Mycoplasma gallisepticum
(
MG
) is a worldwide ruined bacteria affecting different avian species, causing severe economic losses. Consequently, the current research sought to detect the incidence of MG among different commercial broiler, layer chickens and turkey farms, and environmental litter samples in different Egyptian governorates (Damietta, Giza, El-Qalyobia, El-Sharqia, and El-Behera) from January 2019 to December 2020. Four hundred samples (infraorbital sinus aspirates, tracheal swabs, serum from diseased birds, and organ samples; lung tissues, air sacs and tracheal bifurcation from freshly dead birds), and environmental samples (litter) were collected for MG isolation. Samples were subjected to phenotypic and molecular identification. Positive bacteriological samples were subjected for molecular identification using polymerase chain reaction (
PCR
) test to detect MG, then sequencing for PCR amplicon of
mgc
2 gene. Out of 332 samples subjected for bacteriological examination, 206 were bacteriologically positive for MG with an incidence of 62%. The highest incidence of MG was detected in turkey farms at a rate of 83%, followed by broiler chicken farms, layer chicken farms and litter samples at a percentage of 70, 40, and 40, respectively. The highest prevalence of MG in chickens and turkey was recorded during the winter and autumn seasons. Molecular identification of MG isolates revealed that 85% of isolates were positive for
mgc
2 gene using PCR. The Four sequenced strains in this study are closely related and placed in one group with the vaccine strain 6/85 and ts11 strain.
Aim:This research was conducted to evaluate the molluscicidal and mosquitocidal efficacy of silica nanoparticles in the eradication of the larvae and pupa of malaria and filariasis vector as well as vectors of rift-valley fever virus (Culex pipiens); Schistosoma mansoni vector and Biomphlaria alexandrina (snail and egg masses).Materials and Methods:Hydrophilic nanosilica particles (NSPs) were characterized using transmission electron microscope during the preliminary part of the study; the stages were exposed to upgrade concentrations of NSP from 50 to 1200 ppm each for 24-36 h exposure time. The highly effective concentrations were re-evaluated at lower exposure time as 3, 6, and 12 h.Results:Lethal concentration (LC50) and LC90 versus mosquito larvae were (350 ppm/24 h and 1400 ppm/24 h, respectively). C. pipiens pupae proved slight high tolerance versus the effect of these nanoparticles as the two previous doses increased to 680 ppm/6 h and 1300 ppm/24 h. The LC50 and LC90 versus B. alexandrina were increased to 590 ppm/6 h and 980 ppm/48 h, respectively. Moreover, the embryonated snail egg masses appear more susceptible to the toxic effect of these nanoparticles than the non-embryonated eggs as the LC50 and LC90 were increased to 1450 ppm/12 h and 1250 ppm/48 h, respectively, for embryonated eggs, and it was 1400 ppm/24 h and 1890 ppm/48 h, respectively, for non-embryonated one.Conclusion:The results open a new field for controlling the infectious diseases through eradication of their vectors by the way that avoids the resistance recorded from the successive chemical application in this field.
This study evaluates the use of chitosan–silver nanocomposites (CSN) as an insecticide against the bed bug ( Cimex lectularius). Adult bed bugs were collected from infested residential areas and identified using light microscopy and scanning electron microscopy. CSN were prepared and photographed for characterization using transmission electron microscopy, dynamic light scattering, and zeta potential. The insecticidal effect of different concentrations of CSN (400–1000 ppm) was compared to that of 0.1% cypermethrin as a positive control and normal saline as a negative control. The bugs ( n = 25) were immersed for 20 min in the corresponding medium, dried with filter papers, and then incubated at 27–28°C and 70% RH with a 12:12 h light–dark photoperiod. The mortality rates were recorded at different time intervals (2, 4, 6, 12, and 24 h post-incubation (hPI)), and the entire experiment was repeated five times. Image analysis showed round- to spherical-shaped CSN ranging in size from 34 to 72 nm. The mortality rates were positively associated with increasing concentrations of CSN. The mortality rate first reached 100% for concentrations of 800 ppm at 24 hPI and 1000 ppm at 12 hPI. The calculated LC50 was found at a concentration of 1165 ppm at 2 hPI, and the LC99 was found at a concentration of 1914 ppm at 2 hPI. The positive control, cypermethrin, induced 100% mortality among the bugs at 2 hPI, while the negative control caused no mortality. These results clearly show the potential of CSN as an insecticide against C. lectularius. Future studies on best practices for implementing these particles in clinical settings are recommended.
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