Literature DB >> 30701339

Plasmonic gold chips for the diagnosis of Toxoplasma gondii, CMV, and rubella infections using saliva with serum detection precision.

Xiaoyang Li1, Christelle Pomares2, François Peyron3, Cynthia J Press4, Raymund Ramirez4, Gonfrier Geraldine5, Isabelle Cannavo5, Emmanuelle Chapey6, Pauline Levigne3, Martine Wallon3, Jose G Montoya7,8, Hongjie Dai9.   

Abstract

Sampling the blood compartment by an invasive procedure such as phlebotomy is the most common approach used for diagnostic purposes. However, phlebotomy has several drawbacks including pain, vasovagal reactions, and anxiety. Therefore, alternative approaches should be tested to minimize patient's discomfort. Saliva is a reasonable compartment; when obtained, it generates little or no anxiety. We setup a multiplexed serology assay for detection of Toxoplasma gondii IgG and IgM, rubella IgG, and CMV IgG, in serum, whole blood, and saliva using novel plasmonic gold (pGOLD) chips. pGOLD test results in serum, whole blood, and saliva were compared with commercial kits test results in serum. One hundred twenty serum/saliva sets (Lyon) and 28 serum/whole blood/saliva sets (Nice) from France were tested. In serum and whole blood, sensitivity and specificity of multiplex T. gondii, CMV, and rubella IgG were 100% in pGOLD when compared to commercial test results in serum. In saliva, sensitivity and specificity for T. gondii and rubella IgG were 100%, and for CMV IgG, sensitivity and specificity were 92.9% and 100%, respectively, when compared to commercial test results in serum. We were also able to detect T. gondii IgM in saliva with sensitivity and specificity of 100% and 95.4%, respectively, when compared to serum test results. Serological testing by multiplex pGOLD assay for T. gondii, rubella, and CMV in saliva is reliable and likely to be more acceptable for systematic screening of pregnant women, newborn, and immunocompromised patients.

Entities:  

Keywords:  Cytomegalovirus; Multiplexed serologies; Plasmonic gold chips; Rubella; Saliva; Toxoplasmosis

Mesh:

Substances:

Year:  2019        PMID: 30701339     DOI: 10.1007/s10096-019-03487-1

Source DB:  PubMed          Journal:  Eur J Clin Microbiol Infect Dis        ISSN: 0934-9723            Impact factor:   3.267


  25 in total

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Journal:  Nat Commun       Date:  2011-09-13       Impact factor: 14.919

5.  Cytomegalovirus infection in pregnancy: should all women be screened?

Authors:  Amanda Carlson; Errol R Norwitz; Robert J Stiller
Journal:  Rev Obstet Gynecol       Date:  2010

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Journal:  Clin Infect Dis       Date:  2012-03-29       Impact factor: 9.079

7.  Prenatal treatment for serious neurological sequelae of congenital toxoplasmosis: an observational prospective cohort study.

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Journal:  PLoS Med       Date:  2010-10-12       Impact factor: 11.069

8.  Risk factors for retinochoroiditis during the first 2 years of life in infants with treated congenital toxoplasmosis.

Authors:  François Kieffer; Martine Wallon; Patricia Garcia; Philippe Thulliez; François Peyron; Jacqueline Franck
Journal:  Pediatr Infect Dis J       Date:  2008-01       Impact factor: 2.129

9.  Congenital toxoplasma infection: monthly prenatal screening decreases transmission rate and improves clinical outcome at age 3 years.

Authors:  M Wallon; F Peyron; C Cornu; S Vinault; M Abrahamowicz; C Bonithon Kopp; C Binquet
Journal:  Clin Infect Dis       Date:  2013-01-29       Impact factor: 9.079

10.  Maternal serologic screening to prevent congenital toxoplasmosis: a decision-analytic economic model.

Authors:  Eileen Stillwaggon; Christopher S Carrier; Mari Sautter; Rima McLeod
Journal:  PLoS Negl Trop Dis       Date:  2011-09-27
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  4 in total

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