Kiel Life Science

What the metabolism reveals about the origin of life

May 07, 2018

Kiel botanist proposes new theory for the simultaneous evolution of opposing metabolic processes

Which came first, the chicken or the egg? This classical ‘chicken-or-egg’ dilemma applies in particular to the developmental processes of life on earth. The basis of evolution was a gradual transition from purely chemical reactions towards the ability of the first life forms to convert carbon via metabolic processes, with the help of enzymes. In this transition, early life forms soon developed different strategies for energy production and matter conversion. 

In principle, science distinguishes between so-called heterotrophic and autotrophic organisms: the first group, which includes all animals for example, uses various organic substances as energy sources. Their metabolic processes produce CO2 - amongst other things - during respiration. In contrast, autotrophic organisms exclusively use inorganic carbon compounds for their metabolism. This group includes all plants, which carry out photosynthesis and thereby bind CO2 to gain energy from sunlight.

In evolution research, scientists around the world have long discussed which of the two basic metabolic strategies developed first - autotrophy or heterotrophy, i.e. photosynthesis or respiration. Dr Kirstin Gutekunst, research associate in the Plant Cell Physiology and Biotechnology Group at the Botanical Institute at Kiel University, proposes instead that both developments may have occurred simultaneously and in parallel. The Kiel botanist presents this novel theory for discussion, which she has titled "Hypothesis on the Synchronistic Evolution of Autotrophy and Heterotrophy", in the journal Trends in Biochemical Sciences.

Gutekunst argues as follows: in terms of matter conversion, the earth represents a closed system. The quantity of every kind of matter on earth cannot be changed - it is only continuously converted and reassembled. There must therefore be a balance in such a system - otherwise certain substances would be permanently removed and others permanently added. The logical conclusion is that for every metabolic process, there must be a corresponding opposing process - either within the same organism, or in two different organisms which have opposing metabolic processes. A third core argument of the new hypothesis lies in the fact that the main drivers of the metabolism, the enzymes, can inherently act in two directions - so therefore, every metabolic reaction can be reversed by the corresponding opposing reaction. Metabolic processes overall are not linear, but rather cyclical, and have a global balance of materials.

"The current scientific knowledge suggests that heterotrophy and autotrophy cannot have developed independently of each other. In a closed system that is characterised by a balance of materials, then both metabolic processes are interdependent," said Kirstin Gutekunst. "Just like neither the chicken nor the egg could have originated first, so too heterotrophic and autotrophic organisms cannot have developed after each other," continued the Kiel plant researcher. An example of this kind of balance of materials can be found in cyanobacteria, also known as blue-green algae. They combine the metabolic processes of photosynthesis and respiration in one organism, and thus display heterotrophic and autotrophic properties at the same time. Here, these processes are particularly closely linked, and are based on identical molecular components.

The new theory of the Kiel researcher could thus provide impetus to re-evaluating the existing conception of the origin of life on earth in future. In principle, the question of origin can only be viewed hypothetically. However, Gutekunst’s theory offers credible indices against the idea of a singular origin, which in essence is technically based on an unscientific idea of creation. In contrast, the proposed synchronistic hypothesis suggests a duality right from the beginning of evolution. If metabolic processes based on the effect of enzymes are acknowledged as a characteristic of life, then for each reaction there must also be an opposing reaction. Such an evolution can therefore only have started at the same time, and from there onwards developed in parallel. Gutekunst’s thesis is thus a strong argument against the assumption of a singular origin of autotrophy or heterotrophy.

The publication forms part of the plant research conducted within the priority research area "Kiel Life Science" at Kiel University. Currently, the scientists in this area are striving to network with each other better, and to encourage mutual exchange of ideas and information. In this context, together with partner institutions in the region, they are preparing the formation of an independent, interdisciplinary centre for plant research at Kiel University.

