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  1. Article ; Online: Prospective comparison of (1,3)-beta-D-glucan detection using colorimetric and turbidimetric assays for diagnosing invasive fungal disease.

    Alanio, Alexandre / Gits-Muselli, Maud / Guigue, Nicolas / Denis, Blandine / Bergeron, Anne / Touratier, Sophie / Hamane, Samia / Bretagne, Stéphane

    Medical mycology

    2021  Volume 59, Issue 9, Page(s) 882–889

    Abstract: Serum (1→3)-β-D-glucan (BDG), an pan fungal antigen, is detected in some invasive fungal diseases (IFDs). We compared two commercial kits, the Fungitell assay (FA) (colorimetric) and the Wako assay (WA) (turbidimetric) over a 4-month period to ... ...

    Abstract Serum (1→3)-β-D-glucan (BDG), an pan fungal antigen, is detected in some invasive fungal diseases (IFDs). We compared two commercial kits, the Fungitell assay (FA) (colorimetric) and the Wako assay (WA) (turbidimetric) over a 4-month period to prospectively test 171 patients who mainly had hematological conditions (62%) and experienced episodes (n = 175) of suspected invasive fungal infection. Twenty-three episodes due to BDG-producing fungi were diagnosed (pneumocystosis, n = 12; invasive aspergillosis, n = 5; candidemia, n = 3; invasive fusariosis, n = 2; hepato-splenic candidiasis, n = 1).Both assays provided similar areas under the curves (AUC = 0.9). Using the optimized positivity thresholds (≥120 pg/ml for FA and ≥ 4 pg/ml for WA), the sensitivity and specificity were 81.8% (CI95: 61.5-92.7), 94.8% (90.1-97.3) for FA and 81.8% (61.5-92.7), 95.4% (90.9-97.8) for WA. Negative predictive value was 97.3% (93.3-99.0) for both tests. If the manufacturer's positivity threshold (≥11 pg/ml) was applied, the WA sensitivity decreased to 50%. Among 71 patients with bacterial infections, 21.1% were FA-positive and 5.6% were WA-positive (p < 10-2).The WA performed similarly as compared to the FA with an optimized cutoff value. The WA is a single sample test that is clinically relevant when a prompt therapeutic decision is required.
    Lay summary: Serum (1→3)-β-D-glucan testing is dominated by two kits including Fungitell colorimetric assay (FA) and the Wako turbidimetric assay (WA). We compared them prospectively and observed that they both perform similarly when selecting their optimal threshold (≥120 pg/ml for FA and ≥ 4 pg/ml for WA).
    MeSH term(s) Adult ; Colorimetry/methods ; Diagnostic Techniques and Procedures ; Female ; Humans ; Immunoturbidimetry/methods ; Invasive Fungal Infections/diagnosis ; Male ; Middle Aged ; Mycoses/diagnosis ; Prospective Studies ; Proteoglycans/blood ; Sensitivity and Specificity
    Chemical Substances Proteoglycans ; polysaccharide-K (3X48A86C8K)
    Language English
    Publishing date 2021-04-16
    Publishing country England
    Document type Comparative Study ; Journal Article
    ZDB-ID 1421796-x
    ISSN 1460-2709 ; 1369-3786
    ISSN (online) 1460-2709
    ISSN 1369-3786
    DOI 10.1093/mmy/myab016
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  2. Article ; Online: Retrospective study of toxoplasmosis prevalence in pregnant women in Benin and its relation with malaria.

    Dambrun, Magalie / Dechavanne, Célia / Guigue, Nicolas / Briand, Valérie / Candau, Tristan / Fievet, Nadine / Lohezic, Murielle / Manoharan, Saraniya / Sare, Nawal / Viwami, Firmine / Simon, François / Houzé, Sandrine / Migot-Nabias, Florence

    PloS one

    2022  Volume 17, Issue 1, Page(s) e0262018

    Abstract: Background: Globally distributed with variable prevalence depending on geography, toxoplasmosis is a zoonosis caused by an obligate intracellular protozoan parasite, Toxoplasma gondii. This disease is usually benign but poses a risk for ... ...

