Perspective
Rumors of Disease in the Global Village: Outbreak Verification
Emerging infectious diseases and the growth of information technology have produced new demands and possibilities for disease surveillance and response. Increasing numbers of outbreak reports must be assessed rapidly so that control efforts can be initiated and unsubstantiated reports can be identified to protect countries from unnecessary economic damage. The World Health Organization has set up a process for timely outbreak verification to convert large amounts of data into accurate information for suitable action. We describe the context and processes of outbreak verification and information dissemination.
EID | Grein TW, Kamara KO, Rodier G, Plant AJ, Bovier P, Ryan MJ, et al. Rumors of Disease in the Global Village: Outbreak Verification. Emerg Infect Dis. 2000;6(2):97-102. https://doi.org/10.3201/eid0602.000201 |
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AMA | Grein TW, Kamara KO, Rodier G, et al. Rumors of Disease in the Global Village: Outbreak Verification. Emerging Infectious Diseases. 2000;6(2):97-102. doi:10.3201/eid0602.000201. |
APA | Grein, T. W., Kamara, K. O., Rodier, G., Plant, A. J., Bovier, P., Ryan, M. J....Heymann, D. L. (2000). Rumors of Disease in the Global Village: Outbreak Verification. Emerging Infectious Diseases, 6(2), 97-102. https://doi.org/10.3201/eid0602.000201. |
Malaria on the Move: Human Population Movement and Malaria Transmission
Reports of malaria are increasing in many countries and in areas thought free of the disease. One of the factors contributing to the reemergence of malaria is human migration. People move for a number of reasons, including environmental deterioration, economic necessity, conflicts, and natural disasters. These factors are most likely to affect the poor, many of whom live in or near malarious areas. Identifying and understanding the influence of these population movements can improve prevention measures and malaria control programs.
EID | Martens P, Hall L. Malaria on the Move: Human Population Movement and Malaria Transmission. Emerg Infect Dis. 2000;6(2):103-109. https://doi.org/10.3201/eid0602.000202 |
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AMA | Martens P, Hall L. Malaria on the Move: Human Population Movement and Malaria Transmission. Emerging Infectious Diseases. 2000;6(2):103-109. doi:10.3201/eid0602.000202. |
APA | Martens, P., & Hall, L. (2000). Malaria on the Move: Human Population Movement and Malaria Transmission. Emerging Infectious Diseases, 6(2), 103-109. https://doi.org/10.3201/eid0602.000202. |
Synopses
The bdr Gene Families of the Lyme Disease and Relapsing Fever Spirochetes: Potential Influence on Biology, Pathogenesis, and Evolution
Species of the genus Borrelia cause human and animal infections, including Lyme disease, relapsing fever, and epizootic bovine abortion. The borrelial genome is unique among bacterial genomes in that it is composed of a linear chromosome and a series of linear and circular plasmids. The plasmids exhibit significant genetic redundancy and carry 175 paralogous gene families, most of of unknown function. Homologous alleles on different plasmids could influence the organization and evolution of the Borrelia genome by serving as foci for interplasmid homologous recombination. The plasmid-carried Borrelia direct repeat (bdr) gene family encodes polymorphic, acidic proteins with putative phosphorylation sites and transmembrane domains. These proteins may play regulatory roles in Borrelia. We describe recent progress in the characterization of the Borrelia bdr genes and discuss the possible influence of this gene family on the biology, pathogenesis, and evolution of the Borrelia genome.
