Assessment of the hemagglutinating activity of the Porcine orthorubulavirus.

Blue eye disease (BED) in pigs is caused by Porcine orthorubulavirus (PRV) of the Paramyxoviridae family. It is an endemic disease in swine production in the central region of Mexico and causes nervous signs and high mortality in suckling pigs, pneumonia in growing pigs, orchitis in boars and mummification during gestation. PRV hemagglutinates most red blood cells (RBCs) of domestic species. For serological diagnosis, the hemagglutination inhibition test is used, and in this test, guinea pig, bovine and chicken RBCs have been commonly used. In this investigation, hemagglutination with PRV was evaluated using the RBCs of seven domestic species (chicken, bovine, horse, pig, dog, guinea pig and rabbit). In the hemagglutination test, the following parameters were evaluated: temperature (25 °C and 37 °C), bottoms of the wells (V and U), erythrocyte concentration (0.5%, 0.75%, and 1%), and reading time (15, 30, 45, 60 and 90 min). Significant differences (P < 0.001) were found in most of the evaluated treatments. The best hemagglutination results were obtained with chicken, bovine and horse RBCs. The hemagglutination titer is higher (2 dilutions) when using chicken RBCs than when using bovine or horse RBCs. If chicken RBCs are used in the inhibition of hemagglutination, the test will be more sensitive, while it is more specific when bovine or horse RBCs are used. The hemagglutination readings are imprecise when using RBCs from dogs, pigs, guinea pigs and rabbits. RBCs from these species should not be used for the diagnosis or investigation of PRV.

Comparison of hemagglutination inhibition tests, immunoperoxidase monolayer assays, and serum neutralizing tests in detecting antibodies against blue eye disease in pigs.

Blue eye disease (BED) of pigs was identified in the early 1980s in La Piedad, Michoacan, Mexico. The causal agent is Porcine orthorubulavirus (PRV), which affects pigs of all ages, producing nervous, respiratory, and reproductive disorders. BED is geographically endemic to the center of Mexico, where 75% of the country's swine industry is concentrated. Due to its adverse effects on the swine industry and the risk of dissemination to other countries, it is essential to have reliable diagnostic methods for BED. The objective of this study was to establish the optimal conditions for three serological tests, hemagglutination inhibition (HI), immunoperoxidase monolayer assay (IPMA), and serum neutralization (SN), and to compare their sensitivity, specificity, kappa coefficient, and predictive values. Twelve different HI protocols (9408 tests), one SN protocol and one IPMA protocol (784 tests, each) were evaluated. Forty-nine sera were analyzed, and thirty-seven sera showed true positive results, while twelve showed true negative results. The kappa coefficient was used to assess the variation in each test. The best HI protocol registered a sensitivity and specificity of 89 and 100%, respectively, the IPMA test showed values of 85 and 100%, and the SN test registered a sensitivity of 91% and a specificity of 96%. One of the disadvantages of the HI test is that when chicken red blood cells (RBCs) are used, elution occurs in a short incubation time, which would decrease the specificity. The use of bovine RBCs increases the specificity of the testy and makes it more stable, but it decreases the sensitivity. The results of HI and SN revealed the importance of eliminating the complement system of the serum and removing other inhibitors to avoid test nonspecificity. The IPMA test does not use an active virus; hence, it is considered safe and does not present any risk of disseminating PRV.

Ecuadorian mainland industrial poultry production is free of H5/H7 Avian influenza virus: National surveillance program in 2016.

Avian influenza (AI) is a disease caused by influenza viruses type A that belong to the Orthomyxoviridae family. AI induces high economic losses in poultry production worldwide. Due to a possible outbreak, a national surveillance program was needed. From April to July 2016, 152 industrial poultry farms were randomly sampled. All samples were analyzed by competitive ELISA for Influenza type A viruses. Suspicious and positive sera were further analyzed by Hemagglutination Inhibition (HI) in order to serotype H5 or H7 low pathogenic avian influenza virus (LPAIV). The farms sampled showed 94.08%, 3.95% and 1.97% of negative, positive and suspicious results, respectively. However, serotyping revealed all positive and suspicious samples were negative to H5/H7 LPAIV. Our results show the absence of AI in the mainland Ecuadorian industrial poultry production.

