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2.
BMC Infect Dis ; 15: 474, 2015 Oct 29.
Article in English | MEDLINE | ID: mdl-26511098

ABSTRACT

BACKGROUND: Hepatitis E virus (HEV) is the most recently discovered of the hepatotropic viruses, and is considered an emerging pathogen in developed countries with the possibility of fulminant hepatitis in immunocompromised patients. Especially in the latter elevated transaminases should be taken as a clue to consider HEV infection, as it can be treated by discontinuation of immunosuppression and/or ribavirin therapy. To our best knowledge, this is a unique case of autochthonous HEV infection with coincident reactivation of Epstein-Barr virus (EBV) infection in an immunosuppressed patient with rheumatoid arthritis (RA). CASE PRESENTATION: A 68-year-old Swiss woman with RA developed hepatitis initially diagnosed as methotrexate-induced liver injury, but later diagnosed as autochthonous HEV infection accompanied by reactivation of her latent EBV infection. She showed confounding serological results pointing to three hepatotropic viruses (HEV, Hepatitis B virus (HBV) and EBV) that could be resolved by detection of HEV and EBV viraemia. The patient recovered by temporary discontinuation of immunosuppressive therapy. CONCLUSIONS: In immunosuppressed patients with RA and signs of liver injury, HEV infection should be considered, as infection can be treated by discontinuation of immunosuppression. Although anti-HEV-IgM antibody assays can be used as first line virological tools, nucleic acid amplification tests (NAAT) for detection of HEV RNA are recommended--as in our case--if confounding serological results from other hepatotropic viruses are obtained. After discontinuation of immunosuppressive therapy, our patient recovered from both HEV infection and reactivation of latent EBV infection without sequelae.


Subject(s)
Arthritis, Rheumatoid/virology , Epstein-Barr Virus Infections/diagnosis , Hepatitis E/virology , Aged , Arthritis, Rheumatoid/immunology , Coinfection , Epstein-Barr Virus Infections/drug therapy , Female , Hepatitis Antibodies/blood , Hepatitis B virus/immunology , Hepatitis B virus/pathogenicity , Hepatitis E/drug therapy , Herpesvirus 4, Human/immunology , Herpesvirus 4, Human/pathogenicity , Humans , Immunocompromised Host , Immunosuppressive Agents/therapeutic use , Ribavirin/therapeutic use
3.
BMC Infect Dis ; 12: 242, 2012 Oct 04.
Article in English | MEDLINE | ID: mdl-23035948

ABSTRACT

BACKGROUND: Burkholderia pseudomallei, the etiologic agent of melioidosis, is endemic to tropic regions, mainly in Southeast Asia and northern Australia. Melioidosis occurs only sporadically in travellers returning from disease-endemic areas. Severe clinical disease is seen mostly in patients with alteration of immune status. In particular, pericardial effusion occurs in 1-3% of patients with melioidosis, confined to endemic regions. To our best knowledge, this is the first reported case of melioidosis in a traveller complicated by a hemodynamically significant pericardial effusion without predisposing disease. CASE PRESENTATION: A 44-year-old Caucasian man developed pneumonia, with bilateral pleural effusions and complicated by a hemodynamically significant pericardial effusion, soon after his return from Thailand to Switzerland. Cultures from different specimens including blood cultures turned out negative. Diagnosis was only accomplished by isolation of Burkholderia pseudomallei from the pericardial aspirate, thus finally enabling the adequate antibiotic treatment. CONCLUSIONS: Melioidosis is a great mimicker and physicians in non-endemic countries should be aware of its varied manifestations. In particular, melioidosis should be considered in differential diagnosis of pericardial effusion in travellers , even without risk factors predisposing to severe disease.


Subject(s)
Burkholderia pseudomallei/isolation & purification , Melioidosis/complications , Melioidosis/diagnosis , Pericardial Effusion/diagnosis , Pericardial Effusion/etiology , Adult , Humans , Male , Melioidosis/pathology , Pericardial Effusion/pathology , Switzerland , Thailand , Travel
4.
BMC Infect Dis ; 12: 88, 2012 Apr 12.
Article in English | MEDLINE | ID: mdl-22497961

