Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
Epidemiol Infect ; 144(15): 3326-3334, 2016 11.
Article in English | MEDLINE | ID: mdl-27523647

ABSTRACT

Campylobacter is the leading cause of bacterial diarrhoeal disease worldwide, with raw and undercooked poultry meat and products the primary source of infection. Colonization of broiler chicken flocks with Campylobacter has proved difficult to prevent, even with high levels of biosecurity. Dipteran flies are proven carriers of Campylobacter and their ingress into broiler houses may contribute to its transmission to broiler chickens. However, this has not been investigated in the UK. Campylobacter was cultured from 2195 flies collected from four UK broiler farms. Of flies cultured individually, 0·22% [2/902, 95% confidence interval (CI) 0-0·53] were positive by culture for Campylobacter spp. Additionally, 1293 flies were grouped by family and cultured in 127 batches: 4/127 (3·15%, 95% CI 0·11-6·19) from three broiler farms were positive for Campylobacter. Multilocus sequence typing of isolates demonstrated that the flies were carrying broiler-associated sequence types, responsible for human enteric illness. Malaise traps were used to survey the dipteran species diversity on study farms and also revealed up to 612 flies present around broiler-house ventilation inlets over a 2-h period. Therefore, despite the low prevalence of Campylobacter cultured from flies, the risk of transmission by this route may be high, particularly during summer when fly populations are greatest.


Subject(s)
Campylobacter Infections/veterinary , Campylobacter/isolation & purification , Chickens , Diptera/microbiology , Poultry Diseases/transmission , Animal Husbandry , Animals , Campylobacter Infections/epidemiology , Campylobacter Infections/microbiology , Campylobacter Infections/transmission , Poultry Diseases/epidemiology , Poultry Diseases/microbiology , Prevalence , Risk Factors , Seasons , Wales
2.
Lett Appl Microbiol ; 59(1): 122-6, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24666283

ABSTRACT

UNLABELLED: Arcobacter butzleri and Arcobacter cryaerophilus were isolated from samples of raw untreated domestic sewage influent from nine separate wastewater treatment facilities in Cheshire, UK. This is the first report of Arcobacter spp. from sewage in the UK and suggests that Arcobacter spp. may be present in the human community. SIGNIFICANCE AND IMPACT OF THE STUDY: Studies have shown Arcobacter spp. to be present in domestic sewage in several European countries. This study supports previous findings with the first report of Arcobacter spp. in domestic sewage in the UK. This study suggests that Arcobacter spp. is present amongst local human populations, implicating it as an underestimated gastrointestinal pathogen in the UK and contributing to our understanding of this emerging pathogen and its presence within the UK. Providing a confirmation of the presence of Arcobacter in sewage, which supports previous studies, this paper will appeal to fellow researchers of Arcobacter, as well as healthcare and water treatment professionals concerned with microbiology, water safety and gastroenterology, potentially having a wide impact.


Subject(s)
Arcobacter/isolation & purification , Sewage/microbiology , Wastewater/microbiology , Water Microbiology , Animals , England , Humans , Urban Population , Water Purification
3.
Vet Microbiol ; 164(3-4): 246-52, 2013 Jun 28.
Article in English | MEDLINE | ID: mdl-23490561

ABSTRACT

The kobuviruses represent an emerging genus in the Picornaviridae. Here we have used next generation sequencing and conventional approaches to identify the first canine kobuvirus (CaKoV) from outside the USA. Phylogenetic analysis suggests that a single lineage genotype of CaKoV now exists in Europe and the USA with 94% nucleotide similarity in the coding region. CaKoV was only identified in a single case from a case-control study of canine diarrhoea, suggesting this virus was not a frequent cause of disease in this population. Attempts to grow CaKoV in cell culture failed. Sequence analysis suggested CaKoV was distinct from human Aichi virus (AiV), and unlikely to pose a significant zoonotic risk. Serosurveys by ELISA, immunofluorescence and neutralisation tests, using AiV as antigen, suggested kobuvirus infection is prevalent in dogs. In addition, IgG antibody to AiV was also detected in cat sera, indicating for the first time that cats may also be susceptible to kobuvirus infection.


Subject(s)
Cat Diseases/virology , Dog Diseases/virology , Kobuvirus/classification , Phylogeny , Picornaviridae Infections/veterinary , Animals , Cat Diseases/epidemiology , Cats , Dog Diseases/epidemiology , Dogs , Genotype , High-Throughput Nucleotide Sequencing , Kobuvirus/genetics , Molecular Sequence Data , Picornaviridae Infections/epidemiology , Picornaviridae Infections/virology , Prevalence , Sequence Homology, Nucleic Acid , United Kingdom/epidemiology
4.
Appl Environ Microbiol ; 77(5): 1646-50, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21193675

ABSTRACT

The aims of this study were, firstly, to compare five published methods for the isolation of Arcobacter spp. from animal feces in order to determine the most sensitive and specific method. Second, we analyzed the resulting isolates by multilocus sequence typing (MLST) in order to investigate the diversity of the isolates recovered. Third, we investigated the ability to recover Arcobacter spp. from frozen fecal samples. Seventy-seven fecal samples from cattle, sheep, and badgers were subjected to five isolation methods, based on published methods for the isolation of Arcobacter and Campylobacter spp. Thirty-nine Arcobacter butzleri isolates were analyzed using a multilocus sequence typing scheme. The survival of Arcobacter spp. in frozen samples was investigated by freezing the fecal samples at -80°C for 7 days and then applying the same five isolation methods. The most sensitive and specific method used an Arcobacter-specific broth in conjunction with modified charcoal cefoperazone deoxycholate agar (mCCDA) with added antibiotics. Freezing of fecal samples led to a reduction in the recovery of Arcobacter spp. by approximately 50%. The 39 allelic profiles obtained by MLST could be divided into 11 sequence types (STs). We have identified the most sensitive and specific method for the isolation of Arcobacter spp. from animal feces and demonstrated that the freezing of fecal samples prior to isolation reduces arcobacter recovery. MLST analysis of the isolates revealed a high level of diversity.


Subject(s)
Arcobacter/classification , Arcobacter/isolation & purification , Bacteriological Techniques/methods , Feces/microbiology , Genetic Variation , Gram-Negative Bacterial Infections/veterinary , Animals , Bacterial Typing Techniques , Campylobacter/isolation & purification , Cattle , Culture Media/chemistry , Freezing , Gram-Negative Bacterial Infections/microbiology , Microbial Viability , Molecular Typing , Multilocus Sequence Typing , Mustelidae , Sensitivity and Specificity , Sheep , United Kingdom
SELECTION OF CITATIONS
SEARCH DETAIL
...