Research
We analyzed US multiple cause-of-death data for 2003–2006 for demographic and clinical determinants for autopsy in unexplained deaths possibly resulting from infectious causes. For 96,242 deaths, the definition for unexplained death was met and autopsy status was recorded. Most decedents were male, 40–49 years of age, and white. To identify factors associated with unexplained death, we used data from Arizona records. Multivariate analysis of Arizona records suggested that decedents of races other than white and black and decedents who had clinicopathologic syndromes in the cardiovascular, sepsis/shock, and multisyndrome categories recorded on the death certificate were least likely to have undergone autopsy; children with unexplained death were the most likely to have undergone autopsy. Improved understanding of unexplained deaths can provide opportunities for further studies, strengthen collaboration between investigators of unexplained deaths, and improve knowledge and awareness of infectious diseases of public health concern.
EID | Liu L, Callinan LS, Holman RC, Blau DM. Determinants for Autopsy after Unexplained Deaths Possibly Resulting from Infectious Causes, United States. Emerg Infect Dis. 2012;18(4):549-555. https://doi.org/10.3201/eid1804.111311 |
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AMA | Liu L, Callinan LS, Holman RC, et al. Determinants for Autopsy after Unexplained Deaths Possibly Resulting from Infectious Causes, United States. Emerging Infectious Diseases. 2012;18(4):549-555. doi:10.3201/eid1804.111311. |
APA | Liu, L., Callinan, L. S., Holman, R. C., & Blau, D. M. (2012). Determinants for Autopsy after Unexplained Deaths Possibly Resulting from Infectious Causes, United States. Emerging Infectious Diseases, 18(4), 549-555. https://doi.org/10.3201/eid1804.111311. |
In response to pandemic (H1N1) 2009, data were collected on work status and industry of employment of 3,365 adults hospitalized with laboratory-confirmed influenza during the 2009–10 influenza season in the United States. The proportion of workers hospitalized for influenza was lower than their proportion in the general population, reflecting underlying protective characteristics of workers compared with nonworkers. The most commonly represented sectors were transportation and warehousing; administrative and support and waste management and remediation services; health care; and accommodation and food service.
EID | Luckhaupt SE, Sweeney M, Funk R, Calvert GM, Nowell M, D’Mello T, et al. Influenza-associated Hospitalizations by Industry, 2009–10 Influenza Season, United States. Emerg Infect Dis. 2012;18(4):556-562. https://doi.org/10.3201/eid1804.110337 |
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AMA | Luckhaupt SE, Sweeney M, Funk R, et al. Influenza-associated Hospitalizations by Industry, 2009–10 Influenza Season, United States. Emerging Infectious Diseases. 2012;18(4):556-562. doi:10.3201/eid1804.110337. |
APA | Luckhaupt, S. E., Sweeney, M., Funk, R., Calvert, G. M., Nowell, M., D’Mello, T....Jones, T. (2012). Influenza-associated Hospitalizations by Industry, 2009–10 Influenza Season, United States. Emerging Infectious Diseases, 18(4), 556-562. https://doi.org/10.3201/eid1804.110337. |
Identification of Risk Factors for Chronic Q Fever, the Netherlands
Since 2007, the Netherlands has experienced a large Q fever outbreak. To identify and quantify risk factors for development of chronic Q fever after Coxiella burnetii infection, we performed a case–control study. Comorbidity, cardiovascular risk factors, medications, and demographic characteristics from 105 patients with proven (n = 44), probable (n = 28), or possible (n = 33) chronic Q fever were compared with 201 patients who had acute Q fever in 2009 but in whom chronic Q fever did not develop (controls). Independent risk factors for development of proven chronic Q fever were valvular surgery, vascular prosthesis, aneurysm, renal insufficiency, and older age.
EID | Kampschreur LM, Dekker S, Hagenaars J, Lestrade PJ, Renders N, de Jager-Leclercq M, et al. Identification of Risk Factors for Chronic Q Fever, the Netherlands. Emerg Infect Dis. 2012;18(4):563-570. https://doi.org/10.3201/eid1804.111478 |
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AMA | Kampschreur LM, Dekker S, Hagenaars J, et al. Identification of Risk Factors for Chronic Q Fever, the Netherlands. Emerging Infectious Diseases. 2012;18(4):563-570. doi:10.3201/eid1804.111478. |
APA | Kampschreur, L. M., Dekker, S., Hagenaars, J., Lestrade, P. J., Renders, N., de Jager-Leclercq, M....Oosterheert, J. (2012). Identification of Risk Factors for Chronic Q Fever, the Netherlands. Emerging Infectious Diseases, 18(4), 563-570. https://doi.org/10.3201/eid1804.111478. |
Geographic Distribution of Hantaviruses Associated with Neotomine and Sigmodontine Rodents, Mexico
To increase our knowledge of the geographic distribution of hantaviruses associated with neotomine or sigmodontine rodents in Mexico, we tested 876 cricetid rodents captured in 18 Mexican states (representing at least 44 species in the subfamily Neotominae and 10 species in the subfamily Sigmodontinae) for anti-hantavirus IgG. We found antibodies against hantavirus in 35 (4.0%) rodents. Nucleotide sequence data from 5 antibody-positive rodents indicated that Sin Nombre virus (the major cause of hantavirus pulmonary syndrome [HPS] in the United States) is enzootic in the Mexican states of Nuevo León, San Luis Potosí, Tamaulipas, and Veracruz. However, HPS has not been reported from these states, which suggests that in northeastern Mexico, HPS has been confused with other rapidly progressive, life-threatening respiratory diseases. Analyses of nucleotide sequence data from 19 other antibody-positive rodents indicated that El Moro Canyon virus and Limestone Canyon virus are geographically widely distributed in Mexico.
EID | Milazzo ML, Cajimat M, Romo HE, Estrada-Franco JG, Iñiguez-Dávalos L, Bradley RD, et al. Geographic Distribution of Hantaviruses Associated with Neotomine and Sigmodontine Rodents, Mexico. Emerg Infect Dis. 2012;18(4):571-576. https://doi.org/10.3201/eid1804.111028 |
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AMA | Milazzo ML, Cajimat M, Romo HE, et al. Geographic Distribution of Hantaviruses Associated with Neotomine and Sigmodontine Rodents, Mexico. Emerging Infectious Diseases. 2012;18(4):571-576. doi:10.3201/eid1804.111028. |
APA | Milazzo, M. L., Cajimat, M., Romo, H. E., Estrada-Franco, J. G., Iñiguez-Dávalos, L., Bradley, R. D....Fulhorst, C. F. (2012). Geographic Distribution of Hantaviruses Associated with Neotomine and Sigmodontine Rodents, Mexico. Emerging Infectious Diseases, 18(4), 571-576. https://doi.org/10.3201/eid1804.111028. |
Shiga Toxin–producing Escherichia coli Serotype O78:H in Family, Finland, 2009
Shiga toxin–producing Escherichia coli (STEC) is a pathogen that causes gastroenteritis and bloody diarrhea but can lead to severe disease, such as hemolytic uremic syndrome (HUS). STEC serotype O78:H– is rare among humans, and infections are often asymptomatic. We detected a sorbitol-fermenting STEC O78:H–:stx1c:hlyA in blood and fecal samples of a 2-week-old boy who had bacteremia and HUS and in fecal samples of his asymptomatic family members. The phenotypic and genotypic characteristics and the virulence properties of this invasive STEC were investigated. Our findings demonstrate that contrary to earlier suggestions, STEC under certain conditions can invade the human bloodstream. Moreover, this study highlights the need to implement appropriate diagnostic methods for identifying the whole spectrum of STEC strains associated with HUS.
