Bird Flu Resists Fever, Poses Major Human Threat
Author: University of Cambridge
Published: 2025/11/29
Publication Details: Peer-Reviewed, Research, Study, Analysis
Category Topic: Avian Influenza - Related Publications
Page Content: Synopsis - Introduction - Main - Insights, Updates
Synopsis: This paper, published in the peer-reviewed journal Science, reveals a critical discovery about why avian influenza poses such a significant threat to human health: bird flu viruses can replicate effectively at temperatures associated with fever, one of the body's primary defense mechanisms against infection. Researchers from the universities of Cambridge and Glasgow identified that the PB1 gene determines a virus's temperature sensitivity, and during the deadly 1957 and 1968 pandemics, this gene transferred from bird flu to human flu viruses, creating strains that thrived despite elevated body temperatures. Using mouse models, the team demonstrated that while a modest 2°C temperature increase can transform a lethal human flu infection into a mild illness, avian flu viruses remain resistant to fevers reaching 41°C. This research has particular relevance for vulnerable populations, including older adults and those with compromised immune systems, as it explains why bird flu infections in humans have historically shown mortality rates exceeding 40% and underscores the importance of monitoring viral strains that could trigger future pandemics - Disabled World (DW).
Defining Bird Flu Viruses
- Bird Flu Viruses
Bird flu viruses, formally known as avian influenza viruses, are strains of influenza A that naturally circulate among wild and domestic bird populations, particularly waterfowl such as ducks and geese. These viruses have adapted to replicate efficiently in avian hosts, typically infecting the birds' respiratory and gastrointestinal tracts at temperatures considerably higher than those tolerated by human flu strains.
While most avian influenza viruses remain confined to bird populations, certain subtypes - most notably H5N1, H7N9, and H5N8 - have demonstrated the ability to jump species barriers and infect mammals, including humans, though such transmission remains relatively rare. The concern surrounding these viruses stems not only from their high mortality rates when they do infect people, but also from their potential to exchange genetic material with human flu viruses through a process called reassortment, which could produce pandemic strains combining the transmissibility of human flu with the lethality of avian strains.
Ongoing surveillance of bird flu evolution remains a critical component of global pandemic preparedness, as these viruses continue to circulate widely in poultry operations and wild bird populations worldwide.
Introduction
Bird flu viruses are a particular threat to humans because they can replicate at temperatures higher than a typical fever, one of the body's ways of stopping viruses in their tracks, according to new research led by the universities of Cambridge and Glasgow.
In a study published today (November 29th, 2025) in Science, the team identified a gene that plays an important role in setting the temperature sensitivity of a virus. In the deadly pandemics of 1957 and 1968, this gene transferred into human flu viruses, and the resulting virus thrived.
Main Content
Human flu viruses cause millions of infections every year. The most common types of these viruses, which cause seasonal flu, are known as influenza A viruses. They tend to thrive in the upper respiratory tract, where the temperature is around 33C, rather than deep in the lungs in the lower respiratory tract, where the temperature is around 37C.
Unchecked, a virus will replicate and spread throughout the body, where it can cause illness, occasionally severe. One of the body's self-defence mechanisms is fever, which can cause our body temperature to reach as high as 41C, though until now it has not been clear how fever stops viruses - and why some viruses can survive.
Unlike human flu viruses, avian influenza viruses tend to thrive in the lower respiratory tract. In fact, in their natural hosts, which include ducks and seagulls, the virus often infects the gut, where temperatures can be as high as 40-42C.
In previous studies using cultured cells, scientists have shown that avian influenza viruses appear more resistant to temperatures typically seen in fever in humans. Today's study uses in vivo models - mice infected with influenza viruses - to help explain how fever protects us and why it may not be enough to protect us against avian influenza.
An international team led by scientists in Cambridge and Glasgow simulated in mice what happens during a fever in response to influenza infections. To carry out the research, they used a laboratory-adapted influenza virus of human origin, known as PR8, which does not pose a risk to humans.
Although mice do not typically develop fever in response to influenza A viruses, the researchers were able to mimic its effect on the virus by raising the ambient temperature where the mice were housed (elevating the body temperature of the mice).
The researchers showed that raising body temperature to fever levels is effective at stopping human-origin flu viruses from replicating, but it is unlikely to stop avian flu viruses. Fever protected against severe infection from human-origin flu viruses, with just a 2C increase in body temperature enough to turn a lethal infection into a mild disease.
The research also revealed that the PB1 gene of the virus, important in the replication of the virus genome inside infected cells, plays a key role in setting the temperature-sensitivity. Viruses carrying an avian-like PB1 gene were able to withstand the high temperatures associated with fever, and caused severe illness in the mice. This is important, because human and bird flu viruses can 'swap' their genes when they co-infect a host at the same time, for example when both viruses infect pigs.

Dr Matt Turnbull, the first author of the study, from the Medical Research Council Centre for Virus Research at the University of Glasgow said:
"The ability of viruses to swap genes is a continued source of threat for emerging flu viruses. We've seen it happen before during previous pandemics, such as in 1957 and 1968, where a human virus swapped its PB1 gene with that from an avian strain. This may help explain why these pandemics caused serious illness in people."
"It's crucial that we monitor bird flu strains to help us prepare for potential outbreaks. Testing potential spillover viruses for how resistant they are likely to be to fever may help us identify more virulent strains."
Senior author Professor Sam Wilson, from the Cambridge Institute of Therapeutic Immunology and Infectious Disease at the University of Cambridge, said:
"Thankfully, humans don't tend to get infected by bird flu viruses very frequently, but we still see dozens of human cases a year. Bird flu fatality rates in humans have traditionally been worryingly high, such as in historic H5N1 infections that caused more than 40% mortality."
"Understanding what makes bird flu viruses cause serious illness in humans is crucial for surveillance and pandemic preparedness efforts. This is especially important because of the pandemic threat posed by avian H5N1 viruses."
The findings may have implications for the treatment of infections, though the team stresses that more research is needed before changes are considered for treatment guidelines. Fever is often treated with antipyretic medication, which include ibuprofen and aspirin. However, there is clinical evidence that treating fever may not always be beneficial to the patient and may even promote transmission of influenza A viruses in humans.
The research was funded primarily by the Medical Research Council, with additional funding from the Wellcome Trust, Biotechnology and Biological Sciences Research Council, European Research Council, European Union Horizon 2020, UK Department for Environment, Food & Rural Affairs, and US Department of Agriculture.
Reference
Turnbull, ML et al. Avian-origin influenza A viruses tolerate elevated pyrexic temperatures in Mammals. Science; 27 Nov 2025; DOI: 10.1126/science.adq4691
Insights, Analysis, and Developments
Editorial Note: The revelation that fever - our body's ancient and universal defense mechanism - may be powerless against avian influenza represents a sobering reminder that nature's evolutionary processes operate without regard for human vulnerability. As H5N1 viruses continue to circulate globally and gene-swapping between species remains an ever-present possibility, this research moves us beyond theoretical pandemic preparedness into understanding the specific molecular characteristics that could make the next outbreak particularly deadly. The findings challenge us to rethink not only surveillance strategies but also clinical approaches to fever management, suggesting that our instinct to suppress fever with common medications might, in some cases, be working against our body's desperate attempt to halt viral replication - Disabled World (DW).Attribution/Source(s): This peer reviewed publication was selected for publishing by the editors of Disabled World (DW) due to its relevance to the disability community. Originally authored by University of Cambridge and published on 2025/11/29, this content may have been edited for style, clarity, or brevity.