As we grow older we notice declines in our bodies ability to perform as it once did. This decline may refer to a physical or mental decrease. Neuroscientist Tony Wyss-Coray led researchers at Stanford University in a 2014 study that showed how older mice could fight the effects of cognitive and mental decline by receiving infusions of blood from younger mice.
The older mice were joined to the younger mice's circulatory system by a process know as parabiosis. This involved suturing the mice together so that they shared a circulatory system. The older mice who had been joined to a younger mouse started to see changes in the gene system in the hippocampus region of the brain. Not only did the genes start to show improvement the mice also showed increased connections and "increased synaptic plasticity". This increase helped to heal the learning and memory parts of the brain.
Plasma donations from younger mice were also given to the older mice along with the suturing. The improvement in learning and memory was so significant that Wyss-Coray and his colleagues went further and studied the effects that plasma from human umbilical cords and young adults has on the older mice. This breakthrough was significant as it proved to the researchers that humans could benefit from this research. As we are living longer the mental decline of the older generation has increased and become a serious health challenge. My family has suffered with devastating effects of dementia and Alzheimers. My sweet Grandma was the victim of this disease and I was lucky enough to take care of her and see how she hated what the loss of her memory had done to her.
During the study researchers wanted to find which proteins in the plasma were responsible for dramatic increases scientists were seeing when cord or young adult plasma was given to older mice. They were able to find a protein that had not been tested until now for its ability to reverse memory decline. TIMP2 when injected into elderly mice was shown to produce the same effects that cord plasma did on the hippocampus of the brain. The effects of TIMP2 were drastic and clear cut. TIMP2 is one of a family of proteins that regulate a certain class of enzymes that regulate many proteins. This showed the researchers that there was promise in reversing the effects of devastating mental decline in our aging population.
I am excited for this research and also for the hope that there will be a cure for dementia and Alzheimer's. Test studies have been conducted and further research studies are happening by Wyss-Coray. The doors that have been opened by this research are very promising to an aging population that is desperate to remember.
https://www.scientificamerican.com/article/fountain-of-youth-young-blood-infusions-ldquo-rejuvenate-rdquo-old-mice/
Saturday, April 29, 2017
Friday, April 28, 2017
Number of Giraffe Species Quadrouples Overnight
Bryce Broadhead
Dr. Stofer
Thursday Class.
Contrary to my title the population didn't quadruple but our deeper knowledge of the species of giraffes did. In my article it discussed how through more advanced technology and a larger core sample for DNA testing scientists have found that there are four species contrary to the one we thought existed previously. A year ago we thought there was only one species of giraffe with 9 subspecies. The subspecies don't mate with each other however which is interesting as this leads to very distinct populations. Through this further research we have found that there are actually FOUR distinct species, with each having only two subspecies. From 9 subspecies to 8, while the population stayed the same, how is this possible? Through the genetic testing of skin tissue samples we found that two different species were actually genetically identical. I found this article most interesting mainly because it shows very well how little we actually know, and how much more we have to learn. If something this major can be discovered about giraffes, a species that has been in the scientific record for nearly 300 years, then imagine what we can learn about all the other species we currently know about. Leading to further thought in the realm of how little we actually know about ourselves,
Dr. Stofer
Thursday Class.
Contrary to my title the population didn't quadruple but our deeper knowledge of the species of giraffes did. In my article it discussed how through more advanced technology and a larger core sample for DNA testing scientists have found that there are four species contrary to the one we thought existed previously. A year ago we thought there was only one species of giraffe with 9 subspecies. The subspecies don't mate with each other however which is interesting as this leads to very distinct populations. Through this further research we have found that there are actually FOUR distinct species, with each having only two subspecies. From 9 subspecies to 8, while the population stayed the same, how is this possible? Through the genetic testing of skin tissue samples we found that two different species were actually genetically identical. I found this article most interesting mainly because it shows very well how little we actually know, and how much more we have to learn. If something this major can be discovered about giraffes, a species that has been in the scientific record for nearly 300 years, then imagine what we can learn about all the other species we currently know about. Leading to further thought in the realm of how little we actually know about ourselves,
Naked mole-rats “turn into” plants when oxygen is low!
