The endosymbiotic bacteria in the genus Wolbachia are capable of inducing a wide range of reproductive abnormalities in their hosts, including cytoplasmic incompatibility (CI), which could lead to the replacement of uninfected host populations with infected ones. Because of this, Wolbachia have attracted considerable interest as a potential mechanism for spreading disease-blocking transgenes through vector populations. Here we report the establishment of double Wolbachia transinfection by direct adult microinjection of Wolbachia from naturally double-infected Aedes albopictus to Aedes aegypti, the most important mosquito vector of infectious viral diseases, and a mosquito in which natural Wolbachia infections are not known to occur. We further demonstrate that incomplete CI is induced in these double-transinfected mosquitoes. Comparisons of fitness traits between naturally uninfected and transinfected Ae. aegypti lines indicated one significant difference in favor of the latter, namely, an increased number of eggs laid. Levels of CI expression corresponded to the Wolbachia density. There were large differences in relative Wolbachia density between reproductive and nonreproductive tissues in both Ae. albopictus and transinfected Ae. aegypti, except Malpighian tubule, which implied the preferred establishment of Wolbachia within reproductive tissue. Results from a simulation model confirm that population replacement by transinfected Ae. aegypti is possible over time. The establishment of Wolbachia double infections in Ae. aegypti by direct adult microinjection and the demonstration of CI expression in this new host suggest that Wolbachia could be experimentally transferred into vector species and could also be used as a gene-driving system to genetically manipulate vector populations.microinjection ͉ transfer ͉ replacement ͉ tissue tropism ͉ cytoplasmic incompatibility
During a scrub typhus outbreak investigation in Thailand, 4 isolates of O. tsutsugamushi were obtained and established in culture. Phylogenetic analysis based on the 56-kDa type-specific antigen gene demonstrated that the isolates fell into 4 genetic clusters, 3 of which had been previously reported and 1 that represents a new genotype.
The highly sensitive and selective determination of Escherichia coli (E. coli) in urine using SYBRTM Safe loop-mediated Isothermal Amplification (LAMP) method with a distance-based paper device was developed. The new...
Wolbachia are maternally inherited intracellular bacteria that infect a wide range of arthropods and nematodes and are associated with various reproductive abnormalities in their hosts. Insect-associated Wolbachia form a monophyletic clade in the alpha-Proteobacteria and recently have been separated into two supergroups (A and B) and 19 groups. Our recent polymerase chain reaction (PCR) survey using wsp specific primers indicated that various strains of Wolbachia were present in mosquitoes collected from Southeast Asia. Here, we report the phylogenetic relationship of the Wolbachia strains found in these mosquitoes using wsp gene sequences. Our phylogenetic analysis revealed eight new Wolbachia strains, five in the A supergroup and three in the B supergroup. Most of the Wolbachia strains present in Southeast Asian mosquitoes belong to the established Mors, Con, and Pip groups.
Asymptomatic leishmaniasis cases have continuously increased, especially among patients with HIV who are at risk to develop further symptoms of cutaneous and visceral leishmaniasis. Thus, early diagnosis using a simple, sensitive and reliable diagnostic assay is important because populations at risk mostly reside in rural communities where laboratory equipment is limited. In this study, the highly sensitive and selective determination of Leishmania infection in asymptomatic HIV patients was achieved using dual indicators (SYBR safe and gold-nanoparticle probe; AuNP-probe) in one-step LAMP method based on basic instruments. The assay can be simply evaluated under the naked eye due to clear interpretation of fluorescent emission of LAMP-SYBR safe dye-complex and colorimetric precipitate of specific AuNP-probes. The sensitivities and specificities of fluorescent SYBR safe dye and AuNP-probe indicators were equal, which were as high as 94.1 and 97.1%, respectively. Additionally, detection limits were 102 parasites/mL (0.0147 ng/µL), ten times more sensitivity than other related studies. To empower leishmaniasis surveillance, this inexpensive one-step SYBR safe and AuNP-LAMP assay is reliably fast and simple for field diagnostics to point-of-care settings, which can be set up in all levels of health care facilities including resource limited areas, especially in low to middle income countries.
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