EID | Roberts DM, Carlyon J, Theisen M, Marconi RT. The bdr Gene Families of the Lyme Disease and Relapsing Fever Spirochetes: Potential Influence on Biology, Pathogenesis, and Evolution. Emerg Infect Dis. 2000;6(2):110-122. https://doi.org/10.3201/eid0602.000203 |
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AMA | Roberts DM, Carlyon J, Theisen M, et al. The bdr Gene Families of the Lyme Disease and Relapsing Fever Spirochetes: Potential Influence on Biology, Pathogenesis, and Evolution. Emerging Infectious Diseases. 2000;6(2):110-122. doi:10.3201/eid0602.000203. |
APA | Roberts, D. M., Carlyon, J., Theisen, M., & Marconi, R. T. (2000). The bdr Gene Families of the Lyme Disease and Relapsing Fever Spirochetes: Potential Influence on Biology, Pathogenesis, and Evolution. Emerging Infectious Diseases, 6(2), 110-122. https://doi.org/10.3201/eid0602.000203. |
Vaccines for Mucosal Immunity to Combat Emerging Infectious Diseases
The mucosal immune system consists of molecules, cells, and organized lymphoid structures intended to provide immunity to pathogens that impinge upon mucosal surfaces. Mucosal infection by intracellular pathogens results in the induction of cell-mediated immunity, as manifested by CD4-positive (CD4+) T helper-type 1 cells, as well as CD8+ cytotoxic T-lymphocytes. These responses are normally accompanied by the synthesis of secretory immunoglobulin A (S-IgA) antibodies, which provide an important first line of defense against invasion of deeper tissues by these pathogens. New-generation live, attenuated viral vaccines, such as the cold-adapted, recombinant nasal influenza and oral rotavirus vaccines, optimize this form of mucosal immune protection. Despite these advances, new and reemerging infectious diseases are tipping the balance in favor of the parasite; continued mucosal vaccine development will be needed to effectively combat these new threats.
EID | van Ginkel FW, Nguyen HH, McGhee JR. Vaccines for Mucosal Immunity to Combat Emerging Infectious Diseases. Emerg Infect Dis. 2000;6(2):123-132. https://doi.org/10.3201/eid0602.000204 |
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AMA | van Ginkel FW, Nguyen HH, McGhee JR. Vaccines for Mucosal Immunity to Combat Emerging Infectious Diseases. Emerging Infectious Diseases. 2000;6(2):123-132. doi:10.3201/eid0602.000204. |
APA | van Ginkel, F. W., Nguyen, H. H., & McGhee, J. R. (2000). Vaccines for Mucosal Immunity to Combat Emerging Infectious Diseases. Emerging Infectious Diseases, 6(2), 123-132. https://doi.org/10.3201/eid0602.000204. |
Research
Competence of American Robins as Reservoir Hosts for Lyme Disease Spirochetes
To explore the competence of American robins as a reservoir for Lyme disease spirochetes, we determined the susceptibility of these birds to tickborne spirochetes and their subsequent infectivity for larval vector ticks. Robins acquired infection and became infectious to almost all xenodiagnostic ticks soon after exposure to infected nymphal ticks. Although infectivity waned after 2 months, the robins remained susceptible to reinfection, became infectious again, and permitted repeated feeding by vector ticks. In addition, spirochetes passaged through birds retained infectivity for mammalian hosts. American robins become as infectious for vector ticks as do reservoir mice, but infectivity in robins wanes more rapidly.
EID | Richter D, Spielman A, Komar N, Matuschka F. Competence of American Robins as Reservoir Hosts for Lyme Disease Spirochetes. Emerg Infect Dis. 2000;6(2):133-138. https://doi.org/10.3201/eid0602.000205 |
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AMA | Richter D, Spielman A, Komar N, et al. Competence of American Robins as Reservoir Hosts for Lyme Disease Spirochetes. Emerging Infectious Diseases. 2000;6(2):133-138. doi:10.3201/eid0602.000205. |
APA | Richter, D., Spielman, A., Komar, N., & Matuschka, F. (2000). Competence of American Robins as Reservoir Hosts for Lyme Disease Spirochetes. Emerging Infectious Diseases, 6(2), 133-138. https://doi.org/10.3201/eid0602.000205. |
Vibrio cholerae O139 in Calcutta, 1992-1998: Incidence, Antibiograms, and Genotypes
We report results of surveillance for cholera caused by Vibrio cholerae O139 from September 1992, when it was first identified, to December 1998. V. cholerae O139 dominated as the causative agent of cholera in Calcutta during 1992-93 and 1996-97, while the O1 strains dominated during the rest of the period. Dramatic shifts in patterns of resistance to cotrimoxazole, neomycin, and streptomycin were observed. Molecular epidemiologic studies showed clonal diversity among the O139 strains and continuous emergence of new epidemic clones, reflected by changes in the structure, organization, and location of the CTX prophages in the V. cholerae O139 chromosome.
