Digitized DNA

DNA Has Gone Digital — What Could Possibly Go Wrong?

Biology is becoming increasingly digitized. Researchers like us use computers to analyze DNA, operate lab equipment and store genetic information. But new capabilities also mean new risks – and biologists remain largely unaware of the potential vulnerabilities that come with digitizing biotechnology.
The emerging field of cyberbiosecurity explores the whole new category of risks that come with the increased use of computers in the life sciences.
University scientists, industry stakeholders and government agents have begun gathering to discuss these threats. We've even hosted FBI agents from the Weapons of Mass Destruction Directorate here at Colorado State University and previously at Virginia Tech for crash courses on synthetic biology and the associated cyberbiosecurity risks. A year ago, we participated in a U.S. Department of Defense-funded project to assess the security of biotechnology infrastructures. The results are classified, but we disclose some of the lessons learned in our new Trends in Biotechnology paper.
Along with co-authors from Virginia Tech and the University of Nebraska-Lincoln, we discuss two major kinds of threats: sabotaging the machines biologists rely on and creating dangerous biological materials.
In 2010, a nuclear plant in Iran experienced mysterious equipment failures. Months later, a security firm was called in to troubleshoot an apparently unrelated problem. They found a malicious computer virus. The virus, called Stuxnet, was telling the equipment to vibrate. The malfunction shut down a third of the plant's equipment, stunting development of the Iranian nuclear program.
Unlike most viruses, Stuxnet didn't target only computers. It attacked equipment controlled by computers.
The marriage of computer science and biology has opened the door for amazing discoveries. With the help of computers, we're decoding the human genome, creating organisms with new capabilities, automating drug development and revolutionizing food safety.
Stuxnet demonstrated that cybersecurity breaches can cause physical damages. What if those damages had biological consequences? Could bioterrorists target government laboratories studying infectious diseases? What about pharmaceutical companies producing lifesaving drugs? As life scientists become more reliant on digital workflows, the chances are likely rising.
The ease of accessing genetic information online has democratized science, enabling amateur scientists in community laboratories to tackle challenges like developing affordable insulin.
But the line between physical DNA sequences and their digital representation is becoming increasingly blurry. Digital information, including malware, can now be stored and transmitted via DNA. The J. Craig Venter Institute even created an entire synthetic genomewatermarked with encoded links and hidden messages.
Twenty years ago, genetic engineers could only create new DNA molecules by stitching together natural DNA molecules. Today scientists can use chemical processes to produce synthetic DNA.
The sequence of these molecules is often generated using software. In the same way that electrical engineers use software to design computer chipsand computer engineers use software to write computer programs, genetic engineers use software to design genes.
That means that access to specific physical samples is no longer necessary to create new biological samples. To say that all you need to create a dangerous human pathogen is internet access would be an overstatement – but only a slight one. For instance, in 2006, a journalist used publicly available data to order a fragment of smallpox DNA in the mail. The year before, the Centers for Disease Control used published DNA sequences as a blueprint to reconstruct the virus responsible for the Spanish flu, one of the deadliest pandemics of all time.
With the help of computers, editing and writing DNA sequences is almost as easy as manipulating text documents. And it can be done with malicious intent.
The conversations around cyberbiosecurity so far have largely focused on doomsday scenarios. The threats are bidirectional.
On the one hand, computer viruses like Stuxnet could be used to hack into digitally controlled machinery in biology labs. DNA could even be used to deliver the attack by encoding malware that is unlocked when the DNA sequences are translated into digital files by a sequencing computer.
On the other hand, bad actors could use software and digital databases to design or reconstruct pathogens. If nefarious agents hacked into sequence databases or digitally designed novel DNA molecules with the intent to cause harm, the results could be catastrophic.
And not all cyberbiosecurity threats are premeditated or criminal. Unintentional errors that occur while translating between a physical DNA molecule and its digital reference are common. These errors might not compromise national security, but they could cause costly delays or product recalls.
Despite these risks, it is not unusual for researchers to order samples from a collaborator or a company and never bother to confirm that the physical sample they receive matches the digital sequence they were expecting.
Infrastructure changes and new technologies could help increase the security of life science workflows. For instance, voluntary screening guidelines are already in place to help DNA synthesis companies screen orders for known pathogens. Universities could institute similar mandatory guidelines for any outgoing DNA synthesis orders.
There is also currently no simple, affordable way to confirm DNA samples by whole genome sequencing. Simplified protocols and user-friendly software could be developed, so that screening by sequencing becomes routine.
The ability to manipulate DNA was once the privilege of the select few and very limited in scope and application. Today, life scientists rely on a global supply chain and a network of computers that manipulate DNA in unprecedented ways. The time to start thinking about the security of the digital/DNA interface is now, not after a new Stuxnet-like cyberbiosecurity breach.
Jenna E. Gallegos, Postdoctoral Researcher in Chemical and Biological Engineering, Colorado State University and Jean Peccoud, Professor, Abell Chair in Synthetic Biology, Colorado State University
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Love at First site

