Perspective
Effects of Coronavirus Infections in Children
The isolation of the coronavirus (CoV) identified as the cause of severe acute respiratory syndrome and the detection of 2 new human CoVs (HCoV-NL63 and HCoV-HKU1) have led to studies of the epidemiology and clinical and socioeconomic effects of infections caused by all HCoVs, including those known since the late 1960s (HCoV-229E and HCoV-OC43). HCoV infections can be associated with respiratory and extrarespiratory manifestations, including central nervous system involvement. Furthermore, unlike other RNA viruses, HCoVs can easily mutate and recombine when different strains infect the same cells and give rise to a novel virus with unpredictable host ranges and pathogenicity. Thus, circulating HCoVs should be closely monitored to detect the spread of particularly virulent strains in the community at an early stage and to facilitate the development of adequate preventive and therapeutic measures.
EID | Principi N, Bosis S, Esposito S. Effects of Coronavirus Infections in Children. Emerg Infect Dis. 2010;16(2):183-188. https://doi.org/10.3201/eid1602.090469 |
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AMA | Principi N, Bosis S, Esposito S. Effects of Coronavirus Infections in Children. Emerging Infectious Diseases. 2010;16(2):183-188. doi:10.3201/eid1602.090469. |
APA | Principi, N., Bosis, S., & Esposito, S. (2010). Effects of Coronavirus Infections in Children. Emerging Infectious Diseases, 16(2), 183-188. https://doi.org/10.3201/eid1602.090469. |
Research
Imported Methicillin-Resistant Staphylococcus aureus, Sweden
Countries such as Sweden that have a low prevalence of methicillin-resistant Staphylococcus aureus (MRSA) offer the opportunity to discern and study transmission of imported cases of MRSA. We analyzed 444 imported cases of MRSA acquisition reported in Sweden during 2000–2003. Risk for MRSA in returning travelers ranged from 0.1 (95% confidence interval [CI] 0.01–0.4) per 1 million travelers to Nordic countries to 59.4 (95% CI 44.5–79.3) per 1 million travelers to North Africa and the Middle East. Most imported cases (246, 55%) were healthcare acquired, but regions with the highest risk for MRSA in travelers showed a correlation with community acquisition (r = 0.81, p = 0.001). Characteristic differences in MRSA strains acquired were dependent on the region from which they originated and whether they were community or healthcare acquired. Knowledge of differences in transmission of MRSA may improve control measures against imported cases.
EID | Stenhem M, Örtqvist Å, Ringberg H, Larsson L, Olsson-Liljequist B, Hæggman S, et al. Imported Methicillin-Resistant Staphylococcus aureus, Sweden. Emerg Infect Dis. 2010;16(2):189-196. https://doi.org/10.3201/eid1602.081655 |
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AMA | Stenhem M, Örtqvist Å, Ringberg H, et al. Imported Methicillin-Resistant Staphylococcus aureus, Sweden. Emerging Infectious Diseases. 2010;16(2):189-196. doi:10.3201/eid1602.081655. |
APA | Stenhem, M., Örtqvist, Å., Ringberg, H., Larsson, L., Olsson-Liljequist, B., Hæggman, S....Ekdahl, K. (2010). Imported Methicillin-Resistant Staphylococcus aureus, Sweden. Emerging Infectious Diseases, 16(2), 189-196. https://doi.org/10.3201/eid1602.081655. |
We determined estimated incidence of and risk factors for community-associated Clostridium difficile infection (CA-CDI) among patients treated at 6 North Carolina hospitals. CA-CDI case-patients were defined as adults (>18 years of age) with a positive stool test result for C. difficile toxin and no hospitalization within the prior 8 weeks. CA-CDI incidence was 21 and 46 per 100,000 person-years in Veterans Affairs (VA) outpatients and Durham County populations, respectively. VA case-patients were more likely than controls to have received antimicrobial drugs (adjusted odds ratio [aOR] 17.8, 95% confidence interval [CI] 6.6–48] and to have had a recent outpatient visit (aOR 5.1, 95% CI 1.5–17.9). County case-patients were more likely than controls to have received antimicrobial drugs (aOR 9.1, 95% CI 2.9–28.9), to have gastroesophageal reflux disease (aOR 11.2, 95% CI 1.9–64.2), and to have cardiac failure (aOR 3.8, 95% CI 1.1–13.7). Risk factors for CA-CDI overlap with those for healthcare-associated infection.
EID | Kutty PK, Woods CW, Sena AC, Benoit SR, Naggie S, Frederick J, et al. Risk Factors for and Estimated Incidence of Community-associated Clostridium difficile Infection, North Carolina, USA. Emerg Infect Dis. 2010;16(2):198-204. https://doi.org/10.3201/eid1602.090953 |
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AMA | Kutty PK, Woods CW, Sena AC, et al. Risk Factors for and Estimated Incidence of Community-associated Clostridium difficile Infection, North Carolina, USA. Emerging Infectious Diseases. 2010;16(2):198-204. doi:10.3201/eid1602.090953. |
APA | Kutty, P. K., Woods, C. W., Sena, A. C., Benoit, S. R., Naggie, S., Frederick, J....McDonald, L. C. (2010). Risk Factors for and Estimated Incidence of Community-associated Clostridium difficile Infection, North Carolina, USA. Emerging Infectious Diseases, 16(2), 198-204. https://doi.org/10.3201/eid1602.090953. |
Household Responses to Pandemic (H1N1) 2009–related School Closures, Perth, Western Australia
School closure is often purported to reduce influenza transmission, but little is known about its effect on families. We surveyed families affected by pandemic (H1N1) 2009–related school closures in Perth, Western Australia, Australia. Surveys were returned for 233 (58%) of 402 students. School closure was deemed appropriate by 110 parents (47%); however, 91 (45%) parents of 202 asymptomatic students reported taking >1 day off work to care for their child, and 71 (35%) had to make childcare arrangements because of the class closures. During the week, 172 (74%) students participated in activities outside the home on >1 occasion, resulting in an average of 3.7 out-of-home activities for each student. In our survey, activities outside the home were commonly reported by students affected by school closure, the effect on families was substantial, and parental opinion regarding school closures as a means to mitigate the outbreak of pandemic (H1N1) 2009 was divided.
EID | Effler PV, Carcione D, Giele C, Dowse GK, Goggin L, Mak DB. Household Responses to Pandemic (H1N1) 2009–related School Closures, Perth, Western Australia. Emerg Infect Dis. 2010;16(2):205-211. https://doi.org/10.3201/eid1602.091372 |
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AMA | Effler PV, Carcione D, Giele C, et al. Household Responses to Pandemic (H1N1) 2009–related School Closures, Perth, Western Australia. Emerging Infectious Diseases. 2010;16(2):205-211. doi:10.3201/eid1602.091372. |
APA | Effler, P. V., Carcione, D., Giele, C., Dowse, G. K., Goggin, L., & Mak, D. B. (2010). Household Responses to Pandemic (H1N1) 2009–related School Closures, Perth, Western Australia. Emerging Infectious Diseases, 16(2), 205-211. https://doi.org/10.3201/eid1602.091372. |
Employment and Compliance with Pandemic Influenza Mitigation Recommendations
In the event of a serious pandemic influenza outbreak, businesses must play a key role in protecting employees' health and safety. With regard to pandemic influenza mitigation recommendations requiring social distancing, we examined whether some US employees would disproportionately fail to comply because of job insecurity and financial problems associated with missing work. We used the 2006 Harvard School of Public Health Pandemic Influenza Survey and multivariable logistic regression to determine whether employment characteristics such as inability to work from home, lack of pay when absent from work, and self-employment would be associated with less ability to comply with recommendations. We found that inability to work from home, lack of paid sick leave, and income are associated with working adults’ ability to comply and should be major targets for workplace interventions in the event of a serious outbreak.