Complete genome sequence of a novel influenza A H1N2 virus circulating in swine from Central Bajio region, Mexico.

The aim of this study was to perform the complete genome sequence of a swine influenza A H1N2 virus strain isolated from a pig in Guanajuato, México (A/swine/Mexico/GtoDMZC01/2014) and to report its seroprevalence in 86 counties at the Central Bajio zone. To understand the evolutionary dynamics of the isolate, we undertook a phylogenetic analysis of the eight gene segments. These data revealed that the isolated virus is a reassortant H1N2 subtype, as its genes are derived from human (HA, NP, PA) and swine (M, NA, PB1, PB2 and NS) influenza viruses. Pig serum samples were analysed by the hemagglutination inhibition test, using wild H1N2 and H3N2 strains (A/swine/México/Mex51/2010 [H3N2]) as antigen sources. Positive samples to the H1N2 subtype were processed using the field-isolated H1N1 subtype (A/swine/México/Ver37/2010 [H1N1]). Seroprevalence to the H1N2 subtype was 26.74% in the sampled counties, being Jalisco the state with highest seroprevalence to this subtype (35.30%). The results herein reported demonstrate that this new, previously unregistered influenza virus subtype in México that shows internal genes from other swine viral subtypes isolated in the past 5 years, along with human virus-originated genes, is widely distributed in this area of the country.

Screening of feral pigeons (columba livia) for pathogens of veterinary and medical importance

Pathogens of veterinary and medical importance were investigated in 240 feral pigeons (Columba livia) captured in warehouses in São Paulo State, Brazil for one year. Rapid serum agglutination test (RST) was performed for the detection of antibodies against Mycoplasma synoviae, Mycoplasma gallisepticum and Salmonella Pullorum/Gallinarum. Positive samples were submitted to hemagglutination inhibition (HI) and tube seroagglutination tests, respectively. Molecular techniques (RT-PCR and PCR) were performed for Newcastle Diseases Virus (NDV) and Chlamydia psittaci diagnosis. Additionally, HI test was applied to detect antibodies against NDV. Serological results by RST were 3.3% positive for M. synoviae, 2.5% for M. gallisepticum, and 0.4% for S. Pullorum/Gallinarum, all negative on the confirmatory tests performed. NDV RNA or antibodies were not detected. C. psittaci DNA was detected in 13% of the samples. Further research on pigeon health status should be conducted because this species is highly adaptable and their numbers are rapidly rising around the world, posing risks for animals and human beings.

Screening of feral pigeons (columba livia) for pathogens of veterinary and medical importance

Pathogens of veterinary and medical importance were investigated in 240 feral pigeons (Columba livia) captured in warehouses in São Paulo State, Brazil for one year. Rapid serum agglutination test (RST) was performed for the detection of antibodies against Mycoplasma synoviae, Mycoplasma gallisepticum and Salmonella Pullorum/Gallinarum. Positive samples were submitted to hemagglutination inhibition (HI) and tube seroagglutination tests, respectively. Molecular techniques (RT-PCR and PCR) were performed for Newcastle Diseases Virus (NDV) and Chlamydia psittaci diagnosis. Additionally, HI test was applied to detect antibodies against NDV. Serological results by RST were 3.3% positive for M. synoviae, 2.5% for M. gallisepticum, and 0.4% for S. Pullorum/Gallinarum, all negative on the confirmatory tests performed. NDV RNA or antibodies were not detected. C. psittaci DNA was detected in 13% of the samples. Further research on pigeon health status should be conducted because this species is highly adaptable and their numbers are rapidly rising around the world, posing risks for animals and human beings.(AU)

Detection of antibodies to Oropouche virus in non-human primates in Goiânia City, Goiás.

INTRODUCTION: Arboviruses are associated with human disease, and non-human primates (NHPs) are important primary hosts. This study shows the detection of antibodies to Oropouche virus (OROV) in NHPs either living in urban parks or acclimatized at the Wild Animal Screening Center, Goiânia city. METHODS: Fifty blood samples were analyzed by hemagglutination-inhibition and neutralization assays. RESULTS: Two monkeys (Alouatta caraya) had antibodies to OROV by both techniques. CONCLUSIONS: This is the first report demonstrating the detection of OROV antibodies in Goiás State and may represent the introduction/circulation of OROV in the region and a potential risk to the human population.