EID | Basu A, Garg P, Datta S, Chakraborty S, Bhattacharya T, Khan A, et al. Vibrio cholerae O139 in Calcutta, 1992-1998: Incidence, Antibiograms, and Genotypes. Emerg Infect Dis. 2000;6(2):139-147. https://doi.org/10.3201/eid0602.000206 |
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AMA | Basu A, Garg P, Datta S, et al. Vibrio cholerae O139 in Calcutta, 1992-1998: Incidence, Antibiograms, and Genotypes. Emerging Infectious Diseases. 2000;6(2):139-147. doi:10.3201/eid0602.000206. |
APA | Basu, A., Garg, P., Datta, S., Chakraborty, S., Bhattacharya, T., Khan, A....Nair, G. B. (2000). Vibrio cholerae O139 in Calcutta, 1992-1998: Incidence, Antibiograms, and Genotypes. Emerging Infectious Diseases, 6(2), 139-147. https://doi.org/10.3201/eid0602.000206. |
Multivariate Markovian Modeling of Tuberculosis: Forecast for the United States
We have developed a computer-implemented, multivariate Markov chain model to project tuberculosis (TB) incidence in the United States from 1980 to 2010 in disaggregated demographic groups. Uncertainty in model parameters and in the projections is represented by fuzzy numbers. Projections are made under the assumption that current TB control measures will remain unchanged for the projection period. The projections of the model demonstrate an intermediate increase in national TB incidence (similar to that which actually occurred) followed by continuing decline. The rate of decline depends strongly on geographic, racial, and ethnic characteristics. The model predicts that the rate of decline in the number of cases among Hispanics will be slower than among white non-Hispanics and black non-Hispanics--a prediction supported by the most recent data.
EID | Debanne SM, Bielefeld RA, Cauthen GM, Daniel TM, Rowland DY. Multivariate Markovian Modeling of Tuberculosis: Forecast for the United States. Emerg Infect Dis. 2000;6(2):148-157. https://doi.org/10.3201/eid0602.000207 |
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AMA | Debanne SM, Bielefeld RA, Cauthen GM, et al. Multivariate Markovian Modeling of Tuberculosis: Forecast for the United States. Emerging Infectious Diseases. 2000;6(2):148-157. doi:10.3201/eid0602.000207. |
APA | Debanne, S. M., Bielefeld, R. A., Cauthen, G. M., Daniel, T. M., & Rowland, D. Y. (2000). Multivariate Markovian Modeling of Tuberculosis: Forecast for the United States. Emerging Infectious Diseases, 6(2), 148-157. https://doi.org/10.3201/eid0602.000207. |
Serologic Response to Culture Filtrate Antigens of Mycobacterium ulcerans during Buruli Ulcer Disease
Buruli ulcer (BU) is an emerging necrotic skin disease caused by Mycobacterium ulcerans. To assess the potential for a serodiagnostic test, we measured the humoral immune response of BU patients to M. ulcerans antigens and compared this response with delayed-type hypersensitivity responses to both Burulin and PPD. The delayed-type hypersensitivity response generally supported the diagnosis of BU, with overall reactivity to Burulin in 28 (71.8%) of 39 patients tested, compared with 3 (14%) of 21 healthy controls. However, this positive skin test response was observed primarily in patients with healed or active disease, and rarely in patients with early disease (p=0.009). When tested for a serologic response to M. ulcerans culture filtrate, 43 (70.5%) of 61 BU patients had antibodies to these antigens, compared with 10 (37.0%) of 27 controls and 4 (30.8%) of 13 tuberculosis patients. There was no correlation between disease stage and the onset of this serum antibody response. Our findings suggest that serologic testing may be useful in the diagnosis and surveillance of BU.