    Abstract Background: Globally distributed with variable prevalence depending on geography, toxoplasmosis is a zoonosis caused by an obligate intracellular protozoan parasite, Toxoplasma gondii. This disease is usually benign but poses a risk for immunocompromised people and for newborns of mothers with a primary infection during pregnancy because of the risk of congenital toxoplasmosis (CT). CT can cause severe damage to fetuses-newborns. To our knowledge, no study has been conducted in sub-Saharan Africa on toxoplasmosis seroprevalence, seroconversion and CT in a large longitudinal cohort and furthermore, no observation has been made of potential relationships with malaria.
    Methods: We performed a retrospective toxoplasmosis serological study using available samples from a large cohort of 1,037 pregnant women who were enrolled in a malaria follow-up during the 2008-2010 period in a rural area in Benin. We also used some existing data to investigate potential relationships between the maternal toxoplasmosis serological status and recorded malaria infections.
    Results: Toxoplasmosis seroprevalence, seroconversion and CT rates were 52.6%, 3.4% and 0.2%, respectively, reflecting the population situation of toxoplasmosis, without targeted medical intervention. The education level influences the toxoplasmosis serological status of women, with women with little or no formal education have greater immunity than others. Surprisingly, toxoplasmosis seropositive pregnant women tended to present lower malaria infection during pregnancy (number) or at delivery (presence) and to have lower IgG levels to Plasmodium falciparum Apical Membrane Antigen 1, compared to toxoplasmosis seronegative women.
    Conclusions: The high toxoplasmosis seroprevalence indicates that prevention against this parasite remains important to deploy and must be accessible and understandable to and for all individuals (educated and non-educated). A potential protective role against malaria conferred by a preexisting toxoplasmosis infection needs to be explored more precisely to examine the environmental, parasitic and/or immune aspects.
    MeSH term(s) Adolescent ; Adult ; Antibodies, Protozoan/blood ; Antibodies, Protozoan/immunology ; Benin/epidemiology ; Female ; Humans ; Infant, Newborn ; Malaria, Falciparum/blood ; Malaria, Falciparum/epidemiology ; Malaria, Falciparum/parasitology ; Plasmodium falciparum/isolation & purification ; Pregnancy ; Pregnancy Complications, Parasitic/epidemiology ; Pregnancy Complications, Parasitic/parasitology ; Pregnant Women ; Retrospective Studies ; Seroepidemiologic Studies ; Toxoplasma/isolation & purification ; Toxoplasmosis/blood ; Toxoplasmosis/epidemiology ; Toxoplasmosis/parasitology ; Young Adult
    Chemical Substances Antibodies, Protozoan
    Language English
    Publishing date 2022-01-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0262018
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  3. Article ; Online: Entamoeba histolytica DNA Detection in Serum from Patients with Suspected Amoebic Liver Abscess.

    Ghelfenstein-Ferreira, Théo / Gits-Muselli, Maud / Dellière, Sarah / Denis, Blandine / Guigue, Nicolas / Hamane, Samia / Alanio, Alexandre / Bretagne, Stéphane

    Journal of clinical microbiology

    2020  Volume 58, Issue 10

    Abstract: Amoebic liver abscess (ALA) is regularly seen in travelers or immigrants from tropical countries. The diagnosis relies on liver imaging that is not specific and on the detection of anti- ...

    Abstract Amoebic liver abscess (ALA) is regularly seen in travelers or immigrants from tropical countries. The diagnosis relies on liver imaging that is not specific and on the detection of anti-
    MeSH term(s) Antibodies, Protozoan ; Entamoeba histolytica/genetics ; Humans ; Liver Abscess, Amebic/diagnosis ; Retrospective Studies ; Serologic Tests
    Chemical Substances Antibodies, Protozoan
    Language English
    Publishing date 2020-09-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 390499-4
    ISSN 1098-660X ; 0095-1137
    ISSN (online) 1098-660X
    ISSN 0095-1137
    DOI 10.1128/JCM.01153-20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: False positive galactomannan test after ice-pop ingestion.

