Perspective
Reappearance of Chikungunya, Formerly Called Dengue, in the Americas
After an absence of ≈200 years, chikungunya returned to the American tropics in 2013. The virus is maintained in a complex African zoonotic cycle but escapes into an urban cycle at 40- to 50-year intervals, causing global pandemics. In 1823, classical chikungunya, a viral exanthem in humans, occurred on Zanzibar, and in 1827, it arrived in the Caribbean and spread to North and South America. In Zanzibar, the disease was known as kidenga pepo, Swahili for a sudden cramp-like seizure caused by an evil spirit; in Cuba, it was known as dengue, a Spanish homonym of denga. During the eighteenth century, dengue (present-day chikungunya) was distinguished from breakbone fever (present-day dengue), another febrile exanthem. In the twentieth century, experiments resulted in the recovery and naming of present-day dengue viruses. In 1952, chikungunya virus was recovered during an outbreak in Tanzania, but by then, the virus had lost its original name to present-day dengue viruses.
EID | Halstead SB. Reappearance of Chikungunya, Formerly Called Dengue, in the Americas. Emerg Infect Dis. 2015;21(4):561. https://doi.org/10.3201/eid2104.141723 |
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AMA | Halstead SB. Reappearance of Chikungunya, Formerly Called Dengue, in the Americas. Emerging Infectious Diseases. 2015;21(4):561. doi:10.3201/eid2104.141723. |
APA | Halstead, S. B. (2015). Reappearance of Chikungunya, Formerly Called Dengue, in the Americas. Emerging Infectious Diseases, 21(4), 561. https://doi.org/10.3201/eid2104.141723. |
Synopses
Hantavirus Pulmonary Syndrome , Southern Chile, 1995–2012
Hantavirus is endemic to the Region de Los Lagos in southern Chile; its incidence is 8.5 times higher in the communes of the Andean area than in the rest of the region. We analyzed the epidemiologic aspects of the 103 cases diagnosed by serology and the clinical aspects of 80 hospitalized patients during 1995–2012. Cases in this region clearly predominated during winter, whereas in the rest of the country, they occur mostly during summer. Mild, moderate, and severe disease was observed, and the case-fatality rate was 32%. Shock caused death in 75% of those cases; high respiratory frequency and elevated creatinine plasma level were independent factors associated with death. Early clinical suspicion, especially in rural areas, should prompt urgent transfer to a hospital with an intensive care unit and might help decrease the high case-fatality rate.
EID | Riquelme R, Rioseco M, Bastidas L, Trincado D, Riquelme M, Loyola H, et al. Hantavirus Pulmonary Syndrome , Southern Chile, 1995–2012. Emerg Infect Dis. 2015;21(4):562-568. https://doi.org/10.3201/eid2104.141437 |
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AMA | Riquelme R, Rioseco M, Bastidas L, et al. Hantavirus Pulmonary Syndrome , Southern Chile, 1995–2012. Emerging Infectious Diseases. 2015;21(4):562-568. doi:10.3201/eid2104.141437. |
APA | Riquelme, R., Rioseco, M., Bastidas, L., Trincado, D., Riquelme, M., Loyola, H....Valdivieso, F. (2015). Hantavirus Pulmonary Syndrome , Southern Chile, 1995–2012. Emerging Infectious Diseases, 21(4), 562-568. https://doi.org/10.3201/eid2104.141437. |
Among travelers, rabies cases are rare, but animal bites are relatively common. To determine which travelers are at highest risk for rabies, we studied 2,697 travelers receiving care for animal-related exposures and requiring rabies postexposure prophylaxis at GeoSentinel clinics during 1997–2012. No specific demographic characteristics differentiated these travelers from other travelers seeking medical care, making it challenging to identify travelers who might benefit from reinforced pretravel rabies prevention counseling. Median travel duration was short for these travelers: 15 days for those seeking care after completion of travel and 20 days for those seeking care during travel. This finding contradicts the view that preexposure rabies vaccine recommendations should be partly based on longer travel durations. Over half of exposures occurred in Thailand, Indonesia, Nepal, China, and India. International travelers to rabies-endemic regions, particularly Asia, should be informed about potential rabies exposure and benefits of pretravel vaccination, regardless of demographics or length of stay.
EID | Gautret P, Harvey K, Pandey P, Lim P, Leder K, Piyaphanee W, et al. Animal-Associated Exposure to Rabies Virus among Travelers, 1997–2012. Emerg Infect Dis. 2015;21(4):569-577. https://doi.org/10.3201/eid2104.141479 |
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AMA | Gautret P, Harvey K, Pandey P, et al. Animal-Associated Exposure to Rabies Virus among Travelers, 1997–2012. Emerging Infectious Diseases. 2015;21(4):569-577. doi:10.3201/eid2104.141479. |
APA | Gautret, P., Harvey, K., Pandey, P., Lim, P., Leder, K., Piyaphanee, W....Parola, P. (2015). Animal-Associated Exposure to Rabies Virus among Travelers, 1997–2012. Emerging Infectious Diseases, 21(4), 569-577. https://doi.org/10.3201/eid2104.141479. |
Evolution of Ebola Virus Disease from Exotic Infection to Global Health Priority, Liberia, Mid-2014
Over the span of a few weeks during July and August 2014, events in West Africa changed perceptions of Ebola virus disease (EVD) from an exotic tropical disease to a priority for global health security. We describe observations during that time of a field team from the Centers for Disease Control and Prevention and personnel of the Liberian Ministry of Health and Social Welfare. We outline the early epidemiology of EVD within Liberia, including the practical limitations on surveillance and the effect on the country’s health care system, such as infections among health care workers. During this time, priorities included strengthening EVD surveillance; establishing safe settings for EVD patient care (and considering alternative isolation and care models when Ebola Treatment Units were overwhelmed); improving infection control practices; establishing an incident management system; and working with Liberian airport authorities to implement EVD screening of departing passengers.
EID | Arwady M, Bawo L, Hunter JC, Massaquoi M, Matanock A, Dahn B, et al. Evolution of Ebola Virus Disease from Exotic Infection to Global Health Priority, Liberia, Mid-2014. Emerg Infect Dis. 2015;21(4):578-584. https://doi.org/10.3201/eid2104.141940 |
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AMA | Arwady M, Bawo L, Hunter JC, et al. Evolution of Ebola Virus Disease from Exotic Infection to Global Health Priority, Liberia, Mid-2014. Emerging Infectious Diseases. 2015;21(4):578-584. doi:10.3201/eid2104.141940. |
APA | Arwady, M., Bawo, L., Hunter, J. C., Massaquoi, M., Matanock, A., Dahn, B....De Cock, K. M. (2015). Evolution of Ebola Virus Disease from Exotic Infection to Global Health Priority, Liberia, Mid-2014. Emerging Infectious Diseases, 21(4), 578-584. https://doi.org/10.3201/eid2104.141940. |
Research
Population Structure and Antimicrobial Resistance of Invasive Serotype IV Group B Streptococcus, Toronto, Ontario, Canada
We recently showed that 37/600 (6.2%) invasive infections with group B Streptococcus (GBS) in Toronto, Ontario, Canada, were caused by serotype IV strains. We report a relatively high level of genetic diversity in 37 invasive strains of this emerging GBS serotype. Multilocus sequence typing identified 6 sequence types (STs) that belonged to 3 clonal complexes. Most isolates were ST-459 (19/37, 51%) and ST-452 (11/37, 30%), but we also identified ST-291, ST-3, ST-196, and a novel ST-682. We detected further diversity by performing whole-genome single-nucleotide polymorphism analysis and found evidence of recombination events contributing to variation in some serotype IV GBS strains. We also evaluated antimicrobial drug resistance and found that ST-459 strains were resistant to clindamycin and erythromycin, whereas strains of other STs were, for the most part, susceptible to these antimicrobial drugs.