EID | Dobos KM, Spotts EA, Marston BJ, Horsburgh CR, King CH. Serologic Response to Culture Filtrate Antigens of Mycobacterium ulcerans during Buruli Ulcer Disease. Emerg Infect Dis. 2000;6(2):158-164. https://doi.org/10.3201/eid0602.000208 |
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AMA | Dobos KM, Spotts EA, Marston BJ, et al. Serologic Response to Culture Filtrate Antigens of Mycobacterium ulcerans during Buruli Ulcer Disease. Emerging Infectious Diseases. 2000;6(2):158-164. doi:10.3201/eid0602.000208. |
APA | Dobos, K. M., Spotts, E. A., Marston, B. J., Horsburgh, C. R., & King, C. H. (2000). Serologic Response to Culture Filtrate Antigens of Mycobacterium ulcerans during Buruli Ulcer Disease. Emerging Infectious Diseases, 6(2), 158-164. https://doi.org/10.3201/eid0602.000208. |
Haemophilus influenzae Type B and Streptococcus pneumoniae as Causes of Pneumonia among Children in Beijing, China
To determine if Haemophilus influenzae type b (Hib) and S. pneumoniae could be identified more often from the nasopharynx of patients with pneumonia than from control patients, we obtained nasopharyngeal swab specimens from 96 patients with chest x-ray-confirmed pneumonia and 214 age-matched control patients with diarrhea or dermatitis from the outpatient department at Beijing Children's Hospital. Pneumonia patients were more likely to be colonized with Hib and S. pneumoniae than control patients, even after the data were adjusted for possible confounding factors such as day-care attendance, the presence of other children in the household, and recent antibiotic use. In China, where blood cultures from pneumonia patients are rarely positive, the results of these nasopharyngeal cultures provide supporting evidence for the role of Hib and S. pneumoniae as causes of childhood pneumonia.
EID | Levine OS, Liu G, Garman RL, Dowell SF, Yu S, Yang Y. Haemophilus influenzae Type B and Streptococcus pneumoniae as Causes of Pneumonia among Children in Beijing, China. Emerg Infect Dis. 2000;6(2):165-170. https://doi.org/10.3201/eid0602.000209 |
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AMA | Levine OS, Liu G, Garman RL, et al. Haemophilus influenzae Type B and Streptococcus pneumoniae as Causes of Pneumonia among Children in Beijing, China. Emerging Infectious Diseases. 2000;6(2):165-170. doi:10.3201/eid0602.000209. |
APA | Levine, O. S., Liu, G., Garman, R. L., Dowell, S. F., Yu, S., & Yang, Y. (2000). Haemophilus influenzae Type B and Streptococcus pneumoniae as Causes of Pneumonia among Children in Beijing, China. Emerging Infectious Diseases, 6(2), 165-170. https://doi.org/10.3201/eid0602.000209. |
Dispatches
Bacteroides fragilis Enterotoxin Gene Sequences in Patients with Inflammatory Bowel Disease
We identified enterotoxigenic Bacteroides fragilis in stool specimens of patients with inflammatory bowel disease and other gastrointestinal disorders. The organism was detected in 11 (13.2%) of 83 patients with inflammatory bowel disease. Of 57 patients with active disease, 19.3% were toxin positive; none of those with inactive disease had specimens positive for enterotoxigenic Bacteroides fragilis gene sequences.
