Synopses
Invasive Enterobacter sakazakii Disease in Infants
Enterobacter sakazakii kills 40%–80% of infected infants and has been associated with powdered formula. We analyzed 46 cases of invasive infant E. sakazakii infection to define risk factors and guide prevention and treatment. Twelve infants had bacteremia, 33 had meningitis, and 1 had a urinary tract infection. Compared with infants with isolated bacteremia, infants with meningitis had greater birthweight (2,454 g vs. 850 g, p = 0.002) and gestational age (37 weeks vs. 27.8 weeks, p = 0.02), and infection developed at a younger age (6 days vs. 35 days, p<0.001). Among meningitis patients, 11 (33%) had seizures, 7 (21%) had brain abscess, and 14 (42%) died. Twenty-four (92%) of 26 infants with feeding patterns specified were fed powdered formula. Formula samples associated with 15 (68%) of 22 cases yielded E. sakazakii; in 13 cases, clinical and formula strains were indistinguishable. Further clarification of clinical risk factors and improved powdered formula safety is needed.
EID | Bowen A, Braden CR. Invasive Enterobacter sakazakii Disease in Infants. Emerg Infect Dis. 2006;12(8):1185-1189. https://doi.org/10.3201/eid1208.051509 |
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AMA | Bowen A, Braden CR. Invasive Enterobacter sakazakii Disease in Infants. Emerging Infectious Diseases. 2006;12(8):1185-1189. doi:10.3201/eid1208.051509. |
APA | Bowen, A., & Braden, C. R. (2006). Invasive Enterobacter sakazakii Disease in Infants. Emerging Infectious Diseases, 12(8), 1185-1189. https://doi.org/10.3201/eid1208.051509. |
Research
Venezuelan Equine Encephalitis Virus Transmission and Effect on Pathogenesis
Quantifying the dose of an arbovirus transmitted by mosquitoes is essential for designing pathogenesis studies simulating natural infection of vertebrates. Titration of saliva collected in vitro from infected mosquitoes may not accurately estimate titers transmitted during blood feeding, and infection by needle injection may affect vertebrate pathogenesis. We compared the amount of Venezuelan equine encephalitis virus collected from the saliva of Aedes taeniorhynchus to the amount injected into a mouse during blood feeding. Less virus was transmitted by mosquitoes in vivo (geometric mean 11 PFU) than was found for comparable times of salivation in vitro (mean saliva titer 74 PFU). We also observed slightly lower early and late viremia titers in mice that were needle injected with 8 PFU, which represents the low end of the in vivo transmission range. No differences in survival were detected, regardless of the dose or infection route.
EID | Smith DR, Aguilar PV, Coffey LL, Gromowski GD, Wang E, Vasilakis N. Venezuelan Equine Encephalitis Virus Transmission and Effect on Pathogenesis. Emerg Infect Dis. 2006;12(8):1190-1196. https://doi.org/10.3201/eid1208.050841 |
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AMA | Smith DR, Aguilar PV, Coffey LL, et al. Venezuelan Equine Encephalitis Virus Transmission and Effect on Pathogenesis. Emerging Infectious Diseases. 2006;12(8):1190-1196. doi:10.3201/eid1208.050841. |
APA | Smith, D. R., Aguilar, P. V., Coffey, L. L., Gromowski, G. D., Wang, E., & Vasilakis, N. (2006). Venezuelan Equine Encephalitis Virus Transmission and Effect on Pathogenesis. Emerging Infectious Diseases, 12(8), 1190-1196. https://doi.org/10.3201/eid1208.050841. |
Bat-transmitted Human Rabies Outbreaks, Brazilian Amazon
We describe 2 bat-transmitted outbreaks in remote, rural areas of Portel and Viseu Municipalities, Pará State, northern Brazil. Central nervous system specimens were taken after patients' deaths and underwent immunofluorescent assay and histopathologic examination for rabies antigens; also, specimens were injected intracerebrally into suckling mice in an attempt to isolate the virus. Strains obtained were antigenically and genetically characterized. Twenty-one persons died due to paralytic rabies in the 2 municipalities. Ten rabies virus strains were isolated from human specimens; 2 other cases were diagnosed by histopathologic examination. Isolates were antigenically characterized as Desmodus rotundus variant 3 (AgV3). DNA sequencing of 6 strains showed that they were genetically close to D. rotundus–related strains isolated in Brazil. The genetic results were similar to those obtained by using monoclonal antibodies and support the conclusion that the isolates studied belong to the same rabies cycle, the virus variants found in the vampire bat D. rotundus.
EID | da Rosa E, Kotait I, Barbosa T, Carrieri ML, Brandão PE, Pinheiro AS, et al. Bat-transmitted Human Rabies Outbreaks, Brazilian Amazon. Emerg Infect Dis. 2006;12(8):1197-1202. https://doi.org/10.3201/eid1208.050929 |
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AMA | da Rosa E, Kotait I, Barbosa T, et al. Bat-transmitted Human Rabies Outbreaks, Brazilian Amazon. Emerging Infectious Diseases. 2006;12(8):1197-1202. doi:10.3201/eid1208.050929. |
APA | da Rosa, E., Kotait, I., Barbosa, T., Carrieri, M. L., Brandão, P. E., Pinheiro, A. S....Vasconcelos, P. (2006). Bat-transmitted Human Rabies Outbreaks, Brazilian Amazon. Emerging Infectious Diseases, 12(8), 1197-1202. https://doi.org/10.3201/eid1208.050929. |
Streptococcus suis Sequence Type 7 Outbreak, Sichuan, China
An outbreak of Streptococcus suis serotype 2 emerged in the summer of 2005 in Sichuan Province, and sporadic infections occurred in 4 additional provinces of China. In total, 99 S. suis strains were isolated and analyzed in this study: 88 isolates from human patients and 11 from diseased pigs. We defined 98 of 99 isolates as pulse type I by using pulsed-field gel electrophoresis analysis of SmaI-digested chromosomal DNA. Furthermore, multilocus sequence typing classified 97 of 98 members of the pulse type I in the same sequence type (ST), ST-7. Isolates of ST-7 were more toxic to peripheral blood mononuclear cells than ST-1 strains. S. suis ST-7, the causative agent, was a single-locus variant of ST-1 with increased virulence. These findings strongly suggest that ST-7 is an emerging, highly virulent S. suis clone that caused the largest S. suis outbreak ever described.
