24 research outputs found
Anthroponotic transmission of Cryptosporidium parvum predominates in countries with poorer sanitation - a systematic review and meta-analysis
Background: Globally cryptosporidiosis is one of the commonest causes of mortality in children under 24 months old and may be associated with important longterm health effects. Whilst most strains of Cryptosporidium parvum are zoonotic, C. parvum IIc is almost certainly anthroponotic. The global distribution of this potentially important emerging infection is not clear. Methods: We conducted a systematic review of papers identifying the subtype distribution of C. parvum infections globally. We searched PubMed and Scopus using the following key terms Cryptospor* AND parvum AND (genotyp* OR subtyp* OR gp60). Studies were eligible for inclusion if they had found C. parvum within their human study population and had subtyped some or all of these samples using standard gp60 subtyping. Pooled analyses of the proportion of strains being of the IIc subtype were determined using StatsDirect. Meta-regression analyses were run to determine any association between the relative prevalence of IIc and Gross Domestic Product, proportion of the population with access to improved drinking water and improved sanitation. Results: From an initial 843 studies, 85 were included in further analysis. Cryptosporidium parvum IIc was found in 43 of these 85 studies. Across all studies the pooled estimate of relative prevalence of IIc was 19.0% (95% CI: 12.9–25.9%), but there was substantial heterogeneity. In a meta-regression analysis, the relative proportion of all C. parvum infections being IIc decreased as the percentage of the population with access to improved sanitation increased and was some 3.4 times higher in those studies focussing on HIV-positive indivduals. Conclusions: The anthroponotic C. parvum IIc predominates primarily in lower-income countries with poor sanitation and in HIV-positive individuals. Given the apparent enhanced post-infectious virulence of the other main anthroponotic species of Cryptosporidium (C. hominis), it is important to learn about the impact of this subtype on human health
Anthroponotic transmission of Cryptosporidium parvum predominates in countries with poorer sanitation - a systematic review and meta-analysis
Background: Globally cryptosporidiosis is one of the commonest causes of mortality in children under 24 months old and may be associated with important longterm health effects. Whilst most strains of Cryptosporidium parvum are zoonotic, C. parvum IIc is almost certainly anthroponotic. The global distribution of this potentially important emerging infection is not clear. Methods: We conducted a systematic review of papers identifying the subtype distribution of C. parvum infections globally. We searched PubMed and Scopus using the following key terms Cryptospor* AND parvum AND (genotyp* OR subtyp* OR gp60). Studies were eligible for inclusion if they had found C. parvum within their human study population and had subtyped some or all of these samples using standard gp60 subtyping. Pooled analyses of the proportion of strains being of the IIc subtype were determined using StatsDirect. Meta-regression analyses were run to determine any association between the relative prevalence of IIc and Gross Domestic Product, proportion of the population with access to improved drinking water and improved sanitation. Results: From an initial 843 studies, 85 were included in further analysis. Cryptosporidium parvum IIc was found in 43 of these 85 studies. Across all studies the pooled estimate of relative prevalence of IIc was 19.0% (95% CI: 12.9–25.9%), but there was substantial heterogeneity. In a meta-regression analysis, the relative proportion of all C. parvum infections being IIc decreased as the percentage of the population with access to improved sanitation increased and was some 3.4 times higher in those studies focussing on HIV-positive indivduals. Conclusions: The anthroponotic C. parvum IIc predominates primarily in lower-income countries with poor sanitation and in HIV-positive individuals. Given the apparent enhanced post-infectious virulence of the other main anthroponotic species of Cryptosporidium (C. hominis), it is important to learn about the impact of this subtype on human health
Onsite sanitation systems and contamination of groundwater: A systematic review of the evidence for risk using the source-pathway receptor model
