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Ranford-Cartwright, L.

Publications and source records attributed to Ranford-Cartwright, L..

2 recordsLinked to original sources

Prediction of malaria mosquito species and population age structure using mid-infrared spectroscopy and supervised machine learning

Despite the global efforts made in the fight against malaria, the disease is resurging. One of the main causes is the resistance that Anopheles mosquitoes, vectors of the disease, have developed to insecticides. Anopheles must survive for at least 12 days to possibly transmit malaria. Therefore, to evaluate and improve malaria vector control interventions, it is imperative to monitor and accurately estimate the age distribution of mosquito populations as well as total population sizes. However, estimating mosquito age is currently a slow, imprecise, and labour-intensive process that can only distinguish under-from over-four-day-old female mosquitoes. Here, we demonstrate a machine-learning based approach that utilizes mid-infrared spectra of mosquitoes to characterize simultaneously, and with unprecedented accuracy, both age and species identity of females of the malaria vectors Anopheles gambiae and An. arabiensis mosquitoes within their respective populations. The prediction of the age structures was statistically indistinguishable from true modelled distributions. The method has a negligible cost per mosquito, does not require highly trained personnel, is substantially faster than current techniques, and so can be easily applied in both laboratory and field settings. Our results show that, with larger mid-infrared spectroscopy data sets, this technique can be further improved and expanded to vectors of other diseases such as Zika and Dengue.

bioinformatics

Detection Of Human Disease Conditions By Single-Cell Morpho-Rheological Phenotyping Of Whole Blood

Blood is arguably the most important bodily fluid and its analysis provides crucial health status information. A first routine measure to narrow down diagnosis in clinical practice is the differential blood count, determining the frequency of all major blood cells. What is lacking to advance initial blood diagnostics is an unbiased and quick functional assessment of blood that can narrow down the diagnosis and generate specific hypotheses. To address this need, we introduce the continuous, cell-by-cell morpho-rheological (MORE) analysis of whole blood, without labeling, enrichment or separation, at rates of 1,000 cells/sec. In a drop of blood we can identify all major blood cells and characterize their pathological changes in several disease conditions in vitro and in patient samples. This approach takes previous results of mechanical studies on specifically isolated blood cells to the level of application directly in whole blood and adds a functional dimension to conventional blood analysis.

biophysics