2016
DOI: 10.1007/s00436-016-5185-0
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Identification of Eimeria acervulina conoid antigen using chicken monoclonal antibody

Abstract: In the poultry industry, Eimeria spp. is one of the important pathogens which cause significant economic losses. We have previously generated a chicken monoclonal antibody (mAb), 6D-12-G10, with specificity for an antigen located in the apical cytoskeleton of Eimeria acervulina and with cross-reactive among Apicomplexan parasites, including other Eimeria spp., Toxoplasma, Neospora, and Cryptosporidium spp. Furthermore, the protein of Cryptosporidium parvum recognized by the 6D-12-G10 has been identified as elo… Show more

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Cited by 4 publications
(2 citation statements)
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“…Also, antibody may not recognise parasite extracts ab initio [ 72 ] (Fig. 2 ) because of protein self-activation/re-naturation [ 118 , 143 ], isoforms and clusters [ 42 , 134 ]. Various Eimeria stages may show simultaneous or differential expression of some proteins [ 112 , 144 ], which invariably depend on level of expression, importance to parasite stage, host response [ 91 ], limitation (or liberality) of fluorescent antibody [ 66 ] and gene splicing [ 52 ].…”
Section: Hindsightmentioning
confidence: 99%
See 1 more Smart Citation
“…Also, antibody may not recognise parasite extracts ab initio [ 72 ] (Fig. 2 ) because of protein self-activation/re-naturation [ 118 , 143 ], isoforms and clusters [ 42 , 134 ]. Various Eimeria stages may show simultaneous or differential expression of some proteins [ 112 , 144 ], which invariably depend on level of expression, importance to parasite stage, host response [ 91 ], limitation (or liberality) of fluorescent antibody [ 66 ] and gene splicing [ 52 ].…”
Section: Hindsightmentioning
confidence: 99%
“…Eimeria sporozoites, merozoites and trophozoites (zoite stages) possess sub-cellular structures [36] such as apicoplasts, rhoptries, micronemes, conoids, dense granules, polar rings and sub-pellicular microtubules [37] as well as Golgi apparatus, cytoskeleton-associated structures [38][39][40], inner membrane complexes and acidocalcisomes [32,41] and, specifically, refractile bodies (RBs) and amylopectin granules [32,42]. Apical, membrane-bound and heat shock proteins and proteases have been well studied [43].…”
Section: Introductionmentioning
confidence: 99%