scholarly journals Case-control design identifies ecological drivers of endemic coral diseases

2019 ◽  
Author(s):  
Jamie M. Caldwell ◽  
Greta Aeby ◽  
Scott F. Heron ◽  
Megan J. Donahue

AbstractEndemic disease transmission is an important ecological process that is challenging to study because of low occurrence rates. Here, we investigate the ecological drivers of two coral diseases -- growth anomalies and tissue loss -- affecting five coral species. We first show that a statistical framework called the case-control study design, commonly used in epidemiology but rarely applied to ecology, provided high predictive accuracy (67-82%) and disease detection rates (60-83%) compared with a traditional statistical approach that yielded high accuracy (98-100%) but low disease detection rates (0-17%). Using this framework, we found evidence that 1) larger corals have higher disease risk; 2) shallow reefs with low herbivorous fish abundance, limited water motion, and located adjacent to watersheds with high fertilizer and pesticide runoff promote low levels of growth anomalies, a chronic coral disease; and 3) wave exposure, stream exposure, depth, and low thermal stress are associated with tissue loss disease risk during interepidemic periods. Variation in risk factors across host-disease pairs suggests that either different pathogens cause the same gross lesions in different species or that the same disease may arise in different species under different ecological conditions.

2021 ◽  
Author(s):  
◽  
Gareth John Williams

<p>Coral diseases are a major threat to coral reef health and functioning worldwide. Little is known about how coral disease prevalence relates to multiple interacting changes in host densities, abiotic stressors, and levels of human impact. In particular, almost nothing is known about coral disease dynamics under changing abiotic conditions in the absence of direct anthropogenic stressors. Understanding how disease dynamics change relative to shifts in environmental conditions is crucial for the successful management and future survival of coral reefs. With the use of existing and novel field data and statistical modeling I examined the associations (abiotic and biotic) of multiple coral disease states across a variety of spatial scales encompassing a wide range of environmental conditions. Biomedical techniques were then used to relate these environmental associations to potential disease etiology. Study sites included areas with high levels of anthropogenic impact (e.g. Oahu, main Hawaiian Islands); to extremely remote quasi-pristine reefs removed from direct human influence (e.g. Palmyra Atoll National Wildlife Refuge). Over small spatial scales (100s m) at a marine reserve in the main Hawaiian Islands I modelled the spatial patterns of four coral diseases (Porites growth anomalies, Porites tissue loss, Porites trematodiasis and Montipora white syndrome). While Porites tissue loss and Montipora white syndrome were positively associated with poor environmental conditions (poor water quality, low coral cover), Porites growth anomalies and Porites trematodiasis were more prevalent in areas considered to be of superior quality (clearer water, increased host abundance, higher numbers of fish). At Palmyra Atoll, fatal tissue loss diseases were largely absent and although coral growth anomalies were present their prevalence was extremely low. Patterns of growth anomaly prevalence at Palmyra were positively associated with host abundance across four coral genera (Acropora, Astreopora, Montipora and Porites) and generally negatively associated with algal cover. Growth anomalies, although progressive and detrimental to the hosts, were most prevalent in the "healthiest" regions (the highest coral cover regions) of Palmyra. I hypothesised that differences seen in the types and prevalence of coral diseases between heavily populated parts of Hawaii and remote uninhabited locations such as Palmyra Atoll, could be a result of differing levels of either direct (e.g. pollution) or indirect (e.g. pollution leading to loss of key hosts) human stressors, in addition to natural changes in the environment. To begin disentangling the confounding effects of natural variability and human stressors on coral disease prevalence patterns I modelled two diseases (Acropora and Porites growth anomalies) across hundreds of sites throughout the Indo-Pacific Ocean (1000s km). Predictors included host densities, human population numbers, frequency of sea surface temperature anomalies, and input of ultra-violet radiation. Porites growth anomaly prevalence was positively associated with human population density (and to a lesser extent host density), while the prevalence of Acropora growth anomalies was strongly host density dependent. The positive association between the prevalence of Porites growth anomalies and human density suggests the presence and prevalence of the disease are related, directly or indirectly, to some environmental co-factor associated with increased human density at regional spatial scales. Although this association has been widely posited, this is one of the first wide scale studies unambiguously linking a coral disease with human population size. In summary, the types of coral diseases observed, their prevalence, and spatial patterns of distribution within reef systems are the result of multiple abiotic and biotic factors and stressors interacting, in some cases synergistically. Statistical modelling, in conjunction with biomedical techniques and field observations, proved essential to the understanding of coral disease ecology within single reefs and atolls to patterns across entire oceans.</p>


2018 ◽  
Vol 20 (1) ◽  
pp. 17-24
Author(s):  
Hanieh Mohammadi ◽  
Narges Razavi ◽  
Ali Abbasi ◽  
Faezeh Babaei ◽  
Ensiyeh Seyedrezazadeh ◽  
...  

2012 ◽  
Vol 140 (11) ◽  
pp. 1993-2002 ◽  
Author(s):  
B. J. SILK ◽  
M. R. MOORE ◽  
M. BERGTHOLDT ◽  
R. J. GORWITZ ◽  
N. A. KOZAK ◽  
...  

SUMMARYTravel is a risk factor for Legionnaires' disease. In 2008, two cases were reported in condominium guests where we investigated a 2001 outbreak. We reinvestigated to identify additional cases and determine whether ongoing transmission resulted from persistent colonization of potable water. Exposures were assessed by matched case-control analyses (2001) and case-series interviews (2008). We sampled potable water and other water sources. Isolates were compared using sequence-based typing. From 2001 to 2008, 35 cases were identified. Confirmed cases reported after the cluster in 2001–2002 were initially considered sporadic, but retrospective case-finding identified five additional cases. Cases were more likely than controls to stay in tower 2 of the condominium [matched odds ratio (mOR) 6·1, 95% confidence interval (CI) 1·6–22·9]; transmission was associated with showering duration (mOR 23·0, 95% CI 1·4–384). We characterized a clinical isolate as sequence type 35 (ST35) and detected ST35 in samples of tower 2's potable water in 2001, 2002, and 2008. This prolonged outbreak illustrates the importance of striving for permanent Legionella eradication from potable water.