Serological Detection of Newcastle Disease Virus Antibodies in Local Chickens and Guinea Fowls in the Area of Kumasi, Ghana

Newcastle Disease (ND) has been identified as a major constraint to local poultry production with its impact being felt more in rural poultry production which forms about 80% of Ghana poultry population. However documented evidence on ND virus activity in rural poultry in Ghana is still lacking. Hence, this study was conducted to evaluate the level of circulating antibodies against ND using the Haemagglutination Inhibition (HI) technique. Sera collected from unvaccinated 292 chickens and 153 guinea fowls randomly selected from households and a live bird market in Kumasi and its environs were evaluated for Newcastle disease virus antibodies. Results showed 81.8 % (239/292) of local chickens and 24.2 % (37/153) of guinea fowls tested positive for ND antibodies. Comparison was made between the seroprevalence of ND antibodies in household and live bird market as well as between sexes. Significantly higher prevalence rate (p 0.05) was observed with chickens sampled from households compared to those from the live bird market. Higher ranges of titers were also observed in chickens from households than those from live bird markets. The presence of ND antibodies in these unvaccinated local chickens and guinea fowls indicated the presence of the virus amongst the rural poultry population, hence aneed for improvement in vaccine campaignand delivery against ND for rural poultry especially with the use of thermostable and improved oral or feed-based vaccine delivery systems.

Analysis of different diagnostis methods of influenza in horses

Background: Equine Influenza is a serious, acute respiratory illness with characteristical clinical signs. The disease is caused by family of Orthomyxoviridae, genera Influenza virus A by two subtypes H7N7 and H3N8. Currently, there is believe that H7N7 has been replaced as a predominant subtype with the H3N8. Horse infection with influenza virus can be detected by serological tests on paired sera using HI test. Commercial rapid tests could be used for the detection of influenza virus. Recently it is widely use a PCR method as fast and more specific methods. Materials, Methods & Results: Fifty horses and one pony, age between one and 22 years have been included in experiment. Horses were of different race, sex, and age and vaccination status. Ten out of total 51 (10/51) have been regularly vaccinated against EI. Prior to initiation of these study epidemiological survey has been performed. The clinical examination has been followed by blood sampling for blood cell and serum extraction. The serums were evaluated by HI method. Nasal swabs are taken from both nostrils twice, one was frozen for virus detection by RT-qPCR while another was used for detection of EI virus by Directi-gen FLU A rapid test. Analysis of titers of antibody reveled that 7 horses (14%) had specific antibodies (IgG) against subtype H7N7, while 9 horses (18%) had specific antibodies against H3N8 [...]

Analysis of different diagnostis methods of influenza in horses

Background: Equine Influenza is a serious, acute respiratory illness with characteristical clinical signs. The disease is caused by family of Orthomyxoviridae, genera Influenza virus A by two subtypes H7N7 and H3N8. Currently, there is believe that H7N7 has been replaced as a predominant subtype with the H3N8. Horse infection with influenza virus can be detected by serological tests on paired sera using HI test. Commercial rapid tests could be used for the detection of influenza virus. Recently it is widely use a PCR method as fast and more specific methods. Materials, Methods & Results: Fifty horses and one pony, age between one and 22 years have been included in experiment. Horses were of different race, sex, and age and vaccination status. Ten out of total 51 (10/51) have been regularly vaccinated against EI. Prior to initiation of these study epidemiological survey has been performed. The clinical examination has been followed by blood sampling for blood cell and serum extraction. The serums were evaluated by HI method. Nasal swabs are taken from both nostrils twice, one was frozen for virus detection by RT-qPCR while another was used for detection of EI virus by Directi-gen FLU A rapid test. Analysis of titers of antibody reveled that 7 horses (14%) had specific antibodies (IgG) against subtype H7N7, while 9 horses (18%) had specific antibodies against H3N8 [...](AU)

Serological Detection of Newcastle Disease Virus Antibodies in Local Chickens and Guinea Fowls in the Area of Kumasi, Ghana