Original publication:
Kirstin Gutekunst (2018): Hypothesis on the Synchronistic Evolution of Autotrophy and Heterotrophy Trends in Biochemical Sciences
doi.org/10.1016/j.tibs.2018.03.008

Photos are available to download:
www.uni-kiel.de/download/pm/2018/2018-134-1.jpg 
Caption: The Hypothesis on the Synchronistic Evolution of Autotrophy and Heterotrophy assumes that the opposing processes must have developed at the same time.    
Image: Dr Kirstin Gutekunst

Contact:
Dr Kirstin Gutekunst
Plant Cell Physiology and Biotechnology Group,
Botanical Institute and Botanical Gardens, Kiel University
Tel.:         +49 (0)431-880-4237
E-mail:     kgutekunst@bot.uni-kiel.de

More information:
Plant Cell Physiology and Biotechnology Group,
Botanical Institute and Botanical Gardens, Kiel University
www.biotechnologie.uni-kiel.de

Priority research area “Kiel Life Science”, Kiel University
www.kls.uni-kiel.de

Christian-Albrechts-Universität zu Kiel
Press, Communication and Marketing, Dr Boris Pawlowski, Text: Christian Urban
Postal address: D-24098 Kiel, Germany, Telephone: +49 (0)431 880-2104, Fax: +49 (0)431 880-1355
E-mail: presse@uv.uni-kiel.de, Internet: www.uni-kiel.de
Twitter: www.twitter.com/kieluni, Facebook: www.facebook.com/kieluni

 

Conquering the Extreme

Credit: ESO/G. Beccari, License: CC BY 4.0, http://www.eso.org/public/images/eso1723a/

May 04, 2018

How microorganisms support multicellular organisms with the colonisation of hostile environments

From hot and nutrient-poor deserts to alternating dry and wet intertidal zones, right through to the highest water pressure and permanent darkness in the deep sea: in the course of its development over millions of years, life has conquered even the most extreme places on earth. That termites can live off indigestible wood, plants can exist in deserts - seemingly without water and nutrients, or sea anemones can tolerate the constant change between underwater and dry environments in intertidal zones, apparently also depends on close cooperation with their bacterial symbionts. Life scientists around the world are currently investigating the manner in which the symbiotic interaction of microorganisms and hosts, in the functional unit of a metaorganism, supports the colonisation of such extreme habitats. An international research team under the leadership of the Collaborative Research Centre (CRC) 1182 "Origin and Function of Metaorganisms” at Kiel University has now presented an inventory of mechanisms, with which the interactions of hosts and symbionts support life under extreme environmental conditions, or even make it possible at all. Together with colleagues from Saudi Arabia’s King Abdullah University of Science and Technology (KAUST), the researchers have now described in detail for the first time in the scientific journal Zoology how microorganisms can promote the growth and the evolutionary fitness of different organisms in extreme locations.

An important factor in response to changing living conditions is time. If the environment at a particular place changes very quickly, for example through drastic change in physical and chemical conditions such as light or oxygen levels, the more highly-developed multicellular organisms in particular find the adjustment difficult. Their ability to adapt is too slow, because the required genetic change can only be completed over the course of several generations. "Here microorganisms can give their host organisms an advantage," emphasised Professor Thomas Bosch, cell and developmental biologist at Kiel University and spokesperson for the CRC 1182. "With bacteria, for example, the evolutionary processes occur much more rapidly. They can partially transfer this ability to respond much faster to environmental changes to their hosts, and thereby assist the hosts with adaptation," continued Bosch. 

The lack of food or the inability to actually use the available nutrients further limits the available habitats. The metabolisms of many organisms are geared to specific optimal living conditions, and struggle to cope in extreme areas. Here too, it is often the symbiotic relationships with bacteria which enable plants and animals to expand the functioning of their own metabolisms. Thus, different organisms can, for example, exchange nutrients with their bacterial partners, and thereby utilise food sources which their metabolisms otherwise could not process. 

Certain symbiotic bacteria, which colonise the roots of plants, help them to absorb elements such as nitrogen and other minerals in dry and nutrient-poor locations. Other bacteria support plant growth by increasing tolerance to saline soil. In the future, researchers will focus on investigating such helpful bacterial cultures, regarding their applicability to crops. Potentially, a better understanding of plants as metaorganisms could also help to utilise previously-unusable deserts for agriculture in the future.

