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Role of the Nfa1 protein in pathogenic Naegleria fowleri cocultured with CHO target cells.

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dc.contributor.authorKang, SY-
dc.contributor.authorSong, KJ-
dc.contributor.authorJeong, SR-
dc.contributor.authorKim, JH-
dc.contributor.authorPark, S-
dc.contributor.authorKim, K-
dc.contributor.authorKwon, MH-
dc.contributor.authorShin, HJ-
dc.date.accessioned2011-06-16T04:41:50Z-
dc.date.available2011-06-16T04:41:50Z-
dc.date.issued2005-
dc.identifier.issn1071-412X-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/2946-
dc.description.abstractNaegleria fowleri, a free-living amoeba, exists as a virulent pathogen which causes fatal primary amoebic meningoencephalitis in experimental animals and humans. Using infected and immune mouse sera, we previously cloned an nfa1 gene from a cDNA library of N. fowleri by immunoscreening. The nfa1 gene (360 bp) produced a recombinant 13.1-kDa protein, and the Nfa1 protein showed pseudopodium-specific immunolocalization on a trophozoite of N. fowleri. In this study, the role of the Nfa1 protein as a cell contact mechanism of N. fowleri cocultured with target cells was observed by an immunofluorescence assay with an anti-Nfa1 polyclonal antibody. Using confocal microscopic findings, the Nfa1 protein was located on the pseudopodia of N. fowleri trophozoites. The Nfa1 protein in N. fowleri trophozoites cocultured with CHO target cells was also located on pseudopodia, as well as in a food cup formed as a phagocytic structure in close contact with target cells. The amount of nfa1 mRNA of N. fowleri was strongly increased 6 h after coculture.-
dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHAntibodies, Protozoan-
dc.subject.MESHAntigens, Protozoan-
dc.subject.MESHCHO Cells-
dc.subject.MESHCricetinae-
dc.subject.MESHEncephalitis-
dc.subject.MESHMice-
dc.subject.MESHNaegleria fowleri-
dc.subject.MESHPhagocytosis-
dc.subject.MESHProtozoan Proteins-
dc.subject.MESHPseudopodia-
dc.subject.MESHRNA, Messenger-
dc.titleRole of the Nfa1 protein in pathogenic Naegleria fowleri cocultured with CHO target cells.-
dc.typeArticle-
dc.identifier.pmid16002638-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182210/-
dc.contributor.affiliatedAuthor송, 경주-
dc.contributor.affiliatedAuthor정, 석률-
dc.contributor.affiliatedAuthor박, 선-
dc.contributor.affiliatedAuthor김, 경민-
dc.contributor.affiliatedAuthor권, 명희-
dc.contributor.affiliatedAuthor신, 호준-
dc.type.localJournal Papers-
dc.identifier.doi10.1128/CDLI.12.7.873-876.2005-
dc.citation.titleClinical and diagnostic laboratory immunology-
dc.citation.volume12-
dc.citation.number7-
dc.citation.date2005-
dc.citation.startPage873-
dc.citation.endPage876-
dc.identifier.bibliographicCitationClinical and diagnostic laboratory immunology, 12(7). : 873-876, 2005-
dc.identifier.eissn1098-6588-
dc.relation.journalidJ01071412X-
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Journal Papers > School of Medicine / Graduate School of Medicine > Microbiology
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