Thom Lang / Corbis
May 14, 2012 -
Recent controversial experiments and a research paper that detailed how to make an airborne version of the H5N1 avian influenza virus made some people nervous. The fear is that somebody, be it a terrorist group or unethical government, could create a superbug and use it as a biological weapon. But even it the recipe for avian flu hadn't been published, there are still plenty of other viruses to choose from. To be a good biological weapon, a pathogen should be transmitted from person to person, have an incubation or contagious period long enough that the infected patient can spread it and either incapacitate or kill.
Centers for Disease Control
Smallpox Top of the list is smallpox. Historically it's had a mortality rate of 30 to 35 percent, although it was much higher, sometimes 90 percent, in populations that were never exposed to it, such as Native Americans. Smallpox is an airborne virus, which means it can be caught easily from infected people who cough or sneeze, but can also be transmitted through touch. The disease creates a fever, malaise, head and body aches and sometimes vomiting. Two to four days later, a rash develops in the mouth and throat and sores break out on the skin. This is the most contagious period. Usually the rash spreads to the entire body in 24 hours. Ironically, most people feel better at this point. The rash becomes the classic pox after about three days, in which bumps are filled with fluid. The fever rises again at this time. Over the course of another week or two the pustules scab over, and when the last one is gone, the patient is no longer contagious. Smallpox has four varieties; three are often fatal. The last naturally occurring case of the disease was in 1975, in Bangladesh. However, the virus is still in cold storage at two labs, one in the United States and the other in Russia. For now, most people in their 20s and 30s might have no immunity at all. This is especially true in developing nations whose populations are generally younger. "A new outbreak in India or South Africa, for example, would be beyond terrible," said Tara Smith, an assistant professor of epidemiology at the University of Iowa.
Michael Abbey / Visuals Unlimited / Corbis
Resistant Bacteria Diseases that have been historically treated with antibiotics are good candidates for biological weapons because many strains have become resistant to the antibiotics. Methicillin-resistant staph, or MRSA, is one of the more well-known, and is spread by physical contact. MRSA usually stays in the skin, but in some people, it infects vital organs like the heart. Some varieties have caused necrotizing fasciitis, "flesh eating disease." A drug-resistant MRSA that was immune to all of the currently known antibiotics would cause many deaths. Tuberculosis is another that has evolved drug-resistant strains. The first totally drug-resistant form was identified in 2007 in Italy and by 2010, 8.8 million people had contracted it, with 1.4 million dying. Tuberculosis is the second biggest killer behind HIV/AIDS, according to the World Health Organization. It's spread person-to-person by coughing. The bacteria multiplies in the lungs, and patients die from respiratory failure or an excess of fluid in the lungs. Artificially breeding drug-resistant bacteria is no longer that complicated, Smith said. "Antibiotic resistance genes are easy to add to almost any bug, and some plasmids already carry resistance genes for multiple classes of drugs."
Centers for Disease Control
Bubonic Plague The Black Death or bubonic plague -- officially known as Yersina pestis -- killed a third of Europe's population in the 14th century, and it still exists in some parts of the world today. It has a long history as a bioweapon: accounts of the Mongol siege of the Crimean city of Caffa in 1347 say the invaders catapulted the corpses of infected people over the walls. And it isn't just a medieval phenomenon; the last major outbreak in the United States was in 1900 in San Francisco and involved 121 people of which 113 died; cases have appeared sporadically since. The plague is transmitted by fleas, which incubate the bacterium in their gullets. The multiplying Yersina block blood from getting to the fleas' stomachs, and the starving fleas start to feed more aggressively and try to clear the blockage by regurgitating the bacteria. That transmits the disease to hosts, including humans. Symptoms appear in two to six days. The infection causes the lymph nodes to swell (the "buboes"), but sometimes the bacteria invades the bloodstream directly and causes flu-like symptoms, without the swollen lymph nodes. In either case, mortality rates can be 40 to 60 percent if untreated. Infection of the lungs is the most serious form. The patient will cough up bloody sputum and droplets that help spread the disease person-to-person, and unless treated quickly mortality can approach 100 percent. The Black Death is treatable with antibiotics such as streptomycin now, but a resistant strain could be a serious public health problem.
Centers for Disease Control
Anthrax Anthrax is spread by spores, and those spores can survive in many environments, sometimes for years. There are three ways anthrax infects: breathing the spores, eating infected meat or having the spores get into cuts on the skin. Infection through inhalation is the most likely to kill, but anthrax is still quite dangerous. As the bacteria multiply in a person, they release toxins into the blood and tissues that cause swelling and cell death. Fatality rates are high, approaching 50 percent, even with treatment by antibiotics and 90 percent without that. It's not contagious, but a bomb can be made to spread the spores and infect many people at once. The spores can even be sent in the mail, as in the 2001 anthrax attacks. In those cases, envelopes containing anthrax spores were sent to several media outlets and the offices of two senators. Five people died and another 17 were infected. "Anthrax is great from the point of view that it is stable and not usually a suspect until it's too late to treat," Smith said. Anthrax produces symptoms that look like flu and unless there is a reason to think a person is infected, a doctor might not know to test for it. For a bioweapons manufacturer, however, the lack of person-to-person transmission means it needs to be released repeatedly. Anthrax is also vulnerable to antibiotics if caught early, though drug-resistant forms of it were experimented with in the United States until 1972 and the former USSR until the projects were abandoned in 1992. In 1942 the British government tested a strain of anthrax on an island in Scotland; decontamination didn't happen until 1990.
