cloning and sequence analysis of recombinant plasmodium vivax merozoite surface protein 1 (pvmsp-142 kda) in ptz57r/t vector.

نویسندگان

hadi mirahmadi dept. of parasitology and mycology, shahid beheshti university of medical sciences, tehran, iran and infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, iran.

adel spotin dept. of parasitology and mycology, shahid beheshti university of medical sciences, tehran, iran.

shirzad fallahi dept. of parasitology and mycology, shahid beheshti university of medical sciences, tehran, iran.

niloofar taghipour dept. of parasitology and mycology, shahid beheshti university of medical sciences, tehran, iran.

چکیده

background: haemonchosis has a negative effect on the farming industry throughout the world, especially in the tropic and sub-tropic countries. the present study was carried out to differentiate haemonchus species from its main hosts in iran, including sheep, goat and camel.   methods: the identification took place based on the morphometrics of the spic-ules and molecular characters. two hundred seventy adult male nematodes were collected from the abomasums of different ruminants (90 samples from each ani-mal) at the slaughterhouses from different localities in iran. samples were morpho-logically identified according to the spicules’ morphometric measurements. in the section on molecular study, 10 samples of each haemonchus isolates were genetically examined. a simple pcr-restriction fragment length polymorphism (pcr-rflp) assay of the second internal transcribed spacer of ribosomal dna (its2-rdna) were described to confirm the pcr results. results: pcr-rflp profile obtained from the restriction enzyme hpa1 in h. con-tortus and h. longistipes indicated 1 (278 bp) and 2 (113 and 135 bp) different frag-ments, respectively. the morphological parameters clearly distinguish h. contortus from h. longistipes. moreover, regarding the its2-rdna, sequences of 295 bp and 314 bp were obtained from h. contortus and h. longistipes, respectively. conclusion: high similarity of cloned pvmsp-142 kda gene in comparison to reference sequence and other sequences could be beneficial as a remarkable mo-lecular marker for serological diagnostic.

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Cloning and Sequence Analysis of Recombinant Plasmodium vivax Merozoite Surface Protein 1 (PvMSP-142 kDa) In pTZ57R/T Vector

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عنوان ژورنال:
iranian journal of parasitology

جلد ۱۰، شماره ۲، صفحات ۱۹۷-۲۰۵

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