In addition, microbial symbionts enable various organisms to develop a high tolerance towards a rapidly-changing environment: fixed cnidarians in the inter-tidal zones of different oceans can, for example, quickly adapt to the extreme changes in their living conditions because they can also abruptly change the composition of their bacterial colonisation. Behind this lie mechanisms such as the direct exchange of genetic information between different bacterial species, which controls the exclusion or inclusion of specific types of bacteria in the metaorganism. "In sea anemones, their bacterial colonisation changes in accordance with the prevailing site conditions," emphasised Dr Sebastian Fraune, research associate at the Zoological Institute at Kiel University. "The organisms can potentially save this flexible bacterial configuration, and recall it in the event of a change in their habitat, in order to cope with the new conditions," continued Fraune.

From the investigation of this bacterial-controlled ability to adapt to fast-changing environmental conditions, it may be possible in future to draw conclusions about the effects of climate change on organisms and ecosystems, or even to deduce adaptation strategies. Further research will clarify how the health and fitness of a metaorganism depend on the adaptability of its individual partners, and what effects arise from changing individual elements of this complex structure. The new findings thus emphasise the fundamental importance of researching the multi-organismic relationships between hosts and microorganisms, in particular, too, for the understanding of life in a variable and extreme environment.


Original publication:
Corinna Bang, Tal Dagan, Peter Deines, Nicole Dubilier, Wolfgang J. Duschl, Sebastian Fraune, Ute Hentschel, Heribert Hirt, Nils Hülter, Tim Lachnit, Devani Picazo, Lucia Pita, Claudia Pogoreutz, Nils Rädecker, Maged M. Saad, Ruth A. Schmitz, Hinrich Schulenburg, Christian R. Voolstra, Nancy Weiland-Bräuer, Maren Ziegler, Thomas C.G. Bosch (2018): Metaorganisms in extreme environments: do microbes play a role in organismal adaptation? Biology doi.org/10.1016/j.zool.2018.02.004


A photo is available for download under:
www.uni-kiel.de/download/pm/2018/2018-131-1.jpg 
Associated microbiota can promote the host’s vigour and proliferation in extreme environments. Such insights may be informative even when attempting to remotely detect the presence of life in extreme conditions on terrestrial planets. The Photograph shows the spectacular Orion Nebula, 
taken by ESO’s VLT Survey Telescope (VST).
Credit: ESO/G. Beccari, License: CC BY 4.0, http://www.eso.org/public/images/eso1723a/ 

Contact:
Prof. Thomas Bosch
Zoological Institute, Kiel University
Tel.: +49 (0)431-880-4170
E-mail: tbosch@zoologie.uni-kiel.de

More information:
Collaborative Research Centre (CRC) 1182 "Origin and Function of Metaorganisms", Kiel University:
www.metaorganism-research.com

KAUST news release on the related „Metaorganism Frontier Research Workshop“:
www.kaust.edu.sa/en/news/exploring-the-metaorganism-frontier


Christian-Albrechts-Universität zu Kiel
Press, Communication and Marketing, Dr Boris Pawlowski, Text: Christian Urban 
Postal address: D-24098 Kiel, Germany, Telephone: +49 (0)431 880-2104, Fax: +49 (0)431 880-1355
E-mail: presse@uv.uni-kiel.de, Internet: www.uni-kiel.de, Twitter: www.twitter.com/kieluni 
Facebook: www.facebook.com/kieluni, Instagram: www.instagram.com/kieluni

 

Self or nonself?