EID | Lienemann T, Salo E, Rimhanen-Finne R, Rönnholm K, Taimisto M, Hirvonen JJ, et al. Shiga Toxin–producing Escherichia coli Serotype O78:H in Family, Finland, 2009. Emerg Infect Dis. 2012;18(4):577-581. https://doi.org/10.3201/eid1804.111310 |
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AMA | Lienemann T, Salo E, Rimhanen-Finne R, et al. Shiga Toxin–producing Escherichia coli Serotype O78:H in Family, Finland, 2009. Emerging Infectious Diseases. 2012;18(4):577-581. doi:10.3201/eid1804.111310. |
APA | Lienemann, T., Salo, E., Rimhanen-Finne, R., Rönnholm, K., Taimisto, M., Hirvonen, J. J....Siitonen, A. (2012). Shiga Toxin–producing Escherichia coli Serotype O78:H in Family, Finland, 2009. Emerging Infectious Diseases, 18(4), 577-581. https://doi.org/10.3201/eid1804.111310. |
Identification of Intermediate in Evolutionary Model of Enterohemorrhagic Escherichia coli O157
Highly pathogenic enterohemorrhagic Escherichia coli (EHEC) O157 cause a spectrum of clinical signs that include diarrhea, bloody diarrhea, and hemolytic uremic syndrome. The current evolutionary model of EHEC O157:H7/H– consists of a stepwise evolution scenario proceeding from O55:H7 to a node (hypothetical intermediate) that then branches into sorbitol-fermenting (SF) O157:H– and non-SF (NSF) O157:H7. To identify this hypothetical intermediate, we performed single nucleotide polymorphism analysis by sequencing of 92 randomly distributed backbone genomic regions of 40 O157:H7/H– isolates. Overall, 111 single nucleotide polymorphisms were identified in 75/92 partial open reading frames after sequencing 51,041 nt/strain. The EHEC O157:H7 strain LSU-61 from deer occupied an intermediate position between O55:H7 and both O157 branches (SF and NSF O157), complementing the stepwise evolutionary model of EHEC O157:H7/H–. The animal origin of this intermediate emphasizes the value of nonhuman reservoirs in the clarification of the evolution of human pathogens.
EID | Jenke C, Leopold SR, Weniger T, Rothgänger J, Harmsen D, Karch H, et al. Identification of Intermediate in Evolutionary Model of Enterohemorrhagic Escherichia coli O157. Emerg Infect Dis. 2012;18(4):582-588. https://doi.org/10.3201/eid1804.111414 |
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AMA | Jenke C, Leopold SR, Weniger T, et al. Identification of Intermediate in Evolutionary Model of Enterohemorrhagic Escherichia coli O157. Emerging Infectious Diseases. 2012;18(4):582-588. doi:10.3201/eid1804.111414. |
APA | Jenke, C., Leopold, S. R., Weniger, T., Rothgänger, J., Harmsen, D., Karch, H....Mellmann, A. (2012). Identification of Intermediate in Evolutionary Model of Enterohemorrhagic Escherichia coli O157. Emerging Infectious Diseases, 18(4), 582-588. https://doi.org/10.3201/eid1804.111414. |
Emergence of Unusual G6P[6] Rotaviruses in Children, Burkina Faso, 2009–2010
To obtain more information about rotavirus (ROTAV) genotypes in Burkina Faso, we characterized 100 ROTAVs isolated from fecal samples of children with acute gastroenteritis in the capital city of Ouagadougou, during December 2009–March 2010. Of note, 13% of the ROTAV-positive samples, including those with mixed infections, were positive for the unusual G6 genotype ROTAV strain. The genotypes identified were G9P[8], G6P[6], G1P[6], G3P[6], G1P[8], and G2P[4]. G9P[8] subgroup (SG)II strains dominated during the beginning of the ROTAV season, but later in the season, other G types associated with P[6] and SGI specificity emerged. This emergence was related to a shift in the overall age of infected children; ROTAV SGII infected younger children and induced more severe symptoms. The finding of a high incidence of G6P[6] strains highlights the need for long-term surveillance of ROTAV strains in Burkina Faso, especially when ROTAV vaccination is being considered in several African countries.
EID | Nordgren J, Nitiema LW, Sharma S, Ouermi D, Traore AS, Simpore J, et al. Emergence of Unusual G6P[6] Rotaviruses in Children, Burkina Faso, 2009–2010. Emerg Infect Dis. 2012;18(4):589-597. https://doi.org/10.3201/eid1804.110973 |
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AMA | Nordgren J, Nitiema LW, Sharma S, et al. Emergence of Unusual G6P[6] Rotaviruses in Children, Burkina Faso, 2009–2010. Emerging Infectious Diseases. 2012;18(4):589-597. doi:10.3201/eid1804.110973. |
APA | Nordgren, J., Nitiema, L. W., Sharma, S., Ouermi, D., Traore, A. S., Simpore, J....Svensson, L. (2012). Emergence of Unusual G6P[6] Rotaviruses in Children, Burkina Faso, 2009–2010. Emerging Infectious Diseases, 18(4), 589-597. https://doi.org/10.3201/eid1804.110973. |
Comparison of Escherichia coli ST131 Pulsotypes, by Epidemiologic Traits, 1967–2009
Escherichia coli sequence type 131 (ST131), an emerging disseminated public health threat, causes multidrug-resistant extraintestinal infections. Among 579 diverse E. coli ST131 isolates from 1967–2009, we compared pulsotypes (>94% similar XbaI pulsed-field gel electrophoresis profiles) by collection year, geographic origin, source, and antimicrobial drug–resistance traits. Of 170 pulsotypes, 65 had >2 isolates and accounted for 85% of isolates. Although extensively dispersed geographically, pulsotypes were significantly source specific (e.g., had little commonality between humans vs. foods and food animals). The most prevalent pulsotypes were associated with recent isolation, humans, and antimicrobial drug resistance. Predominant pulsotype 968 was associated specifically with fluoroquinolone resistance but not with extended-spectrum β-lactamase production or blaCTX-M-15. Thus, several highly successful antimicrobial drug–resistant lineages within E. coli ST131 have recently emerged and diffused extensively among locales while maintaining a comparatively restricted host/source range. Identification of factors contributing to this behavior of ST131 could help protect public health.