EID | Teatero S, McGeer A, Li A, Gomes J, Seah C, Demczuk W, et al. Population Structure and Antimicrobial Resistance of Invasive Serotype IV Group B Streptococcus, Toronto, Ontario, Canada. Emerg Infect Dis. 2015;21(4):585-591. https://doi.org/10.3201/eid2104.140759 |
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AMA | Teatero S, McGeer A, Li A, et al. Population Structure and Antimicrobial Resistance of Invasive Serotype IV Group B Streptococcus, Toronto, Ontario, Canada. Emerging Infectious Diseases. 2015;21(4):585-591. doi:10.3201/eid2104.140759. |
APA | Teatero, S., McGeer, A., Li, A., Gomes, J., Seah, C., Demczuk, W....Fittipaldi, N. (2015). Population Structure and Antimicrobial Resistance of Invasive Serotype IV Group B Streptococcus, Toronto, Ontario, Canada. Emerging Infectious Diseases, 21(4), 585-591. https://doi.org/10.3201/eid2104.140759. |
Norovirus Genotype Profiles Associated with Foodborne Transmission, 1999–2012
Worldwide, noroviruses are a leading cause of gastroenteritis. They can be transmitted from person to person directly or indirectly through contaminated food, water, or environments. To estimate the proportion of foodborne infections caused by noroviruses on a global scale, we used norovirus transmission and genotyping information from multiple international outbreak surveillance systems (Noronet, CaliciNet, EpiSurv) and from a systematic review of peer-reviewed literature. The proportion of outbreaks caused by food was determined by genotype and/or genogroup. Analysis resulted in the following final global profiles: foodborne transmission is attributed to 10% (range 9%%–11%) of all genotype GII.4 outbreaks, 27% (25%–30%) of outbreaks caused by all other single genotypes, and 37% (24%%–52%) of outbreaks caused by mixtures of GII.4 and other noroviruses. When these profiles are applied to global outbreak surveillance data, results indicate that ≈14% of all norovirus outbreaks are attributed to food.
EID | Verhoef L, Hewitt J, Barclay L, Ahmed SM, Lake R, Hall AJ, et al. Norovirus Genotype Profiles Associated with Foodborne Transmission, 1999–2012. Emerg Infect Dis. 2015;21(4):592-599. https://doi.org/10.3201/eid2104.141073 |
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AMA | Verhoef L, Hewitt J, Barclay L, et al. Norovirus Genotype Profiles Associated with Foodborne Transmission, 1999–2012. Emerging Infectious Diseases. 2015;21(4):592-599. doi:10.3201/eid2104.141073. |
APA | Verhoef, L., Hewitt, J., Barclay, L., Ahmed, S. M., Lake, R., Hall, A. J....Koopmans, M. (2015). Norovirus Genotype Profiles Associated with Foodborne Transmission, 1999–2012. Emerging Infectious Diseases, 21(4), 592-599. https://doi.org/10.3201/eid2104.141073. |
We estimated deaths attributable to influenza and respiratory syncytial virus (RSV) among persons >5 years of age in South Africa during 1998–2009 by applying regression models to monthly deaths and laboratory surveillance data. Rates were expressed per 100,000 person-years. The mean annual number of seasonal influenza–associated deaths was 9,093 (rate 21.6). Persons >65 years of age and HIV-positive persons accounted for 50% (n = 4,552) and 28% (n = 2,564) of overall seasonal influenza-associated deaths, respectively. In 2009, we estimated 4,113 (rate 9.2) influenza A(H1N1)pdm09–associated deaths. The mean of annual RSV-associated deaths during the study period was 511 (rate 1.2); no RSV-associated deaths were estimated in persons >45 years of age. Our findings support the recommendation for influenza vaccination of older persons and HIV-positive persons. Surveillance for RSV should be strengthened to clarify the public health implications and severity of illness associated with RSV infection in South Africa.
EID | Cohen C, Walaza S, Viboud C, Cohen AL, Madhi SA, Venter M, et al. Deaths Associated with Respiratory Syncytial and Influenza Viruses among Persons ≥5 Years of Age in HIV-Prevalent Area, South Africa, 1998–2009. Emerg Infect Dis. 2015;21(4):600-608. https://doi.org/10.3201/eid2104.141033 |
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AMA | Cohen C, Walaza S, Viboud C, et al. Deaths Associated with Respiratory Syncytial and Influenza Viruses among Persons ≥5 Years of Age in HIV-Prevalent Area, South Africa, 1998–2009. Emerging Infectious Diseases. 2015;21(4):600-608. doi:10.3201/eid2104.141033. |
APA | Cohen, C., Walaza, S., Viboud, C., Cohen, A. L., Madhi, S. A., Venter, M....Tempia, S. (2015). Deaths Associated with Respiratory Syncytial and Influenza Viruses among Persons ≥5 Years of Age in HIV-Prevalent Area, South Africa, 1998–2009. Emerging Infectious Diseases, 21(4), 600-608. https://doi.org/10.3201/eid2104.141033. |
Sequence Variability and Geographic Distribution of Lassa Virus, Sierra Leone
Lassa virus (LASV) is endemic to parts of West Africa and causes highly fatal hemorrhagic fever. The multimammate rat (Mastomys natalensis) is the only known reservoir of LASV. Most human infections result from zoonotic transmission. The very diverse LASV genome has 4 major lineages associated with different geographic locations. We used reverse transcription PCR and resequencing microarrays to detect LASV in 41 of 214 samples from rodents captured at 8 locations in Sierra Leone. Phylogenetic analysis of partial sequences of nucleoprotein (NP), glycoprotein precursor (GPC), and polymerase (L) genes showed 5 separate clades within lineage IV of LASV in this country. The sequence diversity was higher than previously observed; mean diversity was 7.01% for nucleoprotein gene at the nucleotide level. These results may have major implications for designing diagnostic tests and therapeutic agents for LASV infections in Sierra Leone.
EID | Leski TA, Stockelman MG, Moses LM, Park M, Stenger DA, Ansumana R, et al. Sequence Variability and Geographic Distribution of Lassa Virus, Sierra Leone. Emerg Infect Dis. 2015;21(4):609-618. https://doi.org/10.3201/eid2104.141469 |
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AMA | Leski TA, Stockelman MG, Moses LM, et al. Sequence Variability and Geographic Distribution of Lassa Virus, Sierra Leone. Emerging Infectious Diseases. 2015;21(4):609-618. doi:10.3201/eid2104.141469. |
APA | Leski, T. A., Stockelman, M. G., Moses, L. M., Park, M., Stenger, D. A., Ansumana, R....Lin, B. (2015). Sequence Variability and Geographic Distribution of Lassa Virus, Sierra Leone. Emerging Infectious Diseases, 21(4), 609-618. https://doi.org/10.3201/eid2104.141469. |
Influenza A(H7N9) Virus Transmission between Finches and Poultry
Low pathogenicity avian influenza A(H7N9) virus has been detected in poultry since 2013, and the virus has caused >450 infections in humans. The mode of subtype H7N9 virus transmission between avian species remains largely unknown, but various wild birds have been implicated as a source of transmission. H7N9 virus was recently detected in a wild sparrow in Shanghai, China, and passerine birds, such as finches, which share space and resources with wild migratory birds, poultry, and humans, can be productively infected with the virus. We demonstrate that interspecies transmission of H7N9 virus occurs readily between society finches and bobwhite quail but only sporadically between finches and chickens. Inoculated finches are better able to infect naive poultry than the reverse. Transmission occurs through shared water but not through the airborne route. It is therefore conceivable that passerine birds may serve as vectors for dissemination of H7N9 virus to domestic poultry.