Feb 23, 2018

Why the interplay of body and microorganisms demands a redefinition of the individual

The individual is synonymous with the human personality, the smallest unit of social structures, and the central concept of existence. In order for science to define this self - which is fundamental to how we see ourselves as humans - biology has traditionally formulated three explanatory approaches, with which the human individual can be clearly set apart from their biologically active environment: the immune system, the brain and the genome make humans unique and distinguishable from all other living beings. However, in light of the new scientific field of metaorganism research, which focuses on the interaction of the organism with its microbial symbionts, this human understanding of being an individual, clearly definable self faces major challenges. Now, an interdisciplinary team of researchers from biology and anthropology, in the framework of the Collaborative Research Centre (CRC) 1182 "Origin and Function of Metaorganisms" at Kiel University, has formulated in a joint essay on why the metaorganism concept - by now broadly accepted in life sciences - demands a redefinition of the traditional concepts of the self. The ground-breaking article was published by Tobias Rees, professor of anthropology at McGill University and director at Berggruen Institute in Los Angeles, Professor Thomas Bosch, spokesperson of the Kiel CRC 1182, and Angela Douglas, professor of molecular biology and genetics at Cornell University, on Thursday 22 February in the journal PLOS Biology.

The basis of their thesis is the now-proven scientific fact that the human body is not a self-contained entity. Instead, both the development and the functioning of the human organism depend on dynamic and interactive cooperation between human and bacterial cells - or in other words, a balance in the so-called metaorganism, which comprises human and microorganisms. The proportion of bacterial cells in this system is approximately 50 percent.

This high degree of interpenetration of human and bacterial life is the reason why science must take a new look at many biological processes, in light of these multi-organismic relationships. "From the functioning of the organs, to the process of metabolism, right through to protection against infectious diseases - these new findings force us to re-examine and develop a new understanding of all life processes in our body as cooperation between humans and microorganisms," emphasised the cell and developmental biologist Bosch.

For this reason, the classical biological explanations of the individual self - the immune system, the brain and the genome - must also be re-evaluated. Defining the human self on the basis of the immune system is due, amongst other things, to its function of protecting the body against harmful external influences. Therefore, it must somehow be able to distinguish between self and nonself at the molecular level. The result is a sharp dividing line between human and non-human organism, for example in the detection and prevention of pathogens. However, it is now clear that bacteria form an essential component of the immune system: what was thus traditionally considered as part of the human self is actually largely of bacterial origin, i.e. nonself.

It is similar with the classical interpretation of the brain as the seat of core human traits like personality, self-awareness, or emotions: the bacterial colonisation of the body communicates with the nervous system, and then directly or indirectly influences cognitive processes, social behaviour and the psyche. How the brain shapes the human individual is therefore also inextricably linked to the close interconnection between organism and bacteria.

The human genome, i.e. the totality of genetic information, is considered to be unchangeable and unique to every human being. However, it has been determined that microbial genes play a major role in the manifestation of human characteristics. As the bacterial colonisation of the body is not static, the microbial genome also behaves in a highly-variable manner - in contrast with the human one. Its properties can thereby change dramatically over time, and contribute in their variability to the genetic make-up of the body. "Bacteria thus not only influence the human genome, they make up a large part of it," emphasised Rees. The definition of the human individual in terms of a fixed genetic make-up is therefore also outdated, according to Rees.

In a broader context, this revision of the human individual challenges the borders between scientific disciplines. Since the areas of human and non-human can no longer be clearly distinguished, it also calls into question the centuries-old divisions between the arts and the sciences, for example. "The era of metaorganism research is therefore not only associated with an upheaval in the life sciences," stressed Rees. "Rather, metaorganism research is an invitation to the humanities to rethink man after the nature-human separation. And that means learning to rethink human domains such as art or technology and poetry." Metaorganism research also shows how an increasingly-detailed understanding of the genetic and molecular processes of life also redefines science as a whole, added Bosch, who together with Rees is part of the interdisciplinary research programme “Humans and the Microbiome” at the Canadian Institute for Advanced Research (CIFAR).

Original publication:
Tobias Rees, Thomas Bosch, Angela E. Douglas (2018): How the microbiome challenges our concept of self. PLOS Biology
dx.doi.org/10.1371/journal.pbio.2005358 

Photos/material is available for download:
www.uni-kiel.de/download/pm/2018/2018-045-1.jpg
Caption: The traditional decoupling of man from nature, such as depicted by Caspar David Friedrich at the beginning of the 19th century, is called into question in the era of the metaorganism: the interactions of body and microorganisms define the human self.

