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1.
Epidemiol Infect ; 152: e89, 2024 Apr 16.
Artigo em Inglês | MEDLINE | ID: mdl-38623863

RESUMO

Following an outbreak of Salmonella Typhimurium in Wales in July 2021 associated with sheep meat and offal, further genetically related cases were detected across the UK. Cases were UK residents with laboratory-confirmed Salmonella Typhimurium in the same 5-single-nucleotide polymorphism (SNP) single-linkage cluster with specimen date between 01/08/2021-2031/12/2022. We described cases using routine (UK) and enhanced (Wales only) surveillance data. Exposures in cases in Wales were compared with non-Typhimurium Salmonella case-controls. Environmental Health Practitioners and the Food Standards Agency investigated supply chains of food premises reported by ≥2 cases. Animal, carcass, and environmental samples taken for diagnostic or monitoring purposes for gastrointestinal pathogens were included in microbiological investigations. We identified 142 cases: 75% in England, 23% in Wales and 3% in Scotland. Median age was 32 years, and 59% were male. Direct contact with sheep was associated with becoming a case (aOR: 14, 95%CI: 1.4-145) but reported by few (6/32 cases). No single food item, premises, or supplier linked all cases. Multi-agency collaboration enabled the identification of isolates in the same 5-SNP single-linkage cluster from a sheep carcass at an English abattoir and in ruminant, wildlife, poultry, and environmental samples, suggesting multiple vehicles and pathways of infection.


Assuntos
Salmonella typhimurium , Humanos , Animais , Reino Unido/epidemiologia , Masculino , Feminino , Adulto , Salmonella typhimurium/genética , Salmonella typhimurium/isolamento & purificação , Adolescente , Adulto Jovem , Criança , Pessoa de Meia-Idade , Ovinos , Infecções por Salmonella/epidemiologia , Infecções por Salmonella/microbiologia , Gado/microbiologia , Surtos de Doenças , Pré-Escolar , Polimorfismo de Nucleotídeo Único , Cadeia Alimentar , Lactente , Idoso , Ruminantes/microbiologia , País de Gales/epidemiologia , Estudos de Casos e Controles
2.
Microb Genom ; 9(4)2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-37052600

RESUMO

Recombination, the process whereby a segment of genetic material from one genome is inserted into another, producing a new chimeric genome, is an important evolutionary mechanism frequently observed in coronaviruses. The risks posed by recombination include the shuffling of advantageous mutations that may increase transmissibility, severity or vaccine escape. We present a genomic and epidemiological description of a new recombinant lineage of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), XR, first identified in Wales. The Pathogen Genomics Unit (Public Health Wales, UK) sequences positive SARS-CoV-2 PCR tests using the ARTIC SARS-CoV-2 sequencing protocol. Recombinants were detected using an in-house pipeline and the epidemiological data analysed in R. Nosocomial cases were defined as those with samples taken after >7 days in hospital. Between February and March 2022, we identified 78 samples with highly similar genomes, comprising a BA.1-like 5' end, a BA.2-like 3' end and a BA.2-like spike protein. This signature is consistent with recombination and was defined as XR by Pangolin (PANGO v1.8). A total of 50 % of cases had a sample collected whilst in hospital and the first three cases were immunocompromised patients. The patient median age was 58 years (range: 4-95 years) and most of the patients were fully vaccinated against SARS-CoV-2 (74 % third dose/booster). Three patients died within 28 days of their sample collection date, one of whom had COVID-19 listed amongst ICD10 (International Classification of Diseases 10) coded causes of death. Our integrated system enabled real-time monitoring of recombinant SARS-CoV-2 for early detection, in order to rapidly risk assess and respond. This work highlights the importance of setting-based surveillance of recombinant SARS-CoV-2, as well as the need to monitor immunocompromised populations through repeat testing and sequencing.