EID | Johnson JR, Nicolas-Chanoine M, DebRoy C, Castanheira M, Robicsek A, Hansen G, et al. Comparison of Escherichia coli ST131 Pulsotypes, by Epidemiologic Traits, 1967–2009. Emerg Infect Dis. 2012;18(4):598-607. https://doi.org/10.3201/eid1804.111627 |
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AMA | Johnson JR, Nicolas-Chanoine M, DebRoy C, et al. Comparison of Escherichia coli ST131 Pulsotypes, by Epidemiologic Traits, 1967–2009. Emerging Infectious Diseases. 2012;18(4):598-607. doi:10.3201/eid1804.111627. |
APA | Johnson, J. R., Nicolas-Chanoine, M., DebRoy, C., Castanheira, M., Robicsek, A., Hansen, G....Kuskowski, M. A. (2012). Comparison of Escherichia coli ST131 Pulsotypes, by Epidemiologic Traits, 1967–2009. Emerging Infectious Diseases, 18(4), 598-607. https://doi.org/10.3201/eid1804.111627. |
Historical Review
Malaria in Highlands of Ecuador since 1900
A recent epidemic of malaria in the highlands of Bolivia and establishment of multiple Anopheles species mosquitoes in the highlands of Ecuador highlights the reemergence of malaria in the Andes Mountains in South America. Because malaria was endemic to many highland valleys at the beginning of the 20th century, this review outlines the 20th century history of malaria in the highlands of Ecuador, and focuses on its incidence (e.g., geographic distribution) and elimination from the northern highland valleys of Pichincha and Imbabura and the role of the Guayaquil to Quito railway in creating highland larval habitat and inadvertently promoting transportation of the vector and parasite. Involvement of control organizations in combating malaria in Ecuador is also outlined in a historical context.
EID | Pinault LL, Hunter FF. Malaria in Highlands of Ecuador since 1900. Emerg Infect Dis. 2012;18(4):615-622. https://doi.org/10.3201/eid1804.111267 |
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AMA | Pinault LL, Hunter FF. Malaria in Highlands of Ecuador since 1900. Emerging Infectious Diseases. 2012;18(4):615-622. doi:10.3201/eid1804.111267. |
APA | Pinault, L. L., & Hunter, F. F. (2012). Malaria in Highlands of Ecuador since 1900. Emerging Infectious Diseases, 18(4), 615-622. https://doi.org/10.3201/eid1804.111267. |
Dengue and US Military Operations from Spanish–American War through Today
Dengue is a major cause of illness among travelers and a threat to military troops operating in areas to which it is endemic. Before and during World War II, dengue frequently occurred in US military personnel in Asia and the South Pacific. From the 1960s into the 1990s, dengue often occurred in US troops in Vietnam, the Philippines, Somalia, and Haiti. We found attack rates as high as 80% and periods of convalescence up to 3-1/2 weeks beyond the acute illness. The increase in dengue throughout the world suggests that it will remain a problem for military personnel until an effective vaccine is licensed.
EID | Gibbons RV, Streitz M, Babina T, Fried JR. Dengue and US Military Operations from Spanish–American War through Today. Emerg Infect Dis. 2012;18(4):623-630. https://doi.org/10.3201/eid1804.110134 |
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AMA | Gibbons RV, Streitz M, Babina T, et al. Dengue and US Military Operations from Spanish–American War through Today. Emerging Infectious Diseases. 2012;18(4):623-630. doi:10.3201/eid1804.110134. |
APA | Gibbons, R. V., Streitz, M., Babina, T., & Fried, J. R. (2012). Dengue and US Military Operations from Spanish–American War through Today. Emerging Infectious Diseases, 18(4), 623-630. https://doi.org/10.3201/eid1804.110134. |
Policy Review
Lessons Learned during Dengue Outbreaks in the United States, 2001–2011
Since 2001, three autochthonous dengue fever outbreaks have occurred in the United States: in Hawaii (2001); Brownsville, Texas (2005); and southern Florida (2009–2011). We sought to characterize and describe the response to these outbreaks from the perspectives of public health and vector control officials. By conducting a medical literature review through PubMed and news media searches through Google, we identified persons involved in managing each outbreak; 26 persons then participated in qualitative, semistructured interviews. After analyzing the 3 outbreaks, we found the following prominent themes in the response efforts: timely detection of illness; communication of up-to-date, correct information; and development of a rapid response that engages the community. We therefore recommend that public health authorities involve the clinical and laboratory community promptly, provide accurate information, and engage the local community in vector control and case identification and reporting.
EID | Adalja AA, Sell T, Bouri N, Franco C. Lessons Learned during Dengue Outbreaks in the United States, 2001–2011. Emerg Infect Dis. 2012;18(4):608-614. https://doi.org/10.3201/eid1804.110968 |
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AMA | Adalja AA, Sell T, Bouri N, et al. Lessons Learned during Dengue Outbreaks in the United States, 2001–2011. Emerging Infectious Diseases. 2012;18(4):608-614. doi:10.3201/eid1804.110968. |
APA | Adalja, A. A., Sell, T., Bouri, N., & Franco, C. (2012). Lessons Learned during Dengue Outbreaks in the United States, 2001–2011. Emerging Infectious Diseases, 18(4), 608-614. https://doi.org/10.3201/eid1804.110968. |
Dispatches
Bartonella spp. in Rats and Zoonoses, Los Angeles, California, USA
Bartonella spp. were detected in rats (Rattus norvegicus) trapped in downtown Los Angeles, California, USA. Of 200 rats tested, putative human pathogens, B. rochalimae and B. tribocorum were found in 37 (18.5%) and 115 (57.5%) rats, respectively. These bacteria among rodents in a densely populated urban area are a public health concern.
EID | Gundi V, Billeter SA, Rood MP, Kosoy MY. Bartonella spp. in Rats and Zoonoses, Los Angeles, California, USA. Emerg Infect Dis. 2012;18(4):631-633. https://doi.org/10.3201/eid1804.110816 |
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AMA | Gundi V, Billeter SA, Rood MP, et al. Bartonella spp. in Rats and Zoonoses, Los Angeles, California, USA. Emerging Infectious Diseases. 2012;18(4):631-633. doi:10.3201/eid1804.110816. |
APA | Gundi, V., Billeter, S. A., Rood, M. P., & Kosoy, M. Y. (2012). Bartonella spp. in Rats and Zoonoses, Los Angeles, California, USA. Emerging Infectious Diseases, 18(4), 631-633. https://doi.org/10.3201/eid1804.110816. |
Detection of Plasmodium spp. in Human Feces
Comparison of diagnostic methods for Plasmodium spp. in humans from Uganda and the Central African Republic showed that parasites can be efficiently detected by PCR in fecal samples. These results, which rely solely on PCR-based examination of feces, validate numerous estimates of the prevalence of malaria in great apes.