EID | Jones JC, Sonnberg S, Webby R, Webster RG. Influenza A(H7N9) Virus Transmission between Finches and Poultry. Emerg Infect Dis. 2015;21(4):619-628. https://doi.org/10.3201/eid2104.141703 |
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AMA | Jones JC, Sonnberg S, Webby R, et al. Influenza A(H7N9) Virus Transmission between Finches and Poultry. Emerging Infectious Diseases. 2015;21(4):619-628. doi:10.3201/eid2104.141703. |
APA | Jones, J. C., Sonnberg, S., Webby, R., & Webster, R. G. (2015). Influenza A(H7N9) Virus Transmission between Finches and Poultry. Emerging Infectious Diseases, 21(4), 619-628. https://doi.org/10.3201/eid2104.141703. |
Highly Pathogenic Avian Influenza A(H5N1) Virus Infection among Workers at Live Bird Markets, Bangladesh, 2009–2010
The risk for influenza A(H5N1) virus infection is unclear among poultry workers in countries where the virus is endemic. To assess H5N1 seroprevalence and seroconversion among workers at live bird markets (LBMs) in Bangladesh, we followed a cohort of workers from 12 LBMs with existing avian influenza surveillance. Serum samples from workers were tested for H5N1 antibodies at the end of the study or when LBM samples first had H5N1 virus–positive test results. Of 404 workers, 9 (2%) were seropositive at baseline. Of 284 workers who completed the study and were seronegative at baseline, 6 (2%) seroconverted (7 cases/100 poultry worker–years). Workers who frequently fed poultry, cleaned feces from pens, cleaned food/water containers, and did not wash hands after touching sick poultry had a 7.6 times higher risk for infection compared with workers who infrequently performed these behaviors. Despite frequent exposure to H5N1 virus, LBM workers showed evidence of only sporadic infection.
EID | Nasreen S, Khan S, Luby SP, Gurley ES, Abedin J, Zaman R, et al. Highly Pathogenic Avian Influenza A(H5N1) Virus Infection among Workers at Live Bird Markets, Bangladesh, 2009–2010. Emerg Infect Dis. 2015;21(4):629-637. https://doi.org/10.3201/eid2104.141281 |
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AMA | Nasreen S, Khan S, Luby SP, et al. Highly Pathogenic Avian Influenza A(H5N1) Virus Infection among Workers at Live Bird Markets, Bangladesh, 2009–2010. Emerging Infectious Diseases. 2015;21(4):629-637. doi:10.3201/eid2104.141281. |
APA | Nasreen, S., Khan, S., Luby, S. P., Gurley, E. S., Abedin, J., Zaman, R....Azziz-Baumgartner, E. (2015). Highly Pathogenic Avian Influenza A(H5N1) Virus Infection among Workers at Live Bird Markets, Bangladesh, 2009–2010. Emerging Infectious Diseases, 21(4), 629-637. https://doi.org/10.3201/eid2104.141281. |
Increased Risk for Group B Streptococcus Sepsis in Young Infants Exposed to HIV, Soweto, South Africa, 2004–2008
Although group B Streptococcus (GBS) is a leading cause of severe invasive disease in young infants worldwide, epidemiologic data and knowledge about risk factors for the disease are lacking from low- to middle-income countries. To determine the epidemiology of invasive GBS disease among young infants in a setting with high maternal HIV infection, we conducted hospital-based surveillance during 2004–2008 in Soweto, South Africa. Overall GBS incidence was 2.72 cases/1,000 live births (1.50 and 1.22, respectively, among infants with early-onset disease [EOD] and late-onset [LOD] disease). Risk for EOD and LOD was higher for HIV-exposed than HIV-unexposed infants. GBS serotypes Ia and III accounted for 84.0% of cases, and 16.9% of infected infants died. We estimate that use of trivalent GBS vaccine (serotypes Ia, Ib, and III) could prevent 2,105 invasive GBS cases and 278 deaths annually among infants in South Africa; therefore, vaccination of all pregnant women in this country should be explored.
EID | Cutland CL, Schrag SJ, Thigpen MC, Velaphi SC, Wadula J, Adrian PV, et al. Increased Risk for Group B Streptococcus Sepsis in Young Infants Exposed to HIV, Soweto, South Africa, 2004–2008. Emerg Infect Dis. 2015;21(4):638-645. https://doi.org/10.3201/eid2104.141562 |
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AMA | Cutland CL, Schrag SJ, Thigpen MC, et al. Increased Risk for Group B Streptococcus Sepsis in Young Infants Exposed to HIV, Soweto, South Africa, 2004–2008. Emerging Infectious Diseases. 2015;21(4):638-645. doi:10.3201/eid2104.141562. |
APA | Cutland, C. L., Schrag, S. J., Thigpen, M. C., Velaphi, S. C., Wadula, J., Adrian, P. V....Madhi, S. A. (2015). Increased Risk for Group B Streptococcus Sepsis in Young Infants Exposed to HIV, Soweto, South Africa, 2004–2008. Emerging Infectious Diseases, 21(4), 638-645. https://doi.org/10.3201/eid2104.141562. |
Dispatches
La Crosse Virus in Aedes japonicus japonicus Mosquitoes in the Appalachian Region, United States
La Crosse virus (LACV), a leading cause of arboviral encephalitis in children in the United States, is emerging in Appalachia. For local arboviral surveillance, mosquitoes were tested. LACV RNA was detected and isolated from Aedes japonicus mosquitoes. These invasive mosquitoes may significantly affect LACV range expansion and dynamics.
EID | Harris M, Dotseth EJ, Jackson B, Zink SD, Marek PE, Kramer LD, et al. La Crosse Virus in Aedes japonicus japonicus Mosquitoes in the Appalachian Region, United States. Emerg Infect Dis. 2015;21(4):646-649. https://doi.org/10.3201/eid2104.140734 |
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AMA | Harris M, Dotseth EJ, Jackson B, et al. La Crosse Virus in Aedes japonicus japonicus Mosquitoes in the Appalachian Region, United States. Emerging Infectious Diseases. 2015;21(4):646-649. doi:10.3201/eid2104.140734. |
APA | Harris, M., Dotseth, E. J., Jackson, B., Zink, S. D., Marek, P. E., Kramer, L. D....Hawley, D. M. (2015). La Crosse Virus in Aedes japonicus japonicus Mosquitoes in the Appalachian Region, United States. Emerging Infectious Diseases, 21(4), 646-649. https://doi.org/10.3201/eid2104.140734. |
Pathogenicity of 2 Porcine Deltacoronavirus Strains in Gnotobiotic Pigs
To verify whether porcine deltacoronavirus infection induces disease, we inoculated gnotobiotic pigs with 2 virus strains (OH-FD22 and OH-FD100) identified by 2 specific reverse transcription PCRs. At 21–120 h postinoculation, pigs exhibited severe diarrhea, vomiting, fecal shedding of virus, and severe atrophic enteritis. These findings confirm that these 2 strains are enteropathogenic in pigs.