EID | Ye C, Zhu X, Jing H, Du H, Segura M, Zheng H, et al. Streptococcus suis Sequence Type 7 Outbreak, Sichuan, China. Emerg Infect Dis. 2006;12(8):1203-1208. https://doi.org/10.3201/eid1208.060232 |
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AMA | Ye C, Zhu X, Jing H, et al. Streptococcus suis Sequence Type 7 Outbreak, Sichuan, China. Emerging Infectious Diseases. 2006;12(8):1203-1208. doi:10.3201/eid1208.060232. |
APA | Ye, C., Zhu, X., Jing, H., Du, H., Segura, M., Zheng, H....Xu, J. (2006). Streptococcus suis Sequence Type 7 Outbreak, Sichuan, China. Emerging Infectious Diseases, 12(8), 1203-1208. https://doi.org/10.3201/eid1208.060232. |
Carbapenem Resistance in Klebsiella pneumoniae Not Detected by Automated Susceptibility Testing
Detecting β-lactamase–mediated carbapenem resistance among Klebsiella pneumoniae isolates and other Enterobacteriaceae is an emerging problem. In this study, 15 blaKPC-positive Klebsiella pneumoniae that showed discrepant results for imipenem and meropenem from 4 New York City hospitals were characterized by isoelectric focusing; broth microdilution (BMD); disk diffusion (DD); and MicroScan, Phoenix, Sensititre, VITEK, and VITEK 2 automated systems. All 15 isolates were either intermediate or resistant to imipenem and meropenem by BMD; 1 was susceptible to imipenem by DD. MicroScan and Phoenix reported 1 (6.7%) and 2 (13.3%) isolates, respectively, as imipenem susceptible. VITEK and VITEK 2 reported 10 (67%) and 5 (33%) isolates, respectively, as imipenem susceptible. By Sensititre, 13 (87%) isolates were susceptible to imipenem, and 12 (80%) were susceptible to meropenem. The VITEK 2 Advanced Expert System changed 2 imipenem MIC results from >16 μg/mL to <2 μg/mL but kept the interpretation as resistant. The recognition of carbapenem-resistant K. pneumoniae continues to challenge automated susceptibility systems.
EID | Tenover FC, Kalsi RK, Williams PP, Carey RB, Stocker S, Lonsway DR, et al. Carbapenem Resistance in Klebsiella pneumoniae Not Detected by Automated Susceptibility Testing. Emerg Infect Dis. 2006;12(8):1209-1213. https://doi.org/10.3201/eid1208.060291 |
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AMA | Tenover FC, Kalsi RK, Williams PP, et al. Carbapenem Resistance in Klebsiella pneumoniae Not Detected by Automated Susceptibility Testing. Emerging Infectious Diseases. 2006;12(8):1209-1213. doi:10.3201/eid1208.060291. |
APA | Tenover, F. C., Kalsi, R. K., Williams, P. P., Carey, R. B., Stocker, S., Lonsway, D. R....Hanna, B. (2006). Carbapenem Resistance in Klebsiella pneumoniae Not Detected by Automated Susceptibility Testing. Emerging Infectious Diseases, 12(8), 1209-1213. https://doi.org/10.3201/eid1208.060291. |
VEB-1 Extended-Spectrum β-lactamase–producing Acinetobacter baumannii, France
VEB-1 extended-spectrum β-lactamase–producing Acinetobacter baumannii was responsible for an outbreak in hospitals in France. A national alert was triggered in September 2003 when 4 hospitals reported clusters of A. baumannii infection with similar susceptibility profiles. Case definitions and laboratory guidelines were disseminated, and prospective surveillance was implemented; strains were sent to a single laboratory for characterization and typing. From April 2003 through June 2004, 53 hospitals reported 290 cases of A. baumannii infection or colonization; 275 isolates were blaVEB-1-positive and clonally related. Cases were first reported in 5 districts of northern France, then in 10 other districts in 4 regions. Within a region, interhospital spread was associated with patient transfer. In northern France, investigation and control measures led to a reduction of reported cases after January 2004. The national alert enabled early control of new clusters, demonstrating the usefulness of early warning about antimicrobial drug resistance.
EID | Naas T, Coignard B, Carbonne A, Blanckaert K, Bajolet O, Bernet C, et al. VEB-1 Extended-Spectrum β-lactamase–producing Acinetobacter baumannii, France. Emerg Infect Dis. 2006;12(8):1214-1222. https://doi.org/10.3201/eid1208.051547 |
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AMA | Naas T, Coignard B, Carbonne A, et al. VEB-1 Extended-Spectrum β-lactamase–producing Acinetobacter baumannii, France. Emerging Infectious Diseases. 2006;12(8):1214-1222. doi:10.3201/eid1208.051547. |
APA | Naas, T., Coignard, B., Carbonne, A., Blanckaert, K., Bajolet, O., Bernet, C....Nordmann, P. (2006). VEB-1 Extended-Spectrum β-lactamase–producing Acinetobacter baumannii, France. Emerging Infectious Diseases, 12(8), 1214-1222. https://doi.org/10.3201/eid1208.051547. |
Macrolide Resistance in Adults with Bacteremic Pneumococcal Pneumonia
We conducted a case-control study of adults with bacteremic pneumococcal pneumonia to identify factors associated with macrolide resistance. Study participants were identified through population-based surveillance in a 5-county region surrounding Philadelphia. Forty-three hospitals contributed 444 patients, who were interviewed by telephone regarding potential risk factors. In multivariable analyses, prior exposure to a macrolide antimicrobial agent (odds ratio [OR] 2.8), prior flu vaccination (OR 2.0), and Hispanic ethnicity (OR 4.1) were independently associated with an increased probability of macrolide resistance, and a history of stroke was independently associated with a decreased probability of macrolide resistance (OR 0.2). Fifty-five percent of patients with macrolide-resistant infections reported no antimicrobial drug exposure in the preceding 6 months. Among patients who reported taking antimicrobial agents in the 6 months preceding infection, failure to complete the course of prescribed drugs was associated with an increased probability of macrolide resistance (OR 3.4).
