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1.
Transbound Emerg Dis ; 69(4): 2390-2397, 2022 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33991179

RESUMO

Taenia hydatigena is a widespread tapeworm of canids (primarily dogs) that causes cysticercosis in ruminants (domestic and wild) and manifests as depression and weakness secondary to various hepatic damages and sometimes mortality in young animals, although, commonly encountered cases are asymptomatic. In most taeniids, genetic polymorphism has been found to impact host preferences, distribution, disease epidemiology and management. Recently, we identified two main mitochondrial lineages of T. hydatigena in China, and here, we examined the mitochondrial nad4-nad5 genes of T. hydatigena from China, Nigeria, Pakistan and Sudan to assess the intraspecies variation of isolates from these countries and also the distribution of the distinct mitochondrial groups. In addition to China, haplogroup B variant was found in Pakistan, while haplogroup A demonstrated a widespread distribution. We then designed a PCR-restriction fragment length polymorphism (PCR-RFLP) assay using XmiI (AccI) and RsaI (AfaI) restriction enzymes to differentiate members of both haplogroups. This result provides more molecular evidence supporting the existence of distinct mitochondrial variants of T. hydatigena. The epidemiological significance of these different mitochondrial groups remains to be explored further. The current PCR-RFLP assay offers a useful molecular approach for investigating the genetic population structure of T. hydatigena in enzootic regions and in identifying/discriminating the different mitochondrial groups (haplogroups A and B).


Assuntos
Cisticercose , Doenças do Cão , Taenia , Animais , Cisticercose/epidemiologia , Cisticercose/veterinária , Cães , Técnicas de Amplificação de Ácido Nucleico/veterinária , Reação em Cadeia da Polimerase/veterinária , Polimorfismo de Fragmento de Restrição , Taenia/genética
2.
J Phys Chem Lett ; 12(42): 10262-10269, 2021 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-34652163

RESUMO

Spin-dependent charge transmission or the so-called chirality-induced spin selectivity (CISS) effect was demonstrated in self-assembled chiral coordinated monolayers. Distinct from the previous CISS phenomenon observed mainly on pure biomolecules, here we expanded this effect to the coordinated complex of chiral biomolecules and metal cations, specifically, cysteine-Cu2+-alanine (Cys/Cu/Ala), in which the complex itself was redox-active. However, the coordinated self-assembled monolayers of cysteine-Cu2+-cysteine did not show any spin-dependent effect. In addition, this phenomenon was explained by developing a theoretical model with spin-orbit coupling. The alanine molecules contributed to multiple transport pathways, leading to experimentally observable spin polarization. Finally, this CISS effect in Cys/Cu/Ala complex was demonstrated to amplify the sensing signal. The enantioselective discrimination efficiency could be improved by controlling the orientation of the external magnetic field.

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