Concentrations of SARS-CoV-2 RNA and physichochemical data on wastewater samples collected from six sites across England and Wales between March and July 2020. Also included are the number of COVID-19 positive tests and COVID-19 related deaths for the same period collated from publicly available records. COVID-19 data relate to the lower tier local authority that the wastewater treatment plant was located within. Full details about this dataset can be found at https://doi.org/10.5285/ce40e62a-21ae-45b9-ba5b-031639a504f7

The resource consists of genome sequence data for the Drosophila C virus that has been serially passaged through different species of Drosophila in the laboratory. The genomes were sequenced and aligned to the reference genome. The frequency of variants at both biallelic and triallelic sites was then calculated. We also generated a phylogeny of the species involved using published data. This data was generated to understand how viruses adapt to new host species by Francis Jiggins and his co workers. The work was carried out between July 2016 and September 2017 and was funded by NERC under award reference NE/L004232/1 Full details about this nonGeographicDataset can be found at https://doi.org/10.5285/4434a27d-5288-4f2e-88ac-4b1372e4d073

This resource holds survival data of human pathogens bound to microplastics during transfer through the freshwater-marine continuum. The survival of Escherichia coli, Enterococcus faecalis and Pseudomonas aeruginosa colonising polyethylene or glass particles was quantified in mesocosm incubation experiments designed to simulate, (1) the direct release of microplastics from wastewater treatment plants (WWTPs) into freshwater and seawater environments; and (2) the movement of microplastics downstream following discharge from the WWTP through the river-estuary-marine-beach continuum. Background bacterial concentrations and crystal violet were also measured. Full details about this nonGeographicDataset can be found at https://doi.org/10.5285/c31c0b2a-ee5b-479f-84c3-ff1b0bfc6d84

These data include results from serological analysis carried out on serum collected from randomly recruited subjects, merged with household and subject level data about the subjects. The subject and household data collected included occupation of the household head, size of the household, and occupation, gender and age of the subject. Samples were collected from 303 people based in irrigated areas, 728 people from pastoral areas and 81 people from riverine areas along River Tana in Tana River and Garissa counties, Kenya. Field surveys were implemented in December 2013 to February 2014 and laboratory analyses were completed in June 2015. Serum samples were harvested from blood samples obtained from randomly recruited subjects and screened for anti-RVF virus immunoglobulin G using inhibition ELISA (enzyme-linked immunosorbent assay) immunoassay. The household and subject metadata was collected using Open Data Kit (ODK) (https://opendatakit.org) loaded into smart phones. The aim of the project was to determine the risk of Rift Valley Fever virus exposure in people living in areas with different land use and socio-ecological settings. The data were collected by experienced researchers from the International Livestock Research Institute (Kenya), the Department of Disease Surveillance and Response, Kenyatta National Hospital This dataset is part of a wider research project, the Dynamic Drivers of Disease in Africa Consortium (DDDAC). The research was funded by NERC project no NE/J001570/1 with support from the Ecosystem Services for Poverty Alleviation Programme (ESPA). Additional funding was provided by the Consultative Group on International Agricultural Research (CGIAR) Research Program Agriculture for Nutrition and Health. Full details about this dataset can be found at https://doi.org/10.5285/8a668a4f-3526-4443-9e77-cea67f04ca19

The dataset provides observational information on events when humans are in contact with poultry in rural and urban Bangladesh. Data were collected during observation periods of three hours duration in three settings where humans and poultry have close interactions: rural households with domestic poultry and small-scale commercial farms in rural areas of Tangail district and market stalls that sell, slaughter and process live poultry in Dhaka city. Observations on hygiene or handwashing behaviours that take place before or after contact with poultry, poultry products (eggs, meat) or poultry waste (bedding, faeces or carcasses) were also recorded. A structured observation sheet was used to record the number of occurrences of pre-defined activities. The objective was to record the types of contact behaviours and proportion of human-poultry interactions that could result in human exposure to antibiotic-resistant bacteria carried by poultry. The research was part of a wider research project, Spatial and Temporal Dynamics of Antimicrobial Resistance (AMR) Transmission from the Outdoor Environment to Humans in Urban and Rural Bangladesh. The research was funded by NERC/BBSRC/MRC on behalf of the Antimicrobial Resistance Cross-Council Initiative, award NE/N019555/1. Full details about this dataset can be found at https://doi.org/10.5285/76f52a38-7a2c-49a3-b86f-cc40205459ef

Mosquito trap data from Kilombero Valley in Tanzania - a global hotspot for malaria. Since 2007, field entomologists working at Ifakara Health Institue (IHI) and at the University of Glasgow have been trapping and collecting primary malaria vectors for four villages in the Kilombero Valley: Lupiro, Kidugalo, Minepa and Sagamaganga. Trapped mosquitoes were identified to species level (Anopheles gambiae and A funestus), their sex recorded (male or female) and their abdominal status (fed or unfed) noted. When available, the daily mosquito data was consistently linked to micro climate data logger data (weather conditions on site, including averaged, minimum and maximum daytime and night time values for temperature, humidity and vapour pressure deficit). This long record allows exploring the relationship between malaria vector dynamics and related environmental conditions. Full details about this dataset can be found at https://doi.org/10.5285/89406b06-d0aa-4120-84db-a5f91b616053