“Deprived of oxygen, naked mole-rats can survive by metabolizing fructose just as plants do, researchers report this week in the journal Science.Understanding how the animals do this could lead to treatments for patients suffering crises of oxygen deprivation, as in heart attacks and strokes.“This is just the latest remarkable discovery about the naked mole-rat — a cold-blooded mammal that lives decades longer than other rodents, rarely gets cancer, and doesn’t feel many types of pain,” says Thomas Park, professor of biological sciences at the University of Illinois at Chicago, who led an international team of researchers from UIC, the Max Delbrück Institute in Berlin and the University of Pretoria in South Africa on the study.”
I chose this article because I have had several family members suffer from strokes and heart attacks. Some of my grandparents and great grandparents have had to drastically change the way they lived their lives due to these tragic life alter events.
When the brain begins to lack oxygen it runs out of energy and starts to die, this happens in humans, lab rats, and all other mammals. Naked mole rats use another source of energy when this happens. Their brain cells begin to burn fructose as a “backup” for energy that produces energy anaerobically through a metabolic pathway that originally scientists thought only plants had.
To test this scientists placed the mole-rats in low oxygen conditions and saw that high fructose levels appeared in the blood stream. The fructose was transported by molecular fructose pumps that is found in all other mammals. The catch is it’s only found in the intestine. “The naked mole-rat has simply rearranged some basic building-blocks of metabolism to make it super-tolerant to low oxygen conditions,” said Park, who has studied the strange species for 18 years.”
Scientists believe that because the mole-rats live in unusual conditions they’ve been able to adapt to their environments. They live in burrows that have little to no ventilation with hundreds of their kind- not the best place to have a large supply of oxygen.
Once scientists can determine how the naked mole-rat “turns into” a plant when oxygen levels are depleted then progress can be made in providing research and help to patients who suffer from oxygen depleted crisis.
https://www.nsf.gov/news/news_summ.jsp?cntn_id=241777&org=NSF&from=news
“The research was supported by National Science Foundation (grant #0744979), the European Research Council (grant 294678), the Deutsche Forschungsgemeinschaft SFB 665, and the National Institutes of Health (grants HL71626 and HL60678).”
- Austin Daines
Sunday, April 9, 2017
23AndMe Disease Testing
BIOL 1610
After years of tug-of-war with the FDA, the ban on selling DNA tests has finally been lifted for unique genetic company 23AndMe. Individuals partaking in the tests can discover risks for developing 10 different disorders, using a simple at home genetic test.
Based in Mountain View California, 23AndMe is a unique service that individuals can order, and send back with a swap of saliva in hopes to receive interesting genetic information. Weeks later, users receive an email describing what their DNA says about them including traits and ancestral information. Beginning in 2006, 23AndMe could also release certain risk factors to developing 240 different health conditions based off of the DNA testing done. The FDA decided to stop this element in 2013, because they were concerned individuals would make important medical decisions based off of the test, regardless how uncertain they were.
Two years later, the FDA allowed results to share whether users children could develop any of 36 diseases. Test results however would not reveal risk factors of the individual's risk of developing each disease. The company vicariously continued their works in hopes to one day get the green light to sell actual DNA tests for specific diseases.
Today, the FDA has finally allowed 23AndMe to determine a person's own risk at developing certain diseases. Consumers can now know up to 10 genetic conditions they have a chance of receiving, including Alzheimers, Parkinson's Disease, Thrombophilia and Coeliac Disease. Such results should not be mistaken for a medical diagnosis, because given factors such as lifestyle and environment play a role in chances of development. This ruling is said to reduce the chances of other companies searching for loopholes around the US Governments requirements for genetic testing, showing that going through the FDA can be a step in the right direction and a way to move forward. 23AndMe will start selling DNA tests in the near months to come. Kathy Hibbs who is an officer at 23AndMe says,"We are really tired and really happy." The long-awaited action is finally in company's favor.
