Read this article in Tackling Global Issues vol.3 Fighting the menace of zoonosis.
Hiroshi Kida, a top authority on zoonoses, has frequently been challenged by naysayers who dispute virtually everything he has asserted about avian, pandemic and seasonal influenzas.
But every time he faced such a challenge, Kida simply concentrated on his pursuit of scientific truths involving influenza – one of the zoonoses – rather than engaging in verbal arguments. “In some cases, it was me against 100 opponents,” Kida recalled. “But influenza can be tackled only by steadily doing careful research. In 10 years, we all will know where the truth lies.”
One recent assertion Kida made is that inactivated whole virus particle vaccines, which are now undergoing clinical studies, should replace conventional split vaccines made of viruses that are disrupted by ether or detergent.
Kida is a long-time proponent of using whole virus particle vaccines after he succeeded in making one as a researcher at Takeda Pharmaceutical Co., Ltd. in the 1970s. Whole virus particle vaccines are more immunogenic than split vaccines, he claims.
“In current clinical trials, whole virus particle vaccines have shown they are effective,” Kida said. “They are also much cheaper to produce because there is no need to disrupt the viruses.”
Since 2015, Kida has been working with all five influenza vaccine producers in Japan to study the introduction of inactivated whole virus particle vaccines. The National Institute of Infectious Diseases in Japan has joined this industry-academia-government joint project, while the Japan Agency for Medical Research and Development has provided much-needed funds for the research. “Failure is not an option,” Kida said, expressing his resolve to make the vaccines available to society.
Identifying natural reservoirs and transmission routes of avian influenza
After a seven-year stint at Takeda, Kida joined Hokkaido University in 1976 to pursue his research on influenza. Kida later established that ducks are the natural host for Type A influenza viruses and identified the transmission route to humans for the first time.
The migratory bird is orally infected with the virus with varying hemagglutinin (HA; a glycoprotein) and neuraminidase (NA; enzyme) subtypes as they nest in lakes and marshes in Siberia, Canada or Alaska near the Arctic in summer. The virus proliferates in the duck’s colon crypts and is discharged with feces, but does not do any harm to the duck. When the duck migrates south in autumn, it infects poultry and livestock on the way to or in its wintering places, such as southern China, Southeast Asia, the southern United States and Mexico. The virus is transmitted by water to domestic ducks and geese and then to terrestrial poultry such as quails, which serve as intermediate hosts that transmit the virus to chickens. While water birds have the receptor to viruses in their intestine, land birds such as chickens have the receptor in their respiratory organs. The infection of quails makes it easier for the virus to spread to chickens.
As the virus is repeatedly transmitted between chickens over more than six months, it can acquire pathogenicity in chickens. Only H5 and H7 subtype viruses become highly pathogenic avian influenza viruses and highly transmittable among chickens. These subtype viruses cause a high fatality rate.
A genetic reassortant virus can cause a pandemic in humans
Humans can rarely be infected with avian influenza viruses. The virus has not been transmitted between humans to date, so it has never caused a pandemic. Then, what caused the pandemics in the past: the Spanish flu in 1918; Asian flu in 1957; Hong Kong flu in 1968; and the 2009 pandemic flu?
Kida strongly suspected influenza was a zoonosis after reading academic articles by overseas researchers pointing to similarities between a viral protein found in ducks and horses, and that of the 1968 Hong Kong pandemic influenza virus strain. He examined feces of migratory birds and finally, in 1977, he isolated a virus (A/duck/Hokkaido/5/77) found in the intestine of a duck that had flown from Siberia to Hokkaido. This virus had HA identical to that of the 1968 Hong Kong influenza virus and NA undistinguishable from that of the 1957 Asian flu virus.
“This duck taught me that the emergence of a new virus is not a result of antigenic variation, but genetic reassortment between different strains,” Kida said. Genetic reassortment is the process by which influenza viruses swap gene segments. Ensuing experiments showed that two of the eight viral genes originated in ducks and the six others were from the Asian flu virus.
“We proved pigs, which have receptors both to the avian and human viruses, serve as a mixing vessel,” Kida said. “When pigs are simultaneously infected with both influenza viruses, the genetic reassortment will take place, producing an ‘avian-human hybrid virus’ that can infect and transmit between humans. Among them, those with HA genes that originated in ducks are pandemic influenza viruses.”
Trying to dispel misunderstanding over influenza
Kida said understanding how people get sick from influenza is crucial. There is a widespread misperception that the virus itself causes sickness in the human body. “Sickness occurs as innate immune responses when the amount of a virus increases in the body,” Kida said. “When excessive responses occur, a person runs a fever or develops serious symptoms. In the most acute cases, blood vessels can be damaged by clots and vascular hyperpermeability, resulting in multiple organ failure, including encephalopathy in children.”
It is vital to control pandemic influenza based on countermeasures against seasonal influenza, Kida stressed. Accordingly, improving seasonal flu vaccines is urgently needed. Kida is determined to realize the introduction of whole virus particle vaccines to replace the weak immunogenic split vaccines that are currently used.
One of Kida’s many contributions is accumulating influenza virus data from duck feces to make a library of pandemic influenza vaccine strain candidates. The library stores more than 4,600 avian influenza virus strains of all 144 combinations of HA and NA subtypes as vaccine strain candidates. Their pathogenicity, antigenicity, genetic information and yield in chicken embryo have been analyzed, put in a database and made available on a website (https://virusdb.czc.hokudai.ac.jp/).
“I declined suggestions that the database be patented,” Kida said. “It is my responsibility to make the database available to whoever needs it, because I cannot achieve much by myself as a researcher.”