The level of risk that onsite sanitation systems (OSS) pose to groundwater quality remains uncertain. The link between contamination and OSS can only be proved if the source, pathway, and receptor are investigated and confirmed when assessing contamination. The literature on the connection between OSS and groundwater contamination has been reviewed several times but with limited assessments of the extent to which the literature confirms that the source of contamination is an OSS, that a pathway has been identified, and that the receptor is groundwater. A systematic review was conducted on published studies and supports previous work that concluded that the removal and transport of contaminants from OSS to groundwater is complex and varies significantly according to local conditions. This variability means simple siting guidelines based on horizontal separation are not reliable. Though not always recognised in the literature, formation of a biological layer is important for removal of microbial pathogens. This layer takes months to form which impacts the performance of OSS that are new or subject to highly variable loading. Under ideal conditions of an unsaturated zone comprising fine material, faecal indicator bacteria can be reduced to detection limits within 10 metres distance. However, ideal conditions are very often not present. Multiple studies showed the presence of viruses in the absence of faecal indicator bacteria. Ingress of contaminated surface water into faulty boreholes/wells and contamination of wells from users are both often significant yet not adequately covered in the included literature. The review established that it is extremely difficult to eliminate the risk of groundwater contamination when OSS effluent is discharged into the subsurface. It is unsafe to assume that contamination can be prevented in areas with high OSS density, and further research is needed to determine the critical density threshold for different ground conditions
Onsite sanitation systems and contamination of groundwater: A systematic review of the evidence for risk using the source-pathway-receptor model.
The level of risk that onsite sanitation systems (OSS) pose to groundwater quality remains uncertain. The link between contamination and OSS can only be proved if the source, pathway, and receptor (SPR) are investigated and confirmed when assessing contamination. The literature on the connection between OSS and groundwater contamination has been reviewed several times. However, previous reviews have made limited assessments of the extent to which the literature confirms that the source of contamination is an OSS, that a pathway has been identified, and that the receptor is groundwater, mainly due to uncertainties or insufficiencies in reported methodologies.
A systematic review was conducted on published studies with the aim of establishing the state of knowledge of groundwater contamination from onsite sanitation systems that infiltrate wastewater into ground, such as pit latrines and septic tank systems. The quality of the methods used to establish the source, pathway and receptor was assessed. The review focussed on three main contaminants: bacteria, viruses and nitrates.
Scopus, PubMed, and Web of Science databases were searched, screening criterion developed and applied, and 60 eligible papers were identified. 35 of these were rated as having a “strong methodology”. The selected studies were assessed to identify areas of knowledge regarding the interaction of OSS with groundwater where there is strong supportive evidence and where there are knowledge gaps.
The review supports previous work that has concluded that the removal and transport of contaminants from OSS to groundwater is complex and varies significantly according to local conditions, including the nature of the ground materials, groundwater levels, ground moisture and other factors. This variability means simple siting guidelines based on horizontal separation are not reliable.
Though not always recognised in the literature, formation of a biological layer is important for removal of microbial pathogens. This layer takes months to form which impacts the performance of OSS that are new or subject to highly variable loading or sudden increases in hydraulic load.
Under ideal conditions of an unsaturated zone comprising fine material (sands, silts, loams with some clay content, Faecal indicator bacteria can be reduced to detection limits within 10 metres distance. However, ideal conditions are very often not present. Multiple studies showed the presence of viruses in the absence of faecal indicator bacteria. Contamination can also occur via localised pathways, but these have not been thoroughly investigated. Contribution of the ingress of contaminated surface water into faulty boreholes/wells and contamination of wells through the spigot or spout from users are both often significant yet not adequately covered in the included literature.