    Guigue, Nicolas / Menotti, Jean / Ribaud, Patricia

    The New England journal of medicine

    2013  Volume 369, Issue 1, Page(s) 97–98

    MeSH term(s) Adult ; False Positive Reactions ; Female ; Food Additives ; Food Analysis ; Food Contamination ; Graft vs Host Disease/blood ; Hematopoietic Stem Cell Transplantation ; Humans ; Mannans/analysis ; Mannans/blood
    Chemical Substances Food Additives ; Mannans ; galactomannan (11078-30-1)
    Language English
    Publishing date 2013-07-04
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMc1210430
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  5. Article ; Online: Time to and differential time to blood culture positivity for assessing catheter-related yeast fungaemia: A longitudinal, 7-year study in a single university hospital.

    Gits-Muselli, Maud / Villiers, Stéphane / Hamane, Samia / Berçot, Béatrice / Donay, Jean-Luc / Denis, Blandine / Guigue, Nicolas / Alanio, Alexandre / Bretagne, Stéphane

    Mycoses

    2019  Volume 63, Issue 1, Page(s) 95–103

    Abstract: Background: Time to positivity (TTP) and differential time to positivity (DTTP) between central and peripheral blood cultures are commonly used for bacteraemia to evaluate the likelihood of central venous catheter (CVC)-related bloodstream infection. ... ...

    Abstract Background: Time to positivity (TTP) and differential time to positivity (DTTP) between central and peripheral blood cultures are commonly used for bacteraemia to evaluate the likelihood of central venous catheter (CVC)-related bloodstream infection. Few studies have addressed these approaches to yeast fungaemia.
    Objectives: This study aimed to evaluate TTP and DTTP to assess CVC-related yeast fungaemia (CVC-RYF).
    Patients/methods: We retrospectively analysed the results from 105 adult patients with incident fungaemia, with CVC removed and cultured, collected from 2010 to 2017. The bottles were incubated in a BioMérieux BacT/ALERT 3D and kept for at least 5 days.
    Results: Of the 105 patients included, most were oncology patients (85.7%) and had of long-term CVC (79.6%); 32 (30.5%) had a culture-positive CVC (defined as CVC-RYF) with the same species as in blood culture, and 69.5% had culture-negative CVC (defined as non-CVC-RYF, NCVC-RYF). Candida albicans represented 46% of the episodes. The median TTP was statistically different between CVC-RYF and NCVC-RYF (16.8 hours interquartile range (IQR) [9.7-28.6] vs 29.4 hours [IQR 20.7-41.3]; P = .001). A TTP <10 hours had the best positive likelihood ratio (21.5) for CVC-RYF, although the sensitivity was only 28%. DTTP was available for 52 patients. A DTTP >5 hours had a sensitivity of 100% and a specificity of 71% for CVC-RYF.
    Conclusions: Since the median TTP was 17 hours and the most performing DTTP >5 hours, these delays are too long to take a decision in the same operational day. More rapid methods for detecting infected catheters should be tested to avoid unnecessary CVC withdrawal.
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Blood Culture ; Candida albicans/isolation & purification ; Candidemia/blood ; Catheter-Related Infections/microbiology ; Catheterization, Central Venous ; Female ; Hospitals, University ; Humans ; Longitudinal Studies ; Male ; Middle Aged ; Retrospective Studies ; Young Adult
    Language English
    Publishing date 2019-11-03
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 392487-7
    ISSN 1439-0507 ; 0933-7407
    ISSN (online) 1439-0507
    ISSN 0933-7407
    DOI 10.1111/myc.13024
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  6. Article ; Online: Variation in copy number of the 28S rDNA of Aspergillus fumigatus measured by droplet digital PCR and analog quantitative real-time PCR.

