas gallinarum and Trichomonas gallinae are found in the digestive tract of birds [23], [24], [25]. Trichomonas gallinae is an etiological agent of avian trichomonosis, a disease especially affecting pigeons and raptors [26], [27], while Tetratrichomonas gallinarum is disputed as a primary pathogen [28], [29] as it is often found together with another parabasalid, Histomonas meleagridis , in the caecum and liver of naturally infected chickens and turkeys [30], [31].…”
Section: Introductionmentioning
confidence: 99%
“…The species involved are not restricted to T. tenax , and the discovery of parasitic species previously unknown in humans raises the possibility that the oral cavity may also harbor other related organisms. In order to identify taxonomically the various trichomonad parasites found, various approaches may be used; for example, DNA fingerprinting and random amplification of polymorphic DNA, where the target sequence to be identified is unknown, have facilitated the identification of species markers (18). Applying these techniques, a Polish research group isolated, from Estonian patients with pulmonary diseases, strains that were different from T. tenax but showed a high similarity to the avian species Tetratrichomonas gallinarum ; they also found that the new strains could be divided into two distinct groups: seven bronchial strains and three oral strains (24).…”
Section: Local Oral Parasitic Infectionsmentioning
confidence: 99%