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Featured researches published by Jonas Behets.


Microbial Ecology | 2005

Impact of Non- Legionella Bacteria on the Uptake and Intracellular Replication of Legionella pneumophila in Acanthamoeba castellanii and Naegleria lovaniensis

Priscilla Declerck; Jonas Behets; Yasmine Delaedt; Anca Margineanu; Elke Lammertyn; Frans Ollevier

In aquatic environments, Legionella pneumophila survives, in association with other bacteria, within biofilms by multiplying in free-living amoebae. The precise mechanisms underlying several aspects of the uptake and intracellular replication of L. pneumophila in amoebae, especially in the presence of other bacteria, remain unknown. In the present study, we examined the competitive effect of selected non-Legionella bacteria (Escherichia coli, Aeromonas hydrophila, Flavobacterium breve, and Pseudomonas aeruginosa) on the uptake of L. pneumophila serogroup 1 by the amoebae Acanthamoeba castellanii and Naegleria lovaniensis. We also investigated their possible influence on the intracellular replication of L. pneumophila in both amoeba species. Our results showed that the non-Legionella bacteria did not compete with L. pneumophila for uptake, suggesting that the amoeba hosts took in L. pneumophila through a specific and presumably highly efficient uptake mechanism. Living and heat-inactivated P. aeruginosa best supported the replication of L. pneumophila in N. lovaniensis and A. castellanii, respectively, whereas for both amoeba species, E. coli yielded the lowest number of replicated L. pneumophila. Furthermore, microscopic examination showed that 100% of the A. castellanii and only 2% of the N. lovaniensis population were infected with L. pneumophila at the end of the experiment. This study clearly shows the influence of some non-Legionella bacteria on the intracellular replication of L. pneumophila in A. castellanii and N. lovaniensis. It also demonstrates the different abilities of the two tested amoeba species to serve as a proper host for the replication and distribution of the human pathogen in man-made aquatic environments such as cooling towers, shower heads, and air conditioning systems with potential serious consequences for human health.


Parasitology Research | 2007

Survey for the presence of specific free-living amoebae in cooling waters from Belgian power plants

Jonas Behets; Priscilla Declerck; Yasmine Delaedt; L Verelst; Frans Ollevier

Free-living amoebae (FLA) are distributed ubiquitously in aquatic environments with increasing importance in hygienic, medical and ecological relationships to man. In this study, water samples from Belgian industrial cooling circuits were quantitatively surveyed for the presence of FLA. Isolated, thermotolerant amoebae were identified morphologically as well as using the following molecular methods: enzyme-linked immunosorbent assay and isoenzyme electrophoresis and PCR. Thermophilic amoebae were present at nearly all collection sites, and the different detection methods gave similar results. Naegleria fowleri was the most frequently encountered thermotolerant species, and concentrations of thermotolerant FLA were correlated with higher temperatures.


Journal of Applied Microbiology | 2007

Receptor‐mediated uptake of Legionella pneumophila by Acanthamoeba castellanii and Naegleria lovaniensis

Priscilla Declerck; Jonas Behets; B. De Keersmaecker; Frans Ollevier

Aims:  Investigation of the attachment and uptake of Legionella pneumophila by Acanthamoeba castellanii and Naegleria lovaniensis, as these are two critical steps in the subsequent bacterial survival in both amoeba hosts.


Current Microbiology | 2006

Quantitative Detection and Differentiation of Free-Living Amoeba Species Using SYBR Green–Based Real-Time PCR Melting Curve Analysis

Jonas Behets; Priscilla Declerck; Yasmine Delaedt; L Verelst; Frans Ollevier

Real-time polymerase chain reaction melting curve analysis (MCA) allows differentiation of several free-living amoebae species. Distinctive characteristics were found for Naegleria fowleri, N. lovaniensis, N. australiensis, N. gruberi, Hartmanella vermiformis, and Willaertia magna. Species specificity of the amplicons was confirmed using agarose gel electrophoresis and sequence-based approaches. Amplification efficiency ranged from 91% to 98%, indicating the quantitative potential of the assay. This MCA approach can be used for quantitative detection of free-living amoebae after cultivation but also as a culture-independent detection method.


Water Research | 2007

Detection of Legionella spp. and some of their amoeba hosts in floating biofilms from anthropogenic and natural aquatic environments

Priscilla Declerck; Jonas Behets; Vincent van Hoef; Frans Ollevier


Microbiological Research | 2009

Replication of Legionella pneumophila in biofilms of water distribution pipes

Priscilla Declerck; Jonas Behets; Anca Margineanu; Vincent van Hoef; Brenda De Keersmaecker; Frans Ollevier


Journal of Microbiological Methods | 2007

Development and evaluation of a Taqman duplex real-time PCR quantification method for reliable enumeration of Legionella pneumophila in water samples

Jonas Behets; Priscilla Declerck; Yasmine Delaedt; Bart Creemers; Frans Ollevier


Water Research | 2007

A duplex real-time PCR assay for the quantitative detection of Naegleria fowleri in water samples

Jonas Behets; Priscilla Declerck; Yasmine Delaedt; L Verelst; Frans Ollevier


Current Microbiology | 2007

Replication of Legionella pneumophila in Floating Biofilms

Priscilla Declerck; Jonas Behets; Vincent van Hoef; Frans Ollevier


Microbiological Research | 2008

The impact of electrochemical disinfection on Escherichia coli and Legionella pneumophila in tap water

Yasmine Delaedt; Arne Daneels; Priscilla Declerck; Jonas Behets; Jaak Ryckeboer; Elmar Peters; Frans Ollevier

Collaboration


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Frans Ollevier

Katholieke Universiteit Leuven

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Priscilla Declerck

Katholieke Universiteit Leuven

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Yasmine Delaedt

Katholieke Universiteit Leuven

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Vincent van Hoef

Katholieke Universiteit Leuven

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Elke Lammertyn

Katholieke Universiteit Leuven

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Arne Daneels

Katholieke Universiteit Leuven

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B. De Keersmaecker

Katholieke Universiteit Leuven

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Brenda De Keersmaecker

Katholieke Universiteit Leuven

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