scholarly journals The efficiency of methods for catching insects - vectors of vector-borne diseases of animals and their species composition

2021 ◽  
Vol 22 (5) ◽  
pp. 761-769
Author(s):  
O. A. Burova ◽  
O. I. Zakharova ◽  
N. N. Toropova ◽  
N. A. Gladkova ◽  
A. A. Blokhin

The article provides the results of study of the effectiveness of collection methods and the taxonomic identification of insects in the regions of Russia. During the research three methods of collecting insects were used: a UV trap, fly strips and a liquid gadfly trap (“death puddle”). The following blood-sucking insects play a key role in the epizootology of transmissible infections - houseflies (Muscidae), black flies (Simuliidae), mosquitoes (Culicidae), biting midges (Ceratopogonidae), gadflies (Tabanidae). There has been obtained new information on the species, territorial and temporal dynamics of the distribution of vectors of lumpy skin disease in cattle in the subjects of the Russian Federation. Data collection of the spatial and temporal spread of the disease visualized using GIS-technologies have been generated on the basis of the statistical reports. As the result of the research, it has been established that in the Nizhny Novgorod region representatives of the Psychodidae family, the percentage of which was 40.9 %, predominate in the nocturnal entomological complex. They are followed by mosquitoes (genus Culex) - 21.6 %, biting midges - 16.4 % manure flies - 7.0 % and black flies - 3.0 %, respectively. In the Saratov region, the nocturnal entomological complex was represented by manure flies (family Sphaeroceridae), black flies (family Simuliidae) and mosquitoes (genus Culex), the percentages were 56,0, 32,0 and 12,0 %, respectively. At the same time, in the Saratov region there were collected 239 times less mosquitoes than in the Nizhny Novgorod region, which was due to an increase in temperature in the conditions of the southern regions. This caused the water bodies to dry out and reduced the pool of insects whose developmental cycle is related to water. It has been established that all-year keeping of cattle in winter cow yards provides the diversity and rise in the number of insect vectors, which increases the risk of lumpy skin disease as compared to the grazing system of cattle keeping. For collection daytime insect vectors, it is recommended to use fly strips covered with rosin and mineral oil. For collection insects of the nocturnal entomocomplex, which are the main transmitters of the lumpy skin disease virus, one should use ultraviolet traps.

2018 ◽  
Vol 20 (88) ◽  
pp. 131-135
Author(s):  
Ya. V. Kisera ◽  
Yu. G. Storchak ◽  
L. Ya. Bozhyk

National biosecurity is a system of organizational and technical measures that help protect humans, animals and the environment from potential and actual biological threats. That is why analysis of the main hazardous biological sources for humans and animals has been carried out. The influence of climate change on the animals’ welfare as well as their predisposition to the deferred type tendency is proved. The prevalence of vector diseases of animals, mycoses and mycotoxicoses, which can manifest themselves in the form of such emergencies as outbreaks of exotic diseases, large-scale epizootics, a sharp increase of the incidence of endemic diseases, etc., are of both ecological and biological danger. Contagious vesicular (nodular) dermatitis (Lumpy skin disease, LSD) is caused by the virus belonging to the genus Capripoxvirus, the Poxviridae family and affects mainly cattle and buffaloes. The virus is distributed mainly by means of mechanical carriers (species of Stomoxys spp. and other flies). Global warming on the European continent facilitates the migration of blood-sucking insects that are carriers of vector diseases. As a result, the insects occupy new ecological niches adapting to the new biocenoses. A poorly controlled movement of large numbers of livestock also creates a risk of disease spreading. The World Organization for Animal Health (OIE) has identified LSD as highly dangerous illnesses subject to notification. The focus is made on policies dealing with the control and eradication of contagious nodular dermatitis in case of its detection. The spread of LSD can be prevented through the introduction of biosafety measures at the farm level and the introduction of restrictions on the movement of infection-susceptible animals and goods from the infected territories. Vaccination is the most effective disease control tool in endemic areas. LSD control and elimination policy in case of disease detection includes sanitary slaughter (stamping-out) of infected animals – a complex of antiepizootic measures that carry out by direction  of the chief state inspector, including the slaughter of sick and infected animals of the herd, and if necessary, animals of another herd that could lead before the transmission of a pathogenic agent – the pathogen of contagious nodular dermatitis of cattle. All animals, that are susceptible to the disease, whether vaccinated or not, are clogged and their carcasses are destroyed by burning, burial with the guarantee of preventing the spread of infection through carcasses or other products of dead animals. Emergency control of outbreaks envisages the ring vaccination of buffer zones within 25–50 km from infected areas, as well as foundation of temporary or permanent slaughter places in the infected areas. Sufficient herd immunity must be created and maintained within large territories both around the infected area and at the borders with infected countries. Such immunity is achieved when 80% of the herd is covered by vaccination.


