
What to Know About the Horned 'Zombie' Rabbits Hopping Around Colorado
The rabbits didn't hop out of the set of a horror flick: They have cottontail rabbit papillomavirus, a skin disease that leads to alarming-looking growths. 'It exhibits as these wart-like growths on their face—sometimes they're smaller, like little nodules, and sometimes they're bigger, like tentacles or horns,' says Kara Van Hoose, a spokesperson with Colorado Parks and Wildlife.
We asked experts what the virus is, how it affects rabbits, and if humans should be concerned.
What exactly is the rabbit papillomavirus?
The rabbit papillomavirus—which is most frequently seen in the Midwest—was identified by the cancer researcher Richard E. Shope in the 1930s. (It's also known as the Shope papillomavirus.) It has since been used as a model to help scientists study the human papillomavirus, or HPV, which can similarly cause genital warts and lead to certain types of cancer.
Rabbits get the virus when they're bitten by ticks, fleas, and mosquitoes, and can spread it to each other through direct contact. Infection tends to be seasonal: It's especially common in the summer, when biting insects are most active. 'We go through this every year,' Van Hoose says. Factors like warm weather and a bad mosquito season (which is the case this summer in Colorado) can influence how prevalent papillomavirus is each year.
Read More: 6 Things to Eat to Reduce Your Cancer Risk
The virus causes warty, black lesions around the neck and shoulders in wild cottontail rabbits, and around the ears and eyelids in domestic rabbits, says A. Alonso Aguirre, dean of Colorado State University's Warner College of Natural Resources and an expert in wildlife diseases. Sometimes, it shows up as a tumor on rabbits' legs, especially on the surface of their hind feet. These tumors are firm, white, and moist on the surface, Aguirre says, and generally persist for up to 150 days—and then disappear. 'It's very painful,' he adds.
Can rabbits recover?
Despite the gruesome way it looks, cottontail rabbit papillomavirus is often benign, and many rabbits end up fighting it off on their own. Research suggests that in about 35% of affected rabbits, papillomas simply disappear within six months. Cottontail rabbits typically aren't treated. 'I don't know if you've ever tried to capture a rabbit, but it's very difficult,' Van Hoose points out. 'They're very fast.'
In other cases, however, the protrusions can affect the rabbits' eyes and mouth, preventing them from being able to eat, drink, or see clearly. That can lead to starvation and other life-ending complications, Van Hoose says. The virus can also turn into squamous cell cancer with metastases.
While wild rabbits mostly just develop warts when infected with cottontail papillomavirus, domestic rabbits experience much more severe illness, says Thomas M. Donnelly, a veterinarian who specializes in laboratory animal medicine and has studied the virus. The majority develop invasive epidermoid carcinomas (meaning they begin in squamous cells), he says, which are typically fatal.
Is there any risk to humans? What about other animals?
The rabbit papillomavirus only affects hares and can't be transmitted to humans or other types of animals. Still, Colorado Parks and Wildlife has instructed residents not to touch or otherwise attempt to help infected rabbits. 'That's what we tell everyone with wildlife,' regardless of whether the animals are sick, Van Hoose says. 'It's just practicing those really smart wildlife principles of keeping your distance, not feeding them, and not trying to step in and help, because there's nothing we can really do.'
A public frenzy
It makes sense why people are so intrigued by the horned rabbits. They're unusual and weird-looking; plus, rabbits are prevalent in many neighborhoods, says Valerie McKenzie, a professor in the department of ecology and evolutionary biology at the University of Colorado. 'You're used to seeing, 'Oh, cute bunny,'' she says. 'Now it's, 'Oh my gosh, crazy bunny with these things all over it.''
While the horned rabbits are currently captivating wildlife observers, the virus isn't the only unique way disease can show up in animals, she adds: 'There's all kinds of parasites and diseases that cause wild things in animals, that are really kind of cool and exciting.' McKenzie hopes the viral nature of the Colorado 'zombie rabbits' inspires more research to better understand the disease.
Read More: What an HPV Diagnosis Really Means
It's been interesting to see the spectrum of reactions play out, Van Hoose says. 'Some people think they look really gross, and they're weirded out by the growths on their face—they don't really want to see it,' she says. 'Other people, myself included, think it looks kind of metal and kind of cool.'