Hank Greely, a bioethiest at Stanford University worries individuals may need help from a genetic coach or counselor in order to correctly understand the information given from the test, as other companies begin to offer the same kind of tests.
When participating in a 23AndMe test, it tells users if any other of their siblings also partook in the program. I have a friend who sent in her swab of spit, and 6-8 weeks later found out her sister also took the test in search of her ancestry information. Except my friend wasn't aware she even had a sister, since she grew up as an only child. After she confronted her parents, it ended up being the best thing that happened to them and completely reunited the family!
- Lindsey Tanner
http://www.nature.com/news/23andme-given-green-light-to-sell-dna-tests-for-10-diseases-1.21802
After years of tug-of-war with the FDA, the ban on selling DNA tests has finally been lifted for unique genetic company 23AndMe. Individuals partaking in the tests can discover risks for developing 10 different disorders, using a simple at home genetic test.
Based in Mountain View California, 23AndMe is a unique service that individuals can order, and send back with a swap of saliva in hopes to receive interesting genetic information. Weeks later, users receive an email describing what their DNA says about them including traits and ancestral information. Beginning in 2006, 23AndMe could also release certain risk factors to developing 240 different health conditions based off of the DNA testing done. The FDA decided to stop this element in 2013, because they were concerned individuals would make important medical decisions based off of the test, regardless how uncertain they were.
Two years later, the FDA allowed results to share whether users children could develop any of 36 diseases. Test results however would not reveal risk factors of the individual's risk of developing each disease. The company vicariously continued their works in hopes to one day get the green light to sell actual DNA tests for specific diseases.
Today, the FDA has finally allowed 23AndMe to determine a person's own risk at developing certain diseases. Consumers can now know up to 10 genetic conditions they have a chance of receiving, including Alzheimers, Parkinson's Disease, Thrombophilia and Coeliac Disease. Such results should not be mistaken for a medical diagnosis, because given factors such as lifestyle and environment play a role in chances of development. This ruling is said to reduce the chances of other companies searching for loopholes around the US Governments requirements for genetic testing, showing that going through the FDA can be a step in the right direction and a way to move forward. 23AndMe will start selling DNA tests in the near months to come. Kathy Hibbs who is an officer at 23AndMe says,"We are really tired and really happy." The long-awaited action is finally in company's favor.
Hank Greely, a bioethiest at Stanford University worries individuals may need help from a genetic coach or counselor in order to correctly understand the information given from the test, as other companies begin to offer the same kind of tests.
When participating in a 23AndMe test, it tells users if any other of their siblings also partook in the program. I have a friend who sent in her swab of spit, and 6-8 weeks later found out her sister also took the test in search of her ancestry information. Except my friend wasn't aware she even had a sister, since she grew up as an only child. After she confronted her parents, it ended up being the best thing that happened to them and completely reunited the family!
- Lindsey Tanner
http://www.nature.com/news/23andme-given-green-light-to-sell-dna-tests-for-10-diseases-1.21802
Saturday, April 1, 2017
Cavefish May Help Humans Evolve to Require Very Little Sleep
Tyler Evans
Bio 1610
Every living organism needs sleep. Sleep is vital in success,health and happiness for everyone and everything. New technologies have lead us to groundbreaking information that humans can evolve and adapt to the sleeping habits of a little cavefish. The Pachón cavefish lives in deep and dark caves in central Mexico. These creatures eat little food and have scarcely any oxygen or light. The cavefish do not have eyes and they get around by lateral lines in the ocean and suppressing sleep.
Florida Atlantic University has been studying these cavefish and learning about the relationship between sleep and the sensory process. In their latest study they found suggests that the inability to block one's environment is one of the ways to lose sleep. Alex C. Keene a professor at FAU said, “ Our study suggests that differences and sensory systems may contribute to the sleep variability. It is possible that evolution drives sensory changes and changes in sleep or a secondary consequence, or that evolution selects for changes in sensory processing in order to change sleep.”
