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2.
Euro Surveill ; 28(3)2023 01.
Article in English | MEDLINE | ID: mdl-36695488

ABSTRACT

In October 2022, an outbreak in Europe of highly pathogenic avian influenza (HPAI) A(H5N1) in intensively farmed minks occurred in northwest Spain. A single mink farm hosting more than 50,000 minks was involved. The identified viruses belong to clade 2.3.4.4b, which is responsible of the ongoing epizootic in Europe. An uncommon mutation (T271A) in the PB2 gene with potential public health implications was found. Our investigations indicate onward mink transmission of the virus may have occurred in the affected farm.


Subject(s)
Influenza A Virus, H5N1 Subtype , Influenza A virus , Influenza in Birds , Influenza, Human , Humans , Animals , Influenza in Birds/epidemiology , Mink , Influenza A Virus, H5N1 Subtype/genetics , Spain/epidemiology , Farms , Influenza, Human/epidemiology , Phylogeny
3.
J Vet Diagn Invest ; 34(2): 190-198, 2022 Mar.
Article in English | MEDLINE | ID: mdl-34852683

ABSTRACT

During the COVID-19 pandemic, infection of farmed mink has become not only an economic issue but also a widespread public health concern. International agencies have advised the use of strict molecular and serosurveillance methods for monitoring the SARS-CoV2 status on mink farms. We developed 2 ELISAs and a duplex protein microarray immunoassay (MI), all in a double-recognition format (DR), to detect SARS-CoV2 antibodies specific to the receptor-binding domain (RBD) of the spike protein and to the full-length nucleoprotein (N) in mink sera. We collected 264 mink serum samples and 126 oropharyngeal samples from 5 Spanish mink farms. In both of the ELISAs and the MI, RBD performed better than N protein for serologic differentiation of mink from SARS-CoV2-positive and -negative farms. Therefore, RBD was the optimal antigenic target for serosurveillance of mink farms.


Subject(s)
COVID-19 , Mink , Animals , Antibodies, Viral , COVID-19/veterinary , Farms , Immunoassay/veterinary , Pandemics , RNA, Viral , SARS-CoV-2 , Spike Glycoprotein, Coronavirus
4.
J Vet Sci ; 21(4): e65, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32735101

ABSTRACT

BACKGROUND: Aleutian mink disease virus (AMDV) causes major economic losses in fur-bearing animal production. The control of most AMDV outbreaks is complex due to the difficulties of establishing the source of infection based only on the available on-farm epidemiological data. In this sense, phylogenetic analysis of the strains present in a farm may help elucidate the origin of the infection and improve the control and biosecurity measures. OBJECTIVES: This study had the following aims: characterize the AMDV strains from most outbreaks produced at Spanish farms between 2012-2019 at the molecular level, and assess the utility of the combined use of molecular and epidemiological data to track the possible routes of infection. METHODS: Thirty-seven strains from 17 farms were partially sequenced for the NS1 and VP2 genes and analyzed phylogenetically with other strains described worldwide. RESULTS: Spanish AMDV strains are clustered in four major clades that generally show a good geographical correlation, confirming that most had been established in Spain a long time ago. The combined study of phylogenetic results and epidemiological information of each farm suggests that most of the AMDV outbreaks since 2012 had been produced by within-farm reservoirs, while a few of them may have been due to the introduction of the virus through international trade. CONCLUSIONS: The combination of phylogenetic inference, together with epidemiological data, helps assess the possible origin of AMDV infections in mink farms and improving the control and prevention of this disease.


Subject(s)
Aleutian Mink Disease Virus/genetics , Aleutian Mink Disease/epidemiology , Disease Outbreaks/veterinary , Mink , Aleutian Mink Disease/virology , Animals , France/epidemiology , Genetic Variation , Molecular Epidemiology , Phylogeny , Portugal/epidemiology , Prevalence , Retrospective Studies , Sequence Analysis, DNA/veterinary , Spain/epidemiology
5.
PLoS One ; 13(8): e0203144, 2018.
Article in English | MEDLINE | ID: mdl-30148883

ABSTRACT

Personal protective equipment (PPE) is an element of biosecurity intended to prevent the access or spread of diseases in farms. Nevertheless, to date no extensive reports exist about the effectiveness of different available PPE on farms. Thus, our aim was to estimate the degree of protection of PPE from viral contamination during farm visits. Two farms, infected with Aleutian mink disease virus and porcine circovirus-2 respectively, were visited by six visitors wearing different combinations of PPE: coveralls with hood and bootcovers, both with a certified barrier to infective agents (certified PPE group) and non-certified bootcover and coverall without hood (non-certified PPE group). Seventy-two swab samples from PPE and both hair and street clothes under PPE were taken after the visit and analysed by qPCR. Our results reveal viral exposure during visits, and the external protections of body and shoes were contaminated in all cases (24/24). In addition, protection from viral contamination varied noticeably according to the biosecurity elements used. A higher number of positives were detected in the non-certified PPE group than in the certified PPE group, both in elements under external protections (14/18 vs 3/18) and also in hair (4/6 vs 0/6). In fact, non-certified bootcovers broke during visits, resulting in viral contamination of the internal elements under them; these are consequently not suitable for using with wrinkled surfaces usually found in farm facilities. Thus, certified coveralls should be used in order to prevent contaminations, and workers and personnel of farms should be trained in their proper use. qPCR is a useful tool in the risk management of biosecurity programmes, and our results may serve as a model to evaluate different biosecurity measures.


Subject(s)
Aleutian Mink Disease Virus , Animal Husbandry , Circovirus , Farms , Personal Protective Equipment/virology , Aleutian Mink Disease/transmission , Animal Husbandry/methods , Animals , Circoviridae Infections/transmission , Circoviridae Infections/veterinary , Hair , Humans , Mink , Shoes , Swine , Swine Diseases/transmission
6.
Vet Microbiol ; 173(3-4): 355-9, 2014 Oct 10.
Article in English | MEDLINE | ID: mdl-25183237

ABSTRACT

The Aleutian Mink Virus (AMDV) causes the Aleutian Mink Disease (AMD) or Mink Plasmacytosis, a disease responsible of high economic losses for industry worldwide. Despite there is evidence of the environmental persistence of the virus, there is not literature on the detection of this virus in environmental samples in farms and this fact would have great importance in the control programs of the disease. In order to detect contamination caused by AMDV on farms, several environmental samples were taken and examined using qPCR. 93.9% of samples taken from farms confirmed to be infected tested positive. The virus was also detected on a farm which, despite having no previous positive results, was sharing personnel with an infected farm. All samples taken from AMD-free farms tested negative, including a farm where an eradication procedure by stamping out had been performed during the preceding months. Higher contamination levels were observed in samples from those surfaces in direct contact with animals. These results are the first demonstration of environmental contamination in farms, hitherto suggested by epidemiological evidences, caused by AMDV on surfaces, furniture and equipments inside mink farms. qPCR is an useful tool for evaluating the spread of AMDV into the environment, and it may have important applications within the disease control programs.


Subject(s)
Aleutian Mink Disease Virus/isolation & purification , Aleutian Mink Disease/epidemiology , Environmental Monitoring/methods , Real-Time Polymerase Chain Reaction/veterinary , Aleutian Mink Disease/genetics , Aleutian Mink Disease Virus/genetics , Animals , Mink , Real-Time Polymerase Chain Reaction/methods , Regression Analysis , Spain/epidemiology
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