Skip to main content
Erschienen in:

18.03.2021 | Original Article

Evaluation of the CARDS toxin and its fragment for the serodiagnosis of Mycoplasma pneumoniae infections

verfasst von: Guanhua Xue, Hanqing Zhao, Chao Yan, Shaoli Li, Jinghua Cui, Yanling Feng, Xianghui Xie, Jing Yuan

Erschienen in: European Journal of Clinical Microbiology & Infectious Diseases | Ausgabe 8/2021

Einloggen, um Zugang zu erhalten

Abstract

Mycoplasma pneumoniae (M. pneumoniae) is an important pathogen in community-acquired pneumonia. The community-acquired respiratory distress syndrome (CARDS) toxin is the only known virulence factor of M. pneumoniae. It is worth exploring whether this toxin can be used as a candidate antigen for the serodiagnosis of M. pneumoniae. In this study, the full-length, N-terminal, and C-terminal regions of the CARDS toxin were expressed and purified, and serological reactions were evaluated using ELISA. A total of 184 serum samples were collected and tested using a commercialized test kit. Eighty-seven samples were positive, and 97 samples were negative for infection. The purified recombinant proteins were used as antigens to test the serum via indirect ELISA. The sensitivity of the CARDS toxin, the N-terminal region, and the C-terminal region were 90.8%, 90.8%, and 92.0%, respectively. The specificity of the CARDS toxin, the N-terminal region, and the C-terminal region were 85.6%, 73.2%, and 93.8%, respectively. All three CARDS toxin proteins exhibited good reactivity, of which the C-terminal region had a good discrimination ability in human sera. This may have a potential diagnostic value for M. pneumoniae infections.
Literatur
1.
Zurück zum Zitat Waites KB, Xiao L, Liu Y, Balish MF, Atkinson TP (2017) Mycoplasma pneumoniae from the respiratory tract and beyond. Clin Microbiol Rev. 30(3):747–809CrossRef Waites KB, Xiao L, Liu Y, Balish MF, Atkinson TP (2017) Mycoplasma pneumoniae from the respiratory tract and beyond. Clin Microbiol Rev. 30(3):747–809CrossRef
2.
Zurück zum Zitat Chaudhry R, Ghosh A, Chandolia A (2016) Pathogenesis of Mycoplasma pneumoniae: an update. Indian J Med Microbiol. 34(1):7–16CrossRef Chaudhry R, Ghosh A, Chandolia A (2016) Pathogenesis of Mycoplasma pneumoniae: an update. Indian J Med Microbiol. 34(1):7–16CrossRef
3.
Zurück zum Zitat Søndergaard MJ, Friis MB, Hansen DS, Jørgensen IM (2018) Clinical manifestations in infants and children with Mycoplasma pneumoniae infection. PLoS One. 13(4):e0195288CrossRef Søndergaard MJ, Friis MB, Hansen DS, Jørgensen IM (2018) Clinical manifestations in infants and children with Mycoplasma pneumoniae infection. PLoS One. 13(4):e0195288CrossRef
4.
Zurück zum Zitat Xue G, Li M, Wang N, Zhao J, Wang B, Ren Z, Yan C, Wu C, Liu Y, Sun H, Xu M, Sun H (2018) Comparison of the molecular characteristics of Mycoplasma pneumoniae from children across different regions of China. PLoS One. 13(8):e0198557CrossRef Xue G, Li M, Wang N, Zhao J, Wang B, Ren Z, Yan C, Wu C, Liu Y, Sun H, Xu M, Sun H (2018) Comparison of the molecular characteristics of Mycoplasma pneumoniae from children across different regions of China. PLoS One. 13(8):e0198557CrossRef
5.
Zurück zum Zitat Daxboeck F, Krause R, Wenisch C (2003) Laboratory diagnosis of Mycoplasma pneumoniae infection. Clin Microbiol Infect. 9(4):263–273CrossRef Daxboeck F, Krause R, Wenisch C (2003) Laboratory diagnosis of Mycoplasma pneumoniae infection. Clin Microbiol Infect. 9(4):263–273CrossRef
6.
Zurück zum Zitat Zhao F, Guan X, Li J, Liu L, Gong J, He L, Meng F, Zhang J (2020) Real-time PCR and quantitative culture for Mycoplasma pneumoniae load in pharyngeal swabs from children at preliminary diagnosis and discharge. Biomed Res Int 3:9814916 Zhao F, Guan X, Li J, Liu L, Gong J, He L, Meng F, Zhang J (2020) Real-time PCR and quantitative culture for Mycoplasma pneumoniae load in pharyngeal swabs from children at preliminary diagnosis and discharge. Biomed Res Int 3:9814916
7.
Zurück zum Zitat Busson L, Van den Wijngaert S, Dahma H, Decolvenaer M, Di Cesare L, Martin A, Vasseur L, Vandenberg O (2013) Evaluation of 10 serological assays for diagnosing Mycoplasma pneumoniae infection. Diagn Microbiol Infect Dis. 76(2):133–137CrossRef Busson L, Van den Wijngaert S, Dahma H, Decolvenaer M, Di Cesare L, Martin A, Vasseur L, Vandenberg O (2013) Evaluation of 10 serological assays for diagnosing Mycoplasma pneumoniae infection. Diagn Microbiol Infect Dis. 76(2):133–137CrossRef
8.
Zurück zum Zitat Montagnani F, De Paolis F, Beghetto E, Gargano N (2010) Use of recombinant chimeric antigens for the serodiagnosis of Mycoplasma pneumoniae infection. Eur J Clin Microbiol Infect Dis. 29(11):1377–1386CrossRef Montagnani F, De Paolis F, Beghetto E, Gargano N (2010) Use of recombinant chimeric antigens for the serodiagnosis of Mycoplasma pneumoniae infection. Eur J Clin Microbiol Infect Dis. 29(11):1