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1.
Clin Diagn Lab Immunol ; 8(6): 1150-5, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11687456

ABSTRACT

An immunochromatographic test that incorporates recombinant antigens (Dengue Duo Rapid Strip Test; PanBio, Brisbane, Australia) has recently become commercially available. This assay is performed in 15 min and detects both immunoglobulin M (IgM) and IgG in a capture format. The four recombinant proteins used represent the N-terminal 80% of the viral envelope glycoproteins of dengue viruses 1, 2, 3, and 4, respectively. The sensitivity and specificity of the recombinant-antigen-based assay were 90 and 86%, respectively. The similar diagnostic performance of these antigens to that of enzyme-linked immunosorbent assays using whole dengue virus suggests that they mimic whole dengue viruses in primary structure and epitope conformation. These results suggest that recombinant proteins can be used in diagnostic assays for dengue to overcome safety issues associated with the use of whole virus.


Subject(s)
Antigens, Viral/immunology , Chromatography/methods , Dengue Virus/isolation & purification , Dengue/diagnosis , Child , Cross Reactions , Dengue/immunology , Dengue Virus/immunology , Encephalitis, Japanese/immunology , Enzyme-Linked Immunosorbent Assay , Humans , Recombinant Proteins/immunology , Sensitivity and Specificity , Serologic Tests , Viral Envelope Proteins/immunology
2.
Clin Diagn Lab Immunol ; 7(5): 850-2, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10973469

ABSTRACT

A commercially available enzyme-linked immunosorbent assay (ELISA) (PanBio Dengue Screening ELISA) that utilized both immunoglobulin M (IgM) and IgG capture in the same microtiter well for the diagnosis of dengue infection was evaluated. Sensitivity in primary and secondary dengue was 95%, while specificity was 94%.


Subject(s)
Antibodies, Viral/blood , Dengue/diagnosis , Immunoglobulin G/blood , Immunoglobulin M/blood , Antibodies, Viral/immunology , Dengue/blood , Dengue/immunology , Enzyme-Linked Immunosorbent Assay/methods , Evaluation Studies as Topic , Humans , Immunoglobulin G/immunology , Immunoglobulin M/immunology , Reagent Kits, Diagnostic , Sensitivity and Specificity
3.
J Clin Microbiol ; 38(4): 1645-7, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10747159

ABSTRACT

A commercially available enzyme-linked immunosorbent assay (ELISA) for the diagnosis of Q fever (PanBio Coxiella burnetii immunoglobulin M [IgM] ELISA, QFM-200) was compared to the indirect fluorescent antibody test (IFAT) for C. burnetii IgM and the complement fixation test (CFT). The ELISA demonstrated 92% agreement with the reference method (IFAT), and gave a sensitivity of 99% (69 of 70 samples) and a specificity of 88% (106 of 121). Specificity can be increased with confirmation by IFAT. CFT was found to have a specificity of 90% (107 of 119), although it was lacking in sensitivity (73%; 51 of 70). No cross-reactivity was observed in the ELISA with serum samples from patients with mycoplasma (n = 6), chlamydia (n = 5), or legionella (n = 4) infections, although 2 of 5 patients with leptospirosis and 1 of 4 samples containing rheumatoid factor (RF) demonstrated positive results in the ELISA. Results indicate that the performance of the PanBio C. burnetii (Q fever) IgM ELISA (F = 187) is superior to that of CFT (F = 163), and consequently the ELISA should be a useful aid in the diagnosis of acute Q fever.


Subject(s)
Coxiella burnetii/immunology , Enzyme-Linked Immunosorbent Assay , Immunoglobulin M/blood , Q Fever/diagnosis , Antibodies, Bacterial/blood , Complement Fixation Tests , Fluorescent Antibody Technique, Indirect , Humans , Q Fever/microbiology , Sensitivity and Specificity
4.
J Clin Microbiol ; 38(4): 1670-1, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10747166

ABSTRACT

An immunochromatographic test for the rapid determination of immunoglobulin M (IgM) and IgG antibodies to Burkholderia pseudomallei was evaluated by using sera from bacteriologically confirmed melioidosis patients and high-risk and clinically suspected patients, along with disease control groups. The sensitivities were 100 and 93% for the IgG and IgM tests, respectively, while the specificity was 95% for both assays. The test was rapid and simple to perform, with results obtained in 10 min.