EID | Jirků M, Pomajbíková K, Petrželková KJ, Hůzová Z, Modrý D, Lukeš J. Detection of Plasmodium spp. in Human Feces. Emerg Infect Dis. 2012;18(4):634-636. https://doi.org/10.3201/eid1804.110984 |
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AMA | Jirků M, Pomajbíková K, Petrželková KJ, et al. Detection of Plasmodium spp. in Human Feces. Emerging Infectious Diseases. 2012;18(4):634-636. doi:10.3201/eid1804.110984. |
APA | Jirků, M., Pomajbíková, K., Petrželková, K. J., Hůzová, Z., Modrý, D., & Lukeš, J. (2012). Detection of Plasmodium spp. in Human Feces. Emerging Infectious Diseases, 18(4), 634-636. https://doi.org/10.3201/eid1804.110984. |
Increase in Extraintestinal Infections Caused by Salmonella enterica Subspecies II–IV
To garner information regarding site of infection and age and sex of persons infected with Salmonella enterica subspecies II–IV, we retrospectively analyzed data on Salmonella spp. infections in California, USA, 1985–2009. These subspecies were found to cause significantly more frequent invasive disease (e.g., bacteremia) than did Salmonella subspecies I strains.
EID | Abbott SL, Ni F, Janda J. Increase in Extraintestinal Infections Caused by Salmonella enterica Subspecies II–IV. Emerg Infect Dis. 2012;18(4):637-639. https://doi.org/10.3201/eid1804.111386 |
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AMA | Abbott SL, Ni F, Janda J. Increase in Extraintestinal Infections Caused by Salmonella enterica Subspecies II–IV. Emerging Infectious Diseases. 2012;18(4):637-639. doi:10.3201/eid1804.111386. |
APA | Abbott, S. L., Ni, F., & Janda, J. (2012). Increase in Extraintestinal Infections Caused by Salmonella enterica Subspecies II–IV. Emerging Infectious Diseases, 18(4), 637-639. https://doi.org/10.3201/eid1804.111386. |
Subclinical Infections with Crimean-Congo Hemorrhagic Fever Virus, Turkey
To investigate Crimean-Congo hemorrhagic fever virus in Turkey, we conducted a seroepidemiologic survey during January–April 2009. Seroprevalence of infection was 10% in a sample from an outbreak region and increased with patient age, indicating that the virus had been previously present in Turkey. We also estimated that 88% of infections were subclinical.
EID | Bodur H, Akinci E, Ascioglu S, Öngürü P, Uyar Y. Subclinical Infections with Crimean-Congo Hemorrhagic Fever Virus, Turkey. Emerg Infect Dis. 2012;18(4):640-642. https://doi.org/10.3201/eid1804.111374 |
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AMA | Bodur H, Akinci E, Ascioglu S, et al. Subclinical Infections with Crimean-Congo Hemorrhagic Fever Virus, Turkey. Emerging Infectious Diseases. 2012;18(4):640-642. doi:10.3201/eid1804.111374. |
APA | Bodur, H., Akinci, E., Ascioglu, S., Öngürü, P., & Uyar, Y. (2012). Subclinical Infections with Crimean-Congo Hemorrhagic Fever Virus, Turkey. Emerging Infectious Diseases, 18(4), 640-642. https://doi.org/10.3201/eid1804.111374. |
Crimean-Congo Hemorrhagic Fever, Kazakhstan, 2009–2010
We evaluated Crimean-Congo hemorrhagic fever (CCHF) surveillance data from southern Kazakhstan during 2009–2010 and found both spatial and temporal association between reported tick bites and CCHF cases. Public health measures should center on preventing tick bites, increasing awareness of CCHF signs and symptoms, and adopting hospital infection control practices.
EID | Knust B, Medetov ZB, Kyraubayev KB, Bumburidi Y, Erickson B, MacNeil A, et al. Crimean-Congo Hemorrhagic Fever, Kazakhstan, 2009–2010. Emerg Infect Dis. 2012;18(4):643-645. https://doi.org/10.3201/eid1804.111503 |
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AMA | Knust B, Medetov ZB, Kyraubayev KB, et al. Crimean-Congo Hemorrhagic Fever, Kazakhstan, 2009–2010. Emerging Infectious Diseases. 2012;18(4):643-645. doi:10.3201/eid1804.111503. |
APA | Knust, B., Medetov, Z. B., Kyraubayev, K. B., Bumburidi, Y., Erickson, B., MacNeil, A....Ospanov, K. S. (2012). Crimean-Congo Hemorrhagic Fever, Kazakhstan, 2009–2010. Emerging Infectious Diseases, 18(4), 643-645. https://doi.org/10.3201/eid1804.111503. |
Vector Blood Meals and Chagas Disease Transmission Potential, United States
A high proportion of triatomine insects, vectors for Trypanosoma cruzi trypanosomes, collected in Arizona and California and examined using a novel assay had fed on humans. Other triatomine insects were positive for T. cruzi parasite infection, which indicates that the potential exists for vector transmission of Chagas disease in the United States.
EID | Stevens L, Dorn PL, Hobson J, de la Rua NM, Lucero DE, Klotz JH, et al. Vector Blood Meals and Chagas Disease Transmission Potential, United States. Emerg Infect Dis. 2012;18(4):646-649. https://doi.org/10.3201/eid1804.111396 |
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AMA | Stevens L, Dorn PL, Hobson J, et al. Vector Blood Meals and Chagas Disease Transmission Potential, United States. Emerging Infectious Diseases. 2012;18(4):646-649. doi:10.3201/eid1804.111396. |
APA | Stevens, L., Dorn, P. L., Hobson, J., de la Rua, N. M., Lucero, D. E., Klotz, J. H....Klotz, S. A. (2012). Vector Blood Meals and Chagas Disease Transmission Potential, United States. Emerging Infectious Diseases, 18(4), 646-649. https://doi.org/10.3201/eid1804.111396. |
Genomic Analysis of emm59 Group A Streptococcus Invasive Strains, United States
Genomic analysis of type emm59 group A Streptococcus invasive strains isolated in the United States discovered higher than anticipated genetic heterogeneity among strains and identified a heretofore unrecognized monoclonal cluster of invasive infections in the San Francisco Bay area. Heightened monitoring for a potential shift in the epidemic behavior of emm59 group A Streptococcus is warranted.