Love at First Sight? It's Probably Just LustWe've all seen that movie moment when two strangers meet and feel an instant romantic connection — in fact, "love at first sight" has been a mainstay of literature for thousands of years, and people in real life often claim to experience a similar spark.
But is that feeling actually love? Not quite, according to the authors of a new study.
In the study, researchers investigated whether people feel love at first sight — LAFS — or whether they believe retroactively that they felt that way, once they've already formed an attachment to a romantic partner. The scientists also questioned whether what people call "love" at a first encounter is truly representative of the complex emotions that make up love — or just a powerful physical attraction
Prior studies have shown that being in love activates certain brain regions, and the location of the activity can vary depending on what type of love the person is feeling, such as emotional, maternal or passionate love. Intense, passionate love activates the same networks in the brain as addiction does, and more long-term love sparked responses in brain regions associated with attachment and reward
Researchers have also previously reported that as many as 1 in 3 people in Western countries claim to have experienced LAFS. And that the feeling is associated with more passion and stronger bonds within the relationship, the scientists wrote in the new study.  
But there was little evidence indicating if LAFS occurred when people thought it did — at the moment of their first meeting ― or if they merely remembered it happening that way through the lens of their current romantic feelings, the study authors explained.
The scientists collected data from about 500 encounters between nearly 400 participants, mostly heterosexual Dutch and German students in their mid-20s. Using three stages of data collection — an online survey, a laboratory study and three dating events lasting up to 90 minutes each — the researchers gathered information from their subjects about meeting prospective romantic partners. They noted whether participants said that they felt something akin to LAFS upon a first meeting, and how physically attractive they ranked the person who inspired those feelings. 
To define what qualified as "love," subjects submitted self-analysis of several key components: "eros" (physical attraction), "intimacy," "passion" and "commitment." During the tests, 32 different individuals reported experiencing LAFS a total of 49 times — and that observation wasn't typically accompanied with high ratings for love components such as intimacy and commitment.
However, reports of LAFS did correspond with a potential partner scoring higher as physically attractive, the researchers discovered. About 60 percent of the study participants were women, but men were more likely to report feeling LAFS "on the spot," the study authors reported. And in every case, their experience of LAFS was unreciprocated, suggesting that mutual, instantaneous LAFS "might generally be rare," according to the study.
The authors determined that LAFS was, in fact, merely "a strong initial attraction" that people identified as love, either at the moment they felt it, or in retrospect. And though some study subjects who were already involved with someone reported that they fell in love at first glance, it's hard to say for sure if that happened the way they remembered. Answering this question would require further investigation into romantic relationships, to see how those initial, powerful feelings of instantaneous love play out over time, the scientists wrote.   
The findings were published online Nov. 17 in the Journal of the International Association for Relationship Research.
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