EID | Prindiville TP, Sheikh RA, Cohen SH, Tang YJ, Cantrell MC, Silva J. Bacteroides fragilis Enterotoxin Gene Sequences in Patients with Inflammatory Bowel Disease. Emerg Infect Dis. 2000;6(2):171-174. https://doi.org/10.3201/eid0602.000210 |
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AMA | Prindiville TP, Sheikh RA, Cohen SH, et al. Bacteroides fragilis Enterotoxin Gene Sequences in Patients with Inflammatory Bowel Disease. Emerging Infectious Diseases. 2000;6(2):171-174. doi:10.3201/eid0602.000210. |
APA | Prindiville, T. P., Sheikh, R. A., Cohen, S. H., Tang, Y. J., Cantrell, M. C., & Silva, J. (2000). Bacteroides fragilis Enterotoxin Gene Sequences in Patients with Inflammatory Bowel Disease. Emerging Infectious Diseases, 6(2), 171-174. https://doi.org/10.3201/eid0602.000210. |
Outbreak among Drug Users Caused by a Clonal Strain of Group A Streptococcus
We describe an outbreak among drug users of severe soft-tissue infections caused by a clonal strain of group A streptococcus of M-type 25. Cases (n = 19) in drug users were defined as infections (mainly needle abscesses) due to the outbreak strain. Comparison with controls showed that infected drug users bought drugs more often at a specific place. Drug purchase and use habits may have contributed to this outbreak.
EID | Böhlen LM, Mühlemann K, Dubuis O, Aebi C, Täuber MG. Outbreak among Drug Users Caused by a Clonal Strain of Group A Streptococcus. Emerg Infect Dis. 2000;6(2):175-179. https://doi.org/10.3201/eid0602.000211 |
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AMA | Böhlen LM, Mühlemann K, Dubuis O, et al. Outbreak among Drug Users Caused by a Clonal Strain of Group A Streptococcus. Emerging Infectious Diseases. 2000;6(2):175-179. doi:10.3201/eid0602.000211. |
APA | Böhlen, L. M., Mühlemann, K., Dubuis, O., Aebi, C., & Täuber, M. G. (2000). Outbreak among Drug Users Caused by a Clonal Strain of Group A Streptococcus. Emerging Infectious Diseases, 6(2), 175-179. https://doi.org/10.3201/eid0602.000211. |
Erythromycin Resistance in Streptococcus pyogenes in Italy
In a prospective study of acute pharyngitis in Italian children, 69 (38.3%) of 180 isolates of Streptococcus pyogenes were resistant to macrolides. S. pyogenes was eradicated in 12 (63.1%) of 19 patients with erythromycin-resistant S. pyogenes treated with clarithromycin and in 22 (88%) of 25 patients with erythromycin-susceptible strains. The constitutive-resistant phenotype was correlated with failure of macrolide treatment.
EID | Bassetti M, Manno G, Collidà A, Ferrando A, Gatti G, Ugolotti E, et al. Erythromycin Resistance in Streptococcus pyogenes in Italy. Emerg Infect Dis. 2000;6(2):180-183. https://doi.org/10.3201/eid0602.000212 |
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AMA | Bassetti M, Manno G, Collidà A, et al. Erythromycin Resistance in Streptococcus pyogenes in Italy. Emerging Infectious Diseases. 2000;6(2):180-183. doi:10.3201/eid0602.000212. |
APA | Bassetti, M., Manno, G., Collidà, A., Ferrando, A., Gatti, G., Ugolotti, E....Bassetti, D. (2000). Erythromycin Resistance in Streptococcus pyogenes in Italy. Emerging Infectious Diseases, 6(2), 180-183. https://doi.org/10.3201/eid0602.000212. |
Sin Nombre Virus (SNV) Ig Isotype Antibody Response during Acute and Convalescent Phases of Hantavirus Pulmonary Syndrome
Serum samples from 22 hantavirus pulmonary syndrome (HPS) patients were tested for Sin Nombre virus (SNV)-reactive antibodies. In the acute phase of HPS, 100% and 67% of the samples tested positive for SNV-specific immunoglobulin (Ig) M and IgA, respectively. Among the virus-specific IgG antibodies, the most prevalent were IgG3 (in 97% of samples), followed by IgG1 (70%), IgG2 (30%), and IgG4 (3%).
