Analysis of Genetic Variation in Ribosomal DNA Internal Transcribed Spacer and the NADH Dehydrogenase Subunit 4 Mitochondrial Genes of the Onchocerciasis Vector Simulium ochraceum

2006 ◽  
Vol 43 (4) ◽  
pp. 701-706 ◽  
Author(s):  
Mario A. Rodríguez-pérez ◽  
Claudia A. Núñez-gonzález ◽  
Cristian Lizarazo-ortega ◽  
Alejandro Sánchez-varela ◽  
Michael C. Wooten ◽  
...  
2006 ◽  
Vol 43 (4) ◽  
pp. 701-706 ◽  
Author(s):  
Mario A. Rodríguez-pérez ◽  
Claudia A. Núñez-gonzález ◽  
Cristian Lizarazo-ortega ◽  
Alejandro Sánchez-varela ◽  
Michael C. Wooten ◽  
...  

2019 ◽  
Vol 12 (1) ◽  
Author(s):  
John A. Ohiolei ◽  
Joshua Luka ◽  
Guo-Qiang Zhu ◽  
Hong-Bin Yan ◽  
Li Li ◽  
...  

Abstract Background Cysticercosis caused by the metacestode larval stage of Taenia hydatigena is a disease of veterinary and economic importance. A considerable level of genetic variation among isolates of different intermediate hosts and locations has been documented. Generally, data on the genetic population structure of T. hydatigena is scanty and lacking in Nigeria. Meanwhile, similar findings in other cestodes like Echinococcus spp. have been found to be of epidemiological importance. Our aim, therefore, was to characterize and compare the genetic diversity of T. hydatigena population in Nigeria based on three mitochondrial DNA markers as well as to assess the phylogenetic relationship with populations from other geographical regions. Methods In the present study, we described the genetic variation and diversity of T. hydatigena isolates from Nigerian sheep and goats using three full-length mitochondrial genes: the cytochrome c oxidase subunit 1 (cox1), NADH dehydrogenase subunit 1 (nad1), and NADH dehydrogenase subunit 5 (nad5). Results The median-joining network of concatenated cox1-nad1-nad5 sequences indicated that T. hydatigena metacestodes of sheep origin were genetically distinct from those obtained in goats and this was supported by high FST values of nad1, cox1, and concatenated cox1-nad1-nad5 sequences. Genetic variation was also found to be higher in isolates from goats than from sheep. Conclusions To the best of our knowledge, the present study described the genetic variation of T. hydatigena population for the first time in Nigeria using full-length mitochondrial genes and suggests the existence of host-specific variants. The population indices of the different DNA markers suggest that analysis of long mitochondrial DNA fragments may provide more information on the molecular ecology of T. hydatigena. We recommend that future studies employ long mitochondrial DNA sequence in order to provide reliable data that would explain the extent of genetic variation in different hosts/locations and the biological and epidemiological significance.


2020 ◽  
Vol 58 (1) ◽  
pp. 93-97 ◽  
Author(s):  
Rosline James Muku ◽  
Hong-Bin Yan ◽  
John Asekhaen Ohiolei ◽  
Abubakar Ahmed Saaid ◽  
Sara Ahmed ◽  
...  

The cestode <i>Taenia hydatigena</i> uses canids, primarily dogs, as definitive hosts, while the metacestode larval stage cysticercus infects a range of intermediate hosts, including domestic animals such as goats, sheep, and pigs. Cysticercosis due to <i>T. hydatigena</i> has large veterinary and economic drawbacks. Like other taeniids, e.g., <i>Echinococcus</i>, intraspecific variation is found among the members of the genus Taenia. In Africa, few studies are available on the epidemiology and distribution of <i>T. hydatigena</i>, and even fewer studies are available on its genetic variation. In this study, we molecularly identified 11 cysticerci from sheep in Sudan and demonstrated the genetic variation based on the NADH dehydrogenase subunit 1 (<i>nad</i>1) and cytochrome c oxidase subunit 1 (<i>cox</i>1) mitochondrial genes. The isolates were correctly identified as <i>T. hydatigena</i> with more than 99% similarity to those in the GenBank database. Low diversity indices and insignificant neutrality indices were observed, with 3 and 2 haplotypes for the <i>nad</i>1 and <i>cox</i>1 genes, respectively. The results suggest the presence of unique <i>T. hydatigena</i> haplotypes in Sudan, as haplotypes with 100% similarity were not found in the GenBank database. With few available studies on the genetic variation of <i>T. hydatigena</i> in Africa, this report represents the first insights into the genetic variation of <i>T. hydatigena</i> in Sudan and constitutes useful data.


2013 ◽  
Vol 27 (6) ◽  
pp. 655 ◽  
Author(s):  
Philip J. Sirvid ◽  
Nicole E. Moore ◽  
Geoffrey K. Chambers ◽  
Kelly Prendergast

We tested competing theories on the origins of the New Zealand fauna using thomisid spiders as a model group. These theories can be broadly described as old and vicariant versus young and recent (dispersal). To test these theories, a phylogenetic analysis was undertaken based on cytochrome c oxidase subunit I (COI) and 28S rRNA sequence data, with smaller datasets (histone H3, nicotinamide adenine dinucleotide (NADH) dehydrogenase subunit 1 and a combined dataset) used to improve resolution of internal branches. The monophyly of New Zealand thomisid subfamilies and of individual taxa were also assessed using these data. Our data supports the separation of New Zealand clades from their Australian counterparts. Evidence of recent dispersal to New Zealand by Australian stephanopines combined with our proposed maximum divergence date of 5.3 mya indicates that the New Zealand thomisids are a younger lineage than previously suspected. Several other gene targets (internal transcribed spacer units 1 and 2, wingless and 18S rRNA) were examined but did not generate sufficient reliable data to contribute to the analysis. Corrected p-distance values for COI indicate that Sidymella angularis, a widely distributed and morphologically variable stephanopine species, is a single taxon. Three undescribed endemic species exhibited molecular and morphological distinctiveness from previously described New Zealand thomisids.


