2017
DOI: 10.1016/j.ijpara.2017.06.008
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Lack of genetic structure in pinworm populations from New World primates in forest fragments

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Cited by 6 publications
(8 citation statements)
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“…A fragment of the mitochondrial cytochrome c oxidase subunit 1 gene ( cox1 ), and a region of the large subunit of the nuclear ribosomal gene ( 28S ) were amplified by polymerase chain reaction (PCR), using the procedure and primers specified in Solórzano-García et al . (2016, 2017). Contig sequences of cox1 were aligned using CLUSTAL W and MESQUITE v. 2.75; two final sets of cox1 alignments were employed, one including all Trypanoxyuris species with available molecular information, consisting of 61 sequences with 707 bp, with 4–12 sequences per Trypanoxyuris species per host subspecies; and a species-specific alignment for each Trypanoxyuris species including all the previously published sequences of pinworms from primates in Mexico (Solórzano-García et al ., 2017).…”
Section: Methodsmentioning
confidence: 99%
See 2 more Smart Citations
“…A fragment of the mitochondrial cytochrome c oxidase subunit 1 gene ( cox1 ), and a region of the large subunit of the nuclear ribosomal gene ( 28S ) were amplified by polymerase chain reaction (PCR), using the procedure and primers specified in Solórzano-García et al . (2016, 2017). Contig sequences of cox1 were aligned using CLUSTAL W and MESQUITE v. 2.75; two final sets of cox1 alignments were employed, one including all Trypanoxyuris species with available molecular information, consisting of 61 sequences with 707 bp, with 4–12 sequences per Trypanoxyuris species per host subspecies; and a species-specific alignment for each Trypanoxyuris species including all the previously published sequences of pinworms from primates in Mexico (Solórzano-García et al ., 2017).…”
Section: Methodsmentioning
confidence: 99%
“…(2016, 2017). Contig sequences of cox1 were aligned using CLUSTAL W and MESQUITE v. 2.75; two final sets of cox1 alignments were employed, one including all Trypanoxyuris species with available molecular information, consisting of 61 sequences with 707 bp, with 4–12 sequences per Trypanoxyuris species per host subspecies; and a species-specific alignment for each Trypanoxyuris species including all the previously published sequences of pinworms from primates in Mexico (Solórzano-García et al ., 2017). The 28S contig sequences were aligned using MUSCLE and consisted of 35 sequences of 1149 bp, with 2–5 sequences per Trypanoxyuris species per host subspecies.…”
Section: Methodsmentioning
confidence: 99%
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“…Despite this, mitochondrial sequence analysis of Trypanoxyuris spp. showed that parasite populations in different forest fragments were not genetically differentiated [ 132 ]. There are two non-mutually-exclusive explanations for this; unexpectedly high Trypanoxyuris gene flow among forest fragments, and/or the failure of Trypanoxyuris populations to detectably differentiate since becoming reproductively isolated.…”
Section: Influence Of Anthropogenic Disruption On Parasitic Nematode mentioning
confidence: 99%
“…Supporting this, Trypanoxyuris spp. and B. schroederi all show genetic evidence of recent population expansion despite marked declines in host population size [ 127 , 132 ], suggesting that prevalence and/or intensity of infection has increased since habitat fragmentation. Hence, population genetic analysis can inform on the biology of parasitic nematodes undergoing changes in range, and can be used to make predictions about how parasite populations might respond genetically to future range changes.…”
Section: Influence Of Anthropogenic Disruption On Parasitic Nematode mentioning
confidence: 99%