Sion Touhig / Corbis
Agricultural Pathogens As bad as pathogens are that kill people, those that attack animals or agriculture can have effects just as devastating. Rinderpest, which was declared wiped out in 2011, killed cattle at mortality rates of 100 percent, if the population had never been exposed previously. Hoof-and-mouth disease, caused by a virus in the genus Aphthovirus, remains active. It can infect cows, pigs, sheep and goats, and causes lesions on the feet and in the mouth. The mouth lesions sometimes keep animals from eating and the foot lesions can cause lameness. Some animals die from heart inflammation. It can be spread via contact with contaminated farming equipment, vehicles, clothing or feed. It also is carried by predators. During the 2001 outbreak in the United Kingdom, anyone traveling to the United States and Europe from there was asked to step onto a disinfectant pad to decontaminate their shoes, and livestock imports from Britain to the European Union were banned. The results were millions of animals being culled and billions of dollars in containment and lost business. To create mayhem, a terrorist could spray aerosols with the virus and devastate herds. "If someone would spray every herd he/she sees from a highway going from New York to San Francisco and then driving North-South (in the middle of the country), that would do it," said Peter Palese, chair of the department of Microbiology at the Mt. Sinai School of Medicine in New York. Other diseases could also become a problem, including H5N1 avian influenza, which infects the respiratory tracts and has a high mortality rate among chickens and poultry.
The Black Death of the 14th century may be written into the DNA of survivors' descendants, new research finds.
The study reveals that Roma people (sometimes known as gypsies, although this is considered a derogatory term) and white Europeans share alterations to their genetic code that occurred after the Roma settled in Europe from northwest India 1,000 years ago. The plague of the 1300s, which killed at least 75 million people, is a likely candidate for forcing this evolutionary change.
"We show that there are some immune receptors that are clearly influenced by evolution in Europe and not in northwest India," said study leader Mihai Netea, a researcher in experimental internal medicine at Radboud University Nijmegen Medical Center in the Netherlands.
"India did not have the medieval plague, as Europe had," Netea told Live Science. "We have also demonstrated that these receptors are recognizing Yersinia pestis, which is the plague bacterium." [In Photos: 14th-Century Black Death Graves Discovered]
Searching for similarities
Netea and his colleagues made their discovery by scanning almost 200,000 single-nucleotide polymorphisms (SNPs), or short segments of DNA that vary among people. They tested people from Romania, as well as Roma people. For social and economic reasons, Netea said, the Roma have lived among Europeans since about A.D. 1000, without much interbreeding between the two groups. That gives researchers a rare opportunity to study two genetically distinct populations in one geographical region.
The researchers looked for genetic variations that appeared in both Europeans and Roma people. Then, they took that list and crossed off the genetic variations that also appeared in a population of northwest Indians, to rule out evolutionary change that originated outside Europe.
The result was a list of about 20 genes that show evidence of convergent evolution between Europeans and Roma -- meaning the two groups started out different but evolved to look more similar because of pressures in their environment.
A plague scene shows a decimated 1600s Rome.SSPL via Getty Images
Black Death genetics
The genes on the list have a variety of functions. One gene, SLC45A2, is known to be involved in skin pigmentation. Others are linked to immune-system function.
One immune-related cluster included three altered genes, making it the most obvious candidate for closer perusal. The cluster, called TLR2, was already known to be involved in building the receptors on the surface of leukocytes, immune cells that recognize and destroy foreign invaders.
Because plague was such a widespread and devastating event in Europe, Netea and his colleagues reasoned that the Black Death outbreak, which occurred after the Roma arrived, might have put pressure on this gene cluster to evolve.
To test the idea, they looked at how cells engineered to express TLR2 would hold up against Y. pestis and Yersinia pseudotuberculosis, an ancestor of Y. pestis. They found that TLR2 caused a heightened immune response when exposed to both bacteria.
Other diseases could have altered the same genes, Netea said, but plague is a strong candidate, because it affected Europe and not northwest India, and because it had such a widespread, devastating influence. The findings could have medical implications even in today's world, where plague is no longer such a danger. For example, autoimmune disorders, in which the body attacks its own tissues, may arise because of immune systems programmed by epidemics to respond strongly to the threat of invasion, Netea said.
Humans "were modified, basically, by the infections," he said.
The researchers report their findings today (Feb. 3) in the journal Proceedings of the National Academy of Sciences.
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