Newcastle Disease (ND) has been identified as a major constraint to local poultry production with its impact being felt more in rural poultry production which forms about 80% of Ghana poultry population. However documented evidence on ND virus activity in rural poultry in Ghana is still lacking. Hence, this study was conducted to evaluate the level of circulating antibodies against ND using the Haemagglutination Inhibition (HI) technique. Sera collected from unvaccinated 292 chickens and 153 guinea fowls randomly selected from households and a live bird market in Kumasi and its environs were evaluated for Newcastle disease virus antibodies. Results showed 81.8 % (239/292) of local chickens and 24.2 % (37/153) of guinea fowls tested positive for ND antibodies. Comparison was made between the seroprevalence of ND antibodies in household and live bird market as well as between sexes. Significantly higher prevalence rate (p 0.05) was observed with chickens sampled from households compared to those from the live bird market. Higher ranges of titers were also observed in chickens from households than those from live bird markets. The presence of ND antibodies in these unvaccinated local chickens and guinea fowls indicated the presence of the virus amongst the rural poultry population, hence aneed for improvement in vaccine campaignand delivery against ND for rural poultry especially with the use of thermostable and improved oral or feed-based vaccine delivery systems.(AU)

Prevalência de anticorpos contra arbovírus da família Bunyaviridae em búfalos de água / Prevalence of arbovirus antibodies against the family Bunyaviridae in water buffaloes

The State of Pará comprises 26% of Brazilian Amazon region where a large diversity of arboviruses has been described. This study sought to assess the prevalence and distribution of haemagglutination-inhibition antibodies against antigens of nine different types of arbovirus of the Bunyaviridae family, where eight were Orthobunyavirus: Guaroa virus, Maguari virus, Tacaiuma virus, Utinga virus, Belem virus, Caraparu virus, Oropouche virus and Catu virus, and one Phlebovirus: Icoaraci virus in sera samples of water buffaloes in Pará State, Brazil. For all Arboviruses investigated there were antibodies, with the exception of Belem virus. Antibodies to Maguari virus were more prevalent (7.33%). The water buffaloes of the present study showed variable levels of antibodies in monotypic and heterotypic reactions that may indicate there are movements from most bunyavirus studied in domestic buffaloes in the state of Pará, and the Maguari virus presents the largest circulation. Therefore, further studies are needed to investigate the role of water buffalo in the maintenance and dispersal of arboviruses, as well as whether these viruses can cause disease in that species, especially in cases of birth defects and abortions.

O Estado do Pará corresponde a 26% da Amazônica brasileira, onde uma grande quantidade de Arbovírus tem sido descrito. O presente trabalho teve como objetivo determinar a prevalência de anticorpos detectados pela técnica de inibição de hemaglutinação contra nove tipos diferentes de arbovírus da família Bunyaviridae, sendo oito do gênero Orthobunyavirus: vírus Guaroa, vírus Maguari, vírus Tacaiuma, vírus Utinga, vírus Belem, vírus Caraparu, vírus Oropouche e vírus Catu e um do gênero Phlebovirus: vírus Icoaraci, em soros de búfalos de água no Estado do Pará, Brasil. Para todos os Arbovírus investigados houve presença de anticorpos, com exceção do vírus Belém. Anticorpos para o vírus Maguari foram mais prevalentes (7,33%). O rebanho bubalino do presente estudo mostrou variáveis níveis de anticorpos em reações heterotípicas e monotípicas podendo indicar que há circulação da maioria dos bunyavírus estudados em búfalos domésticos no estado do Pará, e que o vírus Maguari é o de maior circulação. Por isso, são necessários outros estudos para investigar o papel dos búfalos de água na manutenção e dispersão de arbovírus, assim como se esses vírus podem causar enfermidades na referida espécie, principalmente, em casos de defeitos congênitos e abortamentos.

Prevalência de anticorpos contra arbovírus da família Bunyaviridae em búfalos de água / Prevalence of arbovirus antibodies against the family Bunyaviridae in water buffaloes

The State of Pará comprises 26% of Brazilian Amazon region where a large diversity of arboviruses has been described. This study sought to assess the prevalence and distribution of haemagglutination-inhibition antibodies against antigens of nine different types of arbovirus of the Bunyaviridae family, where eight were Orthobunyavirus: Guaroa virus, Maguari virus, Tacaiuma virus, Utinga virus, Belem virus, Caraparu virus, Oropouche virus and Catu virus, and one Phlebovirus: Icoaraci virus in sera samples of water buffaloes in Pará State, Brazil. For all Arboviruses investigated there were antibodies, with the exception of Belem virus. Antibodies to Maguari virus were more prevalent (7.33%). The water buffaloes of the present study showed variable levels of antibodies in monotypic and heterotypic reactions that may indicate there are movements from most bunyavirus studied in domestic buffaloes in the state of Pará, and the Maguari virus presents the largest circulation. Therefore, further studies are needed to investigate the role of water buffalo in the maintenance and dispersal of arboviruses, as well as whether these viruses can cause disease in that species, especially in cases of birth defects and abortions.(AU)