It's unclear exactly how many infected rabbits are hopping about, but Colorado Parks and Wildlife has received more than a dozen sightings, mostly in the northern part of the state. Since the initial reports, Van Hoose has spent her days on the phone, talking to reporters clamoring for information about the rabbit papillomavirus. 'This is one of the busiest days I've had at Colorado Parks and Wildlife,' she told TIME on Aug. 13. The end of the summer is typically the agency's most hectic time of year anyway, as people flock to the area's outdoor attractions. 'Every day there's a new wildlife question that comes in, and that includes dealing with bears and an invasive bighead carp species that we pulled out of a small pond,' she says. 'I didn't think that rabbits would become our most interesting story.'
Van Hoose hasn't seen an infected rabbit yet, but she hopes that changes soon: 'I feel like I'm kind of owed one now, since I've been talking about it so much,' she says.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
4 hours ago
- Yahoo
Precigen wins immunotherapy approval; Pfizer sickle cell drug fails trial
This story was originally published on BioPharma Dive. To receive daily news and insights, subscribe to our free daily BioPharma Dive newsletter. Today, a brief rundown of news involving Precigen and Pfizer, as well as updates from the Institute for Clinical and Economic Review, Superluminal Medicines and Generation Bio that you may have missed. The Food and Drug Administration granted full approval to a first-of-its-kind treatment for recurrent respiratory papillomatosis, a rare and potentially life-threatening condition caused by persistent HPV infections. Thursday's clearance of Precigen's Papzimeos, an immunotherapy that helps clear HPV-infected cells, was based on study results showing a little more than half of drug recipients didn't need surgery within a year of therapy. Center for Biologics Evaluation and Research director Vinay Prasad, who rejoined the FDA this week, described the approval as proof 'randomized trials are not always needed to approve medical products.' That statement should be 'reassuring' to biotech investors concerned about stricter regulatory standards under Prasad, wrote Cantor Fitzgerald analyst Jennifer Kim. Precigen shares rose higher Friday on the news. — Ben Fidler An experimental Pfizer drug for sickle cell disease failed to meet its goal in a Phase 3 study, the company said Friday. Testing showed that treatment with inclacumab, a drug Pfizer acquired via its 2022 buyout of Global Blood Therapeutics, failed to significantly reduce versus placebo the pain crises people with sickle cell often experience. Pfizer said it would share analyses of the data with the scientific and patient community in 'due course.' Last year, the company pulled from market another sickle cell drug, Oxbryta, that it gained from Global Blood, citing safety concerns. The company plans to provide updates on Oxbryta and a third Global Blood drug, the experimental osivelotor, when they become available. — Ned Pagliarulo Eli Lilly will collaborate with biotechnology startup Superluminal Medicines to develop new drugs for cardiometabolic diseases and obesity. Through the alliance, the two intend to discover and advance small molecule medicines aimed at undisclosed G protein-coupled receptor, or GPCR, targets 'relevant' to those conditions. Lilly will receive exclusive rights to the compounds emerging from the deal, while Superluminal could get up to $1.3 billion in total payouts, including an unspecified upfront payment as well as an equity investment, the companies said Thursday. — Ben Fidler Autolus Therapeutics is delaying launching its leukemia cell therapy Aucatzyl in Europe following approval there as the company 'evaluates potential pricing and feasibility of market entry opportunities' in some countries. Launch in Germany is on hold and Autolus 'does not anticipate any EU sales of Aucatzyl in 2025 and 2026,' the company said in its second quarter earnings report. In the U.K., where Aucatzyl has also been approved, a government cost-effectiveness monitor has initially decided not to pay for it. Autolus said it 'will continue to work towards a pathway for patient access to therapy in the U.K.' Approved by the Food and Drug Administration in November 2024, Aucatzyl earned just shy of $30 million in sales in the first six months of 2025, all from the U.S. — Jonathan Gardner Generation Bio revealed preclinical results suggesting a delivery technology it's developing can effectively send nucleic acid payloads into T cells. But the company also said this week that it may not be able to raise the funds to prove that approach works in humans and, as a result, began a strategic review that could end in a sale or merger. Generation will lay off roughly 90% of its workforce, including all of its research and development staff, by the end of October. Company shares climbed 60%, though they've lost much of their value since the company's initial public offering in 2020. — Ben Fidler Recommended Reading Eli Lilly's Julie Gilmore on finding up-and-coming companies and backing small biotechs Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data


Business Insider
10 hours ago
- Business Insider
Precigen Stock (PGEN) Roars Over 60% Higher on FDA Green Light for Papzimeos Therapy