EID | Blake KD, Blendon RJ, Viswanath K. Employment and Compliance with Pandemic Influenza Mitigation Recommendations. Emerg Infect Dis. 2010;16(2):212-218. https://doi.org/10.3201/eid1602.090638 |
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AMA | Blake KD, Blendon RJ, Viswanath K. Employment and Compliance with Pandemic Influenza Mitigation Recommendations. Emerging Infectious Diseases. 2010;16(2):212-218. doi:10.3201/eid1602.090638. |
APA | Blake, K. D., Blendon, R. J., & Viswanath, K. (2010). Employment and Compliance with Pandemic Influenza Mitigation Recommendations. Emerging Infectious Diseases, 16(2), 212-218. https://doi.org/10.3201/eid1602.090638. |
Human Hendra Virus Encephalitis Associated with Equine Outbreak, Australia, 2008
A recent Hendra virus outbreak at a veterinary clinic in Brisbane, Queensland, Australia, involved 5 equine and 2 human infections. In contrast to previous outbreaks, infected horses had predominantly encephalitic, rather than respiratory, signs. After an incubation period of 9–16 days, influenza-like illnesses developed in the 2 persons before progressing to encephalitis; 1 died. Both patients were given ribavirin. Basal serum and cerebrospinal fluid levels were 10–13 mg/L after intravenous administration and 6 mg/L after oral administration (isolate 90% inhibitory concentration 64 mg/L). Both patients were exposed to infected horses, 1 during the late incubation period in a horse. The attack rate for veterinary clinic staff exposed to infected horses was 10%. An isolate from this outbreak showed genetic heterogeneity with isolates from a concurrent, but geographically remote, outbreak and from previous outbreaks. Emergence of Hendra virus is a serious medical, veterinary, and public health challenge.
EID | Playford EG, McCall B, Smith G, Slinko V, Allen G, Smith I, et al. Human Hendra Virus Encephalitis Associated with Equine Outbreak, Australia, 2008. Emerg Infect Dis. 2010;16(2):219-223. https://doi.org/10.3201/eid1602.090552 |
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AMA | Playford EG, McCall B, Smith G, et al. Human Hendra Virus Encephalitis Associated with Equine Outbreak, Australia, 2008. Emerging Infectious Diseases. 2010;16(2):219-223. doi:10.3201/eid1602.090552. |
APA | Playford, E. G., McCall, B., Smith, G., Slinko, V., Allen, G., Smith, I....Field, H. E. (2010). Human Hendra Virus Encephalitis Associated with Equine Outbreak, Australia, 2008. Emerging Infectious Diseases, 16(2), 219-223. https://doi.org/10.3201/eid1602.090552. |
Cost-effectiveness of Pharmaceutical-based Pandemic Influenza Mitigation Strategies
We used a hybrid transmission and economic model to evaluate the relative merits of stockpiling antiviral drugs and vaccine for pandemic influenza mitigation. In the absence of any intervention, our base-case assumptions generated a population clinical attack rate of 31.1%. For at least some parameter values, population prepandemic vaccination strategies were effective at containing an outbreak of pandemic influenza until the arrival of a matched vaccine. Because of the uncertain nature of many parameters, we used a probabilistic approach to determine the most cost-effective strategies. At a willingness to pay of >A$24,000 per life-year saved, more than half the simulations showed that a prepandemic vaccination program combined with antiviral treatment was cost-effective in Australia.
EID | Newall AT, Wood JG, Oudin N, MacIntyre C. Cost-effectiveness of Pharmaceutical-based Pandemic Influenza Mitigation Strategies. Emerg Infect Dis. 2010;16(2):224-230. https://doi.org/10.3201/eid1602.090571 |
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AMA | Newall AT, Wood JG, Oudin N, et al. Cost-effectiveness of Pharmaceutical-based Pandemic Influenza Mitigation Strategies. Emerging Infectious Diseases. 2010;16(2):224-230. doi:10.3201/eid1602.090571. |
APA | Newall, A. T., Wood, J. G., Oudin, N., & MacIntyre, C. (2010). Cost-effectiveness of Pharmaceutical-based Pandemic Influenza Mitigation Strategies. Emerging Infectious Diseases, 16(2), 224-230. https://doi.org/10.3201/eid1602.090571. |
Domestic Animals and Epidemiology of Visceral Leishmaniasis, Nepal
On the Indian subcontinent, visceral leishmaniasis (VL) is considered an anthroponosis. To determine possible reasons for its persistence during interepidemic periods, we mapped Leishmania infections among healthy persons and animals in an area of active VL transmission in Nepal. During 4 months (September 2007–February 2008), blood was collected from persons, goats, cows, and buffaloes in 1 village. Leishmania infections were determined by using PCR. We found infections among persons (6.1%), cows (5%), buffaloes (4%), and goats (16%). Data were georeferenced and entered into a geographic information system. The bivariate K-function results indicated spatial clustering of Leishmania spp.–positive persons and domestic animals. Classification tree analysis determined that among several possible risk factors for Leishmania infection among persons, proximity of Leishmania spp.–positive goats ranked first. Although our data do not necessarily mean that goats constitute a reservoir host of L. donovani, these observations indicate the need for further investigation of goats’ possible role in VL transmission.
EID | Bhattarai NR, Van der Auwera G, Rijal S, Picado A, Speybroeck N, Khanal B, et al. Domestic Animals and Epidemiology of Visceral Leishmaniasis, Nepal. Emerg Infect Dis. 2010;16(2):231-237. https://doi.org/10.3201/eid1602.090623 |
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AMA | Bhattarai NR, Van der Auwera G, Rijal S, et al. Domestic Animals and Epidemiology of Visceral Leishmaniasis, Nepal. Emerging Infectious Diseases. 2010;16(2):231-237. doi:10.3201/eid1602.090623. |
APA | Bhattarai, N. R., Van der Auwera, G., Rijal, S., Picado, A., Speybroeck, N., Khanal, B....Dujardin, J. (2010). Domestic Animals and Epidemiology of Visceral Leishmaniasis, Nepal. Emerging Infectious Diseases, 16(2), 231-237. https://doi.org/10.3201/eid1602.090623. |
Investigating an Airborne Tularemia Outbreak, Germany
In November 2005, an outbreak of tularemia occurred among 39 participants in a hare hunt in Hesse, Germany. Previously reported tularemia outbreaks in Germany dated back to the 1950s. We conducted a retrospective cohort study among participants and investigated the environment to identify risk factors for infection. Ten participants had serologic evidence of acute Francisella tularensis infection; 1 other participant died before laboratory confirmation was obtained. Presence within 5 meters of the place where disemboweled hares were rinsed with a water hose was the risk factor most strongly associated with infection (risk ratio 22.1; 95% confidence interval 13.2–154.3). Swabs taken at the game chamber and water samples were PCR negative for F. tularensis. Eleven of 14 hare parts showed low-level concentrations of F. tularensis, compatible with cross-contamination. More than half of case-patients may have acquired infection through inhalation of aerosolized droplets containing F. tularensis generated during rinsing of infected hares.
EID | Hauri AM, Hofstetter I, Seibold E, Kaysser P, Eckert J, Neubauer H, et al. Investigating an Airborne Tularemia Outbreak, Germany. Emerg Infect Dis. 2010;16(2):238-243. https://doi.org/10.3201/eid1602.081727 |
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AMA | Hauri AM, Hofstetter I, Seibold E, et al. Investigating an Airborne Tularemia Outbreak, Germany. Emerging Infectious Diseases. 2010;16(2):238-243. doi:10.3201/eid1602.081727. |
APA | Hauri, A. M., Hofstetter, I., Seibold, E., Kaysser, P., Eckert, J., Neubauer, H....Splettstoesser, W. D. (2010). Investigating an Airborne Tularemia Outbreak, Germany. Emerging Infectious Diseases, 16(2), 238-243. https://doi.org/10.3201/eid1602.081727. |
Statewide School-located Influenza Vaccination Program for Children 5–13 Years of Age, Hawaii, USA
New guidance recommends annual influenza vaccination for all children 5–18 years of age in the United States. During 2007–2008, Hawaii offered inactivated and live attenuated influenza vaccine at school-located clinics for grades kindergarten through 8. Most (90%) public and private schools participated, and 622 clinics were conducted at 340 schools. Of 132,775 children 5–13 years of age, 60,760 (46%) were vaccinated. The proportion vaccinated peaked at 54% for those 6 years of age and declined for older cohorts. More than 90% of schoolchildren transited the clinic in <10 minutes. A total of 16,920 staff-hours were expended; estimated cost per dose administered was $27 and included vaccine purchase and administration, health staffing resources, printing costs, data management, and promotion. This program demonstrates the feasibility of conducting mass school-located influenza vaccination programs in public and private schools statewide, as might be indicated to respond to pandemic influenza.