EID | Metlay JP, Fishman NO, Joffe MM, Kallan MJ, Chittams JL, Edelstein PH. Macrolide Resistance in Adults with Bacteremic Pneumococcal Pneumonia. Emerg Infect Dis. 2006;12(8):1223-1230. https://doi.org/10.3201/eid1208.060017 |
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AMA | Metlay JP, Fishman NO, Joffe MM, et al. Macrolide Resistance in Adults with Bacteremic Pneumococcal Pneumonia. Emerging Infectious Diseases. 2006;12(8):1223-1230. doi:10.3201/eid1208.060017. |
APA | Metlay, J. P., Fishman, N. O., Joffe, M. M., Kallan, M. J., Chittams, J. L., & Edelstein, P. H. (2006). Macrolide Resistance in Adults with Bacteremic Pneumococcal Pneumonia. Emerging Infectious Diseases, 12(8), 1223-1230. https://doi.org/10.3201/eid1208.060017. |
Antibody Response to Pneumocystis jirovecii
We conducted a prospective pilot study of the serologic responses to overlapping recombinant fragments of the Pneumocystis jirovecii major surface glycoprotein (Msg) in HIV-infected patients with pneumonia due to P. jirovecii and other causes. Similar baseline geometric mean antibody levels to the fragments measured by an ELISA were found in both groups. Serum antibodies to MsgC in P. jirovecii patients rose to a peak level 3–4 weeks (p<0.001) after recovery from pneumocystosis; baseline CD4+ count >50 cells/μL and first episode of pneumocystosis were the principal host factors associated with this rise (both p<0.001). Thus, MsgC shows promise as a serologic reagent and should be tested further in clinical and epidemiologic studies.
EID | Daly KR, Huang L, Morris A, Koch J, Crothers K, Levin L, et al. Antibody Response to Pneumocystis jirovecii. Emerg Infect Dis. 2006;12(8):1231-1237. https://doi.org/10.3201/eid1208.060230 |
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AMA | Daly KR, Huang L, Morris A, et al. Antibody Response to Pneumocystis jirovecii. Emerging Infectious Diseases. 2006;12(8):1231-1237. doi:10.3201/eid1208.060230. |
APA | Daly, K. R., Huang, L., Morris, A., Koch, J., Crothers, K., Levin, L....Walzer, P. D. (2006). Antibody Response to Pneumocystis jirovecii. Emerging Infectious Diseases, 12(8), 1231-1237. https://doi.org/10.3201/eid1208.060230. |
Policy Review
Virulent Epidemics and Scope of Healthcare Workers' Duty of Care
The phrase "duty of care" is, at best, too vague and, at worst, ethically dangerous. The nature and scope of the duty need to be determined, and conflicting duties must be recognized and acknowledged. Duty of care is neither fixed nor absolute but heavily dependent on context. The normal risk level of the working environment, the healthcare worker's specialty, the likely harm and benefits of treatment, and the competing obligations deriving from the worker's multiple roles will all influence the limits of the duty of care. As experts anticipate the arrival of an avian influenza pandemic in humans, discussion of this matter is urgently needed.
EID | Sokol DK. Virulent Epidemics and Scope of Healthcare Workers' Duty of Care. Emerg Infect Dis. 2006;12(8):1238-1241. https://doi.org/10.3201/eid1208.060360 |
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AMA | Sokol DK. Virulent Epidemics and Scope of Healthcare Workers' Duty of Care. Emerging Infectious Diseases. 2006;12(8):1238-1241. doi:10.3201/eid1208.060360. |
APA | Sokol, D. K. (2006). Virulent Epidemics and Scope of Healthcare Workers' Duty of Care. Emerging Infectious Diseases, 12(8), 1238-1241. https://doi.org/10.3201/eid1208.060360. |
Dispatches
Human and Canine Pulmonary Blastomycosis, North Carolina, 2001–2002
We investigated a cluster of blastomycosis in 8 humans and 4 dogs in a rural North Carolina community. Delayed diagnosis, difficulty isolating Blastomyces dermatitidis in nature, and lack of a sensitive and specific test to assess exposure make outbreaks of this disease difficult to study.
EID | MacDonald P, Langley RL, Gerkin SR, Torok MR, MacCormack J. Human and Canine Pulmonary Blastomycosis, North Carolina, 2001–2002. Emerg Infect Dis. 2006;12(8):1242-1244. https://doi.org/10.3201/eid1208.050781 |
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AMA | MacDonald P, Langley RL, Gerkin SR, et al. Human and Canine Pulmonary Blastomycosis, North Carolina, 2001–2002. Emerging Infectious Diseases. 2006;12(8):1242-1244. doi:10.3201/eid1208.050781. |
APA | MacDonald, P., Langley, R. L., Gerkin, S. R., Torok, M. R., & MacCormack, J. (2006). Human and Canine Pulmonary Blastomycosis, North Carolina, 2001–2002. Emerging Infectious Diseases, 12(8), 1242-1244. https://doi.org/10.3201/eid1208.050781. |
West Nile Virus Epizootiology, Central Red River Valley, North Dakota and Minnesota, 2002–2005
West Nile virus (WNV) epizootiology was monitored from 2002 through 2005 in the area surrounding Grand Forks, North Dakota. Mosquitoes were tested for infection, and birds were surveyed for antibodies. In 2003, WNV was epidemic; in 2004, cool temperatures precluded WNV amplification; and in 2005, immunity in passerines decreased, but did not preclude, WNV amplification.
