Researchers at the University of British Columbia’s Institute for the Oceans and Fisheries (IOF), the Department of Fisheries and Oceans (DFO), University of Toronto, Dalhousie University, and the Hakai Institute examined juvenile sockeye salmon from three locations along their migration route in coastal British Columbia. In 2016 and 2016, the body condition and nutritional health of juvenile sockeye was sampled in the northern Strait of Georgia, the highly tidally mixed Johnstone Strait, and Queen Charlotte Strait.

“We measured the fatty acids in the sockeye salmon tissues, specifically looking at stored fatty acids that are important for mobilizing energy during periods of starvation, such as what these salmon face in Johnstone Strait,” said lead author Dr. Jessica Garzke, an IOF postdoctoral fellow. “We found that short term changes in health differed between years but were not related to zooplankton biomass, abundance, average size, or species composition. Rather it was the quality of the zooplankton that played an important role.”

Leaving the generally productive and good foraging area of the Strait of Georgia, to the typically food-poor conditions of the Johnstone Strait has a powerful impact on the young salmon. When juvenile sockeye salmon entered Johnstone Strait in 2015, they were generally in good body and nutritional condition, and able to use stored energy resources to manage traversing this section, where prey availability was low, to get to Queen Charlotte Strait. In 2016, however, juvenile sockeye salmon entered Johnstone Strait with poor body and nutritional condition, and they struggled to regain condition when they reached Queen Charlotte Strait.

“It was clear from our study that differences in juvenile salmon condition between the two years were due to changes in the food quality available to the fish, more than any other factor. Incorporation of food quality measurements in addition to analysis of quantity of prey is vital to understanding changes in fish condition and survival between years,” Dr. Garzke said.

Understanding how diet affects the salmon’s growth and health during the early part of their lives could help researchers understand the long-term population trends of the species including their decline, says Dr. Garzke. Sockeye salmon are an iconic species in British Columbia, important both commercially and culturally, and are in decline.

The research highlighted how variable the ocean conditions are that juvenile salmon face in British Columbia, said senior author and IOF associate professor Dr. Brian Hunt, with migrating salmon experiencing “boom and bust” feeding conditions. “Importantly, feeding conditions are not consistent from one year to the next. They are impacted by changing climate, and areas that had good feeding conditions in one year can be bad the next. The more areas that switch to bad feeding conditions the tougher it is for juveniles to survive the coastal migration and their first winter at sea.”

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Disruptions to the body’s internal clock — which coordinates the timing of biochemical, physiological and behavioral processes — are associated with a range of diseases, including cancer, cardiovascular conditions and susceptibility to infections, as well as a higher risk for accidents. Common disruptions of circadian rhythms are jet lag and shift work, which is performed by some 30 million people in the U.S.

“We are studying two mutations, both of which affect our ability to respond to shifts of the light cycle,” says neurobiologist Eric Bittman, Professor Emeritus of Biology. “Both of them speed up the clock. They reveal how vulnerable we are to disruptions in the light:dark schedule.”

In mammals, circadian rhythms are generated internally by a master pacemaker in the suprachiasmatic nucleus of the hypothalamus in the brain. In addition, every cell in the body has its own circadian clock, which the master pacemaker coordinates. In the normal, light:dark and fluctuating environment, circadian clocks create 24-hour cycles. However, in constant conditions, such as when hamsters are studied in darkness, the rhythms generate cycles whose period is longer or shorter than 24 hours.

“What this reveals to us is that there’s some internal mechanism that is generating rhythmicity, and that the animals are using cues from the environment, the most powerful of which is the light:dark cycle, to sync it up to exactly 24 hours,” Bittman says.

In previous research, Bittman and team identified a recessive mutation, which they call duper, as a defect in the circadian regulator gene Cryptochrome 1 (CRY1) of Syrian hamsters. By improving the draft of the hamster genome using fast homozygosity mapping, they created a modern genetic research model for investigating human diseases.

In a follow-up paper published recently in the Proceedings of the National Academy of Sciences (PNAS), the research team focuses on the effects of duper in genetically altered hamsters. The scientists identify previously unsuspected functions of CRY1 in circadian entrainment, which is the synching of the biological clock with external signals, and heart disease.

“Duper speeds up the clock in constant conditions and it makes it be able to shift by as much as 180 degrees in response to even a brief pulse of light,” Bittman explains. “We suspect this might be relevant in understanding the effects of jet lag and shift work.”