EID | Effler PV, Chu C, He H, Gaynor K, Sakamoto S, Nagao M, et al. Statewide School-located Influenza Vaccination Program for Children 5–13 Years of Age, Hawaii, USA. Emerg Infect Dis. 2010;16(2):244-250. https://doi.org/10.3201/eid1602.091375 |
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AMA | Effler PV, Chu C, He H, et al. Statewide School-located Influenza Vaccination Program for Children 5–13 Years of Age, Hawaii, USA. Emerging Infectious Diseases. 2010;16(2):244-250. doi:10.3201/eid1602.091375. |
APA | Effler, P. V., Chu, C., He, H., Gaynor, K., Sakamoto, S., Nagao, M....Park, S. Y. (2010). Statewide School-located Influenza Vaccination Program for Children 5–13 Years of Age, Hawaii, USA. Emerging Infectious Diseases, 16(2), 244-250. https://doi.org/10.3201/eid1602.091375. |
Epidemiology of Cryptococcus gattii, British Columbia, Canada, 1999–2007
British Columbia, Canada, has the largest reported population of Cryptococcus gattii–infected persons worldwide. To assess the impact of illness, we retrospectively analyzed demographic and clinical features of reported cases, hospitalizations, and deaths during 1999–2007. A total of 218 cases were reported (average annual incidence 5.8 per million persons). Most persons who sought treatment had respiratory illness (76.6%) or lung cryptococcoma (75.4%). Persons without HIV/AIDS hospitalized with cryptococcosis were more likely than those with HIV/AIDS to be older and admitted for pulmonary cryptococcosis. The 19 (8.7%) persons who died were more likely to be older and to have central nervous system disease and infection from the VGIIb strain. Although incidence in British Columbia is high, the predominant strain (VGIIa) does not seem to cause greater illness or death than do other strains. Further studies are needed to explain host and strain characteristics for regional differences in populations affected and disease outcomes.
EID | Galanis E, MacDougall L, Kidd S, Morshed M. Epidemiology of Cryptococcus gattii, British Columbia, Canada, 1999–2007. Emerg Infect Dis. 2010;16(2):251-257. https://doi.org/10.3201/eid1602.090900 |
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AMA | Galanis E, MacDougall L, Kidd S, et al. Epidemiology of Cryptococcus gattii, British Columbia, Canada, 1999–2007. Emerging Infectious Diseases. 2010;16(2):251-257. doi:10.3201/eid1602.090900. |
APA | Galanis, E., MacDougall, L., Kidd, S., & Morshed, M. (2010). Epidemiology of Cryptococcus gattii, British Columbia, Canada, 1999–2007. Emerging Infectious Diseases, 16(2), 251-257. https://doi.org/10.3201/eid1602.090900. |
Tropheryma whipplei in Patients with Pneumonia
Tropheryma whipplei is the etiologic pathogenic agent of Whipple disease (WD), characterized by various clinical signs, such as diarrhea, weight loss, lymphadenopathy, and polyarthritis. PCR-based methods for diagnosis of WD have been developed. T. whipplei has been identified in saliva and stool samples from patients with WD and from healthy persons. T. whipplei DNA has also been found in bronchoalveolar lavage (BAL) samples of a child with pneumonia. We detected DNA of T. whipplei in 6 (3%) of 210 BAL samples collected in intensive care units by using 16S rDNA and specific quantitative PCR. We identified 4 novel genotypes of T. whipplei. In 1 case, T. whipplei was the only bacterium; in 4 others, it was associated with buccal flora. We suggest that T. whipplei should be investigated as an etiologic agent of pneumonia.
EID | Bousbia S, Papazian L, Auffray J, Fenollar F, Martin C, Li W, et al. Tropheryma whipplei in Patients with Pneumonia. Emerg Infect Dis. 2010;16(2):258-263. https://doi.org/10.3201/eid1602.090610 |
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AMA | Bousbia S, Papazian L, Auffray J, et al. Tropheryma whipplei in Patients with Pneumonia. Emerging Infectious Diseases. 2010;16(2):258-263. doi:10.3201/eid1602.090610. |
APA | Bousbia, S., Papazian, L., Auffray, J., Fenollar, F., Martin, C., Li, W....Raoult, D. (2010). Tropheryma whipplei in Patients with Pneumonia. Emerging Infectious Diseases, 16(2), 258-263. https://doi.org/10.3201/eid1602.090610. |
Emergence of Increased Resistance and Extensively Drug-Resistant Tuberculosis Despite Treatment Adherence, South Africa
We investigated the emergence and evolution of drug-resistant tuberculosis (TB) in an HIV co-infected population at a South African gold mine with a well-functioning TB control program. Of 128 patients with drug-resistant TB diagnosed during January 2003–November 2005, a total of 77 had multidrug-resistant (MDR) TB, 26 had pre–extensively drug-resistant TB (XDR TB), and 5 had XDR TB. Genotyping suggested ongoing transmission of drug-resistant TB, and contact tracing among case-patients in the largest cluster demonstrated multiple possible points of contact. Phylogenetic analysis demonstrated stepwise evolution of drug resistance, despite stringent treatment adherence. These findings suggested that existing TB control measures were inadequate to control the spread of drug-resistant TB in this HIV co-infected population. Diagnosis delay and inappropriate therapy facilitated disease transmission and drug-resistance. These data call for improved infection control measures, implementation of rapid diagnostics, enhanced active screening strategies, and pharmacokinetic studies to determine optimal dosages and treatment regimens.
EID | Calver AD, Falmer AA, Murray MB, Strauss OJ, Streicher EM, Hanekom M, et al. Emergence of Increased Resistance and Extensively Drug-Resistant Tuberculosis Despite Treatment Adherence, South Africa. Emerg Infect Dis. 2010;16(2):264-271. https://doi.org/10.3201/eid1602.090968 |
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AMA | Calver AD, Falmer AA, Murray MB, et al. Emergence of Increased Resistance and Extensively Drug-Resistant Tuberculosis Despite Treatment Adherence, South Africa. Emerging Infectious Diseases. 2010;16(2):264-271. doi:10.3201/eid1602.090968. |
APA | Calver, A. D., Falmer, A. A., Murray, M. B., Strauss, O. J., Streicher, E. M., Hanekom, M....Victor, T. C. (2010). Emergence of Increased Resistance and Extensively Drug-Resistant Tuberculosis Despite Treatment Adherence, South Africa. Emerging Infectious Diseases, 16(2), 264-271. https://doi.org/10.3201/eid1602.090968. |
Associations between Mycobacterium tuberculosis Strains and Phenotypes
To inform development of tuberculosis (TB) control strategies, we characterized a total of 2,261 Mycobacterium tuberculosis complex isolates by using multiple phenotypic and molecular markers, including polymorphisms in repetitive sequences (spoligotyping and variable-number tandem repeats [VNTRs]) and large sequence and single-nucleotide polymorphisms. The Beijing family was strongly associated with multidrug resistance (p = 0.0001), and VNTR allelic variants showed strong associations with spoligotyping families: >5 copies at exact tandem repeat (ETR) A, >2 at mycobacterial interspersed repetitive unit 24, and >3 at ETR-B associated with the East African–Indian and M. bovis strains. All M. tuberculosis isolates were differentiated into 4 major lineages, and a maximum parsimony tree was constructed suggesting a more complex phylogeny for M. africanum. These findings can be used as a model of pathogen global diversity.