O Estado do Pará corresponde a 26% da Amazônica brasileira, onde uma grande quantidade de Arbovírus tem sido descrito. O presente trabalho teve como objetivo determinar a prevalência de anticorpos detectados pela técnica de inibição de hemaglutinação contra nove tipos diferentes de arbovírus da família Bunyaviridae, sendo oito do gênero Orthobunyavirus: vírus Guaroa, vírus Maguari, vírus Tacaiuma, vírus Utinga, vírus Belem, vírus Caraparu, vírus Oropouche e vírus Catu e um do gênero Phlebovirus: vírus Icoaraci, em soros de búfalos de água no Estado do Pará, Brasil. Para todos os Arbovírus investigados houve presença de anticorpos, com exceção do vírus Belém. Anticorpos para o vírus Maguari foram mais prevalentes (7,33%). O rebanho bubalino do presente estudo mostrou variáveis níveis de anticorpos em reações heterotípicas e monotípicas podendo indicar que há circulação da maioria dos bunyavírus estudados em búfalos domésticos no estado do Pará, e que o vírus Maguari é o de maior circulação. Por isso, são necessários outros estudos para investigar o papel dos búfalos de água na manutenção e dispersão de arbovírus, assim como se esses vírus podem causar enfermidades na referida espécie, principalmente, em casos de defeitos congênitos e abortamentos.(AU)

Prevalence of attibodies against influenza viru in non-vaccinated equines fromm the Brazilian pantaall / Prevalência de anticorpos contra o vírus da Influenza em equinos não vacinados do Pantanal Brasileiro

The prevalence of antibodies against Equine Influenza Virus (EIV) was determined in 529 equines living on ranches in the municipality of Poconé, Pantanal area of Brazil, by means of the hemagglutination inhibition test, using subtype H3N8 as antigen. The distribution and possible association among positive animal and ranches were evaluated by the chi-square test, spatial autoregressive and multiple linear regression models. The prevalence of antibodies against EIV was estimated at 45.2% (95% CI 30.2 - 61.1%) with titers ranging from 20 to 1,280 HAU. Seropositive equines were found on 92.0% of the surveyed ranches. Equine from non-flooded ranches (66.5%) and negativity in equine infectious anemia virus (EIAV) (61.7%) were associated with antibodies against EIV. No spatial correlation was found among the ranches, but the ones located in non-flooded areas were associated with antibodies against EIV. A negative correlation was found between the prevalence of antibodies against EIV and the presence of EIAV positive animals on the ranches. The high prevalence of antibodies against EIV detected in this study suggests that the virus is circulating among the animals, and this statistical analysis indicates that the movement and aggregation of animals are factors associated to the transmission of the virus in the region.

A prevalência de anticorpos para o vírus da Influenza Equina (VIE) no município de Poconé, MT. foi determinada em 529 equídeos pela técnica de Inibição da hemaglutinação utilizando como antígeno a variante H3N8 (SP/1/85). A distribuição da positividade e possíveis associações entre os animais e as propriedades foram avaliadas pelo teste do Qui-quadrado e pelos modelos espacial autoregressivo misto e de regressão linear múltipla. A prevalência de anticorpos para o VIE no município de Poconé foi estimada em 45,2% (IC 95% 30,2 - 61,1%) com títulos variando entre 20 e 1280UIH. Das fazendas analisadas 23 (92,0%) apresentaram animais soropositivos. Animais de fazendas não alagadas (66,5%) e negativos para Anemia Infecciosa Equina (AIE) (61,7%) foram associados a soropositividade. Não houve correlação espacial entre as fazendas estudadas, entretanto aquelas localizadas nas áreas não alagadas foram associadas à infecção. Observou-se correlação negativa entre a prevalência de anticorpos para o VIE e a presença de animais positivos para AIE nas propriedades. A elevada prevalência de anticorpos para o VIE detectada neste estudo sugere circulação viral ativa entre os animais, e as análises estatísticas indicam que o trânsito e aglomeração animal são fatores associados à transmissão do vírus na região.