    Alanio, Alexandre / Sturny-Leclère, Aude / Benabou, Marion / Guigue, Nicolas / Bretagne, Stéphane

    Journal of microbiological methods

    2016  Volume 127, Page(s) 160–163

    Abstract: Droplet digital PCR (ddPCR) after DNA digestion yielded a 28S rDNA copy number of 61 to 86 copies/genome when testing 10 unrelated Aspergillus fumigatus isolates, higher than with quantitative PCR. Unfortunately, ddPCR after DNA digestion did not improve ...

    Abstract Droplet digital PCR (ddPCR) after DNA digestion yielded a 28S rDNA copy number of 61 to 86 copies/genome when testing 10 unrelated Aspergillus fumigatus isolates, higher than with quantitative PCR. Unfortunately, ddPCR after DNA digestion did not improve the sensitivity of our PCR assay when testing serum patients with invasive aspergillosis.
    MeSH term(s) Aspergillosis/diagnosis ; Aspergillosis/microbiology ; Aspergillus fumigatus/genetics ; DNA Copy Number Variations ; DNA, Ribosomal/genetics ; DNA, Ribosomal/isolation & purification ; Humans ; RNA, Ribosomal, 28S/genetics ; Real-Time Polymerase Chain Reaction/instrumentation ; Real-Time Polymerase Chain Reaction/methods ; Sensitivity and Specificity
    Chemical Substances DNA, Ribosomal ; RNA, Ribosomal, 28S
    Language English
    Publishing date 2016
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 604916-3
    ISSN 1872-8359 ; 0167-7012
    ISSN (online) 1872-8359
    ISSN 0167-7012
    DOI 10.1016/j.mimet.2016.06.015
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  7. Article: Corrigendum: Continuous Decline of

    Guigue, Nicolas / Léon, Lucie / Hamane, Samia / Gits-Muselli, Maud / Le Strat, Yann / Alanio, Alexandre / Bretagne, Stéphane

    Frontiers in microbiology

    2018  Volume 9, Page(s) 2814

    Abstract: This corrects the article DOI: 10.3389/fmicb.2018.02369.]. ...

    Abstract [This corrects the article DOI: 10.3389/fmicb.2018.02369.].
    Language English
    Publishing date 2018-11-27
    Publishing country Switzerland
    Document type Published Erratum
    ZDB-ID 2587354-4
    ISSN 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2018.02814
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  8. Article: Continuous Decline of

    Guigue, Nicolas / Léon, Lucie / Hamane, Samia / Gits-Muselli, Maud / Le Strat, Yann / Alanio, Alexandre / Bretagne, Stéphane

    Frontiers in microbiology

    2018  Volume 9, Page(s) 2369

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2018-10-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587354-4
    ISSN 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2018.02369
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  9. Article ; Online: Importance of operational factors in the reproducibility of Aspergillus galactomannan enzyme immune assay.

    Guigue, Nicolas / Lardeux, Samuel / Alanio, Alexandre / Hamane, Samia / Tabouret, Marc / Bretagne, Stéphane

    PloS one

    2015  Volume 10, Issue 4, Page(s) e0124044

    Abstract: Background: The Platelia Aspergillus Ag assay (Bio-Rad) is designed for detecting Aspergillus galactomannan (GM) and is widely used for diagnosing invasive aspergillosis but is hampered by variable occurrences of unreproducible positive results. ... ...