EID | Bell JA, Brewer CM, Mickelson NJ, Garman GW, Vaughan JA. West Nile Virus Epizootiology, Central Red River Valley, North Dakota and Minnesota, 2002–2005. Emerg Infect Dis. 2006;12(8):1245-1247. https://doi.org/10.3201/eid1208.060129 |
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AMA | Bell JA, Brewer CM, Mickelson NJ, et al. West Nile Virus Epizootiology, Central Red River Valley, North Dakota and Minnesota, 2002–2005. Emerging Infectious Diseases. 2006;12(8):1245-1247. doi:10.3201/eid1208.060129. |
APA | Bell, J. A., Brewer, C. M., Mickelson, N. J., Garman, G. W., & Vaughan, J. A. (2006). West Nile Virus Epizootiology, Central Red River Valley, North Dakota and Minnesota, 2002–2005. Emerging Infectious Diseases, 12(8), 1245-1247. https://doi.org/10.3201/eid1208.060129. |
O'nyong-nyong Virus, Chad
We report the first laboratory-confirmed human infection with O'nyong-nyong virus in Chad. This virus was isolated from peripheral blood mononuclear cells of a patient with evidence of a seroconversion to a virus related to Chikungunya virus. Genome sequence was partly determined, and phylogenetic studies were conducted.
EID | Bessaud M, Peyrefitte CN, Pastorino B, Gravier P, Tock F, Boete F, et al. O'nyong-nyong Virus, Chad. Emerg Infect Dis. 2006;12(8):1248-1250. https://doi.org/10.3201/eid1208.060199 |
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AMA | Bessaud M, Peyrefitte CN, Pastorino B, et al. O'nyong-nyong Virus, Chad. Emerging Infectious Diseases. 2006;12(8):1248-1250. doi:10.3201/eid1208.060199. |
APA | Bessaud, M., Peyrefitte, C. N., Pastorino, B., Gravier, P., Tock, F., Boete, F....Grandadam, M. (2006). O'nyong-nyong Virus, Chad. Emerging Infectious Diseases, 12(8), 1248-1250. https://doi.org/10.3201/eid1208.060199. |
Human Bocavirus in French Children
Human bocavirus (HBoV), a new member of the genus Bocavirus in the family Parvoviridae, has been recently associated with respiratory tract infections. We report the epidemiologic and clinical features observed from a 1-year retrospective study of HBoV infection in young children hospitalized with a respiratory tract infection.
EID | Foulongne V, Olejnik Y, Perez V, Elaerts S, Rodière M, Segondy M. Human Bocavirus in French Children. Emerg Infect Dis. 2006;12(8):1251-1253. https://doi.org/10.3201/eid1208.060213 |
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AMA | Foulongne V, Olejnik Y, Perez V, et al. Human Bocavirus in French Children. Emerging Infectious Diseases. 2006;12(8):1251-1253. doi:10.3201/eid1208.060213. |
APA | Foulongne, V., Olejnik, Y., Perez, V., Elaerts, S., Rodière, M., & Segondy, M. (2006). Human Bocavirus in French Children. Emerging Infectious Diseases, 12(8), 1251-1253. https://doi.org/10.3201/eid1208.060213. |
Bocavirus Infection in Hospitalized Children, South Korea
This study presents the first evidence of human bocavirus infection in South Korean children. The virus was detected in 27 (8.0%) of 336 tested specimens, including 17 (7.5%) of 225 virus-negative specimens, collected from children with acute lower respiratory tract infection.
EID | Chung J, Han T, Kim C, Kim S. Bocavirus Infection in Hospitalized Children, South Korea. Emerg Infect Dis. 2006;12(8):1254-1256. https://doi.org/10.3201/eid1208.060261 |
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AMA | Chung J, Han T, Kim C, et al. Bocavirus Infection in Hospitalized Children, South Korea. Emerging Infectious Diseases. 2006;12(8):1254-1256. doi:10.3201/eid1208.060261. |
APA | Chung, J., Han, T., Kim, C., & Kim, S. (2006). Bocavirus Infection in Hospitalized Children, South Korea. Emerging Infectious Diseases, 12(8), 1254-1256. https://doi.org/10.3201/eid1208.060261. |
Changing Pattern of Visceral Leishmaniasis, United Kingdom, 1985-2004
A 20-year (1985–2004) retrospective review of 39 patients with imported visceral leishmaniasis found that tourism to Mediterranean countries and HIV infection were associated with visceral leishmaniasis. Diagnosis was often delayed. Treatment with liposomal amphotericin B has improved prognosis. Visceral leishmaniasis should be made a reportable disease.
EID | Malik A, John L, Bryceson A, Lockwood D. Changing Pattern of Visceral Leishmaniasis, United Kingdom, 1985-2004. Emerg Infect Dis. 2006;12(8):1257-1259. https://doi.org/10.3201/eid1208.050486 |
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AMA | Malik A, John L, Bryceson A, et al. Changing Pattern of Visceral Leishmaniasis, United Kingdom, 1985-2004. Emerging Infectious Diseases. 2006;12(8):1257-1259. doi:10.3201/eid1208.050486. |
APA | Malik, A., John, L., Bryceson, A., & Lockwood, D. (2006). Changing Pattern of Visceral Leishmaniasis, United Kingdom, 1985-2004. Emerging Infectious Diseases, 12(8), 1257-1259. https://doi.org/10.3201/eid1208.050486. |
Mental Status after West Nile Virus Infection
Mental status after acute West Nile virus infection has not been examined objectively. We compared Telephone Interview for Cognitive Status scores of 116 patients with West Nile fever or West Nile neuroinvasive disease. Mental status was poorer and cognitive complaints more frequent with West Nile neuroinvasive disease (p = 0.005).
EID | Haaland KY, Sadek J, Pergam SA, Echevarria LA, Davis LE, Goade D, et al. Mental Status after West Nile Virus Infection. Emerg Infect Dis. 2006;12(8):1260-1262. https://doi.org/10.3201/eid1208.060097 |
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AMA | Haaland KY, Sadek J, Pergam SA, et al. Mental Status after West Nile Virus Infection. Emerging Infectious Diseases. 2006;12(8):1260-1262. doi:10.3201/eid1208.060097. |
APA | Haaland, K. Y., Sadek, J., Pergam, S. A., Echevarria, L. A., Davis, L. E., Goade, D....Ettestad, P. (2006). Mental Status after West Nile Virus Infection. Emerging Infectious Diseases, 12(8), 1260-1262. https://doi.org/10.3201/eid1208.060097. |
Human Metapneumovirus, Australia, 2001–2004
We examined 10,025 respiratory samples collected for 4 years (2001–2004) and found a 7.1% average annual incidence of human metapneumovirus. The epidemic peak of infection was late winter to spring, and genotyping showed a change in predominant viral genotype in 3 of the 4 years.