Caspar David Friedrich, Caspar David Friedrich - Wanderer above the Sea Fog, tagged as public domain, details at  Wikimedia Commons  


Contact:
Prof. Thomas Bosch
Zoological Institute, Kiel University
Tel.: +49 (0)431-880-4170
E-mail: tbosch@zoologie.uni-kiel.de

More information:
Priority research area “Kiel Life Science”, Kiel University
www.kls.uni-kiel.de
 
Collaborative Research Centre (CRC) 1182 "Origin and Function of Metaorganisms", Kiel University:
www.metaorganism-research.com

Cell and Developmental Biology (Bosch AG) working group, Zoological Institute, Kiel University:
www.bosch.zoologie.uni-kiel.de

Research Program “Humans & the Microbiome”,
Canadian Institute for Advanced Research (CIFAR):
www.cifar.ca/research/humans-the-microbiome

Kiel University
Press, Communication and Marketing, Dr. Boris Pawlowski
Address: D-24098 Kiel, phone: +49 (0431) 880-2104, fax: +49 (0431) 880-1355
E-Mail: ► presse@uv.uni-kiel.de, Internet: ► www.uni-kiel.de
Twitter: ► www.twitter.com/kieluni, Facebook: ► www.facebook.com/kieluni, Instagram: ► www.instagram.com/kieluni
Text / Redaktion: ► Christian Urban

Bacteria as pacemaker for the intestine

Nov 22, 2017

CAU research team discovers connection between microbiome and tissue contractions that are indispensable for healthy bowel functions

Spontaneous contractions of the digestive tract play an important role in almost all animals, and ensure healthy bowel functions. From simple invertebrates to humans, there are consistently similar patterns of movement, through which rhythmic contractions of the muscles facilitate the transport and mixing of the bowel contents. These contractions, known as peristalsis, are essential for the digestive process. With various diseases of the digestive tract, such as severe inflammatory bowel diseases in humans, there are disruptions to the normal peristalsis. To date, very little research has explored the factors underlying the control of these contractions. Now, for the first time, a research team from the Cell and Developmental Biology (Bosch AG) working group at the Zoological Institute at Kiel University (CAU) has been able to prove that the bacterial colonisation of the intestine plays an important role in controlling peristaltic functions. The scientists published their results yesterday - derived from the example of freshwater polyps - in the latest issue of Scientific Reports.

The triggers for the normal spontaneous contractions of the muscle tissue are so-called pacemaker cells of the nervous system. In a specific rhythm and without any external stimulation, they emit electrical impulses, that ultimately reach the smooth muscles of the intestinal wall, and cause them to contract. Although the impulses as such occur by themselves, their frequency and intensity, however, are subject to external influences. "The example of the simple freshwater polyp Hydra has shown us that the bacterial colonisation of the organism can affect the contractions of its digestive cavity. Most likely they do so by modulating the underlying pacemaker signals," said Professor Thomas Bosch, head of the study and spokesperson for the Collaborative Research Centre (CRC) 1182 "Origin and Function of Metaorganisms". Unlike other more complex organisms, Hydra have no bowel in the true sense of the word. Their simple body cavity assumes, amongst other things, the function of a digestive tract; the surrounding tissue also exhibits the typical contractions associated with more highly-developed intestines.

To find out how peristalsis is regulated in the freshwater polyps, the researchers compared normal Hydra which had typical bacterial colonisation with those that had their microbiome completely removed with an antibiotic cocktail. In comparison, these organisms without bacterial colonisation - also referred to as germ-free polyps - exhibited a reduction in contractions by about half. At the same time, the rhythm of the movements became disrupted, and some of the breaks between the contractions were much longer. Thus, the absence of the typical microbiome in Hydra compromised the peristaltic movements in the body cavity.

