At an SBV information meeting, 60 shepherds >18 years of age were recruited for this study. After obtaining written informed consent, we administered a standardized questionnaire. We collected information about age, sex, SBV infection in their livestock, exposure to sick lambs, frequency of insect bites, personal health, and categories of signs of disease after exposure. In addition, a serum sample was taken from each participant.

We developed an indirect fluorescent antibody test (IFAT) for primary testing of human serum. For this test, antihuman fluorescein isothiocyanate–conjugated secondary antibodies against SBV-specific IgM or IgG (antibovine for positive control) were used. For the IFAT, all heat-inactivated serum specimens were tested in dilutions of 1:20 and 1:80 on glass slides with noninfected and SBV-infected Vero cells. An SBV antibody–positive serum sample from an experimentally infected cow was used as a positive control. To check for background signals and possible cross-reactivity, we tested 80 serum samples from healthy blood donors; none were positive. A serum neutralization test (SNT) was developed for confirmation of indeterminate and positive results. Serial dilutions of the test serum (lowest dilution 1:5) were incubated for 1 h at 37°C with an equal volume of cell culture supernatant containing 100 infectious doses of SBV and subsequently mixed with Vero cells. To detect SBV-specific RNA, we performed a 1-step real-time reverse transcription quantitative PCR (RT-qPCR) on serum, as described (1). The ethics committee of the University Medicine Charité Berlin approved our study.

All 60 participants (75% male; median age 48 years [interquartile range (IQR) 41–56 years]) reported sheep husbandry in the SBV-epizootic area (Table 1). Altogether, 48 (80%) participants had contact with lambs that had characteristic malformations or with the respective birth products (median 10 [IQR 4–20] sick lambs). In livestock from 36 (60%) participants, SBV was laboratory confirmed. Characteristic signs among adult animals had first been noted in September 2011. Median time from first signs in animals to blood withdrawal was 45 days (IQR 39–66 days). A total of 55 (98%) of 56 participants self-reported insect bites during late summer to autumn; among these, 22 (39%) indicated frequent insect bites. Nine (15%) shepherds reported having had signs and symptoms since the disease had appeared in the study area or after handling diseased animals (Table 1): myalgia and arthralgia (7 shepherds), headache (4), fever (4), skin rash (2), and respiratory problems (2). No shepherds reported hospitalization. Of the 36 shepherds whose livestock had laboratory-confirmed SBV infection, 5 (14%) reported signs and symptoms: myalgia and arthralgia (4 shepherds), headache (2), fever (2), skin rash (2), and respiratory problems (2).

No SBV-specific antibodies were detected in any serum specimens (Table 2). Eight specimens showed indeterminate fluorescent signals in the IFAT at a 1:20 serum dilution for IgG (n = 1) or IgM (n = 7) but were not reactive at 1:80 (Figure). These 8 samples were retested by SNT (serum dilution 1:10) and showed no virus inhibition at any serum dilution during 7 days of incubation. Two (25%) of these 8 shepherds reported symptoms. For the bovine control serum, the titer of the SNT was 320. RT-qPCR was negative in all serum samples.

We investigated the risk for human infection after possible high exposure to an emerging vector-borne epizootic disease through contact with infected animals and tissues or through insect bites. No evidence of SBV infection among the shepherds was found by molecular and serologic tests, even though most of the shepherds had received substantial exposure through repeated direct contact with sheep with laboratory-confirmed SBV-infection and with birth products known to contain high virus loads in the SBV-epizootic area. Reported symptoms were compatible with illnesses commonly experienced during the winter (i.e., influenza-like illness caused by human respiratory viruses) without considerable differences between the exposure categories. The likelihood of virus detection by RT-qPCR is certainly limited because SBV viremia in livestock lasts only a few days (4,8). Viremia could be of short duration in humans as well. However, after the end of the viremic phase, detection of specific antibodies can be expected. The period between exposure and sampling was sufficiently long to for antibodies to have developed after infection. Furthermore, a large proportion of the participants indicated having been frequently bitten by insects in the epizootic area. Midge bites are difficult to recall, and therefore this exposure could not be assessed precisely. Recollection of insect bites might not be equivalent to exposure to the vector species. Although SBV has been isolated from certain midge species, entomologic knowledge about the ability of different midge species to transmit SBV, i.e., vector competence and host feeding behavior, is still scarce. Nevertheless, on the basis of results from our study and the phylogenetic relationship of SBV, we conclude that the novel virus is unlikely to pose a threat to humans by transmission from infected livestock or from midges.