EID | Jung K, Hu H, Eyerly B, Lu Z, Chepngeno J, Saif LJ. Pathogenicity of 2 Porcine Deltacoronavirus Strains in Gnotobiotic Pigs. Emerg Infect Dis. 2015;21(4):650-654. https://doi.org/10.3201/eid2104.141859 |
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AMA | Jung K, Hu H, Eyerly B, et al. Pathogenicity of 2 Porcine Deltacoronavirus Strains in Gnotobiotic Pigs. Emerging Infectious Diseases. 2015;21(4):650-654. doi:10.3201/eid2104.141859. |
APA | Jung, K., Hu, H., Eyerly, B., Lu, Z., Chepngeno, J., & Saif, L. J. (2015). Pathogenicity of 2 Porcine Deltacoronavirus Strains in Gnotobiotic Pigs. Emerging Infectious Diseases, 21(4), 650-654. https://doi.org/10.3201/eid2104.141859. |
Multidrug-Resistant Salmonella enterica Serotype Typhi, Gulf of Guinea Region, Africa
We identified 3 lineages among multidrug-resistant (MDR) Salmonella enterica serotype Typhi isolates in the Gulf of Guinea region in Africa during the 2000s. However, the MDR H58 haplotype, which predominates in southern Asia and Kenya, was not identified. MDR quinolone-susceptible isolates contained a 190-kb incHI1 pST2 plasmid or a 50-kb incN pST3 plasmid.
EID | Baltazar M, Ngandjio A, Holt K, Lepillet E, Pardos de la Gandara M, Collard J, et al. Multidrug-Resistant Salmonella enterica Serotype Typhi, Gulf of Guinea Region, Africa. Emerg Infect Dis. 2015;21(4):655-659. https://doi.org/10.3201/eid2104.141355 |
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AMA | Baltazar M, Ngandjio A, Holt K, et al. Multidrug-Resistant Salmonella enterica Serotype Typhi, Gulf of Guinea Region, Africa. Emerging Infectious Diseases. 2015;21(4):655-659. doi:10.3201/eid2104.141355. |
APA | Baltazar, M., Ngandjio, A., Holt, K., Lepillet, E., Pardos de la Gandara, M., Collard, J....Weill, F. (2015). Multidrug-Resistant Salmonella enterica Serotype Typhi, Gulf of Guinea Region, Africa. Emerging Infectious Diseases, 21(4), 655-659. https://doi.org/10.3201/eid2104.141355. |
Candidate New Rotavirus Species in Sheltered Dogs, Hungary
We identified unusual rotavirus strains in fecal specimens from sheltered dogs in Hungary by viral metagenomics. The novel rotavirus species displayed limited genome sequence homology to representatives of the 8 rotavirus species, A–H, and qualifies as a candidate new rotavirus species that we tentatively named Rotavirus I.
EID | Mihalov-Kovács E, Gellért Á, Marton S, Farkas SL, Fehér E, Oldal M, et al. Candidate New Rotavirus Species in Sheltered Dogs, Hungary. Emerg Infect Dis. 2015;21(4):660-663. https://doi.org/10.3201/eid2104.141370 |
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AMA | Mihalov-Kovács E, Gellért Á, Marton S, et al. Candidate New Rotavirus Species in Sheltered Dogs, Hungary. Emerging Infectious Diseases. 2015;21(4):660-663. doi:10.3201/eid2104.141370. |
APA | Mihalov-Kovács, E., Gellért, Á., Marton, S., Farkas, S. L., Fehér, E., Oldal, M....Bányai, K. (2015). Candidate New Rotavirus Species in Sheltered Dogs, Hungary. Emerging Infectious Diseases, 21(4), 660-663. https://doi.org/10.3201/eid2104.141370. |
Severity of Influenza A(H1N1) Illness and Emergence of D225G Variant, 2013–14 Influenza Season, Florida, USA
Despite a regional decline in influenza A(H1N1)pdm09 virus infections during 2013–14, cases at a Florida hospital were more severe than those during 2009–10. Examined strains had a hemagglutinin polymorphism associated with enhanced binding to lower respiratory tract receptors. Genetic changes in this virus must be monitored to predict the effect of future pandemic viruses.
EID | Iovine NM, Morris J, Fredenburg K, Rand KH, Alnuaimat H, Lipori G, et al. Severity of Influenza A(H1N1) Illness and Emergence of D225G Variant, 2013–14 Influenza Season, Florida, USA. Emerg Infect Dis. 2015;21(4):664-667. https://doi.org/10.3201/eid2104.141375 |
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AMA | Iovine NM, Morris J, Fredenburg K, et al. Severity of Influenza A(H1N1) Illness and Emergence of D225G Variant, 2013–14 Influenza Season, Florida, USA. Emerging Infectious Diseases. 2015;21(4):664-667. doi:10.3201/eid2104.141375. |
APA | Iovine, N. M., Morris, J., Fredenburg, K., Rand, K. H., Alnuaimat, H., Lipori, G....Lednicky, J. (2015). Severity of Influenza A(H1N1) Illness and Emergence of D225G Variant, 2013–14 Influenza Season, Florida, USA. Emerging Infectious Diseases, 21(4), 664-667. https://doi.org/10.3201/eid2104.141375. |
Close Relationship of Ruminant Pestiviruses and Classical Swine Fever Virus
To determine why serum from small ruminants infected with ruminant pestiviruses reacted positively to classical swine fever virus (CSFV)–specific diagnostic tests, we analyzed 2 pestiviruses from Turkey. They differed genetically and antigenically from known Pestivirus species and were closely related to CSFV. Cross-reactions would interfere with classical swine fever diagnosis in pigs.
EID | Postel A, Schmeiser S, Oguzoglu T, Indenbirken D, Alawi M, Fischer N, et al. Close Relationship of Ruminant Pestiviruses and Classical Swine Fever Virus. Emerg Infect Dis. 2015;21(4):668-672. https://doi.org/10.3201/eid2104.141441 |
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AMA | Postel A, Schmeiser S, Oguzoglu T, et al. Close Relationship of Ruminant Pestiviruses and Classical Swine Fever Virus. Emerging Infectious Diseases. 2015;21(4):668-672. doi:10.3201/eid2104.141441. |
APA | Postel, A., Schmeiser, S., Oguzoglu, T., Indenbirken, D., Alawi, M., Fischer, N....Becher, P. (2015). Close Relationship of Ruminant Pestiviruses and Classical Swine Fever Virus. Emerging Infectious Diseases, 21(4), 668-672. https://doi.org/10.3201/eid2104.141441. |
Reassortant Avian Influenza A(H9N2) Viruses in Chickens in Retail Poultry Shops, Pakistan, 2009–2010
Phylogenetic analysis of influenza viruses collected during December 2009–February 2010 from chickens in live poultry retail shops in Lahore, Pakistan, showed influenza A(H9N2) lineage polymerase and nonstructural genes generate through inter- and intrasubtypic reassortments. Many amino acid signatures observed were characteristic of human isolates; hence, their circulation could enhance inter- or intrasubtypic reassortment.