EID | Brown T, Nikolayevskyy V, Velji P, Drobniewski F. Associations between Mycobacterium tuberculosis Strains and Phenotypes. Emerg Infect Dis. 2010;16(2):272-280. https://doi.org/10.3201/eid1602.091032 |
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AMA | Brown T, Nikolayevskyy V, Velji P, et al. Associations between Mycobacterium tuberculosis Strains and Phenotypes. Emerging Infectious Diseases. 2010;16(2):272-280. doi:10.3201/eid1602.091032. |
APA | Brown, T., Nikolayevskyy, V., Velji, P., & Drobniewski, F. (2010). Associations between Mycobacterium tuberculosis Strains and Phenotypes. Emerging Infectious Diseases, 16(2), 272-280. https://doi.org/10.3201/eid1602.091032. |
Historical Review
New Hypothesis for Cause of Epidemic among Native Americans, New England, 1616–1619
In the years before English settlers established the Plymouth colony (1616–1619), most Native Americans living on the southeastern coast of present-day Massachusetts died from a mysterious disease. Classic explanations have included yellow fever, smallpox, and plague. Chickenpox and trichinosis are among more recent proposals. We suggest an additional candidate: leptospirosis complicated by Weil syndrome. Rodent reservoirs from European ships infected indigenous reservoirs and contaminated land and fresh water. Local ecology and high-risk quotidian practices of the native population favored exposure and were not shared by Europeans. Reduction of the population may have been incremental, episodic, and continuous; local customs continuously exposed this population to hyperendemic leptospiral infection over months or years, and only a fraction survived. Previous proposals do not adequately account for signature signs (epistaxis, jaundice) and do not consider customs that may have been instrumental to the near annihilation of Native Americans, which facilitated successful colonization of the Massachusetts Bay area.
EID | Marr JS, Cathey JT. New Hypothesis for Cause of Epidemic among Native Americans, New England, 1616–1619. Emerg Infect Dis. 2010;16(2):281-286. https://doi.org/10.3201/eid1602.090276 |
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AMA | Marr JS, Cathey JT. New Hypothesis for Cause of Epidemic among Native Americans, New England, 1616–1619. Emerging Infectious Diseases. 2010;16(2):281-286. doi:10.3201/eid1602.090276. |
APA | Marr, J. S., & Cathey, J. T. (2010). New Hypothesis for Cause of Epidemic among Native Americans, New England, 1616–1619. Emerging Infectious Diseases, 16(2), 281-286. https://doi.org/10.3201/eid1602.090276. |
Dispatches
Clonal Distribution of Invasive Pneumococci, Czech Republic, 1996–2003
We conducted surveillance on invasive pneumococci isolated from adults in the Czech Republic during 1996–2003. The 7 most prevalent serotypes were characterized. Coverage with the 7-valent pneumococcal conjugate vaccine was low. Our observations confirm that detection methods may have modified the expected effect of this vaccine.
EID | Žemličková H, Urbášková P, Jakubů V, Motlová J, Musílek M, Procházka B. Clonal Distribution of Invasive Pneumococci, Czech Republic, 1996–2003. Emerg Infect Dis. 2010;16(2):287-289. https://doi.org/10.3201/eid1602.080535 |
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AMA | Žemličková H, Urbášková P, Jakubů V, et al. Clonal Distribution of Invasive Pneumococci, Czech Republic, 1996–2003. Emerging Infectious Diseases. 2010;16(2):287-289. doi:10.3201/eid1602.080535. |
APA | Žemličková, H., Urbášková, P., Jakubů, V., Motlová, J., Musílek, M., & Procházka, B. (2010). Clonal Distribution of Invasive Pneumococci, Czech Republic, 1996–2003. Emerging Infectious Diseases, 16(2), 287-289. https://doi.org/10.3201/eid1602.080535. |
White-Nose Syndrome Fungus (Geomyces destructans) in Bat, France
White-nose syndrome is caused by the fungus Geomyces destructans and is responsible for the deaths of >1,000,000 bats since 2006. This disease and fungus had been restricted to the northeastern United States. We detected this fungus in a bat in France and assessed the implications of this finding.
EID | Puechmaille SJ, Verdeyroux P, Fuller H, Gouilh MA, Bekaert M, Teeling EC. White-Nose Syndrome Fungus (Geomyces destructans) in Bat, France. Emerg Infect Dis. 2010;16(2):290-293. https://doi.org/10.3201/eid1602.091391 |
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AMA | Puechmaille SJ, Verdeyroux P, Fuller H, et al. White-Nose Syndrome Fungus (Geomyces destructans) in Bat, France. Emerging Infectious Diseases. 2010;16(2):290-293. doi:10.3201/eid1602.091391. |
APA | Puechmaille, S. J., Verdeyroux, P., Fuller, H., Gouilh, M. A., Bekaert, M., & Teeling, E. C. (2010). White-Nose Syndrome Fungus (Geomyces destructans) in Bat, France. Emerging Infectious Diseases, 16(2), 290-293. https://doi.org/10.3201/eid1602.091391. |
Increasing Incidence of Nontuberculous Mycobacteria, Taiwan, 2000–2008
To assess the species distribution and epidemiologic trends of nontuberculous mycobacteria, we examined isolates from patients in Taiwan. During 2000–2008, the proportion increased significantly from 32.3% to 49.8%. Associated disease incidence increased from 2.7 to 10.2 cases per 100,000 patients. Mycobacterium avium complex and M. abscessus were most frequently isolated.
EID | Lai C, Tan C, Chou C, Hsu H, Liao C, Huang Y, et al. Increasing Incidence of Nontuberculous Mycobacteria, Taiwan, 2000–2008. Emerg Infect Dis. 2010;16(2):294-296. https://doi.org/10.3201/eid1602.090675 |
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AMA | Lai C, Tan C, Chou C, et al. Increasing Incidence of Nontuberculous Mycobacteria, Taiwan, 2000–2008. Emerging Infectious Diseases. 2010;16(2):294-296. doi:10.3201/eid1602.090675. |
APA | Lai, C., Tan, C., Chou, C., Hsu, H., Liao, C., Huang, Y....Hsueh, P. (2010). Increasing Incidence of Nontuberculous Mycobacteria, Taiwan, 2000–2008. Emerging Infectious Diseases, 16(2), 294-296. https://doi.org/10.3201/eid1602.090675. |
Bordetella pertussis Clones Identified by Multilocus Variable-Number Tandem-Repeat Analysis
Multilocus variable-number tandem-repeat analysis (MLVA) of 316 Bordetella pertussis isolates collected over 40 years from Australia and 3 other continents identified 66 MLVA types (MTs), including 6 predominant MTs. Typing of genes encoding acellular vaccine antigens showed changes that may be vaccine driven in 2 MTs prevalent in Australia.
EID | Kurniawan J, Maharjan RP, Chan W, Reeves PR, Sintchenko V, Gilbert GL, et al. Bordetella pertussis Clones Identified by Multilocus Variable-Number Tandem-Repeat Analysis. Emerg Infect Dis. 2010;16(2):297-300. https://doi.org/10.3201/eid1602.081707 |
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AMA | Kurniawan J, Maharjan RP, Chan W, et al. Bordetella pertussis Clones Identified by Multilocus Variable-Number Tandem-Repeat Analysis. Emerging Infectious Diseases. 2010;16(2):297-300. doi:10.3201/eid1602.081707. |
APA | Kurniawan, J., Maharjan, R. P., Chan, W., Reeves, P. R., Sintchenko, V., Gilbert, G. L....Lan, R. (2010). Bordetella pertussis Clones Identified by Multilocus Variable-Number Tandem-Repeat Analysis. Emerging Infectious Diseases, 16(2), 297-300. https://doi.org/10.3201/eid1602.081707. |
Plasmodium falciparum Malaria, Southern Algeria, 2007
An outbreak of Plasmodium falciparum malaria occurred in Tinzaouatine in southern Algeria in 2007. The likely vector, Anopheles gambiae mosquitoes, had not been detected in Algeria. Genes for resistance to chloroquine were detected in the parasite. The outbreak shows the potential for an increase in malaria vectors in Algeria.