Subject(s)
Antibodies, Bacterial/blood , Burkholderia pseudomallei/immunology , Immunoassay/methods , Melioidosis/diagnosis , Chromatography/methods , Evaluation Studies as Topic , Fluorescent Antibody Technique, Indirect , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Melioidosis/microbiology , Reagent Kits, Diagnostic , Sensitivity and Specificity
5.
J Clin Virol ; 16(2): 135-44, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10720818

ABSTRACT

BACKGROUND: A number of commercial ELISA for dengue diagnosis have recently become available, though direct comparison between these assays have not been published. OBJECTIVES: The Venture Technologies Dengue IgM and IgG Dot Blot assays and the PanBio Dengue Duo IgM and IgG Capture ELISA were compared. STUDY DESIGN: Paired sera from patients with dengue (n=20) and Japanese encephalitis (JE, n=10), and single sera from patients with typhoid (n=10), leptospirosis (n=10) and scrub typhus (n=10) were assayed according to the manufacturer's instructions. RESULTS: The Dot Blot IgM ELISA showed higher sensitivity than the PanBio IgM ELISA (100 vs. 95%), while the PanBio IgM ELISA showed higher specificity in JE (100 vs. 20%) and non-flavivirus infections (100 vs. 97%). Defining elevation of either IgM or IgG as a positive result, the Dot Blot and ELISA tests both showed 100% sensitivity in dengue infection, while the PanBio test showed superior specificity in JE (70 vs. 0%) and non-flavivirus infections (100 vs. 67%). CONCLUSIONS: Both assays are useful aids to the serological diagnosis of dengue infection. The clinical setting, user preference and local conditions will be important in determining which test is more appropriate.


Subject(s)
Antibodies, Viral/immunology , Dengue/diagnosis , Enzyme-Linked Immunosorbent Assay/methods , Immunoblotting/methods , Antibodies, Viral/blood , Child , Dengue/blood , Dengue/immunology , Humans , Immunoglobulin G/blood , Immunoglobulin G/immunology , Immunoglobulin M/blood , Immunoglobulin M/immunology , Sensitivity and Specificity , Serologic Tests/methods
6.
J Clin Microbiol ; 37(11): 3738-41, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10523589

ABSTRACT

A new commercial enzyme-linked immunosorbent assay (ELISA) for the diagnosis of Japanese encephalitis virus infections showed a sensitivity of 88% with sera and 81% with cerebrospinal fluid and a specificity of 97% with sera from patients with primary and secondary dengue virus infections. Specificity was 100% when samples from nonflavivirus infections were tested.


Subject(s)
Encephalitis, Japanese/diagnosis , Enzyme-Linked Immunosorbent Assay/methods , Antibodies, Viral/blood , Antibodies, Viral/cerebrospinal fluid , Dengue/diagnosis , Dengue/immunology , Encephalitis Virus, Japanese/immunology , Encephalitis, Japanese/immunology , Enzyme-Linked Immunosorbent Assay/statistics & numerical data , Evaluation Studies as Topic , Humans , Immunoglobulin M/blood , Immunoglobulin M/cerebrospinal fluid , Sensitivity and Specificity
7.
Clin Diagn Lab Immunol ; 6(5): 705-12, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10473522

ABSTRACT

The performances of the MRL dengue fever virus immunoglobulin M (IgM) capture enzyme-linked immunosorbent assay (ELISA) and the PanBio Dengue Duo IgM capture and IgG capture ELISA were compared. Eighty sera from patients with dengue virus infections, 24 sera from patients with Japanese encephalitis (JE), and 78 sera from patients with nonflavivirus infections, such as malaria, typhoid, leptospirosis, and scrub typhus, were used. The MRL test showed superior sensitivity for dengue virus infections (94 versus 89%), while the PanBio test showed superior specificity for JE (79 versus 25%) and other infections (100 versus 91%). The PanBio ELISA showed better overall performance, as assessed by the sum of sensitivity and specificity (F value). When dengue virus and nonflavivirus infections were compared, F values of 189 and 185 were obtained for the PanBio and MRL tests, respectively, while when dengue virus infections and JE were compared, F values of 168 and 119 were obtained. The results obtained with individual sera in the PanBio and MRL IgM ELISAs showed good correlation, but this analysis revealed that the cutoff value of the MRL test was set well below that of the PanBio test. Comparing the sensitivity and specificity of the tests at different cutoff values (receiver-operator analysis) revealed that the MRL and PanBio IgM ELISAs performed similarly in distinguishing dengue virus from nonflavivirus infections, although the PanBio IgM ELISA showed significantly better distinction between dengue virus infections and JE. The implications of these findings for the laboratory diagnosis of dengue are discussed.