In a further step, the scientists restored the specific bacterial colonisation in the germ-free organisms. Initially, they introduced each of the five most common bacterial species found in the Hydra microbiome individually back into the sterile polyps. It turned out that this individual bacterial colonisation has no appreciable effect on the frequency and timing of contractions. Only the joint re-introduction of the five main representatives of the microbiome led to a marked improvement in peristalsis, although even then, the pattern of contractions was not fully normalised. Interestingly, an extract produced from the colonising bacteria had a similarly positive influence.

From these observation the Kiel research team concluded that only the natural Hydra microbiome - characterised by a balance between the bacterial species present - can play an important pacemaker role in peristalsis. They discovered that, in this case, certain molecules secreted by the bacteria can intervene in the control mechanism of the pacemaker cells. As such, bacterial signals can have a decisive effect on the pattern of spontaneous peristaltic contractions. "We were able to demonstrate for the first time that in our simple model organism, the microbiome has an indispensable function in the frequency and timing of tissue contractions," emphasised Bosch.

In addition, the example of the evolutionarily ancient model organism Hydra shows us that the control of vital processes of multicellular organisms by their bacterial symbionts already originated very early in the evolution of life, continued Bosch. These ground-breaking results are especially promising for medical research: "The fundamental explanation of the cooperation between organism and microbiome in regulating peristalsis will in future help us to understand the emergence of severe diseases, which arise from disrupted movement of the intestine," summarised Bosch.

Original publication:
Andrea P. Murillo-Rincón, Alexander Klimovich, Eileen Pemöller, Jan Taubenheim, Benedikt Mortzfeld, René Augustin & Thomas C.G. Bosch (2017): “Spontaneous body contractions are modulated by the microbiome of Hydra”. Scientifc Reports, Published on 21.11.2017,
doi:10.1038/s41598-017-16191-x

Photos/material is available for download:

www.uni-kiel.de/download/pm/2017/2017-368-1.gif
Caption: The typical contraction pattern of the freshwater polyp Hydra: Contraction and relaxation of the same animal over the course of three minutes.
Animation: Andrea Murillo-Rincon, Dr. Alexander Klimovich

www.uni-kiel.de/download/pm/2017/2017-368-2.jpg
Caption: Body contractions in Hydra are triggered by nerve cells (in green), while bacteria (rod-shaped cells in red) influence the underlying pacemaker activity.
Image: Christoph Giez, Dr. Alexander Klimovich

www.uni-kiel.de/download/pm/2017/2017-368-3.jpg
Caption: Hydra’s nerve cells (in green) generate electrical impulses that cause contractions of muscle fibers (shown in red) in the gastric cavity wall.
Image: Christoph Giez, Dr. Alexander Klimovich

Contact:
Prof. Thomas Bosch,
Zoological Institute, Kiel University
Tel.: 0431-880-4170
E-Mail: tbosch@zoologie.uni-kiel.de

More information:
Priority research area “Kiel Life Science”, Kiel University
www.kls.uni-kiel.de

Collaborative Research Centre (CRC) 1182 "Origin and Function of Metaorganisms", Kiel University:
www.metaorganism-research.com

Cell and Developmental Biology (Bosch group), Zoological Institute, Kiel University
www.bosch.zoologie.uni-kiel.de

New approach to antibiotic therapy is a dead end for pathogens

Jun 01, 2017

Kiel-based team of researchers uses evolutionary principles to explore sustainable antibiotic treatment strategies

The World Health Organization WHO is currently warning of an antibiotics crisis. The fear is that we are moving into a post-antibiotic era, during which simple bacterial infections would no longer be treatable. According to WHO forecasts, antibiotic-resistant pathogens could become the most frequent cause of unnatural deaths within just a few years. This dramatic threat to public health is due to the rapid evolution of resistance to antibiotics, which continues to reduce the spectrum of effective antibacterial drugs. We urgently need new treatments. In addition to developing new antibiotic drugs, a key strategy is to boost the effectiveness of existing antibiotics by new therapeutic approaches.

