Health & Medical Infectious Diseases

Serologic Evidence of H1 Swine Influenza Virus Infection

Serologic Evidence of H1 Swine Influenza Virus Infection
We evaluated seropositivity to swine and human H1 influenza viruses in 74 swine farm owners, employees, their family members, and veterinarians in rural south-central Wisconsin, compared with 114 urban Milwaukee, Wisconsin, residents. The number of swine farm participants with positive serum hemagglutination-inhibition (HI) antibody titers ≥40 to swine influenza viruses (17/74) was significantly higher (p<0.001) than the number of seropositive urban control samples (1/114). The geometric mean serum HI antibody titers to swine influenza viruses were also significantly higher (p<0.001) among the farm participants. Swine virus seropositivity was significantly (p<0.05) associated with being a farm owner or a farm family member, living on a farm, or entering the swine barn ≥4 days/week. Because pigs can play a role in generating genetically novel influenza viruses, swine farmers may represent an important sentinel population to evaluate the emergence of new pandemic influenza viruses.

Infections with influenza viruses that circulate within the human population are a common and important cause of respiratory disease in people and result in an average of approximately 20,000 deaths and 114,000 hospitalizations per year in the United States alone. Influenza A viruses also infect animals of a wide variety of other species. In particular, influenza is a common and economically important cause of respiratory disease in pigs; subclinically infected wild waterfowl provide a global reservoir of influenza A viruses of all 15 hemagglutinin (HA) and 9 neuraminidase (NA) subtypes.

The occurrence of H5N1 and H9N2 virus infections among people in Asia in 1997-1999 highlighted the potential for avian influenza viruses to cross species barriers to infect humans, but direct avian-to-human transmission of influenza viruses is a rare event. In contrast, the species barrier for transmission of influenza viruses between people and pigs appears to be less stringent, and influenza virus infections in pigs pose important public health concerns at two levels. First, because respiratory tract epithelial cells in pigs contain the sialic acid receptors preferred by both avian (a2,3-N-acetylneuraminic acid-galactose) and human (a2,6-N-acetylneuraminic acid-galactose) influenza viruses, pigs are postulated to serve as the "mixing vessel" hosts in which reassortment between avian and human viruses can generate genetically novel viruses with pandemic potential. Reassortment between human and avian influenza viruses produced the 1957 and 1968 pandemic viruses. More recently, human-avian reassortant viruses have been isolated from pigs in Europe and, thereafter, from children in the Netherlands.

Zoonotic infections of humans with swine influenza viruses, first confirmed by isolation of swine influenza viruses from both pigs and their caretaker on a farm in southern Wisconsin in November 1976, have been diagnosed in the United States, Europe, New Zealand, and Asia. However, the total number of zoonotic infections that have been described is relatively small compared to the number of people worldwide involved directly or indirectly in swine farming. Swine farm workers are likely to be routinely exposed to and infected with swine influenza viruses, but only a small percentage of those zoonotic infections are documented. Zoonotic infections may be recognized if information regarding contact with sick pigs is specifically communicated to physicians, if a patient is hospitalized or dies, or if virus isolation is pursued and yields a virus that is antigenically atypical. In most cases, however, swine influenza virus infections in people may not be clinically distinguishable from routine human influenza virus infections. We developed this study to serologically assess the relative level of exposure to classical H1 swine influenza viruses among people involved in swine farming.



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