EID | Boubidi SC, Gassen I, Khechache Y, Lamali K, Tchicha B, Brengues C, et al. Plasmodium falciparum Malaria, Southern Algeria, 2007. Emerg Infect Dis. 2010;16(2):301-303. https://doi.org/10.3201/eid1602.090914 |
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AMA | Boubidi SC, Gassen I, Khechache Y, et al. Plasmodium falciparum Malaria, Southern Algeria, 2007. Emerging Infectious Diseases. 2010;16(2):301-303. doi:10.3201/eid1602.090914. |
APA | Boubidi, S. C., Gassen, I., Khechache, Y., Lamali, K., Tchicha, B., Brengues, C....Harrat, Z. (2010). Plasmodium falciparum Malaria, Southern Algeria, 2007. Emerging Infectious Diseases, 16(2), 301-303. https://doi.org/10.3201/eid1602.090914. |
Sin Nombre Virus Infection in Field Workers, Colorado, USA
We report 2 cases of Sin Nombre virus (SNV) infection in field workers, possibly contracted through rodent bites. Screening for antibodies to SNV in rodents trapped in 2 seasons showed that 9.77% were seropositive. Quantitative real-time PCR showed that 2 of 79 deer mice had detectable titers of SNV RNA.
EID | Torres-Pérez F, Wilson L, Collinge SK, Harmon H, Ray C, Medina RA, et al. Sin Nombre Virus Infection in Field Workers, Colorado, USA. Emerg Infect Dis. 2010;16(2):308-310. https://doi.org/10.3201/eid1602.090735 |
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AMA | Torres-Pérez F, Wilson L, Collinge SK, et al. Sin Nombre Virus Infection in Field Workers, Colorado, USA. Emerging Infectious Diseases. 2010;16(2):308-310. doi:10.3201/eid1602.090735. |
APA | Torres-Pérez, F., Wilson, L., Collinge, S. K., Harmon, H., Ray, C., Medina, R. A....Hjelle, B. (2010). Sin Nombre Virus Infection in Field Workers, Colorado, USA. Emerging Infectious Diseases, 16(2), 308-310. https://doi.org/10.3201/eid1602.090735. |
Pandemic (H1N1) 2009 Cases, Buenos Aires, Argentina
To determine clinical and virologic characteristics of pandemic (H1N1) 2009 in Buenos Aires, Argentina, we conducted real-time reverse transcription–PCR on samples from patients with influenza-like illness, June 11–30, 2009. Of 513 patients tested, 54% were positive for influenza virus subtype H1N1. Infection rate was lowest for patients ≥60 years of age.
EID | Echavarría M, Querci M, Marcone D, Videla C, Martínez A, Bonvehi P, et al. Pandemic (H1N1) 2009 Cases, Buenos Aires, Argentina. Emerg Infect Dis. 2010;16(2):311-313. https://doi.org/10.3201/eid1602.091114 |
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AMA | Echavarría M, Querci M, Marcone D, et al. Pandemic (H1N1) 2009 Cases, Buenos Aires, Argentina. Emerging Infectious Diseases. 2010;16(2):311-313. doi:10.3201/eid1602.091114. |
APA | Echavarría, M., Querci, M., Marcone, D., Videla, C., Martínez, A., Bonvehi, P....Carballal, G. (2010). Pandemic (H1N1) 2009 Cases, Buenos Aires, Argentina. Emerging Infectious Diseases, 16(2), 311-313. https://doi.org/10.3201/eid1602.091114. |
Extensive Mammalian Ancestry of Pandemic (H1N1) 2009 Virus
We demonstrate that the novel pandemic influenza (H1N1) viruses have human virus–like receptor specificity and can no longer replicate in aquatic waterfowl, their historic natural reservoir. The biological properties of these viruses are consistent with those of their phylogenetic progenitors, indicating longstanding adaptation to mammals.
EID | Ilyushina NA, Kim J, Negovetich NJ, Choi Y, Lang V, Bovin NV, et al. Extensive Mammalian Ancestry of Pandemic (H1N1) 2009 Virus. Emerg Infect Dis. 2010;16(2):314-317. https://doi.org/10.3201/eid1602.091141 |
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AMA | Ilyushina NA, Kim J, Negovetich NJ, et al. Extensive Mammalian Ancestry of Pandemic (H1N1) 2009 Virus. Emerging Infectious Diseases. 2010;16(2):314-317. doi:10.3201/eid1602.091141. |
APA | Ilyushina, N. A., Kim, J., Negovetich, N. J., Choi, Y., Lang, V., Bovin, N. V....Webby, R. J. (2010). Extensive Mammalian Ancestry of Pandemic (H1N1) 2009 Virus. Emerging Infectious Diseases, 16(2), 314-317. https://doi.org/10.3201/eid1602.091141. |
Concurrent Silicosis and Pulmonary Mycosis at Death
To examine risk for mycosis among persons with silicosis, we examined US mortality data for 1979–2004. Persons with silicosis were more likely to die with pulmonary mycosis than were those without pneumoconiosis or those with more common pneumoconioses. Health professionals should consider enhanced risk for mycosis for silica-exposed patients.
EID | Iossifova Y, Bailey R, Wood J, Kreiss K. Concurrent Silicosis and Pulmonary Mycosis at Death. Emerg Infect Dis. 2010;16(2):318-320. https://doi.org/10.3201/eid1602.090824 |
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AMA | Iossifova Y, Bailey R, Wood J, et al. Concurrent Silicosis and Pulmonary Mycosis at Death. Emerging Infectious Diseases. 2010;16(2):318-320. doi:10.3201/eid1602.090824. |
APA | Iossifova, Y., Bailey, R., Wood, J., & Kreiss, K. (2010). Concurrent Silicosis and Pulmonary Mycosis at Death. Emerging Infectious Diseases, 16(2), 318-320. https://doi.org/10.3201/eid1602.090824. |
Coccidioidomycosis among Scholarship Athletes and Other College Students, Arizona, USA
To compare coccidioidomycosis case rates among groups of young adults in a disease-endemic region, we reviewed medical charts for serologic testing and coding. Case rates were higher for scholarship athletes than for other students and paralleled 5× more serologic testing. Our findings underscore the need to routinely test patients for coccidioidomycosis.
EID | Stern NG, Galgiani JN. Coccidioidomycosis among Scholarship Athletes and Other College Students, Arizona, USA. Emerg Infect Dis. 2010;16(2):321-323. https://doi.org/10.3201/eid1602.090918 |
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AMA | Stern NG, Galgiani JN. Coccidioidomycosis among Scholarship Athletes and Other College Students, Arizona, USA. Emerging Infectious Diseases. 2010;16(2):321-323. doi:10.3201/eid1602.090918. |
APA | Stern, N. G., & Galgiani, J. N. (2010). Coccidioidomycosis among Scholarship Athletes and Other College Students, Arizona, USA. Emerging Infectious Diseases, 16(2), 321-323. https://doi.org/10.3201/eid1602.090918. |
Novel Human Bocavirus in Children with Acute Respiratory Tract Infection
Human bocavirus (HBoV) and HBoV2, two human bocavirus species, were found in 18 and 10 of 235 nasopharyngeal aspirates, respectively, from children hospitalized with acute respiratory tract infection. Our results suggest that, like HBoV, HBoV2 is distributed worldwide and may be associated with respiratory and enteric diseases.
