2017
DOI: 10.1016/j.vprsr.2017.10.001
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Redescription and first molecular characterization of the little known feline neurotropic nematode Gurltia paralysans (Nematoda: Metastrongyloidea)

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Cited by 15 publications
(54 citation statements)
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“…in Spain (Jefferies et al, 2010). The morphological and morphometric characteristics of the parasite analyzed in this study are similar to those described for G. paralysans (Muñoz et al, 2017) and molecular analyses confirmed this identity. Gurltia paralysans, first reported in the 1930s (Moroni et al, 2012), is considered a neglected feline neurological parasitosis (Muñoz et al, 2017).…”
Section: Discussionsupporting
confidence: 84%
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“…in Spain (Jefferies et al, 2010). The morphological and morphometric characteristics of the parasite analyzed in this study are similar to those described for G. paralysans (Muñoz et al, 2017) and molecular analyses confirmed this identity. Gurltia paralysans, first reported in the 1930s (Moroni et al, 2012), is considered a neglected feline neurological parasitosis (Muñoz et al, 2017).…”
Section: Discussionsupporting
confidence: 84%
“…The morphological and morphometric characteristics of the parasite analyzed in this study are similar to those described for G. paralysans (Muñoz et al, 2017) and molecular analyses confirmed this identity. Gurltia paralysans, first reported in the 1930s (Moroni et al, 2012), is considered a neglected feline neurological parasitosis (Muñoz et al, 2017). It is a neurotropic metastrongylid nematode of domestic cats that is mainly found in the veins of the spinal cord subarachnoid space and parenchyma (Bowman et al, 2002).…”
Section: Discussionsupporting
confidence: 81%
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“…What we can state unequivocally is that no adult parasites were present in bronchi or bronchioles, a common finding in A. abstrusus infection. Therefore, to ascertain a possible role of G. paralysans in the lung pathology, the paraffin embedded tissues were subjected to nested PCR (Muñoz et al, 2017). Unfortunately, however, the samples did not amplify due to DNA and rRNA degradation, possibly because of prolonged formalin fixation, paraffin embedding time and conservation, processing temperature or PCR inhibitors in the samples (Merkelbach et al, 1997;Macabeo-Ong et al, 2002;Malik et al, 2013;Rodriguez et al, 2014).…”
mentioning
confidence: 99%
“…For the rDNA region we used combinations of the forward primers N18SF1, NF1 and NC1 and the reverse primers D3B, NC2 and NC5BR [ 44 49 ]. For the cox 1 sequence we used the primers MetCOI-F1 and JB4.5 [ 50 52 ]. PCR was performed with HOT FIREPol® Blend Master Mix (Solis BioDyne, Tartu, Estonia), 200 nM final concentration of forward and reverse primers each and 100 ng of nematode DNA in a 50 μl reaction volume.…”
Section: Methodsmentioning
confidence: 99%