The Evolutionary Ecology and Genetics research group at Kiel University uses knowledge gained from evolutionary medicine to develop more efficient treatment approaches. As part of the newly-founded Kiel Evolution Center (KEC) at Kiel University, researchers under the direction of Professor Hinrich Schulenburg are investigating how alternative antibiotic treatments affect the evolutionary adaptation of pathogens. In the joint study with international colleagues now published in the scientific journal Molecular Biology and Evolution, they were able to show that in the case of the pathogen Pseudomonas aeruginosa, the evolution of resistance to certain antibiotics leads to an increased susceptibility to other drugs. This concept of so-called "collateral sensitivity" opens up new perspectives in the fight against multi-resistant pathogens.

Together with colleagues, Camilo Barbosa, a doctoral student in the Schulenburg lab, examined which antibiotics can lead to such drug sensitivities after resistance evolution. He based his work on evolution experiments with Pseudomonas aeruginosa in the laboratory. This bacterium is often multi-resistant and particularly dangerous for immunocompromised patients. In the experiment, the pathogen was exposed to ever-higher doses of eight different antibiotics, in 12-hour intervals. As a consequence, the bacterium evolved resistance to each of the drugs. In the next step, the researchers tested how the resistant pathogens responded to other antibiotics which they had not yet come into contact with. In this way, they were able to determine which resistances simultaneously resulted in a sensitivity to another drug.

The combination of antibiotics with different mechanisms of action was particularly effective - especially if aminoglycosides and penicillins were included. The study of the genetic basis of the evolved resistances showed that three specific genes of the bacterium can make them both resistant and vulnerable at the same time. "The combined or alternating application of antibiotics with reciprocal sensitivities could help to drive pathogens into an evolutionary dead end: as soon as they become resistant to one drug, they are sensitive to the other, and vice versa," said Schulenburg, to emphasize the importance of the work. Even though the results are based on laboratory experiments, there is thus hope: a targeted combination of the currently-effective antibiotics could at least give us a break in the fight against multi-resistant pathogens, continued Schulenburg.

Original publication:
Camilo Barbosa, Vincent Trebosc, Christian Kemmer, Philip Rosenstiel, Robert Beardmore, Hinrich Schulenburg and Gunther Jansen (2017): Alternative Evolutionary Paths to Bacterial Antibiotic Resistance Cause Distinct Collateral Effects. Molecular Biology and Evolution
doi.org/10.1093/molbev/msx158

Photos/material is available for download:

www.uni-kiel.de/download/pm/2017/2017-171-1.jpg
Caption: The pathogen Pseudomonas aeruginosa during the evolution experiment in the laboratory.
Image: Camilo Barbosa/Dr. Philipp Dirksen

www.uni-kiel.de/download/pm/2017/2017-171-2.jpg
Caption: Doctoral student Camilo Barbosa examined the effect of "collateral sensitivity", which can make antibiotic-resistant bacteria treatable.
Photo: Christian Urban, Kiel University

www.uni-kiel.de/download/pm/2017/2017-171-3.jpg
Caption: The research team analysed a total of 180 bacterial populations of the pathogen Pseudomonas aeruginosa.
Photo: Christian Urban, Kiel University

www.uni-kiel.de/download/pm/2017/2017-171-4.jpg
Caption: The bacteria became resistant to certain antibiotics, but at the same time sensitive to other substances.
Photo: Christian Urban, Kiel University

Contact:
Prof. Hinrich Schulenburg
Spokesperson “Kiel Evolution Center” (KEC), Kiel University
Tel.: +49 (0)431-880-4141
E-mail: hschulenburg@zoologie.uni-kiel.de

More information:
Research centre “Kiel Evolution Center”, Kiel University:
www.kec.uni-kiel.de

Evolutionary Ecology and Genetics research group, Zoological Institute, Kiel University:
www.uni-kiel.de/zoologie/evoecogen

Kiel University
Press, Communication and Marketing, Dr. Boris Pawlowski
Address: D-24098 Kiel, phone: +49 (0431) 880-2104, fax: +49 (0431) 880-1355
E-Mail: ► presse@uv.uni-kiel.de, Internet: ► www.uni-kiel.de Twitter: ► www.twitter.com/kieluni, Facebook: ► www.facebook.com/kieluni, Instagram: ► www.instagram.com/kieluni Text / Redaktion: ► Christian Urban