2021 ◽  
Vol 20 (1) ◽  
Author(s):  
C. Airoldi ◽  
C. Magnani ◽  
F. Lazzarato ◽  
D. Mirabelli ◽  
S. Tunesi ◽  
...  

Abstract Background Neighborhood exposure to asbestos increases the risk of developing malignant mesothelioma (MM) in residents who live near asbestos mines and asbestos product plants. The area of Casale Monferrato (Northwest Italy) was impacted by several sources of asbestos environmental pollution, due to the presence of the largest Italian asbestos cement (AC) plant. In the present study, we examined the spatial variation of MM risk in an area with high levels of asbestos pollution and secondly, and we explored the pattern of clustering. Methods A population-based case–control study conducted between 2001 and 2006 included 200 cases and 348 controls. Demographic and occupational data along with residential information were recorded. Bivariate Kernel density estimation was used to map spatial variation in disease risk while an adjusted logistic model was applied to estimate the impact of residential distance from the AC plant. Kulldorf test and Cuzick Edward test were then performed. Results One hundred ninety-six cases and 322 controls were included in the analyses. The contour plot of the cases to controls ratio showed a well-defined peak of MM incidence near the AC factory, and the risk decreased monotonically in all directions when large bandwidths were used. However, considering narrower smoothing parameters, several peaks of increased risk were reported. A constant trend of decreasing OR with increasing distance was observed, with estimates of 10.9 (95% CI 5.32–22.38) and 10.48 (95%CI 4.54–24.2) for 0–5 km and 5–10 km, respectively (reference > 15 km). Finally, a significant (p < 0.0001) excess of cases near the pollution source was identified and cases are spatially clustered relative to the controls until 13 nearest neighbors. Conclusions In this study, we found an increasing pattern of mesothelioma risk in the area around a big AC factory and we detected secondary clusters of cases due to local exposure points, possibly associated to the use of asbestos materials.


1991 ◽  
Vol 89 (1) ◽  
pp. 59-67 ◽  
Author(s):  
Matti Jauhiainen ◽  
Pekka Koskinen ◽  
Christian Ehnholm ◽  
M.Heikki Frick ◽  
Matti Mänttäri ◽  
...  

2015 ◽  
Vol 49 (0) ◽  
Author(s):  
Lorena Dias Monteiro ◽  
Francisco Rogerlândio Martins-Melo ◽  
Aline Lima Brito ◽  
Carlos Henrique Alencar ◽  
Jorg Heukelbach

ABSTRACT OBJECTIVE To describe the spatial patterns of leprosy in the Brazilian state of Tocantins. METHODS This study was based on morbidity data obtained from the Sistema de Informações de Agravos de Notificação (SINAN – Brazilian Notifiable Diseases Information System), of the Ministry of Health. All new leprosy cases in individuals residing in the state of Tocantins, between 2001 and 2012, were included. In addition to the description of general disease indicators, a descriptive spatial analysis, empirical Bayesian analysis and spatial dependence analysis were performed by means of global and local Moran’s indexes. RESULTS A total of 14,542 new cases were recorded during the period under study. Based on the annual case detection rate, 77.0% of the municipalities were classified as hyperendemic (> 40 cases/100,000 inhabitants). Regarding the annual case detection rate in < 15 years-olds, 65.4% of the municipalities were hyperendemic (10.0 to 19.9 cases/100,000 inhabitants); 26.6% had a detection rate of grade 2 disability cases between 5.0 and 9.9 cases/100,000 inhabitants. There was a geographical overlap of clusters of municipalities with high detection rates in hyperendemic areas. Clusters with high disease risk (global Moran’s index: 0.51; p < 0.001), ongoing transmission (0.47; p < 0.001) and late diagnosis (0.44; p < 0.001) were identified mainly in the central-north and southwestern regions of Tocantins. CONCLUSIONS We identified high-risk clusters for transmission and late diagnosis of leprosy in the Brazilian state of Tocantins. Surveillance and control measures should be prioritized in these high-risk municipalities.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Levente Kriston

Abstract Background Infectious disease predictions models, including virtually all epidemiological models describing the spread of the SARS-CoV-2 pandemic, are rarely evaluated empirically. The aim of the present study was to investigate the predictive accuracy of a prognostic model for forecasting the development of the cumulative number of reported SARS-CoV-2 cases in countries and administrative regions worldwide until the end of May 2020. Methods The cumulative number of reported SARS-CoV-2 cases was forecasted in 251 regions with a horizon of two weeks, one month, and two months using a hierarchical logistic model at the end of March 2020. Forecasts were compared to actual observations by using a series of evaluation metrics. Results On average, predictive accuracy was very high in nearly all regions at the two weeks forecast, high in most regions at the one month forecast, and notable in the majority of the regions at the two months forecast. Higher accuracy was associated with the availability of more data for estimation and with a more pronounced cumulative case growth from the first case to the date of estimation. In some strongly affected regions, cumulative case counts were considerably underestimated. Conclusions With keeping its limitations in mind, the investigated model may be used for the preparation and distribution of resources during the initial phase of epidemics. Future research should primarily address the model’s assumptions and its scope of applicability. In addition, establishing a relationship with known mechanisms and traditional epidemiological models of disease transmission would be desirable.


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