ABSTRACT

BACKGROUND: Serologic testing algorithms for recent HIV seroconversion (STARHS) provide important information for HIV surveillance. We have previously demonstrated that a patient's antibody reaction pattern in a confirmatory line immunoassay (INNO-LIA™ HIV I/II Score) provides information on the duration of infection, which is unaffected by clinical, immunological and viral variables. In this report we have set out to determine the diagnostic performance of Inno-Lia algorithms for identifying incident infections in patients with known duration of infection and evaluated the algorithms in annual cohorts of HIV notifications. METHODS: Diagnostic sensitivity was determined in 527 treatment-naive patients infected for up to 12 months. Specificity was determined in 740 patients infected for longer than 12 months. Plasma was tested by Inno-Lia and classified as either incident (< = 12 m) or older infection by 26 different algorithms. Incident infection rates (IIR) were calculated based on diagnostic sensitivity and specificity of each algorithm and the rule that the total of incident results is the sum of true-incident and false-incident results, which can be calculated by means of the pre-determined sensitivity and specificity. RESULTS: The 10 best algorithms had a mean raw sensitivity of 59.4% and a mean specificity of 95.1%. Adjustment for overrepresentation of patients in the first quarter year of infection further reduced the sensitivity. In the preferred model, the mean adjusted sensitivity was 37.4%. Application of the 10 best algorithms to four annual cohorts of HIV-1 notifications totalling 2'595 patients yielded a mean IIR of 0.35 in 2005/6 (baseline) and of 0.45, 0.42 and 0.35 in 2008, 2009 and 2010, respectively. The increase between baseline and 2008 and the ensuing decreases were highly significant. Other adjustment models yielded different absolute IIR, although the relative changes between the cohorts were identical for all models. CONCLUSIONS: The method can be used for comparing IIR in annual cohorts of HIV notifications. The use of several different algorithms in combination, each with its own sensitivity and specificity to detect incident infection, is advisable as this reduces the impact of individual imperfections stemming primarily from relatively low sensitivities and sampling bias.


Subject(s)
Clinical Laboratory Techniques/methods , HIV Antibodies/blood , HIV Infections/diagnosis , HIV-1/isolation & purification , Virology/methods , Adult , Algorithms , Female , HIV Infections/virology , HIV-1/immunology , Humans , Immunoassay/methods , Male , Middle Aged , Plasma/immunology , Sensitivity and Specificity
5.
J Travel Med ; 18(3): 183-90, 2011.
Article in English | MEDLINE | ID: mdl-21539658

ABSTRACT

BACKGROUND: Dengue viruses (DENV) are the most widespread arthropod-borne viruses, which have shown an unexpected geographic expansion, as well as an increase in number and severity of outbreaks in the last decades. Although the emergence of dengue is considered to be due to a number of complex factors, epidemiological studies have shown that some strains of dengue might be associated with increased severity and higher transmission rates than others. In this context, surveillance and identification of the appearance or introduction of more virulent strains, along with fluctuation of DENV among endemic areas are now considered essential public health activities. METHODS: Samples from travelers returning from the tropics with acute dengue infections were analyzed to obtain up-dated information on circulating dengue strains. A short nucleotide fragment located in the carboxyl terminus of the dengue E gene was used for the characterization of DENV strains and the identification of their sero- and genotype. RESULTS: One hundred eighty-six new dengue strains have been classified into 12 distinct genotype groups within the four dengue serotypes. The identification of the emergence of different sero- and genotypes, the appearance of new clades correlating with outbreaks, and the identification of a dengue-4 genotype not previously reported have been achieved. Interestingly, African strains characterized in this study have provided valuable data on dengue circulation on the continent. CONCLUSIONS: This work demonstrates the convenience of routine application of molecular epidemiology analyses in dengue diagnosis laboratories. The use of molecular epidemiology tools on the analysis of imported dengue infections strengthens data acquisition on dengue strain movements correlating with epidemiological changes. The importance of surveillance of imported diseases contributing data for the epidemiological knowledge of infectious diseases in endemic areas has been once more demonstrated.


Subject(s)
Dengue Virus/genetics , Dengue/epidemiology , Dengue/virology , Africa , Base Sequence , Dengue/blood , Dengue Virus/classification , Dengue Virus/isolation & purification , Europe/epidemiology , Genotype , Humans , RNA, Viral , Reverse Transcriptase Polymerase Chain Reaction , Travel
6.
Emerg Infect Dis ; 15(11): 1799-801, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19891868

ABSTRACT

After returning from Thailand, a 35-year-old man from Switzerland was hospitalized with an abscess of the head. Material cultured from the abscess and adjacent bone grew a gram-negative rod, which was misidentified by an automated microbiology system as Burkholderia cepacia. The organism was eventually identified by molecular methods as B. pseudomallei.