Prevalence of antibodies against influenza virus in non-vaccinated equines from the Brazilian Pantanal.

The prevalence of antibodies against Equine Influenza Virus (EIV) was determined in 529 equines living on ranches in the municipality of Poconé, Pantanal area of Brazil, by means of the hemagglutination inhibition test, using subtype H3N8 as antigen. The distribution and possible association among positive animal and ranches were evaluated by the chi-square test, spatial autoregressive and multiple linear regression models. The prevalence of antibodies against EIV was estimated at 45.2% (95% CI 30.2 - 61.1%) with titers ranging from 20 to 1,280 HAU. Seropositive equines were found on 92.0% of the surveyed ranches. Equine from non-flooded ranches (66.5%) and negativity in equine infectious anemia virus (EIAV) (61.7%) were associated with antibodies against EIV. No spatial correlation was found among the ranches, but the ones located in non-flooded areas were associated with antibodies against EIV. A negative correlation was found between the prevalence of antibodies against EIV and the presence of EIAV positive animals on the ranches. The high prevalence of antibodies against EIV detected in this study suggests that the virus is circulating among the animals, and this statistical analysis indicates that the movement and aggregation of animals are factors associated to the transmission of the virus in the region.

Serological evidence for Saint Louis encephalitis virus in free-ranging New World monkeys and horses within the upper Paraná River basin region, Southern Brazil.

INTRODUCTION: Saint Louis encephalitis virus (SLEV) primarily occurs in the Americas and produces disease predominantly in humans. This study investigated the serological presence of SLEV in nonhuman primates and horses from southern Brazil. METHODS: From June 2004 to December 2005, sera from 133 monkeys (Alouatta caraya, n=43; Sapajus nigritus, n=64; Sapajus cay, n=26) trap-captured at the Paraná River basin region and 23 blood samples from farm horses were obtained and used for the serological detection of a panel of 19 arboviruses. All samples were analyzed in a hemagglutination inhibition (HI) assay; positive monkey samples were confirmed in a mouse neutralization test (MNT). Additionally, all blood samples were inoculated into C6/36 cell culture for viral isolation. RESULTS: Positive seroreactivity was only observed for SLEV. A prevalence of SLEV antibodies in sera was detected in Alouatta caraya (11.6%; 5/43), Sapajus nigritus (12.5%; 8/64), and S. cay (30.8%; 8/26) monkeys with the HI assay. Of the monkeys, 2.3% (1/42) of A. caraya, 6.3% 94/64) of S. nigritus, and 15.4% (4/26) of S. cay were positive for SLEV in the MNT. Additionally, SLEV antibodies were detected by HI in 39.1% (9/23) of the horses evaluated in this study. Arboviruses were not isolated from any blood sample. CONCLUSIONS: These results confirmed the presence of SLEV in nonhuman primates and horses from southern Brazil. These findings most likely represent the first detection of this virus in nonhuman primates beyond the Amazon region. The detection of SLEV in animals within a geographical region distant from the Amazon basin suggests that there may be widespread and undiagnosed dissemination of this disease in Brazil.

Serological evidence for Saint Louis encephalitis virus in free-ranging New World monkeys and horses within the upper Paraná River basin region, Southern Brazil

Introduction Saint Louis encephalitis virus (SLEV) primarily occurs in the Americas and produces disease predominantly in humans. This study investigated the serological presence of SLEV in nonhuman primates and horses from southern Brazil. Methods From June 2004 to December 2005, sera from 133 monkeys (Alouatta caraya, n=43; Sapajus nigritus, n=64; Sapajus cay, n=26) trap-captured at the Paraná River basin region and 23 blood samples from farm horses were obtained and used for the serological detection of a panel of 19 arboviruses. All samples were analyzed in a hemagglutination inhibition (HI) assay; positive monkey samples were confirmed in a mouse neutralization test (MNT). Additionally, all blood samples were inoculated into C6/36 cell culture for viral isolation. Results Positive seroreactivity was only observed for SLEV. A prevalence of SLEV antibodies in sera was detected in Alouatta caraya (11.6%; 5/43), Sapajus nigritus (12.5%; 8/64), and S. cay (30.8%; 8/26) monkeys with the HI assay. Of the monkeys, 2.3% (1/42) of A. caraya, 6.3% 94/64) of S. nigritus, and 15.4% (4/26) of S. cay were positive for SLEV in the MNT. Additionally, SLEV antibodies were detected by HI in 39.1% (9/23) of the horses evaluated in this study. Arboviruses were not isolated from any blood sample. Conclusions These results confirmed the presence of SLEV in nonhuman primates and horses from southern Brazil. These findings most likely represent the first detection of this virus in nonhuman primates beyond the Amazon region. The detection of SLEV in animals within a geographical region distant from the Amazon basin suggests that there may be widespread and undiagnosed dissemination of this disease in Brazil. .