EID | Fittipaldi N, Olsen RJ, Beres SB, Van Beneden C, Musser JM. Genomic Analysis of emm59 Group A Streptococcus Invasive Strains, United States. Emerg Infect Dis. 2012;18(4):650-652. https://doi.org/10.3201/eid1804.111803 |
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AMA | Fittipaldi N, Olsen RJ, Beres SB, et al. Genomic Analysis of emm59 Group A Streptococcus Invasive Strains, United States. Emerging Infectious Diseases. 2012;18(4):650-652. doi:10.3201/eid1804.111803. |
APA | Fittipaldi, N., Olsen, R. J., Beres, S. B., Van Beneden, C., & Musser, J. M. (2012). Genomic Analysis of emm59 Group A Streptococcus Invasive Strains, United States. Emerging Infectious Diseases, 18(4), 650-652. https://doi.org/10.3201/eid1804.111803. |
Characterization of Mycobacterium orygis as M. tuberculosis Complex Subspecies
The oryx bacilli are Mycobacterium tuberculosis complex organisms for which phylogenetic position and host range are unsettled. We characterized 22 isolates by molecular methods and propose elevation to subspecies status as M. orygis. M. orygis is a causative agent of tuberculosis in animals and humans from Africa and South Asia.
EID | van Ingen J, Rahim Z, Mulder A, Boeree MJ, Simeone R, Brosch R, et al. Characterization of Mycobacterium orygis as M. tuberculosis Complex Subspecies. Emerg Infect Dis. 2012;18(4):653-655. https://doi.org/10.3201/eid1804.110888 |
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AMA | van Ingen J, Rahim Z, Mulder A, et al. Characterization of Mycobacterium orygis as M. tuberculosis Complex Subspecies. Emerging Infectious Diseases. 2012;18(4):653-655. doi:10.3201/eid1804.110888. |
APA | van Ingen, J., Rahim, Z., Mulder, A., Boeree, M. J., Simeone, R., Brosch, R....van Soolingen, D. (2012). Characterization of Mycobacterium orygis as M. tuberculosis Complex Subspecies. Emerging Infectious Diseases, 18(4), 653-655. https://doi.org/10.3201/eid1804.110888. |
Cosavirus Infection in Persons with and without Gastroenteritis, Brazil
To determine possible cosavirus association with clinical disease, we used real-time reverse transcription PCR to test children and HIV-positive adults in Brazil with and without gastroenteritis. Thirteen (3.6%) of 359 children with gastroenteritis tested positive, as did 69 (33.8%) of 204 controls. Low prevalence, frequent viral co-infections, and low fecal cosavirus RNA concentrations argue against human pathogenicity.
EID | Stöcker A, Souza B, Ribeiro T, Netto E, Araujo L, Corrêa J, et al. Cosavirus Infection in Persons with and without Gastroenteritis, Brazil. Emerg Infect Dis. 2012;18(4):656-659. https://doi.org/10.3201/eid1804.111415 |
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AMA | Stöcker A, Souza B, Ribeiro T, et al. Cosavirus Infection in Persons with and without Gastroenteritis, Brazil. Emerging Infectious Diseases. 2012;18(4):656-659. doi:10.3201/eid1804.111415. |
APA | Stöcker, A., Souza, B., Ribeiro, T., Netto, E., Araujo, L., Corrêa, J....Drexler, J. (2012). Cosavirus Infection in Persons with and without Gastroenteritis, Brazil. Emerging Infectious Diseases, 18(4), 656-659. https://doi.org/10.3201/eid1804.111415. |
Drug Susceptibility of Mycobacterium tuberculosis Beijing Genotype and Association with MDR TB
To determine differences in the ability of Mycobacterium tuberculosis strains to withstand antituberculosis drug treatment, we compared the activity of antituberculosis drugs against susceptible Beijing and East-African/Indian genotype M. tuberculosis strains. Beijing genotype strains showed high rates of mutation within a wide range of drug concentrations, possibly explaining this genotype’s association with multidrug-resistant tuberculosis.
EID | de Steenwinkel J, ten Kate MT, de Knegt GJ, Kremer K, Aarnoutse RE, Boeree MJ, et al. Drug Susceptibility of Mycobacterium tuberculosis Beijing Genotype and Association with MDR TB. Emerg Infect Dis. 2012;18(4):660-663. https://doi.org/10.3201/eid1804.110912 |
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AMA | de Steenwinkel J, ten Kate MT, de Knegt GJ, et al. Drug Susceptibility of Mycobacterium tuberculosis Beijing Genotype and Association with MDR TB. Emerging Infectious Diseases. 2012;18(4):660-663. doi:10.3201/eid1804.110912. |
APA | de Steenwinkel, J., ten Kate, M. T., de Knegt, G. J., Kremer, K., Aarnoutse, R. E., Boeree, M. J....Bakker-Woudenberg, I. (2012). Drug Susceptibility of Mycobacterium tuberculosis Beijing Genotype and Association with MDR TB. Emerging Infectious Diseases, 18(4), 660-663. https://doi.org/10.3201/eid1804.110912. |
Ikoma Lyssavirus, Highly Divergent Novel Lyssavirus in an African Civet
Evidence in support of a novel lyssavirus was obtained from brain samples of an African civet in Tanzania. Results of phylogenetic analysis of nucleoprotein gene sequences from representative Lyssavirus species and this novel lyssavirus provided strong empirical evidence that this is a new lyssavirus species, designated Ikoma lyssavirus.
EID | Marston DA, Horton DL, Ngeleja C, Hampson K, McElhinney LM, Banyard AC, et al. Ikoma Lyssavirus, Highly Divergent Novel Lyssavirus in an African Civet. Emerg Infect Dis. 2012;18(4):664-667. https://doi.org/10.3201/eid1804.111553 |
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AMA | Marston DA, Horton DL, Ngeleja C, et al. Ikoma Lyssavirus, Highly Divergent Novel Lyssavirus in an African Civet. Emerging Infectious Diseases. 2012;18(4):664-667. doi:10.3201/eid1804.111553. |
APA | Marston, D. A., Horton, D. L., Ngeleja, C., Hampson, K., McElhinney, L. M., Banyard, A. C....Lembo, T. (2012). Ikoma Lyssavirus, Highly Divergent Novel Lyssavirus in an African Civet. Emerging Infectious Diseases, 18(4), 664-667. https://doi.org/10.3201/eid1804.111553. |
Coccidioides posadasii Infection in Bats, Brazil
To analyze the eco-epidemiologic aspects of Histoplasma capsulatum in Brazil, we tested 83 bats for this fungus. Although H. capsulatum was not isolated, Coccidioides posadasii was recovered from Carollia perspicillata bat lungs. Immunologic studies detected coccidioidal antibodies and antigens in Glossophaga soricina and Desmodus rotundus bats.