EID | Bostik P, Winter J, Ksiazek TG, Rollin PE, Villinger F, Zaki SR, et al. Sin Nombre Virus (SNV) Ig Isotype Antibody Response during Acute and Convalescent Phases of Hantavirus Pulmonary Syndrome. Emerg Infect Dis. 2000;6(2):184-188. https://doi.org/10.3201/eid0602.000213 |
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AMA | Bostik P, Winter J, Ksiazek TG, et al. Sin Nombre Virus (SNV) Ig Isotype Antibody Response during Acute and Convalescent Phases of Hantavirus Pulmonary Syndrome. Emerging Infectious Diseases. 2000;6(2):184-188. doi:10.3201/eid0602.000213. |
APA | Bostik, P., Winter, J., Ksiazek, T. G., Rollin, P. E., Villinger, F., Zaki, S. R....Ansari, A. A. (2000). Sin Nombre Virus (SNV) Ig Isotype Antibody Response during Acute and Convalescent Phases of Hantavirus Pulmonary Syndrome. Emerging Infectious Diseases, 6(2), 184-188. https://doi.org/10.3201/eid0602.000213. |
Bovine Tuberculosis and the Endangered Iberian Lynx
We report the first case of bovine tuberculosis in a free-living Iberian lynx (Lynx pardina), an extremely endangered feline, from Doñana National Park in Spain. The isolate (Mycobacterium bovis) correlates by molecular characterization with other isolates from wild ungulates in the park, strongly suggesting an epidemiologic link.
EID | Briones V, de Juan L, Sánchez C, Vela A, Galka M, Montero N, et al. Bovine Tuberculosis and the Endangered Iberian Lynx. Emerg Infect Dis. 2000;6(2):189-191. https://doi.org/10.3201/eid0602.000214 |
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AMA | Briones V, de Juan L, Sánchez C, et al. Bovine Tuberculosis and the Endangered Iberian Lynx. Emerging Infectious Diseases. 2000;6(2):189-191. doi:10.3201/eid0602.000214. |
APA | Briones, V., de Juan, L., Sánchez, C., Vela, A., Galka, M., Montero, N....Domínguez, L. (2000). Bovine Tuberculosis and the Endangered Iberian Lynx. Emerging Infectious Diseases, 6(2), 189-191. https://doi.org/10.3201/eid0602.000214. |
Haff Disease: From the Baltic Sea to the U.S. Shore
Haff disease, identified in Europe in 1924, is unexplained rhabdomyolysis in a person who ate fish in the 24 hours before onset of illness. We describe a series of six U.S. patients from 1997 and report new epidemiologic and etiologic aspects. Although Haff disease is traditionally an epidemic foodborne illness, these six cases occurred in two clusters and as one sporadic case.
EID | Buchholz U, Mouzin E, Dickey R, Moolenaar R, Sass N, Mascola L. Haff Disease: From the Baltic Sea to the U.S. Shore. Emerg Infect Dis. 2000;6(2):192-195. https://doi.org/10.3201/eid0602.000215 |
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AMA | Buchholz U, Mouzin E, Dickey R, et al. Haff Disease: From the Baltic Sea to the U.S. Shore. Emerging Infectious Diseases. 2000;6(2):192-195. doi:10.3201/eid0602.000215. |
APA | Buchholz, U., Mouzin, E., Dickey, R., Moolenaar, R., Sass, N., & Mascola, L. (2000). Haff Disease: From the Baltic Sea to the U.S. Shore. Emerging Infectious Diseases, 6(2), 192-195. https://doi.org/10.3201/eid0602.000215. |
Chlamydia pneumoniae Infection in a Breeding Colony of African Clawed Frogs (Xenopus tropicalis)
More than 90% of a breeding colony of clawed frogs (Xenopus tropicalis) imported to the United States from western Africa died in an epizootic of chlamydiosis. Chlamydial inclusions were observed by light and electron microscopy in the liver of an infected frog. Chlamydia pneumoniae was isolated in cell cultures from four frogs. A cutaneous infection by a chytridiomycete fungus observed in two frogs could have been a cofactor in the die-off.