The Pachón cavefish have an environment that differentiates for typical surface fish. Cavefish have evolved to using enhanced sensory systems while having a reduction in sleep. A big reason for this is because nutritional availability and feeding behavior contribute to the evolution of a lack of sleep. If these fish sleep, they could miss out on rare opportunities to eat. Of the 29 different populations of cavefish that have been identified many of them evolved independently. The Pachón cavefish, the population a study, appear to have lost sleep due to increased sensory input, but not the other populations. James Jaggard, the first author on the graduation at FAU working with Keene said, “ this means that there are many different lose sleep or evolve a brain and we are going to search to identify these mechanisms.” This study of neural mechanisms generating this behavioral shift remained elusive.
For this study researchers recorded cavefish under inflated light setup in individual tanks. The video tracking told researchers the fish were inactive and they defined sleep as one minute of immobility. “ Humans block out sensory cues when we enter into sleep-like state,” said Keene he also gave us this example, “ We close our eyes and there are mechanisms in the brain to reduce auditory input. This is one of the reasons why a sensory stimuli like someone entering the room is less likely if you are asleep. Our thinking was that cavefish have to some degree lost this ability and this drives sleep loss.”
I have learned that our sensory inputs can alter our personal definition of sleep. These cavefish have evolved to a lack of immobility creating the same benefits of sleeping. While we sleep our bodies are recovering. It is more than just altering your sleeping environment it is teaching your body that sitting down and laying low is just as beneficial to your body compared to sleep. As humans we block out these sensory cues when we are sleeping. If we could sleep less but still be rested, think about how much we could accomplish.
Tyler Evans
Bio 1610
Every living organism needs sleep. Sleep is vital in success,health and happiness for everyone and everything. New technologies have lead us to groundbreaking information that humans can evolve and adapt to the sleeping habits of a little cavefish. The Pachón cavefish lives in deep and dark caves in central Mexico. These creatures eat little food and have scarcely any oxygen or light. The cavefish do not have eyes and they get around by lateral lines in the ocean and suppressing sleep.
Florida Atlantic University has been studying these cavefish and learning about the relationship between sleep and the sensory process. In their latest study they found suggests that the inability to block one's environment is one of the ways to lose sleep. Alex C. Keene a professor at FAU said, “ Our study suggests that differences and sensory systems may contribute to the sleep variability. It is possible that evolution drives sensory changes and changes in sleep or a secondary consequence, or that evolution selects for changes in sensory processing in order to change sleep.”
The Pachón cavefish have an environment that differentiates for typical surface fish. Cavefish have evolved to using enhanced sensory systems while having a reduction in sleep. A big reason for this is because nutritional availability and feeding behavior contribute to the evolution of a lack of sleep. If these fish sleep, they could miss out on rare opportunities to eat. Of the 29 different populations of cavefish that have been identified many of them evolved independently. The Pachón cavefish, the population a study, appear to have lost sleep due to increased sensory input, but not the other populations. James Jaggard, the first author on the graduation at FAU working with Keene said, “ this means that there are many different lose sleep or evolve a brain and we are going to search to identify these mechanisms.” This study of neural mechanisms generating this behavioral shift remained elusive.
For this study researchers recorded cavefish under inflated light setup in individual tanks. The video tracking told researchers the fish were inactive and they defined sleep as one minute of immobility. “ Humans block out sensory cues when we enter into sleep-like state,” said Keene he also gave us this example, “ We close our eyes and there are mechanisms in the brain to reduce auditory input. This is one of the reasons why a sensory stimuli like someone entering the room is less likely if you are asleep. Our thinking was that cavefish have to some degree lost this ability and this drives sleep loss.”