Assuntos
COVID-19 , SARS-CoV-2 , Humanos , Pessoa de Meia-Idade , SARS-CoV-2/genética , COVID-19/epidemiologia , País de Gales/epidemiologia , Reação em Cadeia da Polimerase , Genômica
3.
Influenza Other Respir Viruses ; 16(6): 986-993, 2022 11.
Artigo em Inglês | MEDLINE | ID: mdl-35822273

RESUMO

BACKGROUND: The Omicron (lineage B.1.1.529) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in Wales, UK, on 3 December 2021. The aim of the study was to describe the first 1000 cases of the Omicron variant by demographic, vaccination status, travel and severe outcome status and compare this to contemporaneous cases of the Delta variant. METHODS: Testing, typing and contact tracing data were collected by Public Health Wales and analysis undertaken by the Communicable Disease Surveillance Centre (CDSC). Risk ratios for demographic factors and symptoms were calculated comparing Omicron cases to Delta cases identified over the same time period. RESULTS: By 14 December 2021, 1000 cases of the Omicron variant had been identified in Wales. Of the first 1000, just 3% of cases had a prior history of travel revealing rapid community transmission. A higher proportion of Omicron cases were identified in individuals aged 20-39, and most cases were double vaccinated (65.9%) or boosted (15.7%). Age-adjusted analysis also revealed that Omicron cases were less likely to be hospitalised (0.4%) or report symptoms (60.8%). Specifically a significant reduction was observed in the proportion of Omicron cases reporting anosmia (8.9%). CONCLUSION: Key findings include a lower risk of anosmia and a reduced risk of hospitalisation in the first 1000 Omicron cases compared with co-circulating Delta cases. We also identify that existing measures for travel restrictions to control importations of new variants identified outside the United Kingdom did not prevent the rapid ingress of Omicron within Wales.


Assuntos
COVID-19 , SARS-CoV-2 , Anosmia , COVID-19/epidemiologia , Humanos , SARS-CoV-2/genética , Reino Unido/epidemiologia , País de Gales/epidemiologia
4.
Epidemiol Infect ; 150: e134, 2022 05 30.
Artigo em Inglês | MEDLINE | ID: mdl-35634739

RESUMO

Prisons are susceptible to outbreaks. Control measures focusing on isolation and cohorting negatively affect wellbeing. We present an outbreak of coronavirus disease 2019 (COVID-19) in a large male prison in Wales, UK, October 2020 to April 2021, and discuss control measures.We gathered case-information, including demographics, staff-residence postcode, resident cell number, work areas/dates, test results, staff interview dates/notes and resident prison-transfer dates. Epidemiological curves were mapped by prison location. Control measures included isolation (exclusion from work or cell-isolation), cohorting (new admissions and work-area groups), asymptomatic testing (case-finding), removal of communal dining and movement restrictions. Facemask use and enhanced hygiene were already in place. Whole-genome sequencing (WGS) and interviews determined the genetic relationship between cases plausibility of transmission.Of 453 cases, 53% (n = 242) were staff, most aged 25-34 years (11.5% females, 27.15% males) and symptomatic (64%). Crude attack-rate was higher in staff (29%, 95% CI 26-64%) than in residents (12%, 95% CI 9-15%).Whole-genome sequencing can help differentiate multiple introductions from person-to-person transmission in prisons. It should be introduced alongside asymptomatic testing as soon as possible to control prison outbreaks. Timely epidemiological investigation, including data visualisation, allowed dynamic risk assessment and proportionate control measures, minimising the reduction in resident welfare.


Assuntos
COVID-19 , Prisões , COVID-19/epidemiologia , Surtos de Doenças , Feminino , Humanos , Masculino , Reino Unido/epidemiologia , Sequenciamento Completo do Genoma
5.
Cell ; 184(20): 5179-5188.e8, 2021 09 30.
Artigo em Inglês | MEDLINE | ID: mdl-34499854

RESUMO

We present evidence for multiple independent origins of recombinant SARS-CoV-2 viruses sampled from late 2020 and early 2021 in the United Kingdom. Their genomes carry single-nucleotide polymorphisms and deletions that are characteristic of the B.1.1.7 variant of concern but lack the full complement of lineage-defining mutations. Instead, the remainder of their genomes share contiguous genetic variation with non-B.1.1.7 viruses circulating in the same geographic area at the same time as the recombinants. In four instances, there was evidence for onward transmission of a recombinant-origin virus, including one transmission cluster of 45 sequenced cases over the course of 2 months. The inferred genomic locations of recombination breakpoints suggest that every community-transmitted recombinant virus inherited its spike region from a B.1.1.7 parental virus, consistent with a transmission advantage for B.1.1.7's set of mutations.