This resource contains anonymised policy interviews on trypanosomiasis in Zambia from 2013 conducted by Catherine Grant (Institute of Development Studies) and Noreen Machila (University of Zambia, Department of Disease Control). These interviews explore the differing opinions of various stakeholders in relation to trypanosomiasis, a widespread and potentially fatal disease spread by tsetse flies which affects both humans and animals. It is an important time to examine this issue as human population growth and other factors have led to migration into new areas which are populated by tsetse flies and this may affect disease levels. This means that there is a greater risk to people and their livestock. Opinions on the best way to manage the disease are deeply divided (Source: Author Summary- Grant, C, Anderson, N and Machila, N [Accepted] Stakeholder narratives on trypanosomiasis, their effect on policy and the scope for One Health, Public Library of Science Neglected Tropical Diseases (PLOS NTD). This was part of a wider research project, the Dynamic Drivers of Disease in Africa Consortium (DDDAC) and these interviews contributed to this consortium. The research was funded by NERC project no NE/J001570/1 with support from the Ecosystem Services for Poverty Alleviation Programme (ESPA). Full details about this dataset can be found at https://doi.org/10.5285/727c1c4e-e097-44a4-abc7-74a4cc9acbfc

These data provide results from serological analysis carried out on serum collected from cattle (sample number = 460), goats (sample number = 949) and sheep (Sample number = 574) combined with data collected at the household and subject/animal levels at the time of serum sampling. The data collected at the household and subject/animal levels were: the total number of livestock owned by a household, altitude, geographical coordinates of the sampling sites; and breed, age, sex and body condition score of an animal. The research was carried out in irrigated and non-irrigated areas in Tana River County, Kenya. Field surveys were implemented in August to November 2013 and laboratory analyses were completed in June 2015. Serum samples were harvested from blood samples obtained from animals and screened for anti-Rift Valley Fever (RVF) virus immunoglobulin G using inhibition (enzyme-linked immunosorbent assay) ELISA immunoassay. The household data was collected using Open Data Kit (ODK) loaded into smart phones. The serological analysis was performed to determine the risk of Rift Valley Fever virus exposure in cattle, sheep and goats. The aim of the survey was to investigate whether land use change, specifically the conversion of rangeland into cropland, affected RVF exposure pattern in livestock. The data were collected by experienced researchers from the Ministry of Livestock Development Nairobi, Kenya and the International Livestock Research Institute (Kenya). This dataset is part of a wider research project, the Dynamic Drivers of Disease in Africa Consortium (DDDAC). The research was funded by NERC project no NE-J001570-1 with support from the Ecosystem Services for Poverty Alleviation Programme (ESPA). Additional funding was provided by Consultative Group on International Agricultural Research (CGIAR) Research Program Agriculture for Nutrition and Health led by International Food Policy Research Institute (IFPRI). Full details about this dataset can be found at https://doi.org/10.5285/b9756c4c-9894-4147-a260-a79067604a06

These dataset files show the calibration of a sensor for mercury (II) ions using a Fluorimeter and either HgCl2 or HgNO3. A range of different sample conditions are tested, including sensor concentrations and relative proportions of water and a methanol co-solvent (required for solubility of the probe). Also tested was the ability of acid to affect the probes sensitivity to mercury as nitric acid is needed for the stability of HgNO3 as an analyte. File names listed show the concentration of sensor and the ratio of water to methanol tested. Inductively coupled plasma mass spectrometry (ICP-MS) data are also given these are used to validate the sensors calibration and also to monitor the levels of soluble mercury content of dental amalgam samples held at either (11⁰C or 37⁰C) in water and saliva. The supernatant of these suspensions is filtered and measured using ICP-MS to give the data as reported. Full details about this nonGeographicDataset can be found at https://doi.org/10.5285/bc82f15b-8db6-4398-bfec-655a1eecf2d7

Antibiotic susceptibility tests are presented as the zone of inhibition using the disc-diffusion method, and categorized as resistant, intermediate or susceptible. DNA samples from antibiotic-resistant bacteria were analysed for the presence or absence of resistance genes using polymerase chain reaction (PCR). Laboratory analyses were conducted by trained staff at the International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b). The aim of the study was to identify the antibiotic-susceptibility profiles and resistance genes of bacteria (Escherichia coli) obtained from humans, poultry and the environment. Bacterial isolates previously identified with resistance to third-generation cephalosporins or carbapenems were included in the analysis. Bacterial samples originated from rural households and poultry farms (broiler chickens) in Mirzapur, Tangail district; and urban food markets in Dhaka city, Bangladesh. Environmental samples included surface water, water supply, wastewater, soil, animal faeces (poultry and cattle) and solid waste. The survey was part of a wider research project, Spatial and Temporal Dynamics of Antimicrobial Resistance Transmission from the Outdoor Environment to Humans in Urban and Rural Bangladesh. The research was funded by NERC/BBSRC/MRC on behalf of the Antimicrobial Resistance Cross-Council Initiative award NE/N019555/1. Full details about this dataset can be found at https://doi.org/10.5285/dda6dd55-f955-4dd5-bc03-b07cc8548a3d