I have learned that our sensory inputs can alter our personal definition of sleep. These cavefish have evolved to a lack of immobility creating the same benefits of sleeping. While we sleep our bodies are recovering. It is more than just altering your sleeping environment it is teaching your body that sitting down and laying low is just as beneficial to your body compared to sleep. As humans we block out these sensory cues when we are sleeping. If we could sleep less but still be rested, think about how much we could accomplish.
Monday, March 27, 2017
Biochemists' discovery could lead to vaccine against 'flesh-eating' bacteria
Necrotizing Fasciitis, also known as 'flesh-eating' bacteria, is a bacterial infection that damages tissues in a short period of time. This infection can cause death in the individual. One of the most common bacteria that causes this infection is group A Streptococcus.
There are some treatments that can be done against this infection, but it mostly involves antibiotics and surgeries (Necrotizing Fasciitis, 2016)
As with other bacteria, group A Streptococcus has a protein coating, and the reason that there is not a vaccine for it is that group A strep has different types of strains. These strains have different protein coatings. The protein coating is called the M protein.
When bacteria enters the body, the immune response of the body immediately tries to fight against the bacteria by using antibodies. The antibodies have to be specific for that bacteria's protein coating. Since there are many strains of group A strep and each have different M proteins, then the body that armed up with antibodies specific to a strain of group A strep will not work for another strain of group A strep. That made it hard for scientists to find a vaccine that fights against this bacteria. However, a group of researchers discovered C4BP. This is a human binding protein. This binding protein binds to not just one M protein, but the majority of M proteins of the group A strep.
Knowing this, biochemist wanted to study the interactions between proteins of the M proteins and C4BP using computers. These studies allowed the biochemists to find patterns that were hidden between all the M proteins that they were studying.
These biochemists now have the idea that a vaccine can be developed that gives antibodies that act like the C4BP in that it recognized many M proteins.
A vaccine is know being developed by chemists at the UC San Diego, and with collaborations of Nizet, an infectious disease expert.
The biochemists' published paper can be found at https://www.ncbi.nlm.nih.gov/pubmed/27595425
When I was younger I remember listening about a 'flesh-eating' bacteria on the news in Bolivia. I remember feeling really scared of it. For a while I was really scared that I would get something like that, or that anybody in my family would get it. Due to this worry of mine, I started reading all sorts of articles about it, but could not find a specific cure for it that does not include amputations. Seeing the title of this article then called my attention.
References
Biochemists' discovery could lead to vaccine against 'flesh-eating' bacteria. (n.d.). Retrieved March 27, 2017, from http://www.biologynews.net/archives/2016/09/05/biochemists_discovery_could_lead_to_vaccine_against_flesheating_bacteria.html?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A%2Bbiologynews%2Fheadlines%2B%28Biology%2BNews%2BNet%29
Necrotizing Fasciitis: A Rare Disease, Especially for the Healthy. (2016, June 15). Retrieved March 27, 2017, from https://www.cdc.gov/features/necrotizingfasciitis/
Study Reveals How Ionising Radiation Damages DNA and Causes Cancer
This article is focused on how ionising radiation in gamma rays and x-ray, which we are frequently exposed to can damage our DNA and cause cancer. Previously, the unfortunate thing is what has yet to be figured out is how tumors are actually cause by these harmful forms of radiation.
From the article it says, "Dr Peter Campbell from the Welcome Trust Sanger Institute who led the study, said: "To find out how radiation could cause cancer, we studied the genomes of cancers caused by radiation in comparison to tumours that arose spontaneously. By comparing the DNA sequences we found two mutational signatures for radiation damage that were independent of cancer type. We then checked the findings with prostate cancers that had or had not been exposed to radiation, and found the same two signatures again. These mutational signatures help us explain how high-energy radiation damages DNA.' "
Often times when DNA is damaged, a mutational signature is shown. Dr. Peter Campbell, through these signatures was then able to track the patterns of the growth of tumors and how radiation reacted to the further growth of cancer is patients.
