Serologic Evidence of Occupational Exposure to Avian Influenza Viruses at the Wildfowl/Poultry/Human Interface.

Maria Alessandra De Marco1 Mauro Delogu2 Marzia Facchini3 Livia Di Trani4 Arianna Boni4 Claudia Cotti2 Giulia Graziosi2 Diana Venturini5 Denise Regazzi6 Valentina Ravaioli7 Fausto Marzadori7 Matteo Frasnelli7 Maria Rita Castrucci4 Elisabetta Raffini7
Affiliations 7 institutions
  1. Institute for Environmental Protection and Research (ISPRA), 40064 Ozzano dell'Emilia (BO), Italy.
  2. Wildlife and Exotic Animal Service, Department of Veterinary Medical Sciences, University of Bologna, 40064 Ozzano dell'Emilia (BO), Italy.
  3. Department of Infectious Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy.
  4. Department of Food Safety, Nutrition, and Veterinary Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.
  5. Animal Health‒Ravenna, Department of Public Health, Azienda Unità Sanitaria Locale della Romagna, 48124 Ravenna, Italy.
  6. Hygiene and Public Health‒Ravenna, Department of Public Health, Azienda Unità Sanitaria Locale della Romagna, 48124 Ravenna, Italy.
  7. Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna B. Ubertini (IZSLER), 48022 Lugo (RA), Italy.

Abstract

Ecological interactions between wild aquatic birds and outdoor-housed poultry can enhance spillover events of avian influenza viruses (AIVs) from wild reservoirs to domestic birds, thus increasing the related zoonotic risk to occupationally exposed workers. To assess serological evidence of AIV infection in workers operating in Northern Italy at the wildfowl/poultry interface or directly exposed to wildfowl, serum samples were collected between April 2005 and November 2006 from 57 bird-exposed workers (BEWs) and from 7 unexposed controls (Cs), planning three sample collections from each individual. Concurrently, AIV surveillance of 3587 reared birds identified 4 AIVs belonging to H10N7, H4N6 and H2N2 subtypes while serological analysis by hemagglutination inhibition (HI) assay showed recent infections caused by H1, H2, H4, H6, H10, H11, H12, and H13 subtypes. Human sera were analyzed for specific antibodies against AIVs belonging to antigenic subtypes from H1 to H14 by using HI and virus microneutralization (MN) assays as a screening and a confirmatory test, respectively. Overall, antibodies specific to AIV-H3, AIV-H6, AIV-H8, and AIV-H9 were found in three poultry workers (PWs) and seropositivity to AIV-11, AIV-H13-still detectable in October 2017-in one wildlife professional (WP). Furthermore, seropositivity to AIV-H2, accounting for previous exposure to the "extinct" H2N2 human influenza viruses, was found in both BEWs and Cs groups. These data further emphasize the occupational risk posed by zoonotic AIV strains and show the possible occurrence of long-lived antibody-based immunity following AIV infections in humans.

Supporting text Virus Host Location
avian influenza virus 59 bird-exposed workers 1 human serology 1 human serosurvey 1 occupational exposure 12 wildlife/poultry/human interface 1

Evidence records

6 total
Zoonotic Surveillance
6 records · 2 evidence types
Evidence type
1 records
Evidence type
5 records
OVE5260
Key finding

Antibodies specific to avian influenza virus subtypes H3, H6, H8, and H9 were detected in three poultry workers, indicating occupational exposure.

Virus
Host
Location
Not specified
Supporting text

Overall, antibodies specific to AIV-H3, AIV-H6, AIV-H8, and AIV-H9 were found in three poultry workers (PWs).

Method
hemagglutination inhibition (HI) assay | virus microneutralization (MN) assay
Sample type
human serum
OVE5262
Key finding

Seropositivity to avian influenza virus H2 was found in both bird-exposed workers and controls, reflecting prior exposure possibly related to extinct H2N2 human influenza viruses.

Virus
Host
Location
Not specified
Supporting text

Seropositivity to AIV-H2, accounting for previous exposure to the "extinct" H2N2 human influenza viruses, was found in both BEWs and Cs groups.

Method
hemagglutination inhibition (HI) assay | virus microneutralization (MN) assay
Sample type
human serum
OVE5259
Key finding

Serological analysis detected avian influenza virus antibodies of multiple hemagglutinin subtypes in reared birds from Northern Italy.

Virus
Host
Location
Not specified
Supporting text

AIV surveillance of 3587 reared birds identified 4 AIVs belonging to H10N7, H4N6 and H2N2 subtypes while serological analysis by hemagglutination inhibition (HI) assay showed recent infections caused by H1, H2, H4, H6, H10, H11, H12, and H13 subtypes.

Method
hemagglutination inhibition (HI) assay
Sample type
serum samples
OVE5261
Key finding

Seropositivity to avian influenza virus subtypes H11 and H13 was detected in one wildlife professional, signifying prior exposure.

Virus
Host
Location
Not specified
Supporting text

Seropositivity to AIV-H11, AIV-H13-still detectable in October 2017-in one wildlife professional (WP).

Method
hemagglutination inhibition (HI) assay | virus microneutralization (MN) assay
Sample type
human serum
OVE5263
Key finding

Serological evidence indicates avian influenza viruses spilled over from wild aquatic birds and poultry to occupationally exposed humans working in Northern Italy.

Virus
Host
Location
Supporting text

Ecological interactions between wild aquatic birds and outdoor-housed poultry can enhance spillover events of avian influenza viruses (AIVs) from wild reservoirs to domestic birds, thus increasing the related zoonotic risk to occupationally exposed workers. To assess serological evidence of AIV infection in workers operating in Northern Italy at the wildfowl/poultry interface or directly exposed to wildfowl.

Method
hemagglutination inhibition (HI) assay | virus microneutralization (MN) assay