EID | Sloots TP, Mackay IM, Bialasiewicz S, Jacob KC, McQueen E, Harnett GB, et al. Human Metapneumovirus, Australia, 2001–2004. Emerg Infect Dis. 2006;12(8):1263-1266. https://doi.org/10.3201/eid1208.051239 |
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AMA | Sloots TP, Mackay IM, Bialasiewicz S, et al. Human Metapneumovirus, Australia, 2001–2004. Emerging Infectious Diseases. 2006;12(8):1263-1266. doi:10.3201/eid1208.051239. |
APA | Sloots, T. P., Mackay, I. M., Bialasiewicz, S., Jacob, K. C., McQueen, E., Harnett, G. B....Nissen, M. D. (2006). Human Metapneumovirus, Australia, 2001–2004. Emerging Infectious Diseases, 12(8), 1263-1266. https://doi.org/10.3201/eid1208.051239. |
Community-acquired Methicillin-resistant Staphylococcus aureus in Children, Taiwan
Highly virulent community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) with Panton-Valentine leukocidin (PVL) is common worldwide. Using antimicrobial drug susceptibility testing, staphylococcal cassette chromosome mec typing, exotoxin profiling, and pulsed-field gel electrophoresis typing, we provide evidence that supports the relationship between nasal strains of PVL-positive MRSA and community-acquired disease.
EID | Lo W, Lin W, Tseng M, Wang S, Chu M, Wang C. Community-acquired Methicillin-resistant Staphylococcus aureus in Children, Taiwan. Emerg Infect Dis. 2006;12(8):1267-1270. https://doi.org/10.3201/eid1208.051570 |
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AMA | Lo W, Lin W, Tseng M, et al. Community-acquired Methicillin-resistant Staphylococcus aureus in Children, Taiwan. Emerging Infectious Diseases. 2006;12(8):1267-1270. doi:10.3201/eid1208.051570. |
APA | Lo, W., Lin, W., Tseng, M., Wang, S., Chu, M., & Wang, C. (2006). Community-acquired Methicillin-resistant Staphylococcus aureus in Children, Taiwan. Emerging Infectious Diseases, 12(8), 1267-1270. https://doi.org/10.3201/eid1208.051570. |
Incubation Period of Hantavirus Cardiopulmonary Syndrome
The potential incubation period from exposure to onset of symptoms was 7–39 days (median 18 days) in 20 patients with a defined period of exposure to Andes virus in a high-risk area. This period was 14–32 days (median 18 days) in 11 patients with exposure for <48 hours.
EID | Vial P, Valdivieso F, Mertz G, Castillo C, Belmar E, Delgado I, et al. Incubation Period of Hantavirus Cardiopulmonary Syndrome. Emerg Infect Dis. 2006;12(8):1271-1273. https://doi.org/10.3201/eid1208.051127 |
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AMA | Vial P, Valdivieso F, Mertz G, et al. Incubation Period of Hantavirus Cardiopulmonary Syndrome. Emerging Infectious Diseases. 2006;12(8):1271-1273. doi:10.3201/eid1208.051127. |
APA | Vial, P., Valdivieso, F., Mertz, G., Castillo, C., Belmar, E., Delgado, I....Ferrés, M. (2006). Incubation Period of Hantavirus Cardiopulmonary Syndrome. Emerging Infectious Diseases, 12(8), 1271-1273. https://doi.org/10.3201/eid1208.051127. |
Bat-associated Rabies Virus in Skunks
Rabies was undetected in terrestrial wildlife of northern Arizona until 2001, when rabies was diagnosed in 19 rabid skunks in Flagstaff. Laboratory analyses showed causative rabies viruses associated with bats, which indicated cross-species transmission of unprecedented magnitude. Public health infrastructure must be maintained to address emerging zoonotic diseases.
EID | Leslie MJ, Messenger S, Rohde RE, Smith J, Cheshier R, Hanlon C, et al. Bat-associated Rabies Virus in Skunks. Emerg Infect Dis. 2006;12(8):1274-1277. https://doi.org/10.3201/eid1208.051526 |
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AMA | Leslie MJ, Messenger S, Rohde RE, et al. Bat-associated Rabies Virus in Skunks. Emerging Infectious Diseases. 2006;12(8):1274-1277. doi:10.3201/eid1208.051526. |
APA | Leslie, M. J., Messenger, S., Rohde, R. E., Smith, J., Cheshier, R., Hanlon, C....Rupprecht, C. E. (2006). Bat-associated Rabies Virus in Skunks. Emerging Infectious Diseases, 12(8), 1274-1277. https://doi.org/10.3201/eid1208.051526. |
Fecal Viral Load and Norovirus-associated Gastroenteritis
We report the median cDNA viral load of norovirus genogroup II is >100-fold higher than that of genogroup I in the fecal specimens of patients with norovirus-associated gastroenteritis. We speculate that increased cDNA viral load accounts for the higher transmissibility of genogroup II strains through the fecal-oral route.
EID | Chan M, Sung J, Lam R, Chan P, Lee N, Lai R, et al. Fecal Viral Load and Norovirus-associated Gastroenteritis. Emerg Infect Dis. 2006;12(8):1278-1280. https://doi.org/10.3201/eid1208.060081 |
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AMA | Chan M, Sung J, Lam R, et al. Fecal Viral Load and Norovirus-associated Gastroenteritis. Emerging Infectious Diseases. 2006;12(8):1278-1280. doi:10.3201/eid1208.060081. |
APA | Chan, M., Sung, J., Lam, R., Chan, P., Lee, N., Lai, R....Leung, W. K. (2006). Fecal Viral Load and Norovirus-associated Gastroenteritis. Emerging Infectious Diseases, 12(8), 1278-1280. https://doi.org/10.3201/eid1208.060081. |
Rickettsia felis in Xenopsylla cheopis, Java, Indonesia
Rickettsia typhi and R. felis, etiologic agents of murine typhus and fleaborne spotted fever, respectively, were detected in Oriental rat fleas (Xenopsylla cheopis) collected from rodents and shrews in Java, Indonesia. We describe the first evidence of R. felis in Indonesia and naturally occurring R. felis in Oriental rat fleas.