Subject(s)
Burkholderia pseudomallei , Communicable Diseases, Emerging/diagnosis , Melioidosis/diagnosis , Abscess/microbiology , Adult , Automation , Bacteriological Techniques , Burkholderia Infections/diagnosis , Burkholderia Infections/microbiology , Burkholderia cepacia/genetics , Burkholderia cepacia/isolation & purification , Burkholderia pseudomallei/genetics , Burkholderia pseudomallei/isolation & purification , Communicable Diseases, Emerging/microbiology , Diagnostic Errors , Genes, Bacterial , Humans , Male , Melioidosis/microbiology , Switzerland , Thailand/ethnology , Travel
7.
PLoS Med ; 4(12): e343, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18052604

ABSTRACT

BACKGROUND: Knowledge of the number of recent HIV infections is important for epidemiologic surveillance. Over the past decade approaches have been developed to estimate this number by testing HIV-seropositive specimens with assays that discriminate the lower concentration and avidity of HIV antibodies in early infection. We have investigated whether this "recency" information can also be gained from an HIV confirmatory assay. METHODS AND FINDINGS: The ability of a line immunoassay (INNO-LIA HIV I/II Score, Innogenetics) to distinguish recent from older HIV-1 infection was evaluated in comparison with the Calypte HIV-1 BED Incidence enzyme immunoassay (BED-EIA). Both tests were conducted prospectively in all HIV infections newly diagnosed in Switzerland from July 2005 to June 2006. Clinical and laboratory information indicative of recent or older infection was obtained from physicians at the time of HIV diagnosis and used as the reference standard. BED-EIA and various recency algorithms utilizing the antibody reaction to INNO-LIA's five HIV-1 antigen bands were evaluated by logistic regression analysis. A total of 765 HIV-1 infections, 748 (97.8%) with complete test results, were newly diagnosed during the study. A negative or indeterminate HIV antibody assay at diagnosis, symptoms of primary HIV infection, or a negative HIV test during the past 12 mo classified 195 infections (26.1%) as recent (< or = 12 mo). Symptoms of CDC stages B or C classified 161 infections as older (21.5%), and 392 patients with no symptoms remained unclassified. BED-EIA ruled 65% of the 195 recent infections as recent and 80% of the 161 older infections as older. Two INNO-LIA algorithms showed 50% and 40% sensitivity combined with 95% and 99% specificity, respectively. Estimation of recent infection in the entire study population, based on actual results of the three tests and adjusted for a test's sensitivity and specificity, yielded 37% for BED-EIA compared to 35% and 33% for the two INNO-LIA algorithms. Window-based estimation with BED-EIA yielded 41% (95% confidence interval 36%-46%). CONCLUSIONS: Recency information can be extracted from INNO-LIA-based confirmatory testing at no additional costs. This method should improve epidemiologic surveillance in countries that routinely use INNO-LIA for HIV confirmation.


Subject(s)
AIDS Serodiagnosis/methods , HIV Antibodies/blood , HIV Infections/diagnosis , HIV Seropositivity/diagnosis , HIV-1/immunology , HIV-2/immunology , Immunoenzyme Techniques , Mass Screening/methods , Algorithms , Antibody Affinity , Antigen-Antibody Reactions , Blotting, Western , Disease Progression , Female , HIV Infections/epidemiology , HIV Infections/immunology , HIV Infections/virology , HIV Seropositivity/epidemiology , HIV Seropositivity/immunology , HIV Seropositivity/virology , HIV Seroprevalence , Humans , Male , Predictive Value of Tests , Prospective Studies , Research Design , Sensitivity and Specificity , Switzerland/epidemiology
8.
Swiss Med Wkly ; 137(1-2): 21-6, 2007 Jan 13.
Article in English | MEDLINE | ID: mdl-17299664

ABSTRACT

BACKGROUND AND OBJECTIVES: In 2002 the first endemic hantavirus infection in Switzerland was detected only by chance following a broad spectrum of diagnostics. This raised the question, whether Hantavirus infection should be included in the differential diagnosis of febrile illness of patients in Switzerland. In order to estimate the frequency of hantavirus infections in Switzerland, this survey on hantaviral seroprevalence was conducted in the Canton St. Gallen. METHODS: A total of 1693 sera from farmers, forestry workers, and young soldiers as well as blood donors, as a cross-section of the average adult population of the Canton St. Gallen, were screened for hantavirus-specific antibodies by a microsphere-based assay. All volunteers with positive screening results obtained a questionnaire for assessment of details of previous rodent encounter and illnesses compatible with hantavirus infection. RESULTS: This first survey on hantavirus-specific IgG in populations of eastern Switzerland revealed low seroprevalence-rates not significantly different among populations with higher risk for hantavirus infection (0.0%-1.9%) and the average adult population (0.5%). CONCLUSIONS: As hantavirus infections among different populations are rare, and no evidence for hantaviral nephropathy could be found, serological investigation of suspected endemic hantavirus infection in eastern Switzerland should be confined to patients with acute nephropathy and/or a history of recent rodent encounter.