EID | Cordeiro R, Rocha de Castro e Silva K, Brilhante R, Moura F, Duarte N, Marques F, et al. Coccidioides posadasii Infection in Bats, Brazil. Emerg Infect Dis. 2012;18(4):668-670. https://doi.org/10.3201/eid1804.111641 |
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AMA | Cordeiro R, Rocha de Castro e Silva K, Brilhante R, et al. Coccidioides posadasii Infection in Bats, Brazil. Emerging Infectious Diseases. 2012;18(4):668-670. doi:10.3201/eid1804.111641. |
APA | Cordeiro, R., Rocha de Castro e Silva, K., Brilhante, R., Moura, F., Duarte, N., Marques, F....Sidrim, J. (2012). Coccidioides posadasii Infection in Bats, Brazil. Emerging Infectious Diseases, 18(4), 668-670. https://doi.org/10.3201/eid1804.111641. |
Surveillance for West Nile, Dengue, and Chikungunya Virus Infections, Veneto Region, Italy, 2010
In 2010, in Veneto Region, Italy, surveillance of summer fevers was conducted to promptly identify autochthonous cases of West Nile fever and increase detection of imported dengue and chikungunya in travelers. Surveillance highlighted the need to modify case definitions, train physicians, and when a case is identified, implement vector control measures
EID | Gobbi F, Barzon L, Capelli G, Angheben A, Pacenti M, Napoletano G, et al. Surveillance for West Nile, Dengue, and Chikungunya Virus Infections, Veneto Region, Italy, 2010. Emerg Infect Dis. 2012;18(4):671-673. https://doi.org/10.3201/eid1804.110753 |
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AMA | Gobbi F, Barzon L, Capelli G, et al. Surveillance for West Nile, Dengue, and Chikungunya Virus Infections, Veneto Region, Italy, 2010. Emerging Infectious Diseases. 2012;18(4):671-673. doi:10.3201/eid1804.110753. |
APA | Gobbi, F., Barzon, L., Capelli, G., Angheben, A., Pacenti, M., Napoletano, G....Bisoffi, Z. (2012). Surveillance for West Nile, Dengue, and Chikungunya Virus Infections, Veneto Region, Italy, 2010. Emerging Infectious Diseases, 18(4), 671-673. https://doi.org/10.3201/eid1804.110753. |
De Novo Daptomycin-Nonsusceptible Enterococcal Infections
Potential emergence of enterococcal daptomycin nonsusceptibility among patients with no prior exposure to daptomycin poses clinical and public health challenges. We found that development of infections with daptomycin-nonsusceptible enterococci in these patients could be associated with sporadic emergence and clonal spread.
EID | Kelesidis T, Humphries R, Uslan DZ, Pegues D. De Novo Daptomycin-Nonsusceptible Enterococcal Infections. Emerg Infect Dis. 2012;18(4):674-676. https://doi.org/10.3201/eid1804.110932 |
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AMA | Kelesidis T, Humphries R, Uslan DZ, et al. De Novo Daptomycin-Nonsusceptible Enterococcal Infections. Emerging Infectious Diseases. 2012;18(4):674-676. doi:10.3201/eid1804.110932. |
APA | Kelesidis, T., Humphries, R., Uslan, D. Z., & Pegues, D. (2012). De Novo Daptomycin-Nonsusceptible Enterococcal Infections. Emerging Infectious Diseases, 18(4), 674-676. https://doi.org/10.3201/eid1804.110932. |
Dengue in Patients with Central Nervous System Manifestations, Brazil
We investigated the prevalence of dengue in patients with suspected viral meningitis/meningoencephalitis in a dengue-endemic area. Cerebrospinal fluid analysis showed positive results and a 6.74× greater likelihood of identifying positive fluid in patients who died. Our findings support testing patients with neurologic manifestations for the virus in dengue-endemic areas.
EID | Araújo F, Nogueira R, Araújo M, Perdigão A, Cavalcanti L, Brilhante R, et al. Dengue in Patients with Central Nervous System Manifestations, Brazil. Emerg Infect Dis. 2012;18(4):677-679. https://doi.org/10.3201/eid1804.111522 |
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AMA | Araújo F, Nogueira R, Araújo M, et al. Dengue in Patients with Central Nervous System Manifestations, Brazil. Emerging Infectious Diseases. 2012;18(4):677-679. doi:10.3201/eid1804.111522. |
APA | Araújo, F., Nogueira, R., Araújo, M., Perdigão, A., Cavalcanti, L., Brilhante, R....Sidrim, J. (2012). Dengue in Patients with Central Nervous System Manifestations, Brazil. Emerging Infectious Diseases, 18(4), 677-679. https://doi.org/10.3201/eid1804.111522. |
Human Parvovirus 4 Infection, Cameroon
In a post hoc analysis of samples collected in 2009, we determined seroprevalence of parvovirus 4 (PARV4) among elderly Cameroonians. PARV4 seropositivity was associated with receipt of intravenous antimalarial drugs, intramuscular streptomycin, or an intramuscular contraceptive, but not hepatitis C virus seropositivity. Findings suggest parenteral acquisition of some PARV4 infections.
EID | Lavoie M, Sharp CP, Pépin J, Pennington C, Foupouapouognigni Y, Pybus OG, et al. Human Parvovirus 4 Infection, Cameroon. Emerg Infect Dis. 2012;18(4):680-683. https://doi.org/10.3201/eid1804.110628 |
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AMA | Lavoie M, Sharp CP, Pépin J, et al. Human Parvovirus 4 Infection, Cameroon. Emerging Infectious Diseases. 2012;18(4):680-683. doi:10.3201/eid1804.110628. |
APA | Lavoie, M., Sharp, C. P., Pépin, J., Pennington, C., Foupouapouognigni, Y., Pybus, O. G....Simmonds, P. (2012). Human Parvovirus 4 Infection, Cameroon. Emerging Infectious Diseases, 18(4), 680-683. https://doi.org/10.3201/eid1804.110628. |
Neuroinvasive Disease and West Nile Virus Infection, North Dakota, USA, 1999–2008
To determine risk for West Nile virus (WNV) neuroinvasive disease in North Dakota, we tested plasma samples from blood donors for WNV IgG and compared infection rates with reported WNV neuroinvasive disease incidence. We estimate that 1 in 244 WNV infections leads to neuroinvasive disease; risk is substantially increased among men and older persons.
