2022
DOI: 10.3390/pathogens11111316
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Prevalence, Infection Intensity and Molecular Diagnosis of Mixed Infections with Metastrongylus spp. (Metastrongylidae) in Wild Boars in Uzbekistan

Abstract: The aim of the present study was to characterize the diversity of Metastrongylus spp. in wild boars and the earthworm intermediate host species contributing to the maintenance of the life cycle. Here, wild boars were subjected to parasitological necropsies, and lungworm species were identified morphologically, followed by confirmation using ITS-2 sequencing and a phylogenetic analysis. Earthworms were collected from wild boar habitats and investigated for the presence of larvae. The prevalence of Metastrongylu… Show more

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Cited by 4 publications
(3 citation statements)
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“…The sequence and results of the primers used to identify RKN and other nematodes are consistent with the results of previous studies (Correa et al, 2013;Janssen et al, 2017;Kuchboev & Krücken, 2022). The species analysis we conducted based on the analysis of morphological and molecular genetic indicators of root-knot nematodes is important because it was conducted for the first time in Central Asia.…”
Section: Discussionsupporting
confidence: 82%
“…The sequence and results of the primers used to identify RKN and other nematodes are consistent with the results of previous studies (Correa et al, 2013;Janssen et al, 2017;Kuchboev & Krücken, 2022). The species analysis we conducted based on the analysis of morphological and molecular genetic indicators of root-knot nematodes is important because it was conducted for the first time in Central Asia.…”
Section: Discussionsupporting
confidence: 82%
“…PCR was performed in 20 µL PCR reaction mixture containing 40 ng of each template, 1.5 µL of each primer, 0.6 µL of dNTP, 0.6 µL of Taq polymerase, 2 µL of PCR buffer (Sileks M (Moscow, Russia)), and 13.8 µL of distilled water with ProFlex PCR system (Applied Biosystems). The thermal conditions consisted of an initial step of 3 min at 95°C followed by 35 cycles of 20 s at 93°C, 30 s at 55°C, and 2 min at 72°C, followed by a final extension of 10 min at 72°C (Kuchboev and Krücken 2022). PCR products were separated by electrophoresis on a 1% agarose gel with edithium bromide and refined by Sileks M (Moscow, Russia).…”
Section: Dna Extraction Polymerase Chain Reaction Amplification and S...mentioning
confidence: 99%
“…This research initiative is driven by the pressing need for accurate and reliable diagnostic tools within the domain of veterinary science. The intricate interplay between host animals and parasitic nematodes necessitates a meticulous understanding of species diversity and distribution [11]. Through the strategic utilization of species-specific markers harnessed from the ITS2 rDNA region, this study seeks to offer a breakthrough solution to this challenge.…”
Section: Introductionmentioning
confidence: 99%