EID | Song J, Jin Y, Xie Z, Gao H, Xiao N, Chen W, et al. Novel Human Bocavirus in Children with Acute Respiratory Tract Infection. Emerg Infect Dis. 2010;16(2):324-327. https://doi.org/10.3201/eid1602.090553 |
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AMA | Song J, Jin Y, Xie Z, et al. Novel Human Bocavirus in Children with Acute Respiratory Tract Infection. Emerging Infectious Diseases. 2010;16(2):324-327. doi:10.3201/eid1602.090553. |
APA | Song, J., Jin, Y., Xie, Z., Gao, H., Xiao, N., Chen, W....Duan, Z. (2010). Novel Human Bocavirus in Children with Acute Respiratory Tract Infection. Emerging Infectious Diseases, 16(2), 324-327. https://doi.org/10.3201/eid1602.090553. |
Lymphocytic Choriomeningitis Virus Meningitis, New York, NY, USA, 2009
We describe a case of lymphocytic choriomeningitis virus (LCMV) meningitis in a New York, NY, resident who had no apparent risk factors. Clues leading to the diagnosis included aseptic meningitis during winter and the finding of hypoglycorrachia and lymphocytosis in the cerebrospinal fluid. LCMV continues to be an underdiagnosed zoonotic disease.
EID | Asnis DS, Muana O, Kim DG, Garcia M, Rollin PE, Slavinski S. Lymphocytic Choriomeningitis Virus Meningitis, New York, NY, USA, 2009. Emerg Infect Dis. 2010;16(2):328-330. https://doi.org/10.3201/eid1602.091347 |
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AMA | Asnis DS, Muana O, Kim DG, et al. Lymphocytic Choriomeningitis Virus Meningitis, New York, NY, USA, 2009. Emerging Infectious Diseases. 2010;16(2):328-330. doi:10.3201/eid1602.091347. |
APA | Asnis, D. S., Muana, O., Kim, D. G., Garcia, M., Rollin, P. E., & Slavinski, S. (2010). Lymphocytic Choriomeningitis Virus Meningitis, New York, NY, USA, 2009. Emerging Infectious Diseases, 16(2), 328-330. https://doi.org/10.3201/eid1602.091347. |
Severe Leptospirosis in Hospitalized Patients, Guadeloupe
We evaluated prognostic factors for leptospirosis in 168 consecutive hospitalized patients in Guadeloupe. Factors independently associated with severity included chronic hypertension or chronic alcoholism, late initiation of antibacterial therapy, abnormal chest auscultation results, icterus, oligoanuria, disorders of consciousness, elevated aspartate aminotransferase levels, hyperamylasemia, and Leptospira interrogans serovar Icterohemorrhagiae.
EID | Herrmann-Storck C, Saint Louis M, Foucand T, Lamaury I, Deloumeaux J, Baranton G, et al. Severe Leptospirosis in Hospitalized Patients, Guadeloupe. Emerg Infect Dis. 2010;16(2):331-334. https://doi.org/10.3201/eid1602.090139 |
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AMA | Herrmann-Storck C, Saint Louis M, Foucand T, et al. Severe Leptospirosis in Hospitalized Patients, Guadeloupe. Emerging Infectious Diseases. 2010;16(2):331-334. doi:10.3201/eid1602.090139. |
APA | Herrmann-Storck, C., Saint Louis, M., Foucand, T., Lamaury, I., Deloumeaux, J., Baranton, G....Cornet, M. (2010). Severe Leptospirosis in Hospitalized Patients, Guadeloupe. Emerging Infectious Diseases, 16(2), 331-334. https://doi.org/10.3201/eid1602.090139. |
Seropositivity for Enterocytozoon bieneusi, Czech Republic
To determine seropositivity for Enterocytozoon bieneusi in the Czech Republic, we tested 115 serum samples from various groups. We found that 20% from HIV-positive persons, 33% from persons with occupational exposure to animals, and 10% from healthy persons were positive by indirect immunofluorescence assay. Proteins of 32 kDa were detected in serum samples from seropositive persons.
EID | Sak B, Kučerová Z, Kváč M, Květoňová D, Rost M, Secor EW. Seropositivity for Enterocytozoon bieneusi, Czech Republic. Emerg Infect Dis. 2010;16(2):335-337. https://doi.org/10.3201/eid1602.090964 |
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AMA | Sak B, Kučerová Z, Kváč M, et al. Seropositivity for Enterocytozoon bieneusi, Czech Republic. Emerging Infectious Diseases. 2010;16(2):335-337. doi:10.3201/eid1602.090964. |
APA | Sak, B., Kučerová, Z., Kváč, M., Květoňová, D., Rost, M., & Secor, E. W. (2010). Seropositivity for Enterocytozoon bieneusi, Czech Republic. Emerging Infectious Diseases, 16(2), 335-337. https://doi.org/10.3201/eid1602.090964. |
Hendra Virus Outbreak with Novel Clinical Features, Australia
To determine the epidemiologic and clinical features of a 2008 outbreak of Hendra virus infection in a veterinary clinic in Australia, we investigated the equine case-series. Four of 5 infected horses died, as did 1 of 2 infected staff members. Clinical manifestation in horses was predominantly neurologic. Preclinical transmission appears likely.
EID | Field HE, Schaaf K, Kung N, Simon C, Waltisbuhl D, Hobert H, et al. Hendra Virus Outbreak with Novel Clinical Features, Australia. Emerg Infect Dis. 2010;16(2):338-340. https://doi.org/10.3201/eid1602.090780 |
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AMA | Field HE, Schaaf K, Kung N, et al. Hendra Virus Outbreak with Novel Clinical Features, Australia. Emerging Infectious Diseases. 2010;16(2):338-340. doi:10.3201/eid1602.090780. |
APA | Field, H. E., Schaaf, K., Kung, N., Simon, C., Waltisbuhl, D., Hobert, H....Lovell, D. (2010). Hendra Virus Outbreak with Novel Clinical Features, Australia. Emerging Infectious Diseases, 16(2), 338-340. https://doi.org/10.3201/eid1602.090780. |
Pandemic (H1N1) 2009 Outbreak on Pig Farm, Argentina
In June–July 2009, an outbreak of pandemic (H1N1) 2009 infection occurred on a pig farm in Argentina. Molecular analysis indicated that the virus was genetically related to the pandemic (H1N1) 2009 influenza virus strain. The outbreak presumably resulted from direct human-to-pig transmission.