EID | Jiang J, Soeatmadji DW, Henry KM, Ratiwayanto S, Bangs MJ, Richards AL. Rickettsia felis in Xenopsylla cheopis, Java, Indonesia. Emerg Infect Dis. 2006;12(8):1281-1283. https://doi.org/10.3201/eid1208.060327 |
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AMA | Jiang J, Soeatmadji DW, Henry KM, et al. Rickettsia felis in Xenopsylla cheopis, Java, Indonesia. Emerging Infectious Diseases. 2006;12(8):1281-1283. doi:10.3201/eid1208.060327. |
APA | Jiang, J., Soeatmadji, D. W., Henry, K. M., Ratiwayanto, S., Bangs, M. J., & Richards, A. L. (2006). Rickettsia felis in Xenopsylla cheopis, Java, Indonesia. Emerging Infectious Diseases, 12(8), 1281-1283. https://doi.org/10.3201/eid1208.060327. |
Avian Influenza among Waterfowl Hunters and Wildlife Professionals
We report serologic evidence of avian influenza infection in 1 duck hunter and 2 wildlife professionals with extensive histories of wild waterfowl and game bird exposure. Two laboratory methods showed evidence of past infection with influenza A/H11N9, a less common virus strain in wild ducks, in these 3 persons.
EID | Gill JS, Webby R, Gilchrist M, Gray GC. Avian Influenza among Waterfowl Hunters and Wildlife Professionals. Emerg Infect Dis. 2006;12(8):1284-1286. https://doi.org/10.3201/eid1208.060492 |
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AMA | Gill JS, Webby R, Gilchrist M, et al. Avian Influenza among Waterfowl Hunters and Wildlife Professionals. Emerging Infectious Diseases. 2006;12(8):1284-1286. doi:10.3201/eid1208.060492. |
APA | Gill, J. S., Webby, R., Gilchrist, M., & Gray, G. C. (2006). Avian Influenza among Waterfowl Hunters and Wildlife Professionals. Emerging Infectious Diseases, 12(8), 1284-1286. https://doi.org/10.3201/eid1208.060492. |
OFFLU Network on Avian Influenza
OFFLU is the name of the network of avian influenza expertise inaugurated jointly in 2005 by the Food and Agriculture Organization of the United Nations and the World Organisation for Animal Health. Achievements and constraints to date and plans for the future are described.
EID | Edwards S. OFFLU Network on Avian Influenza. Emerg Infect Dis. 2006;12(8):1287-1288. https://doi.org/10.3201/eid1208.060380 |
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AMA | Edwards S. OFFLU Network on Avian Influenza. Emerging Infectious Diseases. 2006;12(8):1287-1288. doi:10.3201/eid1208.060380. |
APA | Edwards, S. (2006). OFFLU Network on Avian Influenza. Emerging Infectious Diseases, 12(8), 1287-1288. https://doi.org/10.3201/eid1208.060380. |
Letters
Salmonella Typhimurium DT104, Italy
EID | Cawthorne A, Galetta P, Massari M, Dionisi A, Filetici E, Luzzi I. Salmonella Typhimurium DT104, Italy. Emerg Infect Dis. 2006;12(8):1289. https://doi.org/10.3201/eid1208.050968 |
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AMA | Cawthorne A, Galetta P, Massari M, et al. Salmonella Typhimurium DT104, Italy. Emerging Infectious Diseases. 2006;12(8):1289. doi:10.3201/eid1208.050968. |
APA | Cawthorne, A., Galetta, P., Massari, M., Dionisi, A., Filetici, E., & Luzzi, I. (2006). Salmonella Typhimurium DT104, Italy. Emerging Infectious Diseases, 12(8), 1289. https://doi.org/10.3201/eid1208.050968. |
Echovirus 13 Aseptic Meningitis, Brazil
EID | Kmetzsch CI, Balkie E, Monteiro A, Costa EV, dos Santos G, da Silva EE. Echovirus 13 Aseptic Meningitis, Brazil. Emerg Infect Dis. 2006;12(8):1289-1291. https://doi.org/10.3201/eid1208.051317 |
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AMA | Kmetzsch CI, Balkie E, Monteiro A, et al. Echovirus 13 Aseptic Meningitis, Brazil. Emerging Infectious Diseases. 2006;12(8):1289-1291. doi:10.3201/eid1208.051317. |
APA | Kmetzsch, C. I., Balkie, E., Monteiro, A., Costa, E. V., dos Santos, G., & da Silva, E. E. (2006). Echovirus 13 Aseptic Meningitis, Brazil. Emerging Infectious Diseases, 12(8), 1289-1291. https://doi.org/10.3201/eid1208.051317. |
Nonsteroidal Antiinflammatory Drugs and Group A Streptococcal Infection
EID | Aronoff DM, Mulla ZD. Nonsteroidal Antiinflammatory Drugs and Group A Streptococcal Infection. Emerg Infect Dis. 2006;12(8):1291-129. https://doi.org/10.3201/eid1208.051067 |
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AMA | Aronoff DM, Mulla ZD. Nonsteroidal Antiinflammatory Drugs and Group A Streptococcal Infection. Emerging Infectious Diseases. 2006;12(8):1291-129. doi:10.3201/eid1208.051067. |
APA | Aronoff, D. M., & Mulla, Z. D. (2006). Nonsteroidal Antiinflammatory Drugs and Group A Streptococcal Infection. Emerging Infectious Diseases, 12(8), 1291-129. https://doi.org/10.3201/eid1208.051067. |
Detecting Clostridium botulinum
EID | Karner J, Allerberger F. Detecting Clostridium botulinum. Emerg Infect Dis. 2006;12(8):1292. https://doi.org/10.3201/eid1208.051364 |
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AMA | Karner J, Allerberger F. Detecting Clostridium botulinum. Emerging Infectious Diseases. 2006;12(8):1292. doi:10.3201/eid1208.051364. |
