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"Zombie deer disease" spreads to the US. What is this?



A mad cow-like infectious disease that can turn the talent, elk, and moose into "Swiss cheese" spreads in at least 24 states – and some experts are This warning can eventually make the way to people.

Known as a severely wasted illness – and colloquially called "zombie deer disease" – a severe progressive neurodegenerative disease was first recognized in the 1960s. Like crazy cattle, chronic pain loss is spreading by prions, zombie-like pathogenic proteins that are not alive and can not be killed. When they become infected with an animal, they eat in the brain, causing symptoms similar to dementia and eventually lead to death. While the disease is still rare, researchers believe it is more extensive than ever because, in part, how the people's trade in one and other hoofed mammals.

"What we have seen over the past few decades is that it gradually spreads the deer population gradually," says Peter Larsen, an assistant professor of veterinarians at the University of Minnesota who studies pathogens. It also spreads to captives, elk, and reindeers delivered nationwide and overseas to hunt ranchs, petting zoos, and Christmas-themed farms. That's what happened in South Korea, Larsen said. (It is known in Canada and Norway.)

When new outbreaks start, they are virtually impossible to contain because, unlike viruses and bacteria, prions can not be killed and currently there is no good way to locate it.

Researchers have long wondered if the disease, like crazy cows, could jump people. (Mad maybe people are known as Creutzfeldt-Jakob illness.) Last summer, we had an initial and frightening answer. In a newspaper published in the journal Emerging Infectious Diseases researchers from Scotland and Canada have shown through an experiment in a petri dish that prions from the sick can actually infect cells person.

Since then, there has been no direct evidence of human illness. That research, however, motivated Michael Osterholm, director of the Center for Infectious Disease Research and Policy at the University of Minnesota, to compare the recent acute wasting disease. Osterholm, it turns out, also warned the British government of the dangers of mad cow before hundreds of people were infected in the UK and around the world in the late 1

990's. Seated in front of a state committee in Minnesota On February 7, he called the chances of people being severely affected by wasteful "possible" and "possible," and added: "The number of human cases will be large and not separate events . " [19659007AyonsaLarsenhindipaorasangpagclashngunitnagbabalasiyanaitoayisanglumalakingbantasakalusuganngpublikoAngmgataoayhindidapatkumonsumongkarnengimpeksyonsinabiniyahabangbinabanggitdindoonaytalagangwalangmabutingparaanupangmalamankungangkarneaynahawahan"Sakasalukuyanwalangparaanparamabilisnamasuringmgataoangmgaprionsakarnesaibabawngpagprosesongkarneosalivedeer"sabiniya"Angpangunahinaydapatnakumilostayongayonupangbumuongmgabagongteknolohiyaupangmakitaatsirainangmgaprion"

Let us know about emerging infectious diseases.

1) What is "zombie deer disease"?

Officially called severe wasting disease, zombie deer disease is a deadly progressive neurodegenerative disease that affects one, elk, reindeer, and moose. It was found in edible edible roots in Colorado in 1960, and has become a scientist who has been a scientist since then.

The disease is caused by prions – not viruses or bacteria. Prions are virtually indestructible pathogenic proteins that trigger cells, especially in the brain and spinal cord, to collapse abnormally and start clumping. When that happens, the infected animals begin to produce a lot of pity symptoms – dementia, spells, and difficulty walking, speaking, and eating. The animals eventually became distressed and disturbed. Symptoms are worsening over time, and since there is no cure, they always lead to death.

The reason why this disease is an official name – acute wasting disease – is that when the Prions reach an animal, it starts to lose weight and waste. The prions "opened the brain in Swiss cheese," Larsen says.

But Larsen called the "zombie deer disease" an unfortunate and potentially tricky moniker. "I only saw a deer who died in [chronic wasting disease] and it was skinny," she says. "There are no symptoms like the zombie, but the symptoms are what you expect to see in a sick person: thin, weak, and abnormal.

" It's important to note that [this] a neurodegenerative disease – not a zombie hunter disease. "

2) How does it spread to animals?

An animal with a severe wasting disease can spread to prions with other animals by direct or indirect contact with body fluids such as feces, saliva, blood, or urine.This means that the disease may spread if the deer touches the wound, for example, and its blood is touching an unpalatable animal, or if a healthy animal interacts with the soil, food, or water contaminated with a deer disease.

That's not all, Larsen says, because prions are so powerful , they can survive in the enclosures ran – farms, forests – for years, even decades. "So let's say you have a deer with a severe wasting disease, and it started [prions] on urine, feces, and saliva." If that one dies on the forest floor, prions can survive and bind to the ground, where plants will soak upwards. Plants can spread to prions on their leaves, Larsen said.

"So it spreads in the wild, slowly and every year, we see more and more cases of severe wasting disease."

3) How does this spread to humans?

No documented cases of serious illness in humans – but researchers think it feasible and becomes more likely, because infections are becoming more prevalent among animals.