EID | Carson PJ, Borchardt SM, Custer B, Prince HE, Dunn-Williams J, Winkelman V, et al. Neuroinvasive Disease and West Nile Virus Infection, North Dakota, USA, 1999–2008. Emerg Infect Dis. 2012;18(4):684-686. https://doi.org/10.3201/eid1804.111313 |
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AMA | Carson PJ, Borchardt SM, Custer B, et al. Neuroinvasive Disease and West Nile Virus Infection, North Dakota, USA, 1999–2008. Emerging Infectious Diseases. 2012;18(4):684-686. doi:10.3201/eid1804.111313. |
APA | Carson, P. J., Borchardt, S. M., Custer, B., Prince, H. E., Dunn-Williams, J., Winkelman, V....Busch, M. P. (2012). Neuroinvasive Disease and West Nile Virus Infection, North Dakota, USA, 1999–2008. Emerging Infectious Diseases, 18(4), 684-686. https://doi.org/10.3201/eid1804.111313. |
Letters
West Nile Virus Lineage 2 from Blood Donor, Greece
EID | Papa A, Politis C, Tsoukala A, Eglezou A, Bakaloudi V, Hatzitaki M, et al. West Nile Virus Lineage 2 from Blood Donor, Greece. Emerg Infect Dis. 2012;18(4):688-689. https://doi.org/10.3201/eid1804.110771 |
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AMA | Papa A, Politis C, Tsoukala A, et al. West Nile Virus Lineage 2 from Blood Donor, Greece. Emerging Infectious Diseases. 2012;18(4):688-689. doi:10.3201/eid1804.110771. |
APA | Papa, A., Politis, C., Tsoukala, A., Eglezou, A., Bakaloudi, V., Hatzitaki, M....Tsergouli, K. (2012). West Nile Virus Lineage 2 from Blood Donor, Greece. Emerging Infectious Diseases, 18(4), 688-689. https://doi.org/10.3201/eid1804.110771. |
Tuberculosis Screening before Anti–Hepatitis C Virus Therapy in Prisons
EID | Babudieri S, Soddu A, Murino M, Molicotti P, Muredda AA, Madeddu G, et al. Tuberculosis Screening before Anti–Hepatitis C Virus Therapy in Prisons. Emerg Infect Dis. 2012;18(4):689-691. https://doi.org/10.3201/eid1804.111016 |
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AMA | Babudieri S, Soddu A, Murino M, et al. Tuberculosis Screening before Anti–Hepatitis C Virus Therapy in Prisons. Emerging Infectious Diseases. 2012;18(4):689-691. doi:10.3201/eid1804.111016. |
APA | Babudieri, S., Soddu, A., Murino, M., Molicotti, P., Muredda, A. A., Madeddu, G....Mura, M. (2012). Tuberculosis Screening before Anti–Hepatitis C Virus Therapy in Prisons. Emerging Infectious Diseases, 18(4), 689-691. https://doi.org/10.3201/eid1804.111016. |
Deficient Reporting in Avian Influenza Surveillance, Mali
EID | Molia S, Kamissoko B, Sidibé M, Diakité A, Diall M, N’Diaye M. Deficient Reporting in Avian Influenza Surveillance, Mali. Emerg Infect Dis. 2012;18(4):691-693. https://doi.org/10.3201/eid1804.111102 |
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AMA | Molia S, Kamissoko B, Sidibé M, et al. Deficient Reporting in Avian Influenza Surveillance, Mali. Emerging Infectious Diseases. 2012;18(4):691-693. doi:10.3201/eid1804.111102. |
APA | Molia, S., Kamissoko, B., Sidibé, M., Diakité, A., Diall, M., & N’Diaye, M. (2012). Deficient Reporting in Avian Influenza Surveillance, Mali. Emerging Infectious Diseases, 18(4), 691-693. https://doi.org/10.3201/eid1804.111102. |
Myxozoan Parasite in Brain of Critically Endangered Frog
EID | Hartigan A, Sangster C, Rose K, Phalen DN, Šlapeta J. Myxozoan Parasite in Brain of Critically Endangered Frog. Emerg Infect Dis. 2012;18(4):693-695. https://doi.org/10.3201/eid1804.111606 |
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AMA | Hartigan A, Sangster C, Rose K, et al. Myxozoan Parasite in Brain of Critically Endangered Frog. Emerging Infectious Diseases. 2012;18(4):693-695. doi:10.3201/eid1804.111606. |
APA | Hartigan, A., Sangster, C., Rose, K., Phalen, D. N., & Šlapeta, J. (2012). Myxozoan Parasite in Brain of Critically Endangered Frog. Emerging Infectious Diseases, 18(4), 693-695. https://doi.org/10.3201/eid1804.111606. |
Mayaro Virus Infection in Traveler Returning from Amazon Basin, Northern Peru
EID | Neumayr A, Gabriel M, Fritz J, Günther S, Hatz C, Schmidt-Chanasit J, et al. Mayaro Virus Infection in Traveler Returning from Amazon Basin, Northern Peru. Emerg Infect Dis. 2012;18(4):695-696. https://doi.org/10.3201/eid1804.111717 |
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AMA | Neumayr A, Gabriel M, Fritz J, et al. Mayaro Virus Infection in Traveler Returning from Amazon Basin, Northern Peru. Emerging Infectious Diseases. 2012;18(4):695-696. doi:10.3201/eid1804.111717. |
APA | Neumayr, A., Gabriel, M., Fritz, J., Günther, S., Hatz, C., Schmidt-Chanasit, J....Blum, J. (2012). Mayaro Virus Infection in Traveler Returning from Amazon Basin, Northern Peru. Emerging Infectious Diseases, 18(4), 695-696. https://doi.org/10.3201/eid1804.111717. |
Meningoencephalitis Complicating Relapsing Fever in Traveler Returning from Senegal
EID | Bottieau E, Verbruggen E, Aubry C, Socolovschi C, Vlieghe E. Meningoencephalitis Complicating Relapsing Fever in Traveler Returning from Senegal. Emerg Infect Dis. 2012;18(4):697-698. https://doi.org/10.3201/eid1804.111771 |
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AMA | Bottieau E, Verbruggen E, Aubry C, et al. Meningoencephalitis Complicating Relapsing Fever in Traveler Returning from Senegal. Emerging Infectious Diseases. 2012;18(4):697-698. doi:10.3201/eid1804.111771. |
APA | Bottieau, E., Verbruggen, E., Aubry, C., Socolovschi, C., & Vlieghe, E. (2012). Meningoencephalitis Complicating Relapsing Fever in Traveler Returning from Senegal. Emerging Infectious Diseases, 18(4), 697-698. https://doi.org/10.3201/eid1804.111771. |
Serologic Evidence of Orthopoxvirus Infection in Buffaloes, Brazil
EID | Lopes de Assis F, Pereira G, Oliveira C, Rodrigues G, Cotta M, Silva-Fernandes A, et al. Serologic Evidence of Orthopoxvirus Infection in Buffaloes, Brazil. Emerg Infect Dis. 2012;18(4):698-700. https://doi.org/10.3201/eid1804.111800 |
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AMA | Lopes de Assis F, Pereira G, Oliveira C, et al. Serologic Evidence of Orthopoxvirus Infection in Buffaloes, Brazil. Emerging Infectious Diseases. 2012;18(4):698-700. doi:10.3201/eid1804.111800. |