EID | Chaudhry M, Angot A, Rashid HB, Cattoli G, Hussain M, Trovò G, et al. Reassortant Avian Influenza A(H9N2) Viruses in Chickens in Retail Poultry Shops, Pakistan, 2009–2010. Emerg Infect Dis. 2015;21(4):673-676. https://doi.org/10.3201/eid2104.141570 |
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AMA | Chaudhry M, Angot A, Rashid HB, et al. Reassortant Avian Influenza A(H9N2) Viruses in Chickens in Retail Poultry Shops, Pakistan, 2009–2010. Emerging Infectious Diseases. 2015;21(4):673-676. doi:10.3201/eid2104.141570. |
APA | Chaudhry, M., Angot, A., Rashid, H. B., Cattoli, G., Hussain, M., Trovò, G....Capua, I. (2015). Reassortant Avian Influenza A(H9N2) Viruses in Chickens in Retail Poultry Shops, Pakistan, 2009–2010. Emerging Infectious Diseases, 21(4), 673-676. https://doi.org/10.3201/eid2104.141570. |
Peste des Petits Ruminants Virus in Heilongjiang Province, China, 2014
During March 25–May 5, 2014, we investigated 11 outbreaks of peste des petits ruminants in Heilongjiang Province, China. We found that the most likely source of the outbreaks was animals from livestock markets in Shandong. Peste des petits ruminants viruses belonging to lineages II and IV were detected in sick animals.
EID | Wang J, Wang M, Wang S, Liu Z, Shen N, Si W, et al. Peste des Petits Ruminants Virus in Heilongjiang Province, China, 2014. Emerg Infect Dis. 2015;21(4):677-680. https://doi.org/10.3201/eid2104.141627 |
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AMA | Wang J, Wang M, Wang S, et al. Peste des Petits Ruminants Virus in Heilongjiang Province, China, 2014. Emerging Infectious Diseases. 2015;21(4):677-680. doi:10.3201/eid2104.141627. |
APA | Wang, J., Wang, M., Wang, S., Liu, Z., Shen, N., Si, W....Cai, X. (2015). Peste des Petits Ruminants Virus in Heilongjiang Province, China, 2014. Emerging Infectious Diseases, 21(4), 677-680. https://doi.org/10.3201/eid2104.141627. |
West Nile Virus Infection Incidence Based on Donated Blood Samples and Neuroinvasive Disease Reports, Northern Texas, USA, 2012
During the 2012 outbreak of West Nile virus in the United States, approximately one third of the cases were in Texas. Of those, about half occurred in northern Texas. Models based on infected blood donors and persons with neuroinvasive disease showed, respectively, that ≈0.72% and 1.98% of persons in northern Texas became infected.
EID | Cervantes DT, Chen S, Sutor LJ, Stonecipher S, Janoski N, Wright DJ, et al. West Nile Virus Infection Incidence Based on Donated Blood Samples and Neuroinvasive Disease Reports, Northern Texas, USA, 2012. Emerg Infect Dis. 2015;21(4):681-683. https://doi.org/10.3201/eid2104.141178 |
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AMA | Cervantes DT, Chen S, Sutor LJ, et al. West Nile Virus Infection Incidence Based on Donated Blood Samples and Neuroinvasive Disease Reports, Northern Texas, USA, 2012. Emerging Infectious Diseases. 2015;21(4):681-683. doi:10.3201/eid2104.141178. |
APA | Cervantes, D. T., Chen, S., Sutor, L. J., Stonecipher, S., Janoski, N., Wright, D. J....Murphy, E. L. (2015). West Nile Virus Infection Incidence Based on Donated Blood Samples and Neuroinvasive Disease Reports, Northern Texas, USA, 2012. Emerging Infectious Diseases, 21(4), 681-683. https://doi.org/10.3201/eid2104.141178. |
Influenza A(H10N7) Virus in Dead Harbor Seals, Denmark
Since April 2014, an outbreak of influenza in harbor seals has been ongoing in northern Europe. In Denmark during June–August, 152 harbor seals on the island of Anholt were found dead from severe pneumonia. We detected influenza A(H10N7) virus in 2 of 4 seals examined.
EID | Krog JS, Hansen MS, Holm E, Hjulsager CK, Chriél M, Pedersen K, et al. Influenza A(H10N7) Virus in Dead Harbor Seals, Denmark. Emerg Infect Dis. 2015;21(4):684-687. https://doi.org/10.3201/eid2104.141484 |
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AMA | Krog JS, Hansen MS, Holm E, et al. Influenza A(H10N7) Virus in Dead Harbor Seals, Denmark. Emerging Infectious Diseases. 2015;21(4):684-687. doi:10.3201/eid2104.141484. |
APA | Krog, J. S., Hansen, M. S., Holm, E., Hjulsager, C. K., Chriél, M., Pedersen, K....Larsen, L. E. (2015). Influenza A(H10N7) Virus in Dead Harbor Seals, Denmark. Emerging Infectious Diseases, 21(4), 684-687. https://doi.org/10.3201/eid2104.141484. |
High Seroprevalence of Antibodies against Spotted Fever and Scrub Typhus Bacteria in Patients with Febrile Illness, Kenya
Serum samples from patients in Kenya with febrile illnesses were screened for antibodies against bacteria that cause spotted fever, typhus, and scrub typhus. Seroprevalence was 10% for spotted fever group, <1% for typhus group, and 5% for scrub typhus group. Results should help clinicians expand their list of differential diagnoses for undifferentiated fevers.
EID | Thiga JW, Mutai BK, Eyako WK, Ng’ang’a Z, Jiang J, Richards AL, et al. High Seroprevalence of Antibodies against Spotted Fever and Scrub Typhus Bacteria in Patients with Febrile Illness, Kenya. Emerg Infect Dis. 2015;21(4):688-691. https://doi.org/10.3201/eid2104.141387 |
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AMA | Thiga JW, Mutai BK, Eyako WK, et al. High Seroprevalence of Antibodies against Spotted Fever and Scrub Typhus Bacteria in Patients with Febrile Illness, Kenya. Emerging Infectious Diseases. 2015;21(4):688-691. doi:10.3201/eid2104.141387. |
APA | Thiga, J. W., Mutai, B. K., Eyako, W. K., Ng’ang’a, Z., Jiang, J., Richards, A. L....Waitumbi, J. N. (2015). High Seroprevalence of Antibodies against Spotted Fever and Scrub Typhus Bacteria in Patients with Febrile Illness, Kenya. Emerging Infectious Diseases, 21(4), 688-691. https://doi.org/10.3201/eid2104.141387. |
Prevalence of Hepatitis E Virus Antibodies, Israel, 2009–2010
We investigated prevalence of hepatitis E virus in a sample of the population of Israel. The overall seroprevalence of antibodies to the virus was 10.6% (95% CI 8.4%–13.0%); age-adjusted prevalence was 7.6%. Seropositivity was associated with age, Arab ethnicity, low socioeconomic status, and birth in Africa, Asia, or the former Soviet Union.