Pathogens ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 716
Author(s):  
Yuri V. Saltykov ◽  
Anna A. Kolosova ◽  
Nadezhda N. Filonova ◽  
Alexander N. Chichkin ◽  
Valentina A. Feodorova

Lumpy skin disease virus (LSDV) is the causative agent of lumpy skin disease (LSD) that has been recently reported in the South-East and North Asian parts of the Russian Federation. During 2017–2019, there were more than 30 LSD outbreaks in Saratov Region despite active inoculation of cattle with heterologous vaccine. Importantly, the first case of the novel recombinant LSDV strain was reported here in 2017. This study aimed to determine the main clonal lineage(s) of LSDV strains circulated within Saratov Region and other regions of Russia since the first introduction of LSDV. The molecular typing and subtyping based on the coding regions of the G-protein-coupled chemokine receptor (GPCR) gene resulted in a discrimination of all outbreak-related LSDV strains into two main types, such as Type I and Type II, and subtypes Ia-d and IIa-g. Phylogenetically, eleven LSDV lineages were revealed in Russia including the five ones in Saratov Region. They were the following: (i) the Neethling wild Type Ia/2017; (ii) the recombinant Saratov IIc/2017/2019; (iii) the specific Dergachevskyi IId/2017; (iv) the Khvalynsky IIg/2018, and (v) the Haden-Type IIa lineage for the six LSDV strains detected in cattle immunized with heterologous vaccine during the last LSD outbreak in the Saratov Region, Nesterovo Village, in 2019 (Nesterovo-2019 strains). A single LSDV strain detected in Saratov Region in 2017 had the same Type Ia that was identified in 2016 in the bordered Republic of Kazakhstan. Phylogeographic analysis demonstrated three nominal clusters of LSDV types in the following Russian Federation territories: (I) the Central European part; (II) the South-East of the European part; (III) the North Asian part. Cluster I was represented by mainly Type I strains, while both Clusters 2 and 3 contained predominantly Type II strains. The Clusters I and II partially overlapped, while Cluster 3 was separate. Multiple introductions of LSDV into Saratov Region in 2017–2019 using GPCR-based molecular typing and subtyping were revealed. This scheme is a promising tool for molecular discrimination of LSDV strains derived from both vaccinated and unvaccinated against LSD cattle as well as for molecular epidemiology.


Vaccines ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 473
Author(s):  
Andy Haegeman ◽  
Ilse De Leeuw ◽  
Laurent Mostin ◽  
Willem Van Campe ◽  
Laetitia Aerts ◽  
...  

Vaccines form the cornerstone of any control, eradication and preventative strategy and this is no different for lumpy skin disease. However, the usefulness of a vaccine is determined by a multiplicity of factors which include stability, efficiency, safety and ease of use, to name a few. Although the vaccination campaign in the Balkans against lumpy skin disease virus (LSDV) was successful and has been implemented with success in the past in other countries, data of vaccine failure have also been reported. It was therefore the purpose of this study to compare five homologous live attenuated LSDV vaccines (LSDV LAV) in a standardized setting. All five LSDV LAVs studied were able to protect against a challenge with virulent LSDV. Aside from small differences in serological responses, important differences were seen in side effects such as a local reaction and a Neethling response upon vaccination between the analyzed vaccines. These observations can have important implications in the applicability in the field for some of these LSDV LAVs.


Vaccines ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 4
Author(s):  
Janika Wolff ◽  
Tom Moritz ◽  
Kore Schlottau ◽  
Donata Hoffmann ◽  
Martin Beer ◽  
...  