2005 ◽  
Vol 86 (1) ◽  
pp. 1-11 ◽  
Author(s):  
LAURENCE MOUSSON ◽  
CATHERINE DAUGA ◽  
THOMAS GARRIGUES ◽  
FRANCIS SCHAFFNER ◽  
MARIE VAZEILLE ◽  
...  

Aedes (Stegomyia) aegypti (L.) and Aedes (Stegomyia) albopictus (Skuse) are the most important vectors of the dengue and yellow-fever viruses. Both took advantage of trade developments to spread throughout the tropics from their native area: A. aegypti originated from Africa and A. albopictus from South-East Asia. We investigated the relationships between A. aegypti and A. albopictus mosquitoes based on three mitochondrial-DNA genes (cytochrome b, cytochrome oxidase I and NADH dehydrogenase subunit 5). Little genetic variation was observed for A. albopictus, probably owing to the recent spreading of the species via human activities. For A. aegypti, most populations from South America were found to be genetically similar to populations from South-East Asia (Thailand and Vietnam), except for one sample from Boa Vista (northern Amazonia), which was more closely related to samples from Africa (Guinea and Ivory Coast). This suggests that African populations of A. aegypti introduced during the slave trade have persisted in Boa Vista, resisting eradication campaigns.


2019 ◽  
Vol 12 (1) ◽  
Author(s):  
John Asekhaen Ohiolei ◽  
Chen-Yang Xia ◽  
Li Li ◽  
Jian-Zhi Liu ◽  
Wen-Qiang Tang ◽  
...  

Abstract Background Cystic echinococcosis (CE) in humans and livestock is caused by Echinococcus granulosus (sensu lato). In China where CE is endemic, a number of studies have shown that Echinococcus granulosus (sensu stricto) is majorly responsible for CE. However, E. canadensis (G6) which is the second leading cause of CE is now being detected in most parts of the country. In this study, the species diversity and genetic variation of Echinococcus granulosus (s.l.) in four counties in Tibet Autonomous Region of China were investigated. Methods Infection with Echinococcus granulosus (s.s.) in yaks and sheep was identified using NADH dehydrogenase subunit 1 and 5 (nad1 and nad5) mitochondrial genes while the genotype G6 of E. canadensis initially diagnosed with NADH dehydrogenase subunit 1 (nad1) was further confirmed by analysis of the complete mitochondrial genome and a phylogenetic network constructed based on the nad2 and nad5 genes. Results Out of 85 hydatid cyst samples collected from slaughtered sheep (n = 54) and yaks (n = 31), 83 were identified as E. granulosus (s.s.) G1 (n = 77), G3 (n = 6) and 2 were identified as E. canadensis G6. Analysis of the nad1/nad5 genes revealed 16/17 mutations with 9/14 parsimony informative sites resulting in 15/14 haplotypes, respectively. Haplotype diversity (Hd) and nucleotide diversity (π) of E. granulosus (s.s.) population were 0.650 and 0.00127 for nad1 and 0.782 and 0.00306 for nad5, respectively, with an overall negative Tajima’s D and Fu’s Fs. A low FST indicated no genetic difference between isolates from sheep and yaks. Conclusion Pockets of infection with E. canadensis (G6, G7, G8 and G10) have been previously reported in sheep, goats, yaks and/or humans in different parts of China. While the G6 genotype has been previously reported in sheep in the Tibet Autonomous Region, the detection in a yak in the present study represents the first to the best of our knowledge. Therefore, we recommend future surveys and control efforts to comprehensively investigate other potential intermediate hosts for the prevalence and genetic diversity of the E. canadensis group (G6, G7, G8 and G10) across the country and their inclusion into the existing CE control programme.


Plant Disease ◽  
2016 ◽  
Vol 100 (4) ◽  
pp. 749-757 ◽  
Author(s):  
Jun Myoung Yu ◽  
Ibrahim H. Cafarov ◽  
Mohammad Babadoost

During 2008 to 2009, 255 isolates of Verticillium were obtained from internally discolored horseradish roots collected from California, Illinois, and Ontario. Twenty representative isolates were selected according to morphological features and geographic origin for further characterization. Based on the conidial size, the isolates were divided into two groups: Verticillium dahliae (4.4 ± 1.23 μm) and V. longisporum (7.8 ± 1.76 μm). Genetic diversity of the isolates was determined by sequence analysis of the internal transcribed spacer (ITS) and two mitochondrial genes (cytochrome oxidase subunit III [cox3] and NADH dehydrogenase subunit I [nad1]). Based on ITS analysis, Verticillium isolates were divided into two clades: V. dahliae and V. longisporum. However five isolates of V. longisporum (identified based on conidial size) were clustered with a V. dahliae clade, whereas the other five isolates formed a distinct V. longisporum clade. Combined analysis of the mitochondrial genes cox3 and nad1 showed that the two genetic clades of V. longisporum in ITS region analysis corresponded to the previously reported V. longisporum lineage A1/D3 and A1/D2. Pathogenicity tests revealed that all tested Verticillium isolates caused internal discoloration of horseradish roots, and there were no significant differences in either incidence or severity of root discoloration among the genetic groups.


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