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Highly divergent 18S rRNA gene paralogs in a Cryptosporidium genotype from eastern chipmunks (Tamias striatus)
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SYSNO ASEP 0453300 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Highly divergent 18S rRNA gene paralogs in a Cryptosporidium genotype from eastern chipmunks (Tamias striatus) Tvůrce(i) Stenger, B.L.S. (US)
Clark, M.E. (US)
Kváč, Martin (BC-A) RID, RID, ORCID
Khan, E. (US)
Giddings, C.W. (US)
Dyer, N.W. (US)
Schultz, J.L. (US)
McEvoy, J.M. (US)Zdroj.dok. Infection, Genetics and Evolution. - : Elsevier - ISSN 1567-1348
Roč. 32, JUN 2015 (2015), s. 113-123Poč.str. 11 s. Forma vydání Tištěná - P Jazyk dok. eng - angličtina Země vyd. NL - Nizozemsko Klíč. slova Cryptosporidium ; Paralogy ; 18S rRNA ; 18S rDNA Vědní obor RIV GJ - Choroby a škůdci zvířat, veterinární medicína CEP LH11061 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy Institucionální podpora BC-A - RVO:60077344 UT WOS 000355027300015 DOI 10.1016/j.meegid.2015.03.003 Anotace Cryptosporidium is an apicomplexan parasite that causes the disease cryptosporidiosis in humans, livestock, and other vertebrates. Much of the knowledge on Oyptosporidium diversity is derived from 18S rRNA gene (18S rDNA) phylogenies. Eukaryote genomes generally have multiple 18S rDNA copies that evolve in concert, which is necessary for the accurate inference of phylogenetic relationships. However, 18S rDNA copies in some genomes evolve by a birth-and-death process that can result in sequence divergence among copies. Most notably, divergent 18S rDNA paralogs in the apicomplexan Plasmodium share only 89-95% sequence similarity, encode structurally distinct rRNA molecules, and are expressed at different life cycle stages. In the present study, Cryptosporidium 18S rDNA was amplified from 28/72 (38.9%) eastern chipmunks (Tamias striatus). Phylogenetic analyses showed the co-occurrence of two 18S rDNA types, Type A and Type B, in 26 chipmunks, and Type B clustered with a sequence previously identified as Cryptosporidium chipmunk genotype II. Types A and B had a sister group relationship but shared less than 93% sequence similarity. In contrast, actin and heat shock protein 70 gene sequences were homogeneous in samples with both Types A and B present. It was therefore concluded that Types A and B are divergent 18S rDNA paralogs in Ciyptosporidium chipmunk genotype II. Substitution patterns in Types A and B were consistent with functionally constrained evolution; however, Type B evolved more rapidly than Type A and had a higher G + C content (46.3% versus 41.0%). Oocysts of Oyptosporidium chipmunk genotype II measured 4.17 mu m (3.73-5.04 mu m) x 3.94 mu m (3.50-4.98 mu m) with a length-to-width ratio of 1.06 +/- 0.06 mu m, and infection occurred naturally in the jejunum, cecum, and colon of eastern chipmunks. The findings of this study have implications for the use of 18S rDNA sequences to infer phylogenetic relationships. Pracoviště Biologické centrum (od r. 2006) Kontakt Dana Hypšová, eje@eje.cz, Tel.: 387 775 214 Rok sběru 2016
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