EID | Reed KD, Ruth GR, Meyer JA, Shukla SK. Chlamydia pneumoniae Infection in a Breeding Colony of African Clawed Frogs (Xenopus tropicalis). Emerg Infect Dis. 2000;6(2):196-199. https://doi.org/10.3201/eid0602.000216 |
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AMA | Reed KD, Ruth GR, Meyer JA, et al. Chlamydia pneumoniae Infection in a Breeding Colony of African Clawed Frogs (Xenopus tropicalis). Emerging Infectious Diseases. 2000;6(2):196-199. doi:10.3201/eid0602.000216. |
APA | Reed, K. D., Ruth, G. R., Meyer, J. A., & Shukla, S. K. (2000). Chlamydia pneumoniae Infection in a Breeding Colony of African Clawed Frogs (Xenopus tropicalis). Emerging Infectious Diseases, 6(2), 196-199. https://doi.org/10.3201/eid0602.000216. |
The Impact of Health Communication and Enhanced Laboratory-Based Surveillance on Detection of Cyclosporiasis Outbreaks in California
We investigated the timing of diagnosis, influence of media information on testing for Cyclospora, and the method used to identify cases during eight cyclosporiasis outbreaks in California in spring of 1997. We found that Internet information, media reports, and enhanced laboratory surveillance improved detection of these outbreaks.
EID | Mohle-Boetani JC, Werner SB, Waterman SH, Vugia DJ. The Impact of Health Communication and Enhanced Laboratory-Based Surveillance on Detection of Cyclosporiasis Outbreaks in California. Emerg Infect Dis. 2000;6(2):200-203. https://doi.org/10.3201/eid0602.000217 |
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AMA | Mohle-Boetani JC, Werner SB, Waterman SH, et al. The Impact of Health Communication and Enhanced Laboratory-Based Surveillance on Detection of Cyclosporiasis Outbreaks in California. Emerging Infectious Diseases. 2000;6(2):200-203. doi:10.3201/eid0602.000217. |
APA | Mohle-Boetani, J. C., Werner, S. B., Waterman, S. H., & Vugia, D. J. (2000). The Impact of Health Communication and Enhanced Laboratory-Based Surveillance on Detection of Cyclosporiasis Outbreaks in California. Emerging Infectious Diseases, 6(2), 200-203. https://doi.org/10.3201/eid0602.000217. |
Norwalk-Like Viral Gastroenteritis Outbreak in U.S. Army Trainees
An outbreak of acute gastroenteritis hospitalized 99 (12%) of 835 U.S. Army trainees at Fort Bliss, El Paso, Texas, rom August 27 to September 1, 1998. Reverse transcriptase polymerase chain reaction tests for Norwalk-like virus were positive for genogroup 2. Gastroenteritis was associated with one post dining facility and with soft drinks.