The review established that it is extremely difficult to eliminate the risk of groundwater contamination when OSS effluent is discharged into the subsurface. Generally, it seems unsafe to assume that contamination can be prevented in areas where OSS occur with any frequency
Comparative Epidemiology of <i>Salmonella</i> Paratyphi A and <i>Salmonella</i> Typhi Causing Enteric Fever, Bangladesh, 2018–2020
Enteric fever remains a public health challenge. We analyzed (95% CI 41–117)/100,000 PY for paratyphoid and 887 (95% data from a cluster-randomized Vi-tetanus toxoid conjugate CI 715–1,088)/100,000 PY for typhoid. Lack of private toilets vaccine trial to compare the epidemiology between Salmo- and safe drinking water were associated with both diseases. nella enterica serovars Paratyphi A, which causes para- Prevalence of multidrug resistance was significantly higher typhoid fever, and Typhi, which causes typhoid fever. The in Salmonella Typhi (20.2%) than in Salmonella Paratyphi A overall incidence rate of paratyphoid fever was 27 (95% CI (0.8%) (p<0.001). Our data suggest that integrated control 23–32)/100,000 person-years (PY) and of typhoid fever was measures targeting water, sanitation, and hygiene measures 216 (95% CI 198–236)/100,000 PY. We observed the highest and bivalent vaccine targeting both pathogens are promising incidence for both diseases in children 2–4 years of age: 72 strategies to control both diseases
The Green, Green Grass of Home: an archaeo-ecological approach to pastoralist settlement in central Kenya
© 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This paper considers the ecological residues of pastoralist occupation at the site of Maili Sita in Laikipia, central Kenya, drawing links with the archaeological record so as to contribute a fresh approach to the ephemeral settlement sites of mobile herding communities, a methodological aspect of African archaeology that remains problematic. Variations in the geochemical and micromorphological composition of soils along transects across the site are compared with vegetation distributions and satellite imagery to propose an occupation pattern not dissimilar to contemporary Cushitic-speaking groups further north. We argue that Maili Sita exemplifies the broad migratory and cultural exchange networks in place during the mid- to late second millennium AD, with pastoralist occupants who were both physically and culturally mobile.British Academy (2002-5 Funding)
European Union - Marie Curie Initiatives (EXT grant 2007-11
Age-dependent acquisition of IgG antibodies to Shigella serotypes-a retrospective analysis of seroprevalence in Kenyan children with implications for infant vaccination.
BACKGROUND: Shigellosis mainly affects children under 5 years of age living in low- and middle-income countries, who are the target population for vaccination. There are, however, limited data available to define the appropriate timing for vaccine administration in this age group. Information on antibody responses following natural infection, proxy for exposure, could help guide vaccination strategies. METHODS: We undertook a retrospective analysis of antibodies to five of the most prevalent Shigella serotypes among children aged <5 years in Kenya. Serum samples from a cross-sectional serosurvey in three Kenyan sites (Nairobi, Siaya, and Kilifi) were analyzed by standardized ELISA to measure IgG against Shigella sonnei and Shigella flexneri 1b, 2a, 3a, and 6. We identified factors associated with seropositivity to each Shigella serotype, including seropositivity to other Shigella serotypes. RESULTS: A total of 474 samples, one for each participant, were analyzed: Nairobi (n = 169), Siaya (n = 185), and Kilifi (n = 120). The median age of the participants was 13.4 months (IQR 7.0-35.6), and the male:female ratio was 1:1. Geometric mean concentrations (GMCs) for each serotype increased with age, mostly in the second year of life. The overall seroprevalence of IgG antibodies increased with age except for S. flexneri 6 which was high across all age subgroups. In the second year of life, there was a statistically significant increase of antibody GMCs against all five serotypes (p = 0.01-0.0001) and a significant increase of seroprevalence for S. flexneri 2a (p = 0.006), S. flexneri 3a (p = 0.006), and S. sonnei (p = 0.05) compared with the second part of the first year of life. Among all possible pairwise comparisons of antibody seropositivity, there was a significant association between S. flexneri 1b and 2a (OR = 6.75, 95% CI 3-14, p < 0.001) and between S. flexneri 1b and 3a (OR = 23.85, 95% CI 11-54, p < 0.001). CONCLUSION: Children living in low- and middle-income settings such as Kenya are exposed to Shigella infection starting from the first year of life and acquire serotype-specific antibodies against multiple serotypes. The data from this study suggest that Shigella vaccination should be targeted to infants, ideally at 6 or at least 9 months of age, to ensure children are protected in the second year of life when exposure significantly increases