Today, the only evidence of scientists spread to other animals is not straightforward. In lab experiments, scientists have shown that this disease may spread to monkeys and mice that carry human genes, says Centers for Disease Control and Prevention. In a yet-to-be published study, macaques – a monkey species genetically similar to humans – which fed contaminated meat contracted the disease.

"Experiments were performed [also] where researchers conduct environmental examples, such as stones or pieces of wood, with [pathogenic] prion of them," Larsen says. "Then they put these contaminated items into cages with transgenic hamsters and the hamsters get sick."

Finally, in another published study, researchers discovered that acute wasting disease prions infected human cells on a petri dish. The CDC said that experiments "raised the concern that [chronic wasting disease] could be a hazard to the people and suggest it is important to avoid human exposures in [the disease]." The possible way this can happen is if a person, like a hunter, is eating contaminated meat.

It causes us another disturbing truth about the serious wastage of disease: "In a prion, you can not [cook it off]. The temperature required to destroy it is far from what you can cook in , "said Larsen.

The only way to make non-contagious prions is the use of lye, a powerful alkaline solution that greatly changes the pH balance, and autoclaving – or pressure-treat them – at 270 degrees Fahrenheit. "Most people have no access to this approach," Larsen said, and "the point is that it is difficult to manage [infectious] prions in the environment because we do not know exactly where they lie." That brings us to the next problem with this disease.

4) Where is the zombie deer disease in the US?

Well, we know where the chronic pain loss is . The deer can only be tested after they die (researchers need access to tissues deep into the animal brain, and to try). But animals can carry pathogens for years and do not show any signs or symptoms. "The one who can go on a 40-mile trip, sprinkling [infected] prions in his feces or urine," says Larsen. "If we go and say that it is a [chronic wasting] one at this point on the map, what you do not see on the map is somewhere in the last two years."

As of January 2019, 251 counties in 24 states reported a chronic worsening of deer-free disease, reported by the CDC. You can find them here:


Chronic wasting free-range pain, reported by the county of the United States, in January 2019.
CDC

However, researchers think that the spread range is more extensive. The CDC also states that some states have better animal disease monitoring systems than others, so the current map may be more reflective of where the detective is strongest (and the previous illness) than where the deadly prion is currently spreading to the US.

5) Can we stop the disease from spreading?

Since there is no way to eliminate and cure the disease today, researchers recommend that the states in which it is known to spread are trying to conserve it by identifying the sick.

Now, another problem: The tools available to do that now are very small. Diagnostics for animal disease detection are not always accurate, not all states have access to them, and, again, they can only confirm having an infection with an animal after it is dead. It can also take days or weeks to get results. Which means the pain can move for a while before anyone knows it is there.

That's why Jeremy Schefers, a veterinary pathologist at the University of Minnesota, recently reminded lawmakers of his state for research funding to develop better diagnostic tools and help scientists answer the basic questions about severe wasting disease. Here is Schefers speaking in the Minnesota Post:

We need to find infected animals before their death, but we have no tests. … We need to know how other animals move to CWD prion around the environment, but we have no tests for that.

We need to know if the local meat store is contaminated and if it can be effectively cleaned, but there is no test for it. We need to know whether prions are moving from the soil to plants and potentially contagious, but we have no tests for it. … I want to know how much is on the ground and I want to know how much it takes to get something out, but we have no tests for that.

All Hunters need access to a trial that can be easily bought and quickly discover the CWD in their deers before it can be cut up to 100 pieces and fed into their family. The hunters have no access to a trial.

6) How do humans protect the animals and themselves?

Health officials are most concerned about the potential for hunters exposed to disease by animals carrying prions. So no one finds themselves at care in areas where acute illness is known to spread should take the following precautions, according to the CDC:

  • No shot, handling, or eating elk or deer that does not look bad or "behaves differently."
  • When an animal shapes (or removes the organs of) an animal that is hunted, wear latex or glove gloves, avoid touching animal organs – especially brain and spinal tissues cord – and avoid using the equipment used at home.
  • Get a deer or elk meat tested for prion disease before eating the meat. However, the CDC also warns that because diagnostic tools for illness are still limited, "The negative test results do not guarantee that an individual animal is not contaminated" with severe illness, 39; t "may reduce your risk of exposure." [19659046] When commercially processed meat, ask the killer to handle and process multiple animals at a time (to prevent contamination).

What about buyers of game meat, like veal, and restaurants that serve here? In that case, Larsen did not answer.

He advised that anyone eating a game of meat, or a restaurant serving as a game, would ask about where the meat came from. And restaurants need to make sure their meat is no good. But again, in practice, that is not easy because of how long it takes to get results from diagnostic tests.

"If you are a hunter, and take a deer to feed your family or sell it, will you wait for two weeks [for a test result]?" Larsen asked. "How do you keep the meat fresh?"

So while consumers may have the right to know if their meat is contagious with pathogenic prions, there is currently no good way to get an answer.

"People have been in contact with one of the centuries," says Larsen, "for food, sport, or simply looking at them in the wild." But that tradition is "now under attack because of this pathogen."


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