One type of mutation found is a deletion in the DNA. Another is called balanced inversion. What this means is the DNA is cut in two places and the cut strand of DNA then spins and connects in an opposite orientation. This type of mutation does not occur naturally in the body but high-energy radiation could be strong enough to have this happen.
Of these mutations, Dr Sam Behjati, clinician researcher at the Sanger Institute and the Department of Paediatrics, University of Cambridge, said: "Ionising radiation probably causes all types of mutational damage, but here we can see two specific types of damage and get a sense of what is happening to the DNA. Showers of radiation chop up the genome causing lots of damage simultaneously. This seems to overwhelm the DNA repair mechanism in the cell, leading to the DNA damage we see."
These mutations cause by radiation and the signatures they leave could provide insight into how these tumors would rapidly grow. By following the mutations and looking into the damages cause to the DNA scientists have been able to see the harmful affects of ionising radiation and the affects it has on the body and the risks of cancer it can cause.
-Chad Lords
Friday, March 24, 2017
The Strange World of Nighttime Open-Ocean Diving
Will Ford
BIO 1610
The article that I chose focuses on what to me is a very interesting topic because it shows just how much we still have to discover in biology. It starts off by explaining how at night deep sea plankton migrate up closer to the surface than usual. Along with these plankton many of the othere deep sea fish who feed on them also go up closer to the surface. This causes a huge variety of fish to be much more easily observed by people because they are so much closer, all you need is your basic scuba diving skills. However with this "Blackwater Diving" even the most seasoned scuba diver can be thrown completely out of his element because you encounter animals that you would have never ever seen like that in their natural habitat.
This type of deep water diving started first in Hawaii and is currently practiced in only a handful of locations around the globe. In Hawaii dives are lead weekly just a short boat ride off the shore. However after arriving to the dive zone it usually still takes a while for someone to summon the courage to get in from the fear of the unknown below them.
This fear of the unknown has caused many to speak out saying that this type of diving should be avoided because there are so many potentially dangerous sea creatures that you may encounter and there is evidence of these encounters. The author gives an explanation of why he doesn't fear Blackwater Diving any more than regular writing how in reality we come in contact with just as many highly dangerous animals during the daytime when diving and just as in the light they are normally scared of us.Photographer Jeff Milisen is who gathered the data and he makes the claim that really what causes the fear of Blackwater Diving is really just the fear of so much that we are unfamiliar with.
I really enjoy this article in relation to biology because it goes beyond just looking at and studying things in a lab and takes us to what biology really is, it shows us life in its different forms. After all that what biology is all about, teaching us how life itself keeps functioning and with so many things that we still dont know in the ocean its really cool to see that we have access to some of that and that we have only scratched the surface with the studies so far.
BIO 1610
The article that I chose focuses on what to me is a very interesting topic because it shows just how much we still have to discover in biology. It starts off by explaining how at night deep sea plankton migrate up closer to the surface than usual. Along with these plankton many of the othere deep sea fish who feed on them also go up closer to the surface. This causes a huge variety of fish to be much more easily observed by people because they are so much closer, all you need is your basic scuba diving skills. However with this "Blackwater Diving" even the most seasoned scuba diver can be thrown completely out of his element because you encounter animals that you would have never ever seen like that in their natural habitat.
This type of deep water diving started first in Hawaii and is currently practiced in only a handful of locations around the globe. In Hawaii dives are lead weekly just a short boat ride off the shore. However after arriving to the dive zone it usually still takes a while for someone to summon the courage to get in from the fear of the unknown below them.
This fear of the unknown has caused many to speak out saying that this type of diving should be avoided because there are so many potentially dangerous sea creatures that you may encounter and there is evidence of these encounters. The author gives an explanation of why he doesn't fear Blackwater Diving any more than regular writing how in reality we come in contact with just as many highly dangerous animals during the daytime when diving and just as in the light they are normally scared of us.Photographer Jeff Milisen is who gathered the data and he makes the claim that really what causes the fear of Blackwater Diving is really just the fear of so much that we are unfamiliar with.