The body’s organs reset their clocks at different rates after circadian disruption. This temporal misalignment is believed to cause the adverse health effects associated with shift work. “Almost all of our physiological processes are rhythmic,” Bittman says.

The researchers found that circadian re-entrainment is accelerated in duper mutant hamsters, independent of the speeding up of the clock. In an effort to understand more about the health consequences of circadian misalignment, the researchers examined effects of duper and phase shifts on a hamster model of heart disease known to be aggravated by phase shifts.

Simulated jet lag, in the form of eight-hour phase shifts every second week, shortened the lifespan of cardiomyopathic hamsters. However, the shortened lifespan was reversed in duper hamsters as the mutation accelerated their adjustment to the shift of the light:dark cycles. Bittman says the findings have implications for pinpointing the pathways involved in human biological clocks.

“For people with jet lag or the millions of shift workers, it can take days and sometimes weeks for the body — the different organs — to come back into their normal temporal relationship,” he says. Many of us disrupt our circadian system when we are exposed to light late in the evening, such as by looking at cell phones and computer screens. “It can take a couple of weeks until your brain is having the right relationship to your liver and kidneys,” Bittman adds.

The research suggests that we all need to be mindful of how the environment affects our biological clocks. Specifically, hospitals need to be sensitive to the timing of lights and darkness in patients’ rooms. “We need to pay attention to the temporal relationship between organs and between the master clock and the brain, and how it regulates the clock in the brain, as well as in the peripheral organs, and be sensitive to the light:dark environment,” Bittman says.

Additionally, understanding the rhythms of the organs is a crucial aspect in the timing of medical treatment. “An awful lot of drugs that are administered are more effective at one time of the day than another because the circadian clock is regulating all these metabolic pathways that in fact are being targeted by these drugs,” Bittman says.

Ongoing research will focus on identifying the underlying mechanisms of the biological clocks and their role in disease.

But surprising new research published in Nature is adding a new, early chapter to the evolutionary story of gills.

“Our work suggests that the early, simplified gills of our worm-like ancestors played an important role in ion regulation. And that role might have originated as early as the very inception of gills, well before they played any role in breathing,” says Dr. Michael Sackville, a zoologist who led the study while with the University of British Columbia (UBC).

“This really does flip the script on our understanding of how gills and gill function evolved.”

The evolution of gills and lungs has fascinated biologists, including Darwin, for more than 100 years. Prior to this study, gills were thought to be first used for breathing and ion regulation near the very beginning of vertebrate life. In this traditional timeline, these two functions shifted from the skin to the gills in tandem, helping vertebrates transition from small, worm-like creatures to larger, active fishes. This transition from “small and wormy” to “big and fishy” is an iconic event in vertebrate evolution.

The study traced the evolutionary journey of gills by comparing three animals that are alive today, but belong to different lineages: lampreys, which are vertebrates, and amphioxus and acorn worms, which are close relatives of vertebrates. The researchers assumed that any gill functions shared between the animals were inherited from a common ancestor, which is believed to be when simple gills first appeared well over 500 million years ago.

“We found that gills were used for breathing in only our vertebrate representative, and only with increasing body size and activity,” says Dr. Colin Brauner, a UBC zoologist and senior author on the paper.

“But we found ion regulating cells in the gills of all three of our animals. This allowed us to trace the origin of ion regulation at gills all the way back to early deuterostome animals, when very simple gill structures are thought to have first evolved. The finding supports the classic story that gills were first used for breathing in early vertebrates, but adds an exciting new, earlier chapter to the story, clearly worthy of further study.”

The study was conducted in collaboration with researchers at the University of Montreal and Cambridge University, and funded by the Natural Sciences and Engineering Council of Canada and Royal Society.

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Last year, a team led by Jill Banfield discovered DNA structures within a methane-consuming microbe called Methanoperedens that appear to supercharge the organism’s metabolic rate. They named the genetic elements “Borgs” because the DNA within them contains genes assimilated from many organisms. In a study published today as the cover item in Nature, the researchers describe the curious collection of genes within Borgs and begin to investigate the role these DNA packages play in environmental processes, such as carbon cycling.