EID | Pereda A, Cappuccio J, Quiroga MA, Baumeister E, Insarralde L, Ibar M, et al. Pandemic (H1N1) 2009 Outbreak on Pig Farm, Argentina. Emerg Infect Dis. 2010;16(2):304-307. https://doi.org/10.3201/eid1602.091230 |
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AMA | Pereda A, Cappuccio J, Quiroga MA, et al. Pandemic (H1N1) 2009 Outbreak on Pig Farm, Argentina. Emerging Infectious Diseases. 2010;16(2):304-307. doi:10.3201/eid1602.091230. |
APA | Pereda, A., Cappuccio, J., Quiroga, M. A., Baumeister, E., Insarralde, L., Ibar, M....Perfumo, C. J. (2010). Pandemic (H1N1) 2009 Outbreak on Pig Farm, Argentina. Emerging Infectious Diseases, 16(2), 304-307. https://doi.org/10.3201/eid1602.091230. |
Commentaries
The Critical Role of Permanent Voucher Specimens of Hosts and Vectors in Public Health and Epidemiology
EID | Peterson AT. The Critical Role of Permanent Voucher Specimens of Hosts and Vectors in Public Health and Epidemiology. Emerg Infect Dis. 2010;16(2):341-342. https://doi.org/10.3201/eid1602.091241 |
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AMA | Peterson AT. The Critical Role of Permanent Voucher Specimens of Hosts and Vectors in Public Health and Epidemiology. Emerging Infectious Diseases. 2010;16(2):341-342. doi:10.3201/eid1602.091241. |
APA | Peterson, A. T. (2010). The Critical Role of Permanent Voucher Specimens of Hosts and Vectors in Public Health and Epidemiology. Emerging Infectious Diseases, 16(2), 341-342. https://doi.org/10.3201/eid1602.091241. |
Letters
Perinatal Pandemic (H1N1) 2009 Infection, Thailand
EID | Dulyachai W, Makkoch J, Rianthavorn P, Changpinyo M, Prayangprecha S, Payungporn S, et al. Perinatal Pandemic (H1N1) 2009 Infection, Thailand. Emerg Infect Dis. 2010;16(2):343-344. https://doi.org/10.3201/eid1602.091733 |
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AMA | Dulyachai W, Makkoch J, Rianthavorn P, et al. Perinatal Pandemic (H1N1) 2009 Infection, Thailand. Emerging Infectious Diseases. 2010;16(2):343-344. doi:10.3201/eid1602.091733. |
APA | Dulyachai, W., Makkoch, J., Rianthavorn, P., Changpinyo, M., Prayangprecha, S., Payungporn, S....Poovorawan, Y. (2010). Perinatal Pandemic (H1N1) 2009 Infection, Thailand. Emerging Infectious Diseases, 16(2), 343-344. https://doi.org/10.3201/eid1602.091733. |
Bronchial Casts and Pandemic (H1N1) 2009 Virus Infection
EID | Hasegawa M, Inamo Y, Fuchigami T, Hashimoto K, Morozumi M, Ubukata K, et al. Bronchial Casts and Pandemic (H1N1) 2009 Virus Infection. Emerg Infect Dis. 2010;16(2):344-346. https://doi.org/10.3201/eid1602.091607 |
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AMA | Hasegawa M, Inamo Y, Fuchigami T, et al. Bronchial Casts and Pandemic (H1N1) 2009 Virus Infection. Emerging Infectious Diseases. 2010;16(2):344-346. doi:10.3201/eid1602.091607. |
APA | Hasegawa, M., Inamo, Y., Fuchigami, T., Hashimoto, K., Morozumi, M., Ubukata, K....Takahashi, T. (2010). Bronchial Casts and Pandemic (H1N1) 2009 Virus Infection. Emerging Infectious Diseases, 16(2), 344-346. https://doi.org/10.3201/eid1602.091607. |
Methicillin-Resistant Staphylococcus aureus ST398, Italy
EID | Soavi L, Stellini R, Signorini L, Antonini B, Pedroni P, Zanetti L, et al. Methicillin-Resistant Staphylococcus aureus ST398, Italy. Emerg Infect Dis. 2010;16(2):346-348. https://doi.org/10.3201/eid1602.091478 |
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AMA | Soavi L, Stellini R, Signorini L, et al. Methicillin-Resistant Staphylococcus aureus ST398, Italy. Emerging Infectious Diseases. 2010;16(2):346-348. doi:10.3201/eid1602.091478. |
APA | Soavi, L., Stellini, R., Signorini, L., Antonini, B., Pedroni, P., Zanetti, L....Carosi, G. (2010). Methicillin-Resistant Staphylococcus aureus ST398, Italy. Emerging Infectious Diseases, 16(2), 346-348. https://doi.org/10.3201/eid1602.091478. |
Neisseria meningitidis Serogroup W135, China
EID | Shao Z, Zhou H, Gao Y, Ren H, Xu L, Kan B, et al. Neisseria meningitidis Serogroup W135, China. Emerg Infect Dis. 2010;16(2):348-349. https://doi.org/10.3201/eid1602.090901 |
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AMA | Shao Z, Zhou H, Gao Y, et al. Neisseria meningitidis Serogroup W135, China. Emerging Infectious Diseases. 2010;16(2):348-349. doi:10.3201/eid1602.090901. |
APA | Shao, Z., Zhou, H., Gao, Y., Ren, H., Xu, L., Kan, B....Xu, J. (2010). Neisseria meningitidis Serogroup W135, China. Emerging Infectious Diseases, 16(2), 348-349. https://doi.org/10.3201/eid1602.090901. |
Avian Influenza (H5N1) Outbreak among Wild Birds, Russia, 2009
EID | Sharshov K, Silko N, Sousloparov I, Zaykovskaya AV, Shestopalov A, Drozdov I. Avian Influenza (H5N1) Outbreak among Wild Birds, Russia, 2009. Emerg Infect Dis. 2010;16(2):349-351. https://doi.org/10.3201/eid1602.090974 |
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AMA | Sharshov K, Silko N, Sousloparov I, et al. Avian Influenza (H5N1) Outbreak among Wild Birds, Russia, 2009. Emerging Infectious Diseases. 2010;16(2):349-351. doi:10.3201/eid1602.090974. |
APA | Sharshov, K., Silko, N., Sousloparov, I., Zaykovskaya, A. V., Shestopalov, A., & Drozdov, I. (2010). Avian Influenza (H5N1) Outbreak among Wild Birds, Russia, 2009. Emerging Infectious Diseases, 16(2), 349-351. https://doi.org/10.3201/eid1602.090974. |
Detection of Pandemic (H1N1) 2009 Virus in Patients Treated with Oseltamivir
EID | Boutolleau D, Houhou N, Deback C, Agut H, Brun-Vézinet F. Detection of Pandemic (H1N1) 2009 Virus in Patients Treated with Oseltamivir. Emerg Infect Dis. 2010;16(2):351-352. https://doi.org/10.3201/eid1602.091328 |
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AMA | Boutolleau D, Houhou N, Deback C, et al. Detection of Pandemic (H1N1) 2009 Virus in Patients Treated with Oseltamivir. Emerging Infectious Diseases. 2010;16(2):351-352. doi:10.3201/eid1602.091328. |
APA | Boutolleau, D., Houhou, N., Deback, C., Agut, H., & Brun-Vézinet, F. (2010). Detection of Pandemic (H1N1) 2009 Virus in Patients Treated with Oseltamivir. Emerging Infectious Diseases, 16(2), 351-352. https://doi.org/10.3201/eid1602.091328. |
Marburg Virus in Fruit Bat, Kenya
EID | Kuzmin IV, Niezgoda M, Franka R, Agwanda B, Markotter W, Breiman RF, et al. Marburg Virus in Fruit Bat, Kenya. Emerg Infect Dis. 2010;16(2):352-354. https://doi.org/10.3201/eid1602.091269 |
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AMA | Kuzmin IV, Niezgoda M, Franka R, et al. Marburg Virus in Fruit Bat, Kenya. Emerging Infectious Diseases. 2010;16(2):352-354. doi:10.3201/eid1602.091269. |
APA | Kuzmin, I. V., Niezgoda, M., Franka, R., Agwanda, B., Markotter, W., Breiman, R. F....Rupprecht, C. E. (2010). Marburg Virus in Fruit Bat, Kenya. Emerging Infectious Diseases, 16(2), 352-354. https://doi.org/10.3201/eid1602.091269. |
Human African Trypanosomiasis in Areas without Surveillance
EID | Chappuis F, Lima MA, Flevaud L, Ritmeijer K. Human African Trypanosomiasis in Areas without Surveillance. Emerg Infect Dis. 2010;16(2):354-356. https://doi.org/10.3201/eid1602.090967 |
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AMA | Chappuis F, Lima MA, Flevaud L, et al. Human African Trypanosomiasis in Areas without Surveillance. Emerging Infectious Diseases. 2010;16(2):354-356. doi:10.3201/eid1602.090967. |
APA | Chappuis, F., Lima, M. A., Flevaud, L., & Ritmeijer, K. (2010). Human African Trypanosomiasis in Areas without Surveillance. Emerging Infectious Diseases, 16(2), 354-356. https://doi.org/10.3201/eid1602.090967. |