EID | Mor O, Bassal R, Michaeli M, Wax M, Ram D, Cohen-Ezra O, et al. Prevalence of Hepatitis E Virus Antibodies, Israel, 2009–2010. Emerg Infect Dis. 2015;21(4):692-694. https://doi.org/10.3201/eid2104.140245 |
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AMA | Mor O, Bassal R, Michaeli M, et al. Prevalence of Hepatitis E Virus Antibodies, Israel, 2009–2010. Emerging Infectious Diseases. 2015;21(4):692-694. doi:10.3201/eid2104.140245. |
APA | Mor, O., Bassal, R., Michaeli, M., Wax, M., Ram, D., Cohen-Ezra, O....Shohat, T. (2015). Prevalence of Hepatitis E Virus Antibodies, Israel, 2009–2010. Emerging Infectious Diseases, 21(4), 692-694. https://doi.org/10.3201/eid2104.140245. |
Outbreak of Severe Zoonotic Vaccinia Virus Infection, Southeastern Brazil
In 2010, a vaccinia virus isolate caused an atypically severe outbreak that affected humans and cattle in Brazil. Of 26 rural workers affected, 12 were hospitalized. Our data raise questions about the risk factors related to the increasing number and severity of vaccinia virus infections.
EID | Abrahão J, Campos R, Trindade G, Guimarães da Fonseca F, Ferreira P, Lima M. Outbreak of Severe Zoonotic Vaccinia Virus Infection, Southeastern Brazil. Emerg Infect Dis. 2015;21(4):695-698. https://doi.org/10.3201/eid2104.140351 |
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AMA | Abrahão J, Campos R, Trindade G, et al. Outbreak of Severe Zoonotic Vaccinia Virus Infection, Southeastern Brazil. Emerging Infectious Diseases. 2015;21(4):695-698. doi:10.3201/eid2104.140351. |
APA | Abrahão, J., Campos, R., Trindade, G., Guimarães da Fonseca, F., Ferreira, P., & Lima, M. (2015). Outbreak of Severe Zoonotic Vaccinia Virus Infection, Southeastern Brazil. Emerging Infectious Diseases, 21(4), 695-698. https://doi.org/10.3201/eid2104.140351. |
Lack of Middle East Respiratory Syndrome Coronavirus Transmission from Infected Camels
To determine risk for Middle East respiratory syndrome coronavirus transmission from camels to humans, we tested serum from 191 persons with various levels of exposure to an infected dromedary herd. We found no serologic evidence of human infection, suggesting that zoonotic transmission of this virus from dromedaries is rare.
EID | Hemida MG, Al-Naeem A, Perera R, Chin A, Poon L, Peiris M. Lack of Middle East Respiratory Syndrome Coronavirus Transmission from Infected Camels. Emerg Infect Dis. 2015;21(4):699-701. https://doi.org/10.3201/eid2104.141949 |
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AMA | Hemida MG, Al-Naeem A, Perera R, et al. Lack of Middle East Respiratory Syndrome Coronavirus Transmission from Infected Camels. Emerging Infectious Diseases. 2015;21(4):699-701. doi:10.3201/eid2104.141949. |
APA | Hemida, M. G., Al-Naeem, A., Perera, R., Chin, A., Poon, L., & Peiris, M. (2015). Lack of Middle East Respiratory Syndrome Coronavirus Transmission from Infected Camels. Emerging Infectious Diseases, 21(4), 699-701. https://doi.org/10.3201/eid2104.141949. |
Safety of Recombinant VSV–Ebola Virus Vaccine Vector in Pigs
The ongoing Ebola outbreak in West Africa has resulted in fast-track development of vaccine candidates. We tested a vesicular stomatitis virus vector expressing Ebola virus glycoprotein for safety in pigs. Inoculation did not cause disease and vaccine virus shedding was minimal, which indicated that the vaccine virus does not pose a risk of dissemination in pigs.
EID | de Wit E, Marzi A, Bushmaker T, Brining D, Scott D, Richt JA, et al. Safety of Recombinant VSV–Ebola Virus Vaccine Vector in Pigs. Emerg Infect Dis. 2015;21(4):702-704. https://doi.org/10.3201/eid2104.142012 |
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AMA | de Wit E, Marzi A, Bushmaker T, et al. Safety of Recombinant VSV–Ebola Virus Vaccine Vector in Pigs. Emerging Infectious Diseases. 2015;21(4):702-704. doi:10.3201/eid2104.142012. |
APA | de Wit, E., Marzi, A., Bushmaker, T., Brining, D., Scott, D., Richt, J. A....Feldmann, H. (2015). Safety of Recombinant VSV–Ebola Virus Vaccine Vector in Pigs. Emerging Infectious Diseases, 21(4), 702-704. https://doi.org/10.3201/eid2104.142012. |
Letters
Enterovirus A71 Subgenotype B5, France, 2013
EID | Mirand A, Molet L, Hassel C, Peigue-Lafeuille H, Rozenberg F, Bailly J, et al. Enterovirus A71 Subgenotype B5, France, 2013. Emerg Infect Dis. 2015;21(4):707-709. https://doi.org/10.3201/eid2104.141093 |
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AMA | Mirand A, Molet L, Hassel C, et al. Enterovirus A71 Subgenotype B5, France, 2013. Emerging Infectious Diseases. 2015;21(4):707-709. doi:10.3201/eid2104.141093. |
APA | Mirand, A., Molet, L., Hassel, C., Peigue-Lafeuille, H., Rozenberg, F., Bailly, J....Henquell, C. (2015). Enterovirus A71 Subgenotype B5, France, 2013. Emerging Infectious Diseases, 21(4), 707-709. https://doi.org/10.3201/eid2104.141093. |
Avian Influenza A(H7N9) Virus Antibodies in Close Contacts of Infected Persons, China, 2013–2014
EID | Ma M, Ma G, Yang X, Chen S, Gray GC, Zhao T, et al. Avian Influenza A(H7N9) Virus Antibodies in Close Contacts of Infected Persons, China, 2013–2014. Emerg Infect Dis. 2015;21(4):709-711. https://doi.org/10.3201/eid2104.141442 |
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AMA | Ma M, Ma G, Yang X, et al. Avian Influenza A(H7N9) Virus Antibodies in Close Contacts of Infected Persons, China, 2013–2014. Emerging Infectious Diseases. 2015;21(4):709-711. doi:10.3201/eid2104.141442. |
APA | Ma, M., Ma, G., Yang, X., Chen, S., Gray, G. C., Zhao, T....Cao, W. (2015). Avian Influenza A(H7N9) Virus Antibodies in Close Contacts of Infected Persons, China, 2013–2014. Emerging Infectious Diseases, 21(4), 709-711. https://doi.org/10.3201/eid2104.141442. |
Hepatitis E Epidemic, Biratnagar, Nepal, 2014
EID | Shrestha A, Lama TK, Karki S, Sigdel DR, Rai U, Rauniyar SK, et al. Hepatitis E Epidemic, Biratnagar, Nepal, 2014. Emerg Infect Dis. 2015;21(4):711-713. https://doi.org/10.3201/eid2104.141512 |
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AMA | Shrestha A, Lama TK, Karki S, et al. Hepatitis E Epidemic, Biratnagar, Nepal, 2014. Emerging Infectious Diseases. 2015;21(4):711-713. doi:10.3201/eid2104.141512. |