Age-dependent acquisition of IgG antibodies to Shigella serotypes—a retrospective analysis of seroprevalence in Kenyan children with implications for infant vaccination
BackgroundShigellosis mainly affects children under 5 years of age living in low- and middle-income countries, who are the target population for vaccination. There are, however, limited data available to define the appropriate timing for vaccine administration in this age group. Information on antibody responses following natural infection, proxy for exposure, could help guide vaccination strategies.MethodsWe undertook a retrospective analysis of antibodies to five of the most prevalent Shigella serotypes among children aged <5 years in Kenya. Serum samples from a cross-sectional serosurvey in three Kenyan sites (Nairobi, Siaya, and Kilifi) were analyzed by standardized ELISA to measure IgG against Shigella sonnei and Shigella flexneri 1b, 2a, 3a, and 6. We identified factors associated with seropositivity to each Shigella serotype, including seropositivity to other Shigella serotypes.ResultsA total of 474 samples, one for each participant, were analyzed: Nairobi (n = 169), Siaya (n = 185), and Kilifi (n = 120). The median age of the participants was 13.4 months (IQR 7.0–35.6), and the male:female ratio was 1:1. Geometric mean concentrations (GMCs) for each serotype increased with age, mostly in the second year of life. The overall seroprevalence of IgG antibodies increased with age except for S. flexneri 6 which was high across all age subgroups. In the second year of life, there was a statistically significant increase of antibody GMCs against all five serotypes (p = 0.01–0.0001) and a significant increase of seroprevalence for S. flexneri 2a (p = 0.006), S. flexneri 3a (p = 0.006), and S. sonnei (p = 0.05) compared with the second part of the first year of life. Among all possible pairwise comparisons of antibody seropositivity, there was a significant association between S. flexneri 1b and 2a (OR = 6.75, 95% CI 3–14, p < 0.001) and between S. flexneri 1b and 3a (OR = 23.85, 95% CI 11–54, p < 0.001).ConclusionChildren living in low- and middle-income settings such as Kenya are exposed to Shigella infection starting from the first year of life and acquire serotype-specific antibodies against multiple serotypes. The data from this study suggest that Shigella vaccination should be targeted to infants, ideally at 6 or at least 9 months of age, to ensure children are protected in the second year of life when exposure significantly increases
Multiple introductions of multidrug-resistant typhoid associated with acute infection and asymptomatic carriage, Kenya
BACKGROUND: Understanding the dynamics of infection and carriage of typhoid in endemic settings is critical to finding solutions to prevention and control. METHODS: In a 3-year case-control study, we investigated typhoid among children aged <16 years (4670 febrile cases and 8549 age matched controls) living in an informal settlement, Nairobi, Kenya. RESULTS: 148 S. Typhi isolates from cases and 95 from controls (stool culture) were identified; a carriage frequency of 1 %. Whole-genome sequencing showed 97% of cases and 88% of controls were genotype 4.3.1 (Haplotype 58), with the majority of each (76% and 88%) being multidrug-resistant strains in three sublineages of the H58 genotype (East Africa 1 (EA1), EA2, and EA3), with sequences from cases and carriers intermingled. CONCLUSIONS: The high rate of multidrug-resistant H58 S. Typhi, and the close phylogenetic relationships between cases and controls, provides evidence for the role of carriers as a reservoir for the community spread of typhoid in this setting. FUNDING: National Institutes of Health (R01AI099525); Wellcome Trust (106158/Z/14/Z); European Commission (TyphiNET No 845681); National Institute for Health Research (NIHR); Bill and Melinda Gates Foundation (OPP1175797)