EID | Arness MK, Feighner BH, Canham ML, Taylor DN, Monroe SS, Cieslak TJ, et al. Norwalk-Like Viral Gastroenteritis Outbreak in U.S. Army Trainees. Emerg Infect Dis. 2000;6(2):204-207. https://doi.org/10.3201/eid0602.009918 |
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AMA | Arness MK, Feighner BH, Canham ML, et al. Norwalk-Like Viral Gastroenteritis Outbreak in U.S. Army Trainees. Emerging Infectious Diseases. 2000;6(2):204-207. doi:10.3201/eid0602.009918. |
APA | Arness, M. K., Feighner, B. H., Canham, M. L., Taylor, D. N., Monroe, S. S., Cieslak, T. J....Skillman, D. R. (2000). Norwalk-Like Viral Gastroenteritis Outbreak in U.S. Army Trainees. Emerging Infectious Diseases, 6(2), 204-207. https://doi.org/10.3201/eid0602.009918. |
Letters
Preventing Zoonotic Diseases in Immunocompromised Persons: The Role of Physicians and Veterinarians
EID | Nowotny N, Deutz A. Preventing Zoonotic Diseases in Immunocompromised Persons: The Role of Physicians and Veterinarians. Emerg Infect Dis. 2000;6(2):208. https://doi.org/10.3201/eid0602.000219 |
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AMA | Nowotny N, Deutz A. Preventing Zoonotic Diseases in Immunocompromised Persons: The Role of Physicians and Veterinarians. Emerging Infectious Diseases. 2000;6(2):208. doi:10.3201/eid0602.000219. |
APA | Nowotny, N., & Deutz, A. (2000). Preventing Zoonotic Diseases in Immunocompromised Persons: The Role of Physicians and Veterinarians. Emerging Infectious Diseases, 6(2), 208. https://doi.org/10.3201/eid0602.000219. |
Reply to Drs. Nowotny and Deutz
EID | Olsen CW, Barton LL. Reply to Drs. Nowotny and Deutz. Emerg Infect Dis. 2000;6(2):209. https://doi.org/10.3201/eid0602.000220 |
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AMA | Olsen CW, Barton LL. Reply to Drs. Nowotny and Deutz. Emerging Infectious Diseases. 2000;6(2):209. doi:10.3201/eid0602.000220. |
APA | Olsen, C. W., & Barton, L. L. (2000). Reply to Drs. Nowotny and Deutz. Emerging Infectious Diseases, 6(2), 209. https://doi.org/10.3201/eid0602.000220. |
Books and Media
International Law and Infectious Diseases
EID | Patterson D. International Law and Infectious Diseases. Emerg Infect Dis. 2000;6(2):210. https://doi.org/10.3201/eid0602.000221 |
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AMA | Patterson D. International Law and Infectious Diseases. Emerging Infectious Diseases. 2000;6(2):210. doi:10.3201/eid0602.000221. |
APA | Patterson, D. (2000). International Law and Infectious Diseases. Emerging Infectious Diseases, 6(2), 210. https://doi.org/10.3201/eid0602.000221. |
Oxford Handbook of Tropical Medicine
EID | Beharry R, Keystone JS. Oxford Handbook of Tropical Medicine. Emerg Infect Dis. 2000;6(2):211-212. https://doi.org/10.3201/eid0602.000222 |
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AMA | Beharry R, Keystone JS. Oxford Handbook of Tropical Medicine. Emerging Infectious Diseases. 2000;6(2):211-212. doi:10.3201/eid0602.000222. |
APA | Beharry, R., & Keystone, J. S. (2000). Oxford Handbook of Tropical Medicine. Emerging Infectious Diseases, 6(2), 211-212. https://doi.org/10.3201/eid0602.000222. |
Conference Summaries
Institute of Medicine's Forum on Emerging Infections: Workshop on Managed-Care Systems and Emerging Infections
EID | Davis JR, Lederberg J. Institute of Medicine's Forum on Emerging Infections: Workshop on Managed-Care Systems and Emerging Infections. Emerg Infect Dis. 2000;6(2):213-214. https://doi.org/10.3201/eid0602.000223 |
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AMA | Davis JR, Lederberg J. Institute of Medicine's Forum on Emerging Infections: Workshop on Managed-Care Systems and Emerging Infections. Emerging Infectious Diseases. 2000;6(2):213-214. doi:10.3201/eid0602.000223. |
APA | Davis, J. R., & Lederberg, J. (2000). Institute of Medicine's Forum on Emerging Infections: Workshop on Managed-Care Systems and Emerging Infections. Emerging Infectious Diseases, 6(2), 213-214. https://doi.org/10.3201/eid0602.000223. |
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Owl on a Tree Trunk and Two Robins