Levantamento soroepidemiológico para arbovírus em macaco-prego-galego (Cebus flavius) de vida livre no estado da Paraíba e em macaco-prego (Cebus libidinosus) de cativeiro do nordeste do Brasil / Epidemiologic survey for arbovirus in galician capuchin monkeys (Cebus flavius) free living in Paraíba and captive capuchin monkey (Cebus libidinosus) from northeast Brazil

Este estudo descreve a primeira investigação de anticorpos para arbovírus em primatas não humanos do Novo Mundo no nordeste brasileiro. No período de março de 2008 a setembro de 2010 foram colhidos soros sanguíneos de 31 macacos-prego-galegos (Cebus flavius) de vida livre na Paraíba e de 100 macacos-prego (Cebus libidinosus) em cativeiro nos estados de Alagoas, Paraíba, Pernambuco, Piauí e Rio Grande do Norte. Para a pesquisa de anticorpos utilizou-se o teste de inibição da hemaglutinação (IH), usando antígenos de 19 diferentes tipos de arbovírus, pertencentes aos gêneros Flavivirus,Alphavirus e Bunyavirus. As amostras de soro foram testadas nas diluições de 1:20 a 1:1280. Dentre as amostras examinadas, todas as de C. flavius foram negativas e 46 por cento das de C. libidinosus em cativeiro apresentaram anticorpos para arbovírus. Foram detectados anticorpos para nove (9/19) arbovírus. Foram observadas 17 reações heterotípicas, para dois ou mais vírus, do gênero Flavivirus, e 15 para o gênero Alphavirus, com títulos variando de 1:20 a 1:1280. Quinze amostras apresentaram reação monotípica para ILHV (n=4), MAYV (n=6), SLEV (n=1), ROCV (n=2), OROV (n=1) e MUCV (n=1). Estes resultados sugerem que houve intensa circulação de arbovírus na população estudada de macacos-prego em cativeiro.

This paper describes the first investigation of arbovirus antibodies on New World non-human primates from Northeast Brazil. From March 2008 to September 2010 blood serum samples were collected from 31 wild blond capuchin monkeys (Cebus flavius) from Paraíba and 100 captive capuchin monkeys from Alagoas, Paraíba, Pernambuco, Piauí and Rio Grande do Norte. The haemagglutination-inhibition test (HI) was employed for 19 arbovirus of the Flavivirus,Alphavirus and Bunyavirus genus. Serum samples were tested from 1:20 to 1:1280 dilutions. Among the primates tested all C. flavius were negative and 46 percent C. libidinosus presented antibodies to arbovirus. Antibodies were detected for nine arbovirus (9/19). Seventeen heterotypic reactions were observed for at least two Or Flavirus and 15 for Alphavirus, at titers varying between 1:20 to 1:1280. Fifteen samples presented monotypic reaction for ILHV (n=4), MAYV (n=6), SLEV (n=1), ROCV (n=2), OROV (n=1) and MUCV (n=1). These results suggest that there was an intense arbovirus circulation in the studied population of captive capuchin monkeys.