 

Switching mutations on and off again

Apr 12, 2016

Kiel research team facilitates functional genomics with new procedure

 

Mould is primarily associated with various health risks. However, it also plays a lesser-known role, but one which is particularly important in biotechnology. The mould (ascomycete) Aspergillus niger, for example, has been used for for around 100 years to industrially produce citric acid, which is used as a preservative additive in many foodstuffs. In order to research the genetic mechanisms which could shed light on the potential application spectrum of mould and its metabolic products, a research team from Kiel University has developed a new procedure in collaboration with colleagues from Leiden University in the Netherlands.  Read more...

Why the Japanese live longer

Nov 13, 2015

Kiel-based research team shows positive influence on life span of bioactive plant compounds in green tea and soy

A research team at the Institute of Human Nutrition and Food Science at Kiel University has discovered promising links between life expectancy and two phytochemicals - the so-called catechins and isoflavones. The underlying research by the Kiel-based scientists recently appeared in the two journals Oncotarget and The FASEB Journal. Read more...

Marine fungi contain promising anti-cancer compounds

Oct 28, 2015

A Kiel-based research team has identified fungi genes that can develop anti-cancer compounds

To date, the ocean is one of our planet's least researched habitats. Researchers suspect that the seas and oceans hold an enormous knowledge potential and are therefore searching for new substances to treat diseases here. In the EU "Marine Fungi" project, international scientists have now systematically looked for such substances specifically in fungi from the sea, with help from Kiel University and the GEOMAR Helmholtz Centre for Ocean Research Kiel. Read more...

New strategy for fighting antibiotic-resistant pathogens

Oct 16, 2015

Daily switching of antibiotics inhibits the evolution of resistance

Rapid evolution of resistance to antibiotics represents an increasingly dramatic risk for public health. In fewer than 20 years from now, antibiotic-resistant pathogens could become one of the most frequent causes of unnatural deaths. Medicine is therefore facing the particular challenge of continuing to ensure the successful treatment of bacterial infections - despite an ever-shrinking spectrum of effective antibiotics. Recent research by a group of scientists at Kiel University has now shown that there are possible ways to prolong the effectiveness of the antibiotics that are currently available. Read more...

Nematode worms hitch a ride on slugs

Jul 13, 2015

Kiel scientists expand the understanding of Caenorhabditis elegans’ natural ecology


Slugs and other invertebrates provide essential public transport for small worms including Caenorhabditis elegans in the search for food, as researchers from Kiel University have now found out. These worms are around a millimeter long and commonly found in short-lived environments, such as decomposing fruit or other rotting plant material. Read more...

Live from the Evolution Lab

Jun 05, 2015

Study on coevolution between host and pathogens sheds new light on evolutionary dynamics.

 

Every year, new cold and flu pathogens occur and problematic pathogens such as Ebola cause global alarm at regular intervals. The key to a better understanding of disease epidemics lies in the adaptability and thus in the evolution of the pathogens that cause disease. With the aid of innovative experiments in the lab, researchers in the research group Evolutionary Ecology and Genetics at the Christian Albrecht University of Kiel (CAU) have now been able to gain important insights into the evolution of pathogens. Read more...

Hidden safety switch: New findings on death receptors in cancer cells

Jun 10, 2015

Achieving a better molecular understanding of the role played in the occurrence of cancer of so-called death receptors which make the progression of pancreatic cancer in particular especially aggressive and almost always fatal – this is the goal of scientists at the Institute for Experimental Tumor Research at the Christian Albrecht University of Kiel (CAU). Read more...

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  • all day: III. International PP1530 Symposium: Genetic Variation of Flowering Time Genes and Applications for Crop Improvement
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  • all day: III. International PP1530 Symposium: Genetic Variation of Flowering Time Genes and Applications for Crop Improvement
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