Subject(s)
Hantavirus Infections/epidemiology , Orthohantavirus/isolation & purification , Adult , Cross-Sectional Studies , Humans , Immunoassay , Microspheres , Middle Aged , Occupations , Seroepidemiologic Studies , Switzerland/epidemiology
9.
J Clin Virol ; 38(2): 172-5, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17204453

ABSTRACT

In Switzerland, reports of tick-borne encephalitis virus (TBEV) infections to the Federal Office of Public Health have increased by 100% in 2005 compared to the annual mean from 1999 to 2004. This might be partly due to unspecificity in serological testing. In order to make diagnostics more specific and to improve patient management, we recommend to consider the first phase of the biphasic course of TBE, that can be suspected in a trias of tick bite, followed by a feverish illness associated with thrombocytopenia and/or leucocytopenia. In this phase, detection of viremia by TBEV-specific polymerase chain reaction assay (PCR) will enable diagnosis as well as prediction of the second phase of TBEV infection, developing in the majority of patients. Circumstances suggesting detection of TBE viremia are exemplified by two case reports.


Subject(s)
Encephalitis Viruses, Tick-Borne/immunology , Encephalitis, Tick-Borne/diagnosis , Child , Encephalitis Viruses, Tick-Borne/isolation & purification , Encephalitis, Tick-Borne/immunology , Encephalitis, Tick-Borne/virology , Humans , Male , Middle Aged
10.
Swiss Med Wkly ; 134(47-48): 700-4, 2004 Nov 27.
Article in English | MEDLINE | ID: mdl-15616903

ABSTRACT

BACKGROUND AND OBJECTIVES: The optimal strategy for the diagnosis of herpes simplex virus (HSV) and varizella-zoster virus (VZV) disease of the central nervous system is the detection of viral DNA by polymerase chain reaction assay (PCR) in cerebrospinal fluid (CSF) and the examination of intrathecal production of specific antibodies. However, in acute neurological disease caused by either HSV or VZV, dual intrathecal synthesis of HSV-1, 2- as well as VZV-specific antibodies may be detectable and thus can hamper accurate aetiological diagnosis. This paper illustrates such equivocal findings in two case reports, investigates their frequency and discusses the possible reasons. METHODS: Consecutive CSF/serum pairs of two patients with central nervous system (CNS) disease were tested by HSV-1-, HSV-2-, and VZV-specific PCR and by different serological assays for detection of neurotropic viruses and bacteria. Additionally, the results of microbiological investigations of 1'155 CSF/serum samples were retrospectively analyzed for coincident intrathecal antibody synthesis against HSV-1, 2 and VZV. RESULTS: Although only HSV-1 and VZV-specific DNA was detectable in the CSF of two patients with encephalitis and chronic meningitis, respectively, increasing intrathecal antibody production against both virus species could be demonstrated. Retrospective analysis of 1155 CSF/serum pairs revealed 55 (4.8%) pairs with evidence for intrathecally produced antibodies against either HSV-1, 2 (30/55) or VZV (14/55). Eleven of these 55 (20%) pairs showed intrathecal antibody-production against both virus species. CONCLUSIONS: Patients with CNS infection with HSV and VZV can be diagnosed by detecting intrathecally produced virus-specific antibodies, in addition to virus-specific PCR. However, in an appreciable proportion of patients a correct diagnosis is hampered by coincidentally detected antibodies in CSF against both virus species. Possible reasons for these equivocal findings are given.


Subject(s)
Antibodies, Viral/cerebrospinal fluid , Central Nervous System Viral Diseases/diagnosis , Herpes Simplex/diagnosis , Herpes Zoster/diagnosis , Herpesvirus 3, Human/immunology , Simplexvirus/immunology , Adult , Aged , Aged, 80 and over , Antibodies, Viral/blood , Antibody Specificity , Central Nervous System Viral Diseases/cerebrospinal fluid , Cerebrospinal Fluid/cytology , DNA, Viral/cerebrospinal fluid , Encephalitis, Viral/cerebrospinal fluid , Encephalitis, Viral/diagnosis , Female , Herpes Simplex/cerebrospinal fluid , Herpes Zoster/cerebrospinal fluid , Herpesvirus 3, Human/genetics , Humans , Immunoglobulin G/blood , Immunoglobulin G/cerebrospinal fluid , Male , Middle Aged , Polymerase Chain Reaction , Retrospective Studies , Simplexvirus/genetics
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