First contact

Methanoperedens are a type of archaea (unicellular organisms that resemble bacteria but represent a distinct branch of life) that break down methane (CH₄) in soils, groundwater, and the atmosphere to support cellular metabolism. Methanoperedens and other methane-consuming microbes live in diverse ecosystems around the world but are believed to be less common than microbes that use photosynthesis, oxygen, or fermentation for energy. Yet they play an outsized role in Earth system processes by removing methane — the most potent greenhouse gas — from the atmosphere. Methane traps 30 times more heat than carbon dioxide and is estimated to account for about 30 percent of human-driven global warming. The gas is emitted naturally through geological processes and by methane-generating archaea; however, industrial processes are releasing stored methane back into the atmosphere in worrying quantities.

Banfield, a faculty scientist at Lawrence Berkeley National Laboratory (Berkeley Lab) and professor of Earth & Planetary Science and Environmental Science, Policy & Management at UC Berkeley, studies how microbial activities shape large-scale environmental processes and how, in turn, environmental fluctuations alter the planet’s microbiomes. As part of this work, she and her colleagues regularly sample microbes in different habitats to see what interesting genes microbes are using for survival, and how these genes might affect global cycles of key elements, such as carbon, nitrogen, and sulfur. The team looks at the genomes within cells as well as the portable packets of DNA known as extra-chromosomal elements (ECEs) that transfer genes between bacteria, archaea, and viruses. These elements allow microbes to quickly gain beneficial genes from their neighbors, including those that are only distantly related.

While studying Methanoperedens sampled from seasonal wetland pool soil in California, the scientists found evidence of an entirely new type of ECE. Unlike the circular strands of DNA that make up most plasmids, the most well-known type of extra-chromosomal element, the new ECEs are linear and very long — up to one-third the length of the entire Methanoperedens genome. After analyzing additional samples from underground soil, aquifers, and riverbeds in California and Colorado that contain methane-consuming archaea, the team uncovered a total of 19 distinct ECEs they dubbed Borgs. Using advanced genome analysis tools, the scientists determined that many of the sequences within the Borgs are similar to the methane-metabolizing genes within the actual Methanoperedens genome. Some of the Borgs even encode all the necessary cellular machinery to eat methane on their own, so long as they are inside a cell that can express the genes.

“Imagine a single cell that has the ability to consume methane. Now you add genetic elements within that cell that can consume methane in parallel and also add genetic elements that give the cell higher capacity. It basically creates a condition for methane consumption on steroids, if you will,” explained co-author Kenneth Williams, a senior scientist and Banfield’s colleague in Berkeley Lab’s Earth and Environmental Sciences Area. Williams led research at the Rifle, Colorado site where the best characterized Borg was recovered, and is also chief field scientist of a research site on the East River, near Crested Butte, Colorado, where some of Banfield’s current sampling takes place.

The East River field site is part of the Department of Energy’s Watershed Function Scientific Focus Area, a multidisciplinary research project led by Berkeley Lab that aims to link microbiology and biochemistry with hydrology and climate science. “Our expertise is bringing together what are often thought of and treated as completely disparate fields of inquiry — big science that links everything from genes all the way up to watershed and atmospheric processes.”

Resistance is futile a disadvantage

Banfield and her fellow researchers at UC Berkeley’s Innovative Genomics Institute, including co-author and longtime collaborator Jennifer Doudna, hypothesize that the Borgs could be residual fragments of entire microbes that were engulfed by Methanoperedens to aid metabolism, similar to how plant cells harnessed formerly free-living photosynthetic microbes to gain what we now call chloroplasts, and how an ancient eukaryotic cell consumed the ancestors of today’s mitochondria. Based on the similarities in sequences, the engulfed cell could have been a relative of Methanoperedens, but the overall diversity of genes found in the Borgs indicates that these DNA packages were assimilated from a wide range of organisms.

No matter the origin, it is clear that Borgs have existed alongside these archaea, shuttling genes back and forth, for a very long time.

Notably, some Methanoperedens were found with no Borgs. And, in addition to recognizable genes, the Borgs also contain unique genes encoding other metabolic proteins, membrane proteins, and extracellular proteins almost certainly involved in electron conduction required for energy generation, as well as other proteins that have unknown effects on their hosts. Until the scientists can culture Methanoperedens in a laboratory environment, they won’t know for sure what capabilities the different Borgs confer, why some microbes use them, and why others don’t.

One likely explanation is that Borgs act as a storage locker for metabolic genes that are only needed at certain times. Ongoing methane monitoring research has shown that methane concentrations can vary significantly throughout the year, usually peaking in the fall and dropping to the lowest levels in early spring. The Borgs therefore provide a competitive advantage to methane-eating microbes like Methanoperedens during periods of abundancewhen there is more methane than their native cellular machinery can break down.

