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1.
Korean J Parasitol ; 57(1): 61-67, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30840802

ABSTRACT

Cystic echinococcosis (CE) in sheep is a hazardous zoonotic parasitic disease that is caused by Echinococcus granulosus (Eg). At present, serological test is an important diagnostic method for Eg infection in domestic animals. Here, a fusion protein Eg mefAg-1 harboring 8 dominant B-cell epitopes of Eg such as antigen B, tetraspanin 1, tetraspanin 6, reticulon and Eg95 was produced in E. coli and evaluated for CE in sheep by indirect ELISA. Eg mefAg-1 showed in ELISA a high sensitivity (93.41%) and specificity (99.31%), with a coincidence rate of 97.02%. Overall, it is suggested that the Eg mefAg-1 could be a potential antigen candidate for CE serodiagnosis in sheep.


Subject(s)
Antibodies, Helminth/blood , Antigens, Helminth/immunology , Echinococcosis/veterinary , Echinococcus/isolation & purification , Enzyme-Linked Immunosorbent Assay/methods , Serologic Tests/methods , Sheep Diseases/diagnosis , Animals , Antigens, Helminth/genetics , Echinococcosis/diagnosis , Echinococcosis/parasitology , Echinococcus/immunology , Epitopes/genetics , Epitopes/immunology , Escherichia coli/genetics , Escherichia coli/metabolism , Incidence , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/immunology , Sensitivity and Specificity , Sheep , Sheep Diseases/parasitology
2.
Trop Anim Health Prod ; 48(4): 863-9, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26898687

ABSTRACT

Porcine sapovirus (PoSaV) is one of the important pathogens that cause acute gastroenteritis in piglets. A survey on the infection and epidemic status of PoSaV in Xinjiang Province, Northwest China, was conducted in this study. We applied indirect viral protein 1 (VP1)-ELISA method to detect specific antibodies in 1218 serum samples of 3-month-old piglets collected from eight regions in Xinjiang during 2013-2014 and also detected PoSaV in 146 diarrhea stools of piglets in these eight regions using RT-PCR technology. The results showed that the PoSaV-serological positive rates in piglets in eight different regions in Xinjiang were between 32.82 and 47.06% with a mean rate of 37.68%. The average positive rate of PCR in stools of piglets was 3.42%. Sequencing and comparative analysis of five PCR-amplified DNA fragments revealed that four epidemic strains of PoSaV (swine/XJ-KO1, swine/XJ-AK2, swine/XJ-KS1, and swine/XJ-SHZ1) shared high nucleotide and amino acid identities with Cowden strain, while strain swine/XJ-AK1 shared higher high identities with Po/OH-JJ681/2000/US isolate. Phylogenetic clustering further verified that the epidemic strains of PoSaVs, i.e., swine/XJ-KO1, swine/XJ-AK2, swine/XJ-KS1, and swine/XJ-SHZ1, belong to genogroup (GIII) while swine/XJ-AK1 belongs to GVI. This survey confirmed for the first time that PoSaV infection was common in piglets in Xinjiang, China, and that the epidemic strains exist at least in both GIII and GVI clusters. This study provided the useful epidemiological data for scientific control and prevention of this disease.


Subject(s)
Animal Husbandry , Caliciviridae Infections/veterinary , Gastroenteritis/veterinary , Sapovirus/isolation & purification , Swine Diseases/epidemiology , Animals , Animals, Newborn , Caliciviridae Infections/epidemiology , Caliciviridae Infections/virology , China/epidemiology , Cluster Analysis , Demography , Enzyme-Linked Immunosorbent Assay/veterinary , Feces/virology , Gastroenteritis/epidemiology , Gastroenteritis/virology , Phylogeny , Polymerase Chain Reaction/veterinary , Sapovirus/genetics , Swine , Swine Diseases/blood , Swine Diseases/virology
3.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-415676

ABSTRACT

Objective To investigate the clinical application of multiplex allele-specific PCR assays for simultaneous detection of the mitochondrial 12S rRNA A1555G and C1494T mutations associated with aminoglycoside-induced hearing impairment.Methods Three standard plasmids of different genotypes (wild-type, A1555G mutant and C1494T mutant) were constructed for templates and allele-specific primers aiming directly at wild-type and mutant of mitochondrial DNA nt1555 and nt1494 were designed for developing a multiplex allele-specific PCR technique to detect the A1555G and C1494T mutations.Then the method was applied to clinical screening of 138 non-syndromic hearing loss subjects and confirmed by DNA sequencing.Results Multiplex allele-specific PCR was successfully applied to the detection of A1555G and C1494T mutations in a cohort of 138 Han Chinese genetically unrelated hearing-loss subjects.Finally, 11(7.97%) unrelated affected subjects harbored the A1555G and C1494T mutations in the 12S rRNA gene(10 cases for A1555G and 1 cases for C1494T), which was well consistent with results of DNA sequencing [7.97%(11/138), Kappa=1.000, P<0.01].Conclusion This study indicates that the multiplex allele-specific PCR assay is useful, convenient and reliable in the detection of the A1555G and C1494T mutations, which could identify the subjects at risk and effectively prevent of aminoglycoside-induced hearing loss.

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