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Woods Hole Oceanographic Institution

Tim Verslycke
Tim A. G. Verslycke's photoTim Verslycke
Guest Investigator
Biology

Contact Information:
Work: 508 289 3729
tverslycke@whoi.edu
Building: Redfield 310

http://gradientcorp.com/people/talent.php?last=Verslycke

Mailing Address:
Mailstop 32
Woods Hole Oceanographic Institution
Woods Hole, MA 02543

Background
I graduated from Ghent University (Ghent, Belgium) in 1999 as a Bio-engineer with a Master in Environmental Technology. I received a Ph.D. in Applied Biological Sciences from the same university in September 2003 through my research on the effects of hormone disruptors on estuarine invertebrate species in the Laboratory of Environmental Toxicology and Aquatic Ecology. In November 2003, I started an 18-month position as a postdoctoral scholar in the Biology Department at the Woods Hole Oceanographic Institution (Woods Hole, USA). My goals are to continue to investigate chemical effects in marine invertebrates at the molecular, organismal and population level using interdisciplinary approaches. At WHOI, I am currently a Visiting Investigator in Dr. Stegeman's Toxicology lab which has a long and established expertise in studying the presence, function and inducibility of cytochrome P-450 enzymes in marine animals.  Since my arrival, I have been awarded a Belgian American Educational Foundation Fellowship and several other research grants (see projects section) to continue my research on endocrine disruption in marine invertebrates. In January 2008, I joined the environmental consultancy Gradient Corporation (www.gradientcorp.com) in Cambridge (MA) as a Senior Environmental Toxicologist, where I am involved in environmental risk assessments, product safety studies, pharmaceuticals in the environment, and endocrine disruptor projects.

Outreach and Teaching
Tim Verslycke has allocated a significant amount of his time to bringing science to the public, decision-makers and other potential users. He was member of the scientific expert group of the 'Centre for Health and Environment' which provides information to the Flemish authorities on the impact of the environment on the health of the Flemish society. He has presented his research and marine ecotoxicological research in general at several venues, such as the annual Flemish Science Week and Science Fair, Ostend Fisheries Festival, Project Expeditie Zeeleeuw (an e-learning project), Faculty Open House days,... In addition, he has written publications in gray literature to inform general public about chemical effects on our marine ecosystems.
Tim Verslycke has taught field and laboratory classes in marine ecotoxicology and marine ecology to graduate and master-level students at Ghent University. In addition, he has supervised the graduate thesis research of several students in the Laboratory of Environmental Toxicology and Aquatic Ecology (Ghent University).

Research Interests - Endocrine disruption in invertebrates
I wrote this commentary for the e.hormone website at Tulane University (http://e.hormone.tulane.edu/newsAndViews.html) and it broadly talks about my research interests.

In December 1998, more than 40 scientists from Europe, Japan, and North America joined forces during a workshop in The Netherlands on endocrine disruption in invertebrates.  The driving force behind this workshop was the observation that all ongoing discussions and debates at that time omitted the majority of animals on our planet - the invertebrates.  While I didn’t attend that workshop, it is not hard to imagine that the participants hoped their views and ideas would quickly right this wrong.  Now, almost seven years later, the story continues …

It is frustrating, and frankly not a very nice thing, to keep beating a dead horse, but here’s my attempt.  In many ways, it is not surprising to see a bias in any discussion or debate, regulatory or funding program that deals with animals.  The animals we commonly think of, such as mammals, fish and birds, all belong to a single subgroup within the 30 some phyla comprising the animal Kingdom.  On the other hand, hundreds of thousands of invertebrate species make up most of the animal diversity on earth and account for more than 95% of all known species.  These animals are virtually unknown to non-scientists.  Despite their huge abundance, they live secret lives, generously providing us with food, clean environments, and life itself. 

First and for the ecological reasons described above, one would hope that any comprehensive program that seeks to protect our environment from the potential harmful effects of endocrine disruptors includes the invertebrates.  Secondly, hormonal regulation is a characteristic common to all animals, and invertebrates generally use their endocrine systems to regulate processes similar to those found in the vertebrates, processes such as growth, development and reproduction.  Thirdly, a growing (though still very limited) number of field examples of endocrine disruption affecting invertebrate populations have been published, and it is suspected that many more cases are still undetected.  Finally, invertebrates have been used for decades as important models for research, and they are crucial components of chemical regulatory screening and testing programs all over the world.  So, what is the present and potential future role of invertebrates in endocrine disruptor research and in testing and screening programs?    

