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1.
J Microsc ; 294(3): 397-410, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38691400

ABSTRACT

In the dynamic landscape of scientific research, imaging core facilities are vital hubs propelling collaboration and innovation at the technology development and dissemination frontier. Here, we present a collaborative effort led by Global BioImaging (GBI), introducing international recommendations geared towards elevating the careers of Imaging Scientists in core facilities. Despite the critical role of Imaging Scientists in modern research ecosystems, challenges persist in recognising their value, aligning performance metrics and providing avenues for career progression and job security. The challenges encompass a mismatch between classic academic career paths and service-oriented roles, resulting in a lack of understanding regarding the value and impact of Imaging Scientists and core facilities and how to evaluate them properly. They further include challenges around sustainability, dedicated training opportunities and the recruitment and retention of talent. Structured across these interrelated sections, the recommendations within this publication aim to propose globally applicable solutions to navigate these challenges. These recommendations apply equally to colleagues working in other core facilities and research institutions through which access to technologies is facilitated and supported. This publication emphasises the pivotal role of Imaging Scientists in advancing research programs and presents a blueprint for fostering their career progression within institutions all around the world.


Subject(s)
Research Personnel , Humans , Career Mobility , Biomedical Research/methods , Career Choice
2.
Nat Microbiol ; 4(6): 941-947, 2019 06.
Article in English | MEDLINE | ID: mdl-30911126

ABSTRACT

Malaria, a major cause of child mortality in Africa, is engendered by Plasmodium parasites that are transmitted by anopheline mosquitoes. Fitness of Plasmodium parasites is closely linked to the ecology and evolution of its anopheline vector. However, whether the genetic structure of vector populations impacts malaria transmission remains unknown. Here, we describe a partitioning of the African malaria vectors into generalists and specialists that evolve along ecological boundaries. We next identify the contribution of mosquito species to Plasmodium abundance using Granger causality tests for time-series data collected over two rainy seasons in Mali. We find that mosquito microevolution, defined by changes in the genetic structure of a population over short ecological timescales, drives Plasmodium dynamics in nature, whereas vector abundance, infection prevalence, temperature and rain have low predictive values. Our study demonstrates the power of time-series approaches in vector biology and highlights the importance of focusing local vector control strategies on mosquito species that drive malaria dynamics.


Subject(s)
Evolution, Molecular , Mosquito Vectors/genetics , Mosquito Vectors/parasitology , Plasmodium falciparum/physiology , Animals , Anopheles/genetics , Ecosystem , Genotype , Humans , Insect Proteins/genetics , Malaria/epidemiology , Malaria/transmission , Mali , Prevalence , Rain , Seasons , Species Specificity , Temperature
3.
PLoS One ; 7(1): e28694, 2012.
Article in English | MEDLINE | ID: mdl-22272225

ABSTRACT

Mitochondria exist as a network of interconnected organelles undergoing constant fission and fusion. Current approaches to study mitochondrial morphology are limited by low data sampling coupled with manual identification and classification of complex morphological phenotypes. Here we propose an integrated mechanistic and data-driven modeling approach to analyze heterogeneous, quantified datasets and infer relations between mitochondrial morphology and apoptotic events. We initially performed high-content, multi-parametric measurements of mitochondrial morphological, apoptotic, and energetic states by high-resolution imaging of human breast carcinoma MCF-7 cells. Subsequently, decision tree-based analysis was used to automatically classify networked, fragmented, and swollen mitochondrial subpopulations, at the single-cell level and within cell populations. Our results revealed subtle but significant differences in morphology class distributions in response to various apoptotic stimuli. Furthermore, key mitochondrial functional parameters including mitochondrial membrane potential and Bax activation, were measured under matched conditions. Data-driven fuzzy logic modeling was used to explore the non-linear relationships between mitochondrial morphology and apoptotic signaling, combining morphological and functional data as a single model. Modeling results are in accordance with previous studies, where Bax regulates mitochondrial fragmentation, and mitochondrial morphology influences mitochondrial membrane potential. In summary, we established and validated a platform for mitochondrial morphological and functional analysis that can be readily extended with additional datasets. We further discuss the benefits of a flexible systematic approach for elucidating specific and general relationships between mitochondrial morphology and apoptosis.


Subject(s)
Apoptosis/physiology , Mitochondria/physiology , Models, Biological , Signal Transduction/physiology , Apoptosis/drug effects , Camptothecin/pharmacology , Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology , Cell Line, Tumor , Electron Transport Complex IV/genetics , Electron Transport Complex IV/metabolism , Fuzzy Logic , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Humans , Membrane Potential, Mitochondrial/drug effects , Microscopy, Fluorescence , Mitochondria/drug effects , Mitochondria/metabolism , Mitochondrial Proteins/genetics , Mitochondrial Proteins/metabolism , Oligomycins/pharmacology , Protein Transport/drug effects , Signal Transduction/drug effects , Thapsigargin/pharmacology , Tumor Necrosis Factor-alpha/pharmacology , bcl-2-Associated X Protein/genetics , bcl-2-Associated X Protein/metabolism
4.
Vet Parasitol ; 146(3-4): 352-6, 2007 May 31.
Article in English | MEDLINE | ID: mdl-17418951

ABSTRACT

Besnoitia besnoiti, an apicomplexan protozoan parasite, is the causative agent of bovine besnoitiosis. This infection may dramatically affect body condition, and, in males, lead to irreversible infertility. While identification of clinical cases and their histopathological confirmation is relatively simple to carry out, finding subclinical forms of infection is more difficult, thus a more sensitive test for the identification of the etiological agent may be an appropriate diagnostic tool. We have developed the ITS1 rDNA-sequence-based conventional and real-time PCR which are highly sensitive and specific for the detection of B. besnoiti infection in cattle. A recombinant internal positive control was introduced to assess possible sample-related inhibitory effects during the amplification reaction and, in order to prevent false-positive results, a pre-PCR treatment of potentially contaminating dU-containing PCR product with uracil-DNA-glycosylase (UDG) was followed.


Subject(s)
Cattle Diseases/parasitology , Coccidiosis/veterinary , DNA, Ribosomal Spacer/genetics , Polymerase Chain Reaction/veterinary , Sarcocystidae/genetics , Sarcocystidae/isolation & purification , Skin/parasitology , Animals , Cattle , Cattle Diseases/diagnosis , Coccidiosis/diagnosis , Coccidiosis/parasitology , DNA, Ribosomal Spacer/analysis , Sensitivity and Specificity
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