APA | Shrestha, A., Lama, T. K., Karki, S., Sigdel, D. R., Rai, U., Rauniyar, S. K....Mishiro, S. (2015). Hepatitis E Epidemic, Biratnagar, Nepal, 2014. Emerging Infectious Diseases, 21(4), 711-713. https://doi.org/10.3201/eid2104.141512. |
Human Parvovirus 4 Infection among Mothers and Children in South Africa
EID | Matthews PC, Sharp CP, Malik A, Gregory WF, Adland E, Jooste P, et al. Human Parvovirus 4 Infection among Mothers and Children in South Africa. Emerg Infect Dis. 2015;21(4):713-715. https://doi.org/10.3201/eid2104.141545 |
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AMA | Matthews PC, Sharp CP, Malik A, et al. Human Parvovirus 4 Infection among Mothers and Children in South Africa. Emerging Infectious Diseases. 2015;21(4):713-715. doi:10.3201/eid2104.141545. |
APA | Matthews, P. C., Sharp, C. P., Malik, A., Gregory, W. F., Adland, E., Jooste, P....Klenerman, P. (2015). Human Parvovirus 4 Infection among Mothers and Children in South Africa. Emerging Infectious Diseases, 21(4), 713-715. https://doi.org/10.3201/eid2104.141545. |
Co-infection with Avian (H7N9) and Pandemic (H1N1) 2009 Influenza Viruses, China
EID | Zhang W, Zhu D, Tian D, Xu L, Zhu Z, Teng Z, et al. Co-infection with Avian (H7N9) and Pandemic (H1N1) 2009 Influenza Viruses, China. Emerg Infect Dis. 2015;21(4):715-718. https://doi.org/10.3201/eid2104.141560 |
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AMA | Zhang W, Zhu D, Tian D, et al. Co-infection with Avian (H7N9) and Pandemic (H1N1) 2009 Influenza Viruses, China. Emerging Infectious Diseases. 2015;21(4):715-718. doi:10.3201/eid2104.141560. |
APA | Zhang, W., Zhu, D., Tian, D., Xu, L., Zhu, Z., Teng, Z....Hu, Y. (2015). Co-infection with Avian (H7N9) and Pandemic (H1N1) 2009 Influenza Viruses, China. Emerging Infectious Diseases, 21(4), 715-718. https://doi.org/10.3201/eid2104.141560. |
Nairobi Sheep Disease Virus RNA in Ixodid Ticks, China, 2013
EID | Gong S, He B, Wang Z, Shang L, Wei F, Liu Q, et al. Nairobi Sheep Disease Virus RNA in Ixodid Ticks, China, 2013. Emerg Infect Dis. 2015;21(4):718-720. https://doi.org/10.3201/eid2104.141602 |
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AMA | Gong S, He B, Wang Z, et al. Nairobi Sheep Disease Virus RNA in Ixodid Ticks, China, 2013. Emerging Infectious Diseases. 2015;21(4):718-720. doi:10.3201/eid2104.141602. |
APA | Gong, S., He, B., Wang, Z., Shang, L., Wei, F., Liu, Q....Tu, C. (2015). Nairobi Sheep Disease Virus RNA in Ixodid Ticks, China, 2013. Emerging Infectious Diseases, 21(4), 718-720. https://doi.org/10.3201/eid2104.141602. |
Avian Influenza A(H10N7) Virus–Associated Mass Deaths among Harbor Seals
EID | Bodewes R, Bestebroer TM, van der Vries E, Verhagen JH, Herfst S, Koopmans M, et al. Avian Influenza A(H10N7) Virus–Associated Mass Deaths among Harbor Seals. Emerg Infect Dis. 2015;21(4):720-722. https://doi.org/10.3201/eid2104.141675 |
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AMA | Bodewes R, Bestebroer TM, van der Vries E, et al. Avian Influenza A(H10N7) Virus–Associated Mass Deaths among Harbor Seals. Emerging Infectious Diseases. 2015;21(4):720-722. doi:10.3201/eid2104.141675. |
APA | Bodewes, R., Bestebroer, T. M., van der Vries, E., Verhagen, J. H., Herfst, S., Koopmans, M....Osterhaus, A. (2015). Avian Influenza A(H10N7) Virus–Associated Mass Deaths among Harbor Seals. Emerging Infectious Diseases, 21(4), 720-722. https://doi.org/10.3201/eid2104.141675. |
Zika Virus Infection, Philippines, 2012
EID | Alera M, Hermann L, Tac-An IA, Klungthong C, Rutvisuttinunt W, Manasatienkij W, et al. Zika Virus Infection, Philippines, 2012. Emerg Infect Dis. 2015;21(4):722-724. https://doi.org/10.3201/eid2104.141707 |
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AMA | Alera M, Hermann L, Tac-An IA, et al. Zika Virus Infection, Philippines, 2012. Emerging Infectious Diseases. 2015;21(4):722-724. doi:10.3201/eid2104.141707. |
APA | Alera, M., Hermann, L., Tac-An, I. A., Klungthong, C., Rutvisuttinunt, W., Manasatienkij, W....Yoon, I. (2015). Zika Virus Infection, Philippines, 2012. Emerging Infectious Diseases, 21(4), 722-724. https://doi.org/10.3201/eid2104.141707. |
Chikungunya Outbreak, French Polynesia, 2014
EID | Aubry M, Teissier A, Roche C, Richard V, Yan A, Zisou K, et al. Chikungunya Outbreak, French Polynesia, 2014. Emerg Infect Dis. 2015;21(4):724-726. https://doi.org/10.3201/eid2104.141741 |
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AMA | Aubry M, Teissier A, Roche C, et al. Chikungunya Outbreak, French Polynesia, 2014. Emerging Infectious Diseases. 2015;21(4):724-726. doi:10.3201/eid2104.141741. |
APA | Aubry, M., Teissier, A., Roche, C., Richard, V., Yan, A., Zisou, K....Musso, D. (2015). Chikungunya Outbreak, French Polynesia, 2014. Emerging Infectious Diseases, 21(4), 724-726. https://doi.org/10.3201/eid2104.141741. |
Influenza A and B Viruses but Not MERS-CoV in Hajj Pilgrims, Austria, 2014
EID | Aberle JH, Popow-Kraupp T, Kreidl P, Laferl H, Heinz FX, Aberle SW. Influenza A and B Viruses but Not MERS-CoV in Hajj Pilgrims, Austria, 2014. Emerg Infect Dis. 2015;21(4):726-727. https://doi.org/10.3201/eid2104.141745 |
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AMA | Aberle JH, Popow-Kraupp T, Kreidl P, et al. Influenza A and B Viruses but Not MERS-CoV in Hajj Pilgrims, Austria, 2014. Emerging Infectious Diseases. 2015;21(4):726-727. doi:10.3201/eid2104.141745. |
APA | Aberle, J. H., Popow-Kraupp, T., Kreidl, P., Laferl, H., Heinz, F. X., & Aberle, S. W. (2015). Influenza A and B Viruses but Not MERS-CoV in Hajj Pilgrims, Austria, 2014. Emerging Infectious Diseases, 21(4), 726-727. https://doi.org/10.3201/eid2104.141745. |
Enterovirus D68 Infection, Chile, Spring 2014
EID | Torres JP, Farfan MJ, Izquierdo G, Piemonte P, Henriquez J, O’Ryan ML. Enterovirus D68 Infection, Chile, Spring 2014. Emerg Infect Dis. 2015;21(4):728-729. https://doi.org/10.3201/eid2104.141766 |
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AMA | Torres JP, Farfan MJ, Izquierdo G, et al. Enterovirus D68 Infection, Chile, Spring 2014. Emerging Infectious Diseases. 2015;21(4):728-729. doi:10.3201/eid2104.141766. |