Subject(s)
Dengue Virus/isolation & purification , Dengue/diagnosis , Enzyme-Linked Immunosorbent Assay/methods , Immunoglobulin M/analysis , Adolescent , Adult , Alphavirus Infections/diagnosis , Alphavirus Infections/immunology , Antibodies, Viral/analysis , Antibody Specificity , Asia, Southeastern , Chikungunya virus/immunology , Child , Child, Preschool , Dengue/immunology , Dengue Virus/immunology , Diagnosis, Differential , Encephalitis Virus, Japanese/immunology , Encephalitis, Japanese/diagnosis , Encephalitis, Japanese/immunology , Female , Humans , Immunoglobulin G/analysis , Infant , Male , Sensitivity and Specificity
8.
J Clin Microbiol ; 36(12): 3737-9, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9817913

ABSTRACT

Saliva was collected prospectively from patients presenting with suspected dengue infection 4 to 8 days after the onset of symptoms and assayed by a commercial dengue immunoglobulin M (IgM) and IgG capture enzyme-linked immunosorbent assay (ELISA) (PanBio Dengue Duo ELISA). Laboratory diagnosis was based on virus isolation and on hemagglutination inhibition (HAI) assay and an in-house IgM and IgG capture ELISA. With a positive result defined as either salivary IgM or IgG levels above the cutoff value, an overall sensitivity of 92% was obtained for both primary- and secondary-dengue patients (22 of 24), while no patients with non-flavivirus infections (n = 11) and no healthy laboratory donors (n = 17) showed elevation of salivary antidengue antibody (100% specificity). Salivary IgG levels correlated well with serum HAI titer (r = 0.78), and salivary IgG levels could be used to distinguish between primary- and secondary-dengue virus infections.


Subject(s)
Antibodies, Viral/analysis , Dengue Virus/immunology , Dengue/diagnosis , Saliva/virology , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin A, Secretory/analysis , Immunoglobulin G/analysis , Immunoglobulin M/analysis , Prospective Studies , Sensitivity and Specificity
9.
Clin Diagn Lab Immunol ; 5(1): 7-10, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9455871

ABSTRACT

A commercially available capture enzyme-linked immunosorbent assay (ELISA) for the detection of specific immunoglobulin M (IgM) and IgG antibodies produced during dengue infection (PanBio Dengue Duo) was evaluated with paired serum specimens from 176 patients. Diagnosis was based on a hemagglutination inhibition (HAI) assay, with patients having either primary dengue (n = 90), secondary dengue (n = 58), or no dengue (n = 28) infection. The combined use of IgM and IgG (sensitivity, 99%; specificity, 96%) was superior to the use of IgM alone (sensitivity, 88%; specificity, 96%) or IgG alone (sensitivity, 85%; specificity, 96%). Furthermore, with the first serum sample of the pair of serum samples, the ELISA was able to diagnose significantly more cases of dengue than the HAI assay (55% versus 14%). The results of the IgG capture ELISA gave a significant correlation with those of the HAI assay (r = 0.91; P < 0.0001), and the IgG capture ELISA could be used to distinguish between primary and secondary infection. The best distinction was observed when an IgG cutoff ratio of 3.0 was used, with 88% of primary infections and 98% of secondary infections being correctly classified. This ELISA should prove to be useful in the clinical diagnosis of dengue infection.


Subject(s)
Antibodies, Anti-Idiotypic/blood , Dengue/blood , Enzyme-Linked Immunosorbent Assay/methods , Dengue/diagnosis , Dengue/immunology , Hemagglutination Inhibition Tests , Humans , Immunoglobulin G/immunology , Immunoglobulin M/immunology , Sensitivity and Specificity
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