2010
DOI: 10.1016/j.ijfoodmicro.2010.08.011
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Molecular identification of Anisakis type I larvae isolated from hairtail fish off the coasts of Taiwan and Japan

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Cited by 49 publications
(40 citation statements)
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“…The high prevalence of Anisakis species in fish hosts in this study is therefore thought to reflect the richness of micro/macroinvertebrates and possibly subsequently have relations with the biomass of other predators such as pinnipeds and cetaceans in waters investigated. Several papers also reported relatively a high prevalence of anisakid nematodes larvae in the largehead hairtail (Borges et al 2012;Kong et al 2015;Umehara et al 2010), as in this study. The low number of the nematodes larvae in the previous study (Lee et al 2009) may just reflect the low abundance of micro/macroinvertebrates in the areas where the largehead hairtail were caught.…”
Section: Discussionsupporting
confidence: 83%
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“…The high prevalence of Anisakis species in fish hosts in this study is therefore thought to reflect the richness of micro/macroinvertebrates and possibly subsequently have relations with the biomass of other predators such as pinnipeds and cetaceans in waters investigated. Several papers also reported relatively a high prevalence of anisakid nematodes larvae in the largehead hairtail (Borges et al 2012;Kong et al 2015;Umehara et al 2010), as in this study. The low number of the nematodes larvae in the previous study (Lee et al 2009) may just reflect the low abundance of micro/macroinvertebrates in the areas where the largehead hairtail were caught.…”
Section: Discussionsupporting
confidence: 83%
“…Several papers described anisakid nematodes L3 from the largehead hairtail (Borges et al 2012;Kong et al 2015;Lee et al 2009;Shih 2004;Umehara et al 2010;Zhang et al, 2013), but there was no report in which T. japonicus was mentioned as host species, except for our study. It is not clear if the host species mentioned was in fact T. japonicus or other Trichiurus species in their studies because the identification of host species was not clearly conducted.…”
Section: Discussionmentioning
confidence: 55%
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“…In PCR-RFLP analysis, primer pairs A-B and NC2-NC5 were used for the amplification of ITS region, AniF-Ani1R for 5.8 rRNA and JB3-JB4.5 for mt-CO1 genes 7,8,[14][15][16][22][23][24][25] . The most used restriction enzymes were HinfI, HhaI and TagI for the analysis of both ribosomal and mitochondrial genes 7,8,[14][15][16][22][23][24][25] 7,[14][15][16]22,25 .…”
Section: Umehara Et Almentioning
confidence: 99%
“…The most used restriction enzymes were HinfI, HhaI and TagI for the analysis of both ribosomal and mitochondrial genes 7,8,[14][15][16][22][23][24][25] 7,[14][15][16]22,25 . In this study, we used universal primers A and B for the amplification of ITS region, and HinfI for digestion of ITS products.…”
Section: Umehara Et Almentioning
confidence: 99%