Assuntos
COVID-19/epidemiologia , COVID-19/transmissão , Pandemias , Recombinação Genética , SARS-CoV-2/genética , Sequência de Bases/genética , COVID-19/virologia , Biologia Computacional/métodos , Frequência do Gene , Genoma Viral , Genótipo , Humanos , Mutação , Filogenia , Polimorfismo de Nucleotídeo Único , Reino Unido/epidemiologia , Sequenciamento Completo do Genoma/métodos
6.
Cell ; 184(1): 64-75.e11, 2021 01 07.
Artigo em Inglês | MEDLINE | ID: mdl-33275900

RESUMO

Global dispersal and increasing frequency of the SARS-CoV-2 spike protein variant D614G are suggestive of a selective advantage but may also be due to a random founder effect. We investigate the hypothesis for positive selection of spike D614G in the United Kingdom using more than 25,000 whole genome SARS-CoV-2 sequences. Despite the availability of a large dataset, well represented by both spike 614 variants, not all approaches showed a conclusive signal of positive selection. Population genetic analysis indicates that 614G increases in frequency relative to 614D in a manner consistent with a selective advantage. We do not find any indication that patients infected with the spike 614G variant have higher COVID-19 mortality or clinical severity, but 614G is associated with higher viral load and younger age of patients. Significant differences in growth and size of 614G phylogenetic clusters indicate a need for continued study of this variant.


Assuntos
Substituição de Aminoácidos , COVID-19/transmissão , COVID-19/virologia , SARS-CoV-2/genética , SARS-CoV-2/patogenicidade , Glicoproteína da Espícula de Coronavírus/genética , Ácido Aspártico/análise , Ácido Aspártico/genética , COVID-19/epidemiologia , Genoma Viral , Glicina/análise , Glicina/genética , Humanos , Mutação , SARS-CoV-2/crescimento & desenvolvimento , Reino Unido/epidemiologia , Virulência , Sequenciamento Completo do Genoma
7.
J Exp Psychol Anim Learn Cogn ; 46(1): 40-46, 2020 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-31259576

RESUMO

Texture is often used as a convenient stimulus dimension to study aspects of discrimination learning in rodents. However, the basis of texture discrimination learning is often left untested: Although learning could involve the whisker system, it could also be based on other senses (e.g., olfactory or visual). Here, we investigated whether mice use their whisker system to learn texture discriminations. Mice were placed in an apparatus illuminated with a dim red light, and the mice had to learn which of 2 sawdust-filled bowls contained a buried reward. The outer surfaces of the bowls were 3-D printed with different textures (grooved or smooth). Within a 60-min session, mice learned to dig in 1 bowl (e.g., grooved) rather than the other (e.g., smooth) to gain the reward. This texture discrimination and an equivalent odor discrimination were retained overnight (Experiments 1 and 2); and whisker trimming disrupted learning based on the texture of the bowls but not learning based on the odor of the sawdust in the bowls (Experiments 3 and 4). These results provide a secure basis upon which to investigate the behavioral and brain basis of texture learning in rodents. (PsycINFO Database Record (c) 2019 APA, all rights reserved).


Assuntos
Comportamento Animal/fisiologia , Aprendizagem por Discriminação/fisiologia , Percepção Olfatória/fisiologia , Percepção do Tato/fisiologia , Vibrissas/fisiologia , Animais , Masculino , Camundongos , Camundongos Endogâmicos C57BL
8.
Learn Behav ; 45(2): 107-114, 2017 06.
Artigo em Inglês | MEDLINE | ID: mdl-28432592

RESUMO

The animal kingdom contains species with a wide variety of sensory systems that have been selected to function in different environmental niches, but that are also subject to modification by experience during an organism's lifetime. The modification of such systems by experience is often called perceptual learning. In rodents, the classic example of perceptual learning is the observation that simple preexposure to two visual stimuli facilitates a subsequent (reinforced) discrimination between them. However, until recently very little behavioral research had investigated perceptual learning with tactile stimuli in rodents, in marked contrast to the wealth of information about plasticity in the rodent somatosensory system. Here we present a selective review of behavioral analyses of perceptual learning with tactile stimuli, alongside evidence concerning the potential bases of such effects within the somatosensory system.


Assuntos
Aprendizagem , Percepção , Animais
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