I really enjoy this article in relation to biology because it goes beyond just looking at and studying things in a lab and takes us to what biology really is, it shows us life in its different forms. After all that what biology is all about, teaching us how life itself keeps functioning and with so many things that we still dont know in the ocean its really cool to see that we have access to some of that and that we have only scratched the surface with the studies so far.
Wednesday, March 22, 2017
A Virus, Fished out of a Lake, May Have Saved a Man's Life
The most common forms of medicine used to fight bacterial infections are antiobiotics; however, in the case of a man Dr. Ali Khodadoust, a virus was used to kill the serious infection that was nearly killing him. Clearly, a virus doesn't seem like the best form of medicine, but a virus-using method called phage therapy has actually been used for over a century. Back before antibiotics were discovered, bacteria-infecting viruses called bacteriophages were used to treat infections. This method became outdated and was never studied enough because of the submergence of antibiotics. But, when the bacteria killing Dr. Ali Khodadoust was resistant to antibiotics, the use of page therapy was turned to.
In 2012, Khodadoust had to have a coronary artery bypass, in which there was a piece of plastic mesh patching placed on his aorta. The mash patch end up having a bacteria on it called Pseudomonas aerugino that created a massive infection on the aorta. This bacteria is virtually harmless to healthy people, but can be extremely harmful to someone with a weakened immune-system, such as someone with cystic fibrosis, which we talked about in our first case study.
Antibiotics were tried, but the bacteria was resistant to them. A fistula, which is essentially a hole, formed on his chest. The hole became infected by the bacteria as well. For three months he was on large amounts of antibiotics that were only helping a little bit, and carrying an IV port with him. The doctors didn't know what to do because they were scared of spreading the bacteria. Just as Khodadoust was falling into a "miserable medical limbo", a scientist named Benjamin Chan came with an idea. He wanted to try phage therapy on the infection. All they had to do was find bacteriophages that killed infections like Pseudomonas aeruginosa.
After searching for weeks, a sample of water from a Dodge Pond in Connecticut came up. Bacteriophages from the water were tested and worked on the Pseudomonas aeruginosa sample! They called this perfect virus OMKO1. Chan and the other doctors made a plan to use this OMKO1 on the infection and then kill off any remaining bacteria with strong antibiotics. This plan was a risky one to be tried on Khodadoust, but something had to be done -- it was do or die for him. Chan and the other doctors got the operation approved by the FDA and did it.
Five weeks after the surgery, Khodadoust was in his homeland of Iran and had to be rushed into surgery to stop massive bleeding from a bone poke in his fistula. After the surgery, they tested him for Pseudomonas, and there was no trace at all. The phage therapy had worked! Miraculously, the virus had worked against the bacteria and they concluded that OMKO1 was capable and worth studying much further.
I found this article incredibly intriguing and awesome. I never knew that viruses, which are normally looked at in a negative aspect, could be used in a positive way. I think it shows how cool biology is -- how the medicine we may need could be all around us. This article and assignment definitely make me want to read more on these websites.
-Connor Lemmon
-Connor Lemmon
Can Facebook’s Machine-Learning Algorithms Accurately Predict Suicide?
Joshua Reber
Biology 1610
Can Facebook’s Machine-Learning Algorithms Accurately Predict Suicide?
We as humans love our social media. Many of us are avid users-for example there are 1.23 billion active Facebook users daily. Why? Talking face-to-face is messy and emotionally
involved–we don’t have time to think about what to say, we have to read facial
cues and body language.
This article begins by talking about a story of a young girl who through Facebooks new live video feature filmed herself talking, and even showing signs that she was about to commit suicide. Her friend saw this and alarmed the police, but they weren’t able to get there in time to save her life. This caused a lot of alarm in the Florida area, and Facebook is the first to start doing something about it.
Online, we have time to construct and and be open. This gives us the opportunity to position ourselves the way we want to
be seen. We hear daily about how the current generation is struggling with bullying, and how it has turned into something digital.