APA | Karner, J., & Allerberger, F. (2006). Detecting Clostridium botulinum. Emerging Infectious Diseases, 12(8), 1292. https://doi.org/10.3201/eid1208.051364. |
Echinococcus multilocularis in Dogs, Japan
EID | Morishima Y, Sugiyama H, Arakawa K, Kawanaka M. Echinococcus multilocularis in Dogs, Japan. Emerg Infect Dis. 2006;12(8):1292-1294. https://doi.org/10.3201/eid1208.051241 |
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AMA | Morishima Y, Sugiyama H, Arakawa K, et al. Echinococcus multilocularis in Dogs, Japan. Emerging Infectious Diseases. 2006;12(8):1292-1294. doi:10.3201/eid1208.051241. |
APA | Morishima, Y., Sugiyama, H., Arakawa, K., & Kawanaka, M. (2006). Echinococcus multilocularis in Dogs, Japan. Emerging Infectious Diseases, 12(8), 1292-1294. https://doi.org/10.3201/eid1208.051241. |
New World Hantavirus in Humans, French Guiana
EID | Matheus S, Meynard J, Rollin PE, Maubert B, Morvan J. New World Hantavirus in Humans, French Guiana. Emerg Infect Dis. 2006;12(8):1294-1295. https://doi.org/10.3201/eid1208.051619 |
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AMA | Matheus S, Meynard J, Rollin PE, et al. New World Hantavirus in Humans, French Guiana. Emerging Infectious Diseases. 2006;12(8):1294-1295. doi:10.3201/eid1208.051619. |
APA | Matheus, S., Meynard, J., Rollin, P. E., Maubert, B., & Morvan, J. (2006). New World Hantavirus in Humans, French Guiana. Emerging Infectious Diseases, 12(8), 1294-1295. https://doi.org/10.3201/eid1208.051619. |
Qinghai-like H5N1 from Domestic Cats, Northern Iraq
EID | Yingst SL, Saad MD, Felt SA. Qinghai-like H5N1 from Domestic Cats, Northern Iraq. Emerg Infect Dis. 2006;12(8):1295-1297. https://doi.org/10.3201/eid1208.060264 |
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AMA | Yingst SL, Saad MD, Felt SA. Qinghai-like H5N1 from Domestic Cats, Northern Iraq. Emerging Infectious Diseases. 2006;12(8):1295-1297. doi:10.3201/eid1208.060264. |
APA | Yingst, S. L., Saad, M. D., & Felt, S. A. (2006). Qinghai-like H5N1 from Domestic Cats, Northern Iraq. Emerging Infectious Diseases, 12(8), 1295-1297. https://doi.org/10.3201/eid1208.060264. |
Classifying Escherichia coli
EID | Girão DM, Girão V, Irino K, Gomes TA. Classifying Escherichia coli. Emerg Infect Dis. 2006;12(8):1297-1299. https://doi.org/10.3201/eid1208.051654 |
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AMA | Girão DM, Girão V, Irino K, et al. Classifying Escherichia coli. Emerging Infectious Diseases. 2006;12(8):1297-1299. doi:10.3201/eid1208.051654. |
APA | Girão, D. M., Girão, V., Irino, K., & Gomes, T. A. (2006). Classifying Escherichia coli. Emerging Infectious Diseases, 12(8), 1297-1299. https://doi.org/10.3201/eid1208.051654. |
Toscana Virus RNA in Sergentomyia minuta Flies
EID | Charrel RN, Izri A, Temmam S, de Lamballerie X, Parola P. Toscana Virus RNA in Sergentomyia minuta Flies. Emerg Infect Dis. 2006;12(8):1299-1300. https://doi.org/10.3201/eid1208.060345 |
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AMA | Charrel RN, Izri A, Temmam S, et al. Toscana Virus RNA in Sergentomyia minuta Flies. Emerging Infectious Diseases. 2006;12(8):1299-1300. doi:10.3201/eid1208.060345. |
APA | Charrel, R. N., Izri, A., Temmam, S., de Lamballerie, X., & Parola, P. (2006). Toscana Virus RNA in Sergentomyia minuta Flies. Emerging Infectious Diseases, 12(8), 1299-1300. https://doi.org/10.3201/eid1208.060345. |
Rat-bite Fever, Canada
EID | Schachter ME, Wilcox L, Rau N, Yamamura D, Brown S, Lee CH. Rat-bite Fever, Canada. Emerg Infect Dis. 2006;12(8):1301-1302. https://doi.org/10.3201/eid1208.060044 |
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AMA | Schachter ME, Wilcox L, Rau N, et al. Rat-bite Fever, Canada. Emerging Infectious Diseases. 2006;12(8):1301-1302. doi:10.3201/eid1208.060044. |
APA | Schachter, M. E., Wilcox, L., Rau, N., Yamamura, D., Brown, S., & Lee, C. H. (2006). Rat-bite Fever, Canada. Emerging Infectious Diseases, 12(8), 1301-1302. https://doi.org/10.3201/eid1208.060044. |
Cutaneous Injury and Vibrio vulnificus Infection
EID | Chung P, Chuang S, Tsang T, Wai-man L, Yung R, Lo J. Cutaneous Injury and Vibrio vulnificus Infection. Emerg Infect Dis. 2006;12(8):1302-1303. https://doi.org/10.3201/eid1208.051495 |
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AMA | Chung P, Chuang S, Tsang T, et al. Cutaneous Injury and Vibrio vulnificus Infection. Emerging Infectious Diseases. 2006;12(8):1302-1303. doi:10.3201/eid1208.051495. |
APA | Chung, P., Chuang, S., Tsang, T., Wai-man, L., Yung, R., & Lo, J. (2006). Cutaneous Injury and Vibrio vulnificus Infection. Emerging Infectious Diseases, 12(8), 1302-1303. https://doi.org/10.3201/eid1208.051495. |
Neorickettsia helminthoeca in Dog, Brazil
EID | Headley SA, Scorpio DG, Barat NC, Vidotto O, Dumler J. Neorickettsia helminthoeca in Dog, Brazil. Emerg Infect Dis. 2006;12(8):1303-1305. https://doi.org/10.3201/eid1208.060130 |