Plasmids are known to serve a similar purpose, quickly spreading genes for resistance to toxic molecules (like heavy metals and antibiotics) when the toxins are present in high enough concentrations to exert evolutionary pressure.

“There is evidence that different types of Borgs sometimes coexist in the same host Methanopreredens cell. This opens the possibility that Borgs could be spreading genes across lineages,” said Banfield.

Boldly exploring the (microbial) universe

Since posting their article as a pre-print last year, the team has begun follow-up work to better understand how Borgs may affect biological and geological processes. Some researchers are combing through data sets of genetic material from other microorganisms, looking for evidence that Borgs exist in association with other species.

While her colleagues are using lab-based methods, co-author Susan Mullen, a graduate student in Banfield’s lab, will be getting her feet wet with some very picturesque field work. She recently started a project to sample microbes from the floodplains of the East River throughout the year to assess how seasonal changes in Borg abundance and other microbes known to be involved in methane cycling correlate to seasonal fluxes of methane.

According to the authors, years down the line, carefully cultured microbes chock full of Borgs could be used to reduce methane and curb global warming. It’s all to benefit the collective — life on Earth.

Opiates cause addiction, new substances do not

They are a blessing for patients suffering from severe pain, but they also have serious side effects: Opioids, and above all morphine, can cause nausea, dizziness and constipation and can also often cause slowed breathing that can even result in respiratory failure. In addition, opiates are addictive — a high percentage of the drug problem in the USA is caused by pain medication, for example.

In order to tackle the unwanted medical and social effects of opioids, researchers all over the world are searching for alternative analgesics. Prof. Dr. Peter Gmeiner, Chair of Pharmaceutical Chemistry is one of these researchers. “We are focusing particularly on the molecular structures of the receptors that dock onto the pharmaceutical substances,” says Gmeiner. “It is only when we understand these on the atomic level that we can develop effective and safe active substances.” Collaborating with an international team of researchers, Prof. Gmeiner discovered an active substance in 2016 that bonds to known opioid receptors and that offers the same level of pain relief as morphine, even though it has no chemical similarity to opiates.

New approach: Adrenaline receptors instead of opioid receptors

Peter Gmeiner is currently following a lead that seems very promising: “Many non-opioid receptors are involved in pain processing, but only a small number of these alternatives have as yet been validated for use in therapies,” he explains. Gmeiner and a team of researchers from Erlangen, China, Canada and the USA have now turned their attention to a new receptor that is responsible for binding adrenaline — the alpha 2A adrenergic receptor. There are already some analgesics that target this receptor such as brimonidine, clonidine and dexmedetomidine. Gmeiner: “Dexmedetomidine relieves pain, but has a strong sedative effect, which means its use is restricted to intensive care in hospital settings and is not suitable for broader patient groups.”

The aim of the research consortium is to find a chemical compound that activates the receptor in the central nervous system without a sedative effect. In a virtual library of more than 300 million different and easily accessible molecules, the researchers looked for compounds that physically match the receptor but are not chemically related to known medication. After a series of complex virtual docking simulations, around 50 molecules were selected for synthesis and testing and two of these fulfilled the desired criteria. They had good bonding characteristics, activated only certain protein sub-types and thus a very selective set of cellular signal pathways, whereas dexmedetomidine responds to a significantly wider range of proteins.

Pain relief without sedation in animal models

By further optimizing the identified molecules, for which extremely high-resolution cryo-electron microscopic imaging was used, the researchers were able to synthesize agonists that produced high concentrations in the brain and reduced the sensation of pain effectively in investigations with animal models. “Various tests confirmed that docking on the receptor was responsible for the analgesic effect,” explains Gmeiner. “We are particularly pleased about the fact that none of the new compounds caused sedation, even at considerably higher doses than those that would be required for pain relief.”

The successful separation of analgesic properties and sedation is a milestone in the development of non-opioid pain medication, especially as the newly-identified agonists are comparatively easy to manufacture and administer orally to patients. However, Prof. Gmeiner has to dampen any hopes of rapid widespread use in human medicine: “We are currently still talking about basic research. The development of medication is subject to strict controls and in addition to significant amounts of funding, it takes a long time. However, these results still make us very optimistic.”