Capripox virus (CaPV)-induced diseases (lumpy skin disease, sheeppox, goatpox) are described as the most serious pox diseases of livestock animals, and therefore are listed as notifiable diseases under guidelines of the World Organisation for Animal Health (OIE). Until now, only live-attenuated vaccines are commercially available for the control of CaPV. Due to numerous potential problems after vaccination (e.g., loss of the disease-free status of the respective country, the possibility of vaccine virus shedding and transmission as well as the risk of recombination with field strains during natural outbreaks), the use of these vaccines must be considered carefully and is not recommended in CaPV-free countries. Therefore, innocuous and efficacious inactivated vaccines against CaPV would provide a great tool for control of these diseases. Unfortunately, most inactivated Capripox vaccines were reported as insufficient and protection seemed to be only short-lived. Nevertheless, a few studies dealing with inactivated vaccines against CaPV are published, giving evidence for good clinical protection against CaPV-infections. In our studies, a low molecular weight copolymer-adjuvanted vaccine formulation was able to induce sterile immunity in the respective animals after severe challenge infection. Our findings strongly support the possibility of useful inactivated vaccines against CaPV-infections, and indicate a marked impact of the chosen adjuvant for the level of protection.


2021 ◽  
pp. 109046
Author(s):  
Youness Es-sadeqy ◽  
Zahra Bamouh ◽  
Abderrahim Ennahli ◽  
Najete Safini ◽  
Soufiane El Mejdoub ◽  
...  

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Halima Rhazi ◽  
Najete Safini ◽  
Karima Mikou ◽  
Meryeme Alhyane ◽  
Khalid Omari Tadlaoui ◽  
...  

Abstract Background Animal vaccination is an important way to stop the spread of diseases causing immense damage to livestock and economic losses and the potential transmission to humans. Therefore effective method for vaccine production using simple and inexpensive bioprocessing solutions is very essential. Conventional culture systems currently in use, tend to be uneconomic in terms of labor and time involved. Besides, they offer a limited surface area for growth of cells. In this study, the CelCradle™-500A was evaluated as an alternative to replace conventional culture systems in use such as Cell factories for the production of viral vaccines against small ruminant morbillivirus (PPR), rift valley fever virus (RVF) and lumpy skin disease virus (LSD). Results Two types of cells Vero and primary Lamb Testis cells were used to produce these viruses. The study was done in 2 phases as a) optimization of cell growth and b) virus cultivation. Vero cells could be grown to significantly higher cell densities of 3.04 × 109 using the CelCradle™-500A with a shorter doubling time as compared to 9.45 × 108 cells in Cell factories. This represents a 19 fold increase in cell numbers as compared to seeding vs only 3.7 fold in Cell factories. LT cells achieved modestly higher cell densities of 6.7 × 108 as compared to 6.3 × 108 in Cell factories. The fold change in densities for these cells was 3 fold in the CelCradle™-500A vs 2.5 fold in Cell factories. The titers in the conventional system and the bioreactor were not significantly different. However, the Cell-specific virus yield for rift valley fever virus and lumpy skin disease virus are higher (25 virions/cell for rift valley fever virus, and 21.9 virions/cell for lumpy skin disease virus versus 19.9 virions/cell for rift valley fever virus and 10 virions/cell for lumpy skin disease virus). Conclusions This work represents a novel study for primary lamb testis cell culture in CellCradle™-500A bioreactors. In addition, on account of the high cell densities obtained and the linear scalability the titers could be further optimized using other culture process such us perfusion.


2021 ◽  
Vol 53 (1) ◽  
Author(s):  
Mukhit B. Orynbayev ◽  
Raikhan K. Nissanova ◽  
Berik M. Khairullin ◽  
Arman Issimov ◽  
Kunsulu D. Zakarya ◽  
...  

AbstractThis study describes the registration of the first cases of lumpy skin disease in July 2016 in the Republic of Kazakhstan. In the rural district of Makash, Kurmangazinsky district of Atyrau region, 459 cattle fell ill and 34 died (morbidity 12.9% and mortality 0.96%). To determine the cause of the disease, samples were taken from sick and dead animals, as well as from insects and ticks. LSDV DNA was detected by PCR in all samples from dead animals and ticks (Dermacentor marginatus and Hyalomma asiaticum), in 14.29% of samples from horseflies (Tabanus bromius), and in one of the samples from two Stomoxys calcitrans flies. The reproductive LSD virus was isolated from organs of dead cattle and insects in the culture of LT and MDBK cells. The virus accumulated in cell cultures of LT and MDBK at the level of the third passage with titers in the range of 5.5–5.75 log 10 TCID50/cm3. Sequencing of the GPCR gene allowed us to identify this virus as a lumpy skin disease virus.


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