APA | Torres, J. P., Farfan, M. J., Izquierdo, G., Piemonte, P., Henriquez, J., & O’Ryan, M. L. (2015). Enterovirus D68 Infection, Chile, Spring 2014. Emerging Infectious Diseases, 21(4), 728-729. https://doi.org/10.3201/eid2104.141766. |
Bat Coronavirus in Brazil Related to Appalachian Ridge and Porcine Epidemic Diarrhea Viruses
EID | Simas P, Barnabé A, Durães-Carvalho R, Neto D, Caserta L, Artacho L, et al. Bat Coronavirus in Brazil Related to Appalachian Ridge and Porcine Epidemic Diarrhea Viruses. Emerg Infect Dis. 2015;21(4):729-731. https://doi.org/10.3201/eid2104.141783 |
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AMA | Simas P, Barnabé A, Durães-Carvalho R, et al. Bat Coronavirus in Brazil Related to Appalachian Ridge and Porcine Epidemic Diarrhea Viruses. Emerging Infectious Diseases. 2015;21(4):729-731. doi:10.3201/eid2104.141783. |
APA | Simas, P., Barnabé, A., Durães-Carvalho, R., Neto, D., Caserta, L., Artacho, L....Arns, C. (2015). Bat Coronavirus in Brazil Related to Appalachian Ridge and Porcine Epidemic Diarrhea Viruses. Emerging Infectious Diseases, 21(4), 729-731. https://doi.org/10.3201/eid2104.141783. |
Tandem Repeat Insertion in African Swine Fever Virus, Russia, 2012
EID | Goller KV, Malogolovkin A, Katorkin S, Kolbasov D, Titov I, Höper D, et al. Tandem Repeat Insertion in African Swine Fever Virus, Russia, 2012. Emerg Infect Dis. 2015;21(4):731-732. https://doi.org/10.3201/eid2104.141792 |
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AMA | Goller KV, Malogolovkin A, Katorkin S, et al. Tandem Repeat Insertion in African Swine Fever Virus, Russia, 2012. Emerging Infectious Diseases. 2015;21(4):731-732. doi:10.3201/eid2104.141792. |
APA | Goller, K. V., Malogolovkin, A., Katorkin, S., Kolbasov, D., Titov, I., Höper, D....Blome, S. (2015). Tandem Repeat Insertion in African Swine Fever Virus, Russia, 2012. Emerging Infectious Diseases, 21(4), 731-732. https://doi.org/10.3201/eid2104.141792. |
Norovirus GII.21 in Children with Diarrhea, Bhutan
EID | Yahiro T, Wangchuk S, Wada T, Dorji C, Matsumoto T, Mynak M, et al. Norovirus GII.21 in Children with Diarrhea, Bhutan. Emerg Infect Dis. 2015;21(4):732-734. https://doi.org/10.3201/eid2104.141856 |
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AMA | Yahiro T, Wangchuk S, Wada T, et al. Norovirus GII.21 in Children with Diarrhea, Bhutan. Emerging Infectious Diseases. 2015;21(4):732-734. doi:10.3201/eid2104.141856. |
APA | Yahiro, T., Wangchuk, S., Wada, T., Dorji, C., Matsumoto, T., Mynak, M....Ahmed, K. (2015). Norovirus GII.21 in Children with Diarrhea, Bhutan. Emerging Infectious Diseases, 21(4), 732-734. https://doi.org/10.3201/eid2104.141856. |
Another Dimension
Lives of a Cell: 40 Years Later, A Third Interpretation
EID | Dato VM. Lives of a Cell: 40 Years Later, A Third Interpretation. Emerg Infect Dis. 2015;21(4):705-706. https://doi.org/10.3201/eid2104.110793 |
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AMA | Dato VM. Lives of a Cell: 40 Years Later, A Third Interpretation. Emerging Infectious Diseases. 2015;21(4):705-706. doi:10.3201/eid2104.110793. |
APA | Dato, V. M. (2015). Lives of a Cell: 40 Years Later, A Third Interpretation. Emerging Infectious Diseases, 21(4), 705-706. https://doi.org/10.3201/eid2104.110793. |
Books and Media
Australia’s War against Rabbits: The Story of Rabbit Haemorrhagic Disease
EID | Effler P. Australia’s War against Rabbits: The Story of Rabbit Haemorrhagic Disease. Emerg Infect Dis. 2015;21(4):735. https://doi.org/10.3201/eid2104.142009 |
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AMA | Effler P. Australia’s War against Rabbits: The Story of Rabbit Haemorrhagic Disease. Emerging Infectious Diseases. 2015;21(4):735. doi:10.3201/eid2104.142009. |
APA | Effler, P. (2015). Australia’s War against Rabbits: The Story of Rabbit Haemorrhagic Disease. Emerging Infectious Diseases, 21(4), 735. https://doi.org/10.3201/eid2104.142009. |
Etymologia
Etymologia: Varicella Zoster Virus
EID | Etymologia: Varicella Zoster Virus. Emerg Infect Dis. 2015;21(4):698. https://doi.org/10.3201/eid2104.et2104 |
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AMA | Etymologia: Varicella Zoster Virus. Emerging Infectious Diseases. 2015;21(4):698. doi:10.3201/eid2104.et2104. |
APA | (2015). Etymologia: Varicella Zoster Virus. Emerging Infectious Diseases, 21(4), 698. https://doi.org/10.3201/eid2104.et2104. |
Online Reports
Global Avian Influenza Surveillance in Wild Birds: A Strategy to Capture Viral Diversity
Wild birds play a major role in the evolution, maintenance, and spread of avian influenza viruses. However, surveillance for these viruses in wild birds is sporadic, geographically biased, and often limited to the last outbreak virus. To identify opportunities to optimize wild bird surveillance for understanding viral diversity, we reviewed responses to a World Organisation for Animal Health–administered survey, government reports to this organization, articles on Web of Knowledge, and the Influenza Research Database. At least 119 countries conducted avian influenza virus surveillance in wild birds during 2008–2013, but coordination and standardization was lacking among surveillance efforts, and most focused on limited subsets of influenza viruses. Given high financial and public health burdens of recent avian influenza outbreaks, we call for sustained, cost-effective investments in locations with high avian influenza diversity in wild birds and efforts to promote standardized sampling, testing, and reporting methods, including full-genome sequencing and sharing of isolates with the scientific community.
About the Cover
“Welcome to the World of the Plastic Beach”
EID | Breedlove B. “Welcome to the World of the Plastic Beach”. Emerg Infect Dis. 2015;21(4):736-737. https://doi.org/10.3201/eid2104.ac2104 |
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AMA | Breedlove B. “Welcome to the World of the Plastic Beach”. Emerging Infectious Diseases. 2015;21(4):736-737. doi:10.3201/eid2104.ac2104. |
APA | Breedlove, B. (2015). “Welcome to the World of the Plastic Beach”. Emerging Infectious Diseases, 21(4), 736-737. https://doi.org/10.3201/eid2104.ac2104. |