APA | Lopes de Assis, F., Pereira, G., Oliveira, C., Rodrigues, G., Cotta, M., Silva-Fernandes, A....Abrahão, J. (2012). Serologic Evidence of Orthopoxvirus Infection in Buffaloes, Brazil. Emerging Infectious Diseases, 18(4), 698-700. https://doi.org/10.3201/eid1804.111800. |
Methicillin-Susceptible Staphylococcus aureus ST398, New York and New Jersey, USA
EID | Mediavilla JR, Chen L, Uhlemann A, Hanson BM, Rosenthal M, Stanak K, et al. Methicillin-Susceptible Staphylococcus aureus ST398, New York and New Jersey, USA. Emerg Infect Dis. 2012;18(4):700-702. https://doi.org/10.3201/eid1804.111419 |
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AMA | Mediavilla JR, Chen L, Uhlemann A, et al. Methicillin-Susceptible Staphylococcus aureus ST398, New York and New Jersey, USA. Emerging Infectious Diseases. 2012;18(4):700-702. doi:10.3201/eid1804.111419. |
APA | Mediavilla, J. R., Chen, L., Uhlemann, A., Hanson, B. M., Rosenthal, M., Stanak, K....Kreiswirth, B. N. (2012). Methicillin-Susceptible Staphylococcus aureus ST398, New York and New Jersey, USA. Emerging Infectious Diseases, 18(4), 700-702. https://doi.org/10.3201/eid1804.111419. |
Rickettsia monacensis as Cause of Mediterranean Spotted Fever–like Illness, Italy
EID | Madeddu G, Mancini F, Caddeo A, Ciervo A, Babudieri S, Maida I, et al. Rickettsia monacensis as Cause of Mediterranean Spotted Fever–like Illness, Italy. Emerg Infect Dis. 2012;18(4):702-704. https://doi.org/10.3201/eid1804.111583 |
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AMA | Madeddu G, Mancini F, Caddeo A, et al. Rickettsia monacensis as Cause of Mediterranean Spotted Fever–like Illness, Italy. Emerging Infectious Diseases. 2012;18(4):702-704. doi:10.3201/eid1804.111583. |
APA | Madeddu, G., Mancini, F., Caddeo, A., Ciervo, A., Babudieri, S., Maida, I....Mura, M. (2012). Rickettsia monacensis as Cause of Mediterranean Spotted Fever–like Illness, Italy. Emerging Infectious Diseases, 18(4), 702-704. https://doi.org/10.3201/eid1804.111583. |
Leishmania Resistance to Miltefosine Associated with Genetic Marker
EID | Cojean S, Houzé S, Haouchine D, Huteau F, Lariven S, Hubert V, et al. Leishmania Resistance to Miltefosine Associated with Genetic Marker. Emerg Infect Dis. 2012;18(4):704-706. https://doi.org/10.3201/eid1804.110841 |
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AMA | Cojean S, Houzé S, Haouchine D, et al. Leishmania Resistance to Miltefosine Associated with Genetic Marker. Emerging Infectious Diseases. 2012;18(4):704-706. doi:10.3201/eid1804.110841. |
APA | Cojean, S., Houzé, S., Haouchine, D., Huteau, F., Lariven, S., Hubert, V....Matheron, S. (2012). Leishmania Resistance to Miltefosine Associated with Genetic Marker. Emerging Infectious Diseases, 18(4), 704-706. https://doi.org/10.3201/eid1804.110841. |
Prolonged KI Polyomavirus Infection in Immunodeficient Child
EID | Falcone V, Panning M, Strahm B, Vraetz T, Bierbaum S, Neumann-Haefelin D, et al. Prolonged KI Polyomavirus Infection in Immunodeficient Child. Emerg Infect Dis. 2012;18(4):706-708. https://doi.org/10.3201/eid1804.111588 |
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AMA | Falcone V, Panning M, Strahm B, et al. Prolonged KI Polyomavirus Infection in Immunodeficient Child. Emerging Infectious Diseases. 2012;18(4):706-708. doi:10.3201/eid1804.111588. |
APA | Falcone, V., Panning, M., Strahm, B., Vraetz, T., Bierbaum, S., Neumann-Haefelin, D....Huzly, D. (2012). Prolonged KI Polyomavirus Infection in Immunodeficient Child. Emerging Infectious Diseases, 18(4), 706-708. https://doi.org/10.3201/eid1804.111588. |
High Virulence of African Swine Fever Virus Caucasus Isolate in European Wild Boars of All Ages
EID | Blome S, Gabriel C, Dietze K, Breithaupt A, Beer M. High Virulence of African Swine Fever Virus Caucasus Isolate in European Wild Boars of All Ages. Emerg Infect Dis. 2012;18(4):708. https://doi.org/10.3201/eid1804.111813 |
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AMA | Blome S, Gabriel C, Dietze K, et al. High Virulence of African Swine Fever Virus Caucasus Isolate in European Wild Boars of All Ages. Emerging Infectious Diseases. 2012;18(4):708. doi:10.3201/eid1804.111813. |
APA | Blome, S., Gabriel, C., Dietze, K., Breithaupt, A., & Beer, M. (2012). High Virulence of African Swine Fever Virus Caucasus Isolate in European Wild Boars of All Ages. Emerging Infectious Diseases, 18(4), 708. https://doi.org/10.3201/eid1804.111813. |
Another Dimension
Leaving the Hospital
EID | Silver A. Leaving the Hospital. Emerg Infect Dis. 2012;18(4):687. https://doi.org/10.3201/eid1804.ad1804 |
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AMA | Silver A. Leaving the Hospital. Emerging Infectious Diseases. 2012;18(4):687. doi:10.3201/eid1804.ad1804. |
APA | Silver, A. (2012). Leaving the Hospital. Emerging Infectious Diseases, 18(4), 687. https://doi.org/10.3201/eid1804.ad1804. |
Online Reports
Multidisciplinary and Evidence-based Method for Prioritizing Diseases of Food-producing Animals and Zoonoses
To prioritize 100 animal diseases and zoonoses in Europe, we used a multicriteria decision-making procedure based on opinions of experts and evidence-based data. Forty international experts performed intracategory and intercategory weighting of 57 prioritization criteria. Two methods (deterministic with mean of each weight and probabilistic with distribution functions of weights by using Monte Carlo simulation) were used to calculate a score for each disease. Consecutive ranking was established. Few differences were observed between each method. Compared with previous prioritization methods, our procedure is evidence based, includes a range of fields and criteria while considering uncertainty, and will be useful for analyzing diseases that affect public health.
About the Cover
Military Magic or Nature’s Fool
EID | Potter P. Military Magic or Nature’s Fool. Emerg Infect Dis. 2012;18(4):709-710. https://doi.org/10.3201/eid1804.ac1804 |
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AMA | Potter P. Military Magic or Nature’s Fool. Emerging Infectious Diseases. 2012;18(4):709-710. doi:10.3201/eid1804.ac1804. |
APA | Potter, P. (2012). Military Magic or Nature’s Fool. Emerging Infectious Diseases, 18(4), 709-710. https://doi.org/10.3201/eid1804.ac1804. |