Current regulatory efforts to screen and test chemicals for endocrine toxicity largely focus on effects on humans.  In the US, the Environmental Protection Agency (EPA) identified endocrine disruptors as one of its top six research priorities in 1996.  The EPA was mandated to develop a screening program, using appropriate validated test systems and other scientifically relevant information, to determine whether certain substances may have an effect in humans similar to the effect produced by naturally occurring estrogen.  Since then, EPA’s focus has been extended to include effects on vertebrate androgen and thyroid systems, and non-vertebrate animals.   Specifically, one arthropod assay is being proposed for in vivo testing, a mysid assay (mysids are small crustaceans).  On an international level, a task force on endocrine disruptor testing and assessment was established at the request of the Organization for Economic Cooperation and Development (OECD) in 1998.  OECD recently published a draft detailed review paper on the use of aquatic arthropods for endocrine disruptor studies, which includes specifics on life cycle and multi-generation testing with mysids, daphnids, copepods, and chironomids.  A number of other countries (notably Japan) and non-governmental organizations have set up programs addressing policy, regulation and scientific research that include one or more arthropod models.  Unfortunately, the focus of current testing programs on three vertebrate signaling pathways (estrogen, androgen, and thyroid) poses the risk of seriously underestimating the ecological effects of endocrine disruptors.  None of these three pathways nor their respective receptors, have been identified in the invertebrate species that are presently being considered for in vivo testing.  Most likely, estrogens, androgens, and thyroid hormones play a less important, if not trivial, role in most invertebrates.  As such, a ‘quick’ in vitro chemical triage based on estrogen/androgen/thyroid receptor interaction (e.g., binding), as is presently being proposed by regulatory agencies, seems scientifically unsupported.  So, what should be done?

Fortunately, we do have a fairly good understanding of arthropod endocrinology, and we have full genome sequences for an ever-increasing number of arthropod species (honey bee, fruit fly, mosquito).   The Daphnia genome is being sequenced, and hopefully other invertebrates commonly used in toxicity testing will follow.  What’s more, the molecular targets of many insecticides have been studied in great detail for the purpose of developing specific pesticides.  These studies provide those of us in the invertebrate endocrine disruption business, with a wealth of data on how chemicals disrupt specific hormone pathways in certain animal pests.  We know, to some extent, which hormone receptors are being targeted by these chemicals and how they affect physiological processes such as molting, embryonic development, growth, and reproduction.  We have a unique opportunity to exploit this knowledge in the study of chemical effects on hormone regulation in other (non-target) arthropods, such as the model organisms presently being considered in screening and testing programs.  This should allow us to study hormone regulation and its chemical disruption in mysids, daphnids, copepods, and other animals, in ways previously not possible.  A number of significant advances I see, or hope to see, are (1) the identification of the molecular targets (e.g., receptors) of endocrine toxicants in the species presently proposed in screening programs; (2) a mechanistic understanding of hormone regulation and signal disruption by chemicals in these animals; (3) better predictive and modeling power within a species (across levels of biological organization, i.e., from receptor to population), and across species; (4) assays that look at chemical effects on hormone systems that are specifically relevant to invertebrates (such as effects on molting, metamorphosis, etc.).

I am hopeful that the initial inclusion of invertebrates in regulatory screening programs worldwide wasn’t just an easy-way-out approach to covering the ecological bases.  In vitro assays that are relevant for non-vertebrate species need to be included in the initial rapid screening phase of chemicals.  The proposed invertebrate in vivo assays will need to be optimized using information that will be made available over the next few years by studies using new genomic approaches.  It makes sense to start with animals that are already incorporated or proposed in existing testing and screening programs, such as mysids, daphnids, and copepods.  There are many reasons why these animals would make a good first start, many of these are the reasons that make them great toxicity testing models.  However, the use of a limited number of species as representatives of the enormous invertebrate diversity is a naive approach destined to failure in the absence of suitable safeguards.  As more information becomes available, other invertebrate models will need to be included.  This inclusion could be based on evolutionary considerations (i.e., pick animals from important time points in evolution).    Prime candidates would be invertebrate deuterostomes such as sea stars and urchins (genome projects are underway for these animals) and members of the Lophotrochozoa, the other big protostome clade (next to the Ecdysozoa or molting animals) that includes annelids and mollusks.  Ideally, greater integration of toxicology and molecular biology should lead to greater incorporation of established toxicity testing models in future genome sequencing plans.  This would allow us to expand our battery of invertebrate endocrine disruption assays with well-established toxicity testing models. 

A number of good things have happened since that 1998 meeting in The Netherlands.  Most importantly, the invertebrate community has taken a step back from trying to sell their invertebrates as a quick and easy way to do vertebrate risk assessment.  This doesn’t mean that invertebrates cannot enhance our understanding of hormone regulation and its chemical disruption in ways relevant to vertebrates.  It generally was, and unfortunately still is, a necessary evil for us to ‘sell our science’.   However, it is an oversimplification that has not done us much good.  We will never come to a thorough understanding of invertebrate endocrine disruption if we do not incorporate all the diversity, difficulties, and uncertainties that come with it.  We need to sell our invertebrates for what they are.  And let’s face it, it shouldn’t be a hard sell.   We just need to train our ‘buyers’, whether they are our fellow scientists, the public, or regulatory and funding agencies.              




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