Using Museum Collections to Detect Pathogens
EID | Pinto CM, Baxter BD, Hanson JD, Méndez-Harclerode FM, Suchecki JR, Grijalva MJ, et al. Using Museum Collections to Detect Pathogens. Emerg Infect Dis. 2010;16(2):356-357. https://doi.org/10.3201/eid1602.090998 |
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AMA | Pinto CM, Baxter BD, Hanson JD, et al. Using Museum Collections to Detect Pathogens. Emerging Infectious Diseases. 2010;16(2):356-357. doi:10.3201/eid1602.090998. |
APA | Pinto, C. M., Baxter, B. D., Hanson, J. D., Méndez-Harclerode, F. M., Suchecki, J. R., Grijalva, M. J....Bradley, R. D. (2010). Using Museum Collections to Detect Pathogens. Emerging Infectious Diseases, 16(2), 356-357. https://doi.org/10.3201/eid1602.090998. |
Aggression and Rabid Coyotes, Massachusetts, USA
EID | Wang X, Brown CM, Smole S, Werner BG, Han L, Farris M, et al. Aggression and Rabid Coyotes, Massachusetts, USA. Emerg Infect Dis. 2010;16(2):357-369. https://doi.org/10.3201/eid1602.090731 |
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AMA | Wang X, Brown CM, Smole S, et al. Aggression and Rabid Coyotes, Massachusetts, USA. Emerging Infectious Diseases. 2010;16(2):357-369. doi:10.3201/eid1602.090731. |
APA | Wang, X., Brown, C. M., Smole, S., Werner, B. G., Han, L., Farris, M....DeMaria, A. (2010). Aggression and Rabid Coyotes, Massachusetts, USA. Emerging Infectious Diseases, 16(2), 357-369. https://doi.org/10.3201/eid1602.090731. |
Neisseria meningitidis Serogroup X Sequence Type 2888, Italy
EID | Fazio C, Starnino S, Dal Soldà M, Sofia T, Neri A, Mastrantonio P, et al. Neisseria meningitidis Serogroup X Sequence Type 2888, Italy. Emerg Infect Dis. 2010;16(2):359-360. https://doi.org/10.3201/eid1602.091553 |
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AMA | Fazio C, Starnino S, Dal Soldà M, et al. Neisseria meningitidis Serogroup X Sequence Type 2888, Italy. Emerging Infectious Diseases. 2010;16(2):359-360. doi:10.3201/eid1602.091553. |
APA | Fazio, C., Starnino, S., Dal Soldà, M., Sofia, T., Neri, A., Mastrantonio, P....Stefanelli, P. (2010). Neisseria meningitidis Serogroup X Sequence Type 2888, Italy. Emerging Infectious Diseases, 16(2), 359-360. https://doi.org/10.3201/eid1602.091553. |
Antiphospholipid Syndrome and Acute HIV Infection
EID | Díaz JS, Octavio JG, Guerrero ML. Antiphospholipid Syndrome and Acute HIV Infection. Emerg Infect Dis. 2010;16(2):360-361. https://doi.org/10.3201/eid1602.090728 |
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AMA | Díaz JS, Octavio JG, Guerrero ML. Antiphospholipid Syndrome and Acute HIV Infection. Emerging Infectious Diseases. 2010;16(2):360-361. doi:10.3201/eid1602.090728. |
APA | Díaz, J. S., Octavio, J. G., & Guerrero, M. L. (2010). Antiphospholipid Syndrome and Acute HIV Infection. Emerging Infectious Diseases, 16(2), 360-361. https://doi.org/10.3201/eid1602.090728. |
Mycobacterium tuberculosis Beijing Strain, Bamako, Mali
EID | Diarra B, Siddiqui S, Sogoba D, Traore B, Maiga M, Washington J, et al. Mycobacterium tuberculosis Beijing Strain, Bamako, Mali. Emerg Infect Dis. 2010;16(2):362-363. https://doi.org/10.3201/eid1602.090501 |
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AMA | Diarra B, Siddiqui S, Sogoba D, et al. Mycobacterium tuberculosis Beijing Strain, Bamako, Mali. Emerging Infectious Diseases. 2010;16(2):362-363. doi:10.3201/eid1602.090501. |
APA | Diarra, B., Siddiqui, S., Sogoba, D., Traore, B., Maiga, M., Washington, J....Polis, M. A. (2010). Mycobacterium tuberculosis Beijing Strain, Bamako, Mali. Emerging Infectious Diseases, 16(2), 362-363. https://doi.org/10.3201/eid1602.090501. |
Hemorrhagic Fever with Renal Syndrome, Vietnam
EID | Huong VT, Yoshimatsu K, Luan VD, Van Tuan L, Nhi L, Arikawa J, et al. Hemorrhagic Fever with Renal Syndrome, Vietnam. Emerg Infect Dis. 2010;16(2):363-365. https://doi.org/10.3201/eid1602.091204 |
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AMA | Huong VT, Yoshimatsu K, Luan VD, et al. Hemorrhagic Fever with Renal Syndrome, Vietnam. Emerging Infectious Diseases. 2010;16(2):363-365. doi:10.3201/eid1602.091204. |
APA | Huong, V. T., Yoshimatsu, K., Luan, V. D., Van Tuan, L., Nhi, L., Arikawa, J....Nguyen, T. M. (2010). Hemorrhagic Fever with Renal Syndrome, Vietnam. Emerging Infectious Diseases, 16(2), 363-365. https://doi.org/10.3201/eid1602.091204. |
Origin of Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus, China
EID | An T, Tian Z, Xiao Y, Li R, Peng J, Wei T, et al. Origin of Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus, China. Emerg Infect Dis. 2010;16(2):365-367. https://doi.org/10.3201/eid1602.090005 |
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AMA | An T, Tian Z, Xiao Y, et al. Origin of Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus, China. Emerging Infectious Diseases. 2010;16(2):365-367. doi:10.3201/eid1602.090005. |
APA | An, T., Tian, Z., Xiao, Y., Li, R., Peng, J., Wei, T....Tong, G. (2010). Origin of Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus, China. Emerging Infectious Diseases, 16(2), 365-367. https://doi.org/10.3201/eid1602.090005. |
Evidence-based Tool for Triggering School Closures during Influenza Outbreaks
EID | Vogt RL. Evidence-based Tool for Triggering School Closures during Influenza Outbreaks. Emerg Infect Dis. 2010;16(2):367-368. https://doi.org/10.3201/eid1602.091628 |
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AMA | Vogt RL. Evidence-based Tool for Triggering School Closures during Influenza Outbreaks. Emerging Infectious Diseases. 2010;16(2):367-368. doi:10.3201/eid1602.091628. |
APA | Vogt, R. L. (2010). Evidence-based Tool for Triggering School Closures during Influenza Outbreaks. Emerging Infectious Diseases, 16(2), 367-368. https://doi.org/10.3201/eid1602.091628. |
Another Dimension
Personal Log, Stardate 42552.6
EID | Kim C. Personal Log, Stardate 42552.6. Emerg Infect Dis. 2010;16(2):368. https://doi.org/10.3201/eid1602.ad1602 |
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AMA | Kim C. Personal Log, Stardate 42552.6. Emerging Infectious Diseases. 2010;16(2):368. doi:10.3201/eid1602.ad1602. |
APA | Kim, C. (2010). Personal Log, Stardate 42552.6. Emerging Infectious Diseases, 16(2), 368. https://doi.org/10.3201/eid1602.ad1602. |
Etymologia
Etymologia: Cryptococcus gattii
EID | Snarey C. Etymologia: Cryptococcus gattii. Emerg Infect Dis. 2010;16(2):286. https://doi.org/10.3201/eid1602.et1602 |
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AMA | Snarey C. Etymologia: Cryptococcus gattii. Emerging Infectious Diseases. 2010;16(2):286. doi:10.3201/eid1602.et1602. |
APA | Snarey, C. (2010). Etymologia: Cryptococcus gattii. Emerging Infectious Diseases, 16(2), 286. https://doi.org/10.3201/eid1602.et1602. |
About the Cover
Bird’s Eye View of Emerging Zoonoses
EID | Potter P. Bird’s Eye View of Emerging Zoonoses. Emerg Infect Dis. 2010;16(2):369-370. https://doi.org/10.3201/eid1602.ac1602 |
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AMA | Potter P. Bird’s Eye View of Emerging Zoonoses. Emerging Infectious Diseases. 2010;16(2):369-370. doi:10.3201/eid1602.ac1602. |
APA | Potter, P. (2010). Bird’s Eye View of Emerging Zoonoses. Emerging Infectious Diseases, 16(2), 369-370. https://doi.org/10.3201/eid1602.ac1602. |