Shares in biopharmaceutical company Precigen (PGEN) rocketed higher today after the U.S. Food and Drug Administration gave the green light to a therapy to treat a rare respiratory disease. Elevate Your Investing Strategy: Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence. The approval of the therapy, called Papzimeos, is the first treatment for the condition to receive the health regulator's nod. Fatal Tumors Papzimeos has been approved to treat recurrent respiratory papillomatosis (RRP) — a condition that causes growth of wart-like tumors in the respiratory tract due to human papillomavirus (HPV) infection. RRP can lead to severe voice disturbance, a compromised airway, and recurrent post-obstructive pneumonias. Precigen estimates that there are about 27,000 adult RRP patients in the U.S. RRP can be fatal as there is no cure and the current standard-of-care is repeated surgeries. However, despite being removed in these surgeries, the growth has a tendency to return. 'For more than a century, since RRP was first recognized as a distinct disease, patients have had to rely on repeated surgeries to manage this relentless condition. Today marks a historic turning point. With the landmark FDA approval all adult RRP patients are now eligible for access to the first and only approved therapy that targets the root cause of the disease,' said Helen Sabzevari, PhD, President and CEO of Precigen. Analyst Upgrade Simon Best, associate professor of Otolaryngology at Johns Hopkins Hospital, added: 'Everybody is anxiously awaiting a new treatment for this disease. The patients are and the surgeons are. There's nothing more frustrating than doing a surgery and then having the patient come back six months later.' The approval was based on an early-to-mid-stage study data that showed 51% of patients required no surgeries in the 12 months after the treatment. upgraded Precigen to Neutral from Underweight on the news. It cited the removal of Precigen's 'major regulatory overhang' and its revenue potential for the upgrade. It estimates that peak sales for the drug in the U.S. to be about $250 million. Precigen is certainly making strides when it comes to its financials – as can be seen below. Precigen recently reported a Q2 net loss of $26.6 million, a significant improvement from the $58.8 million loss in the same period last year. Total revenues for the quarter were $856,000, up from $717,000 in the previous year, driven by increased service revenues. Is PGEN a Good Stock to Buy Now? On TipRanks, PGEN has a Hold consensus based on 2 Buy, 1 Hold and 1 Sell ratings. Its highest price target is $6. PGEN stock's consensus price target is $4.50, implying a 143.24% upside.


Axios
18 hours ago
- Axios
At-home cervical cancer test rolls out in California
The first FDA-approved at-home cervical cancer screening device launched this week in California. Why it matters: Cervical cancer is largely preventable, yet 1 in 4 U.S. women aren't up to date on screenings for the disease, per the CDC. Teal Health's goal is to make the testing experience feel less invasive than a Pap smear, which can often cause pain. Driving the news: The Teal Wand allows people to self-collect a vaginal sample to test for HPV, the virus that causes nearly all cervical cancers. The San Francisco women's health company spearheading the device says it uses the same HPV test used in clinics and merely differs in the method of collection. The big picture: California records about 7.3 cervical cancer cases per 100,000 people every year, slightly under the national rate of 7.5. The incidence rate varies among racial groups, however, with Hispanics generally seeing higher figures. Nationwide, Black and Indigenous people also experience higher rates of cervical cancer and mortality compared to white women. "Several studies have shown that the availability of self-screening can boost participation in cervical cancer screening among underscreened persons—a population most likely to benefit in terms of cancer prevention," UCSF obstetrician-gynecologist George F. Sawaya told Axios via email. In 2023, cervical cancer screenings in the U.S. remained 14% lower than pre-pandemic levels, per a March journal article. Yes, but: It's equally critical to ensure those with positive test results get reliable follow-ups and treatment, Sawaya added. How it works: To take a sample, the wand — similar to a tampon in its dimensions — is inserted into the vagina and deploys a sponge to collect cells from the cervix. Once the sponge is extracted, it's placed in a vial and mailed to the lab. Teal medical providers then review the results and follow up via telehealth. The kit, which is shipped to your door, is available for purchase online and costs $99 with in-network insurance and $249 via credit card or HSA/FSA payment. By the numbers: Self-collected samples using the wand have proven to detect cervical precancer 96% of the time, similar to clinician-collected ones, Teal Health's 16-site clinical trials found. Eighty-six percent of participants said they'd be more likely to stay up to date with screenings if they could do it at home, per the trials. What they're saying: A lot of people don't recognize the importance of getting tested regularly because it's not always clear what a Pap smear is for, Teal Health co-founder and CEO Kara Egan told Axios. Lack of appointments, time conflicts and discomfort with the exam are also top reasons for not screening, Egan added. The wand was designed to alleviate those concerns, she said, offering the "same accuracy, but just comfortably and privately from home."