This article begins by talking about a story of a young girl who through Facebooks new live video feature filmed herself talking, and even showing signs that she was about to commit suicide. Her friend saw this and alarmed the police, but they weren’t able to get there in time to save her life. This caused a lot of alarm in the Florida area, and Facebook is the first to start doing something about it.
The article says this: “To reach its at-risk users, Facebook says it is expanding its services that allow friends to report posts containing signs of any suicidal or self-mutilation plans and it provides a menu of options for both those individuals and the friend who reported them. Choices include hotlines to call, prompts to reach out to friends and tips on what to do in moments of crisis. This tool will now be available for Facebook live streams as well. Similar reporting systems exist on a number of social media platforms including Twitter, Pinterest and YouTube. Facebook is now also piloting a program that will let people use Messenger, its instant messaging app, to directly connect with counselors from crisis support organizations including Crisis Text Line and the National Suicide Prevention Lifeline (NSPL).”
Various programmers are working on developing software that acts as a robot to identify keywords and behavior expected from a victim of suicide. These robots and software will then be able to provide various hotlines and numbers and resources that lead to help. Facebook stated that tens of thousands cases are reported by friends who are concerned by a friend to see if they can get some help with suicide prevention.
“This ultimately is an effort that makes a lot of sense,”
says Jessica Ribeiro, who is a psychologist at Florida State University. I am
in complete agreeance with her. I really like this article because I know many
people who really do struggle with these things, and are having hard trials
with it all. This article also interests me because I am a social media user,
and find it interesting to hear about what kind of protection the various
platforms are offering their users so they can feel safer. I believe if they can
dominate this software, without it being pushy on people, it really could be
beneficial and serve a lot of people. It's also interesting to think on a biological level about the various chemicals that are being secreted when we post online, and how we react to reading posts from friends/family. Suicide in this nation is one of the top
10 reasons for death, and is now 2nd overall cause of death for
youth. I encourage everyone to read this article, not only to hear about this
cool idea, but to also be aware of the issue.
The reference came from Scientific American: http://biologyinthenewsspring2017-tuesday.blogspot.com/2017/03/joshua-reber-biology-1610-can.html
The reference came from Scientific American: http://biologyinthenewsspring2017-tuesday.blogspot.com/2017/03/joshua-reber-biology-1610-can.html
Ethical Guidelines on Lab-Grown Embryos Beg for Revamping, Scientists Say
Ethical Guidelines on Lab-Grown Embryos Beg for
Revamping, Scientists Say, it
may be time to update the currently observed 14-day rule as a benchmark
This article was
about synthetic biology and the growing of an embryo that passed the 14-day
observation mark. Which is usually the time when the embryo is developing
tissues and right before they start developing a nervous system. The article
also explained that during this time it is the last time an embryo can divide. The
article goes on with George Church who is a synthetic biologist and geneticist,
he explains what he does in his lab. For example, growing organoids to function
like hearts, lungs, kidneys, and the brain. He uses them to test out drugs and
hoping one day they can be used for failing body parts. The idea of going over
the 14-day mark triggered some opinions from the bioethicists. Insoo Hyun for
example says, “Between synthetic biology and artificial intelligence a
future might not be far off in which we have to ask whether something created
in a lab is truly alive.” He goes on by saying that we are getting into experiments
that question what it means, to be human
and what it means to deserve moral respect. That being said there are some
committees that regulate embryonic research, but lit it states in the article, “Synthetic biology falls between the cracks,
though, with no one having such clear authority to regulate the work,” Finally
the article comes to a close with church saying that from his experience he has
seen more problems come from under regulation as oppose to overregulation.
I found this article really interesting, because of a few
reasons. The first being that synthetic biology is growing day by day. New
discoveries for synthetic organs that are being used was really interesting. Reading
other scientist views on synthetic biology was interesting as well because, not
all of them believe this new discovery is not ethical. I really liked reading
this article, I liked seeing scientist tell share their own opinions and
backing them up as well.
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