Levantamento soroepidemiológico para arbovírus em macaco-prego-galego (Cebus flavius) de vida livre no estado da Paraíba e em macaco-prego (Cebus libidinosus) de cativeiro do nordeste do Brasil / Epidemiologic survey for arbovirus in galician capuchin monkeys (Cebus flavius) free living in Paraíba and captive capuchin monkey (Cebus libidinosus) from northeast Brazil

Este estudo descreve a primeira investigação de anticorpos para arbovírus em primatas não humanos do Novo Mundo no nordeste brasileiro. No período de março de 2008 a setembro de 2010 foram colhidos soros sanguíneos de 31 macacos-prego-galegos (Cebus flavius) de vida livre na Paraíba e de 100 macacos-prego (Cebus libidinosus) em cativeiro nos estados de Alagoas, Paraíba, Pernambuco, Piauí e Rio Grande do Norte. Para a pesquisa de anticorpos utilizou-se o teste de inibição da hemaglutinação (IH), usando antígenos de 19 diferentes tipos de arbovírus, pertencentes aos gêneros Flavivirus,Alphavirus e Bunyavirus. As amostras de soro foram testadas nas diluições de 1:20 a 1:1280. Dentre as amostras examinadas, todas as de C. flavius foram negativas e 46 por cento das de C. libidinosus em cativeiro apresentaram anticorpos para arbovírus. Foram detectados anticorpos para nove (9/19) arbovírus. Foram observadas 17 reações heterotípicas, para dois ou mais vírus, do gênero Flavivirus, e 15 para o gênero Alphavirus, com títulos variando de 1:20 a 1:1280. Quinze amostras apresentaram reação monotípica para ILHV (n=4), MAYV (n=6), SLEV (n=1), ROCV (n=2), OROV (n=1) e MUCV (n=1). Estes resultados sugerem que houve intensa circulação de arbovírus na população estudada de macacos-prego em cativeiro.(AU)

This paper describes the first investigation of arbovirus antibodies on New World non-human primates from Northeast Brazil. From March 2008 to September 2010 blood serum samples were collected from 31 wild blond capuchin monkeys (Cebus flavius) from Paraíba and 100 captive capuchin monkeys from Alagoas, Paraíba, Pernambuco, Piauí and Rio Grande do Norte. The haemagglutination-inhibition test (HI) was employed for 19 arbovirus of the Flavivirus,Alphavirus and Bunyavirus genus. Serum samples were tested from 1:20 to 1:1280 dilutions. Among the primates tested all C. flavius were negative and 46 percent C. libidinosus presented antibodies to arbovirus. Antibodies were detected for nine arbovirus (9/19). Seventeen heterotypic reactions were observed for at least two Or Flavirus and 15 for Alphavirus, at titers varying between 1:20 to 1:1280. Fifteen samples presented monotypic reaction for ILHV (n=4), MAYV (n=6), SLEV (n=1), ROCV (n=2), OROV (n=1) and MUCV (n=1). These results suggest that there was an intense arbovirus circulation in the studied population of captive capuchin monkeys.(AU)

Epidemiology and ecology of H3N8 canine influenza viruses in US shelter dogs.

BACKGROUND: H3N8 canine influenza virus (CIV) infection might contribute to increased duration of shelter stay for dogs. Greater understanding of factors contributing to CIV within shelters could help veterinarians identify control measures for CIV. OBJECTIVES: To assess community to shelter dog CIV transmission, estimate true prevalence of CIV, and determine risk factors associated with CIV in humane shelters. ANIMALS: 5,160 dogs upon intake or discharge from 6 US humane shelters, December 2009 through January 2012. METHODS: A cross-sectional study was performed with prospective convenience sampling of 40 dogs from each shelter monthly. Nasal swabs and serum samples were collected. Hemagglutination inhibition and real-time reverse transcriptase-polymerase chain reaction assays were performed for each nasal and serum sample. True prevalence was estimated by stochastic latent class analysis. Logistic regression was used to identify risk factors associated with CIV shedding and seropositivity. RESULTS: Nasal swabs were positive from 4.4% of New York (NY), 4.7% of Colorado (CO), 3.2% of South Carolina, 1.2% of Florida, and 0% of California and Texas shelter dogs sampled. Seropositivity was the highest in the CO shelter dogs at 10%, and NY at 8.5%. Other shelters had 0% seropositivity. Information-theoretic analyses suggested that CIV shedding was associated with region, month, and year (model weight = 0.95) and comingling/cohousing (model weight = 0.92). CONCLUSIONS AND CLINICAL IMPORTANCE: Community dogs are a likely source of CIV introduction into humane shelters and once CIV has become established, dog-to-dog transmission maintains the virus within a shelter.