    Abstract Background: The Platelia Aspergillus Ag assay (Bio-Rad) is designed for detecting Aspergillus galactomannan (GM) and is widely used for diagnosing invasive aspergillosis but is hampered by variable occurrences of unreproducible positive results. Frequency and origin of these unreproducible results have not been formally studied.
    Methods: Different technicians simultaneously performed four tests on 550 consecutive sera from adult patients (Test#1-Test#2 for extraction#1 and Test#3-Test#4 for extraction#2). The samples were classified as confirmed negative [all tests with GM optical density index (GM-ODI) <0.5], confirmed positive (all tests with GM-ODI ≥0.5), extraction unreproducible positive (Test#1 and Test#2 ODIs ≥0.5, and Test#3 and Test#4 GM-ODIs <0.5, or conversely), and ELISA unreproducible positive (only one test with GM-ODI ≥0.5). The samples with positive and negative GM-ODIs within the assay coefficient of variation values were classified as non-conclusive. Four similar additional tests were performed after ≤72h storage at 4 °C and a new GM test after 8 months at -20 °C.
    Results: Five-hundred-twenty sera (94.5%) were confirmed negative, 15 (2.7%) confirmed positive, 4 (0.7%) extraction unreproducible positive, 6 (1.1%) ELISA unreproducible positive, and 5 (0.9%) non-conclusive. Upon retesting, the unreproducible positive results turned negative except for one which turned non-conclusive. The confirmed positive and non-conclusive had similar GM-ODIs (p>0.4) upon retesting after storage ≤72h at 4 °C (n = 20) or eight months at -20 °C (n = 17).
    Conclusions: Operational unreproducible positives represent 33% of the GM-positive results and a second sample evaluation appears mandatory to avoid useless investigations or treatments. When operational artifacts are excluded, GM remains stable at standard storage conditions.
    MeSH term(s) Adult ; Antigens, Fungal/blood ; Aspergillosis/diagnosis ; Aspergillosis/microbiology ; Aspergillus/chemistry ; Aspergillus/immunology ; Enzyme-Linked Immunosorbent Assay/methods ; False Positive Reactions ; Humans ; Mannans/blood ; Mannans/immunology ; Reproducibility of Results
    Chemical Substances Antigens, Fungal ; Mannans ; galactomannan (11078-30-1)
    Language English
    Publishing date 2015-04-10
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0124044
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  10. Article: Performance of the Liaison® XL Murex recHTLV-I/II Immunoassay in the Detection of HTLV-1/2 Antibodies in Serum.

    Gantner, Pierre / Velay, Aurelie / Guigue, Nicolas / Barth, Heidi / Wendling, Marie-Josee / Delaugerre, Constance / Fafi-Kremer, Samira

    Clinical laboratory

    2017  Volume 63, Issue 5, Page(s) 997–1001

    Abstract: Background: Human T-cell lymphotropic virus type 1 and 2 (HTLV-1/2) immunoassays are used for blood screen- ing from blood products, milk, and organ donors.: Methods: We assessed the performance of the DiaSorin Liaison® XL murex recHTLV-I/II ... ...

    Abstract Background: Human T-cell lymphotropic virus type 1 and 2 (HTLV-1/2) immunoassays are used for blood screen- ing from blood products, milk, and organ donors.
    Methods: We assessed the performance of the DiaSorin Liaison® XL murex recHTLV-I/II immunoassay relative to the Abbott Architect® rHTLV-I/II immunoassay and with the Innogenetics immunoblot as confirmation.
    Results: A panel of HTLV positive (n = 66) and negative (n = 30) sera was tested in both techniques within the same freeze/thaw cycle. The specificity and sensitivity of DiaSorin immunoassay were 100% and 78.8%, respectively. Abbott and DiaSorin immunoassays showed a correlation in chemiluminiscent signals to cutoff (S/CO) (Pearson r = 0.92). Half of the samples (34/66) from the seropositive panel were not confirmed by immunoblot (S/CO < 5 in both techniques).
    Conclusions: Our data confirmed that the DiaSorin Liaison® XL murex recHTLV-I/II immunoassay is an effective platform for HTLV screening. Due to false-positive reaction, especially for samples with low S/CO, each seropositive sample should be confirmed by immunoblot.
    MeSH term(s) Antibodies, Viral/analysis ; Blood Donors ; False Positive Reactions ; HTLV-I Infections/diagnosis ; Human T-lymphotropic virus 1 ; Human T-lymphotropic virus 2 ; Humans ; Immunoassay ; Immunologic Tests ; Sensitivity and Specificity ; Serum
    Chemical Substances Antibodies, Viral
    Language English
    Publishing date 2017-05-01
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1307629-2
    ISSN 1433-6510 ; 0941-2131
    ISSN 1433-6510 ; 0941-2131
    DOI 10.7754/Clin.Lab.2017.161026
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