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AMA | Headley SA, Scorpio DG, Barat NC, et al. Neorickettsia helminthoeca in Dog, Brazil. Emerging Infectious Diseases. 2006;12(8):1303-1305. doi:10.3201/eid1208.060130. |
APA | Headley, S. A., Scorpio, D. G., Barat, N. C., Vidotto, O., & Dumler, J. (2006). Neorickettsia helminthoeca in Dog, Brazil. Emerging Infectious Diseases, 12(8), 1303-1305. https://doi.org/10.3201/eid1208.060130. |
Another Dimension
Grandmother Speaks of the Old Country
EID | Haskins L. Grandmother Speaks of the Old Country. Emerg Infect Dis. 2006;12(8):1202. https://doi.org/10.3201/eid1208.ad1208 |
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AMA | Haskins L. Grandmother Speaks of the Old Country. Emerging Infectious Diseases. 2006;12(8):1202. doi:10.3201/eid1208.ad1208. |
APA | Haskins, L. (2006). Grandmother Speaks of the Old Country. Emerging Infectious Diseases, 12(8), 1202. https://doi.org/10.3201/eid1208.ad1208. |
Books and Media
Mycobacterium bovis Infection in Animals and Humans, 2nd Edition
EID | Palmer MV. Mycobacterium bovis Infection in Animals and Humans, 2nd Edition. Emerg Infect Dis. 2006;12(8):1306. https://doi.org/10.3201/eid1208.060526 |
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AMA | Palmer MV. Mycobacterium bovis Infection in Animals and Humans, 2nd Edition. Emerging Infectious Diseases. 2006;12(8):1306. doi:10.3201/eid1208.060526. |
APA | Palmer, M. V. (2006). Mycobacterium bovis Infection in Animals and Humans, 2nd Edition. Emerging Infectious Diseases, 12(8), 1306. https://doi.org/10.3201/eid1208.060526. |
Evolution of Microbial Pathogens
EID | Xu J. Evolution of Microbial Pathogens. Emerg Infect Dis. 2006;12(8):1306-1307. https://doi.org/10.3201/eid1208.060579 |
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AMA | Xu J. Evolution of Microbial Pathogens. Emerging Infectious Diseases. 2006;12(8):1306-1307. doi:10.3201/eid1208.060579. |
APA | Xu, J. (2006). Evolution of Microbial Pathogens. Emerging Infectious Diseases, 12(8), 1306-1307. https://doi.org/10.3201/eid1208.060579. |
Etymologia
Etymologia: O’nyong-nyong virus
EID | Etymologia: O’nyong-nyong virus. Emerg Infect Dis. 2006;12(8):1250. https://doi.org/10.3201/eid1208.et1208 |
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AMA | Etymologia: O’nyong-nyong virus. Emerging Infectious Diseases. 2006;12(8):1250. doi:10.3201/eid1208.et1208. |
APA | (2006). Etymologia: O’nyong-nyong virus. Emerging Infectious Diseases, 12(8), 1250. https://doi.org/10.3201/eid1208.et1208. |
Conference Summaries
Pathogenesis of Verocytotoxin/Shiga Toxin–producing Escherichia coli Infection
Corrections
Correction, Vol. 12, No. 4
EID | Correction, Vol. 12, No. 4. Emerg Infect Dis. 2006;12(8):1305. https://doi.org/10.3201/eid1208.c11208 |
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AMA | Correction, Vol. 12, No. 4. Emerging Infectious Diseases. 2006;12(8):1305. doi:10.3201/eid1208.c11208. |
APA | (2006). Correction, Vol. 12, No. 4. Emerging Infectious Diseases, 12(8), 1305. https://doi.org/10.3201/eid1208.c11208. |
Correction: Vol. 12, No. 6
EID | Correction: Vol. 12, No. 6. Emerg Infect Dis. 2006;12(8):1307. https://doi.org/10.3201/eid1208.c21208 |
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AMA | Correction: Vol. 12, No. 6. Emerging Infectious Diseases. 2006;12(8):1307. doi:10.3201/eid1208.c21208. |
APA | (2006). Correction: Vol. 12, No. 6. Emerging Infectious Diseases, 12(8), 1307. https://doi.org/10.3201/eid1208.c21208. |
Correction: Vol. 12 No. 7
EID | Correction: Vol. 12 No. 7. Emerg Infect Dis. 2006;12(8):1307. https://doi.org/10.3201/eid1208.c31208 |
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AMA | Correction: Vol. 12 No. 7. Emerging Infectious Diseases. 2006;12(8):1307. doi:10.3201/eid1208.c31208. |
APA | (2006). Correction: Vol. 12 No. 7. Emerging Infectious Diseases, 12(8), 1307. https://doi.org/10.3201/eid1208.c31208. |
Correction: Vol. 12, No. 7
EID | Correction: Vol. 12, No. 7. Emerg Infect Dis. 2006;12(8):1307. https://doi.org/10.3201/eid1208.c41208 |
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AMA | Correction: Vol. 12, No. 7. Emerging Infectious Diseases. 2006;12(8):1307. doi:10.3201/eid1208.c41208. |
APA | (2006). Correction: Vol. 12, No. 7. Emerging Infectious Diseases, 12(8), 1307. https://doi.org/10.3201/eid1208.c41208. |
About the Cover
Art, Science, and Life’s Enigmas
EID | Potter P. Art, Science, and Life’s Enigmas. Emerg Infect Dis. 2006;12(8):1308-1309. https://doi.org/10.3201/eid1208.ac1208 |
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AMA | Potter P. Art, Science, and Life’s Enigmas. Emerging Infectious Diseases. 2006;12(8):1308-1309. doi:10.3201/eid1208.ac1208. |
APA | Potter, P. (2006). Art, Science, and Life’s Enigmas. Emerging Infectious Diseases, 12(8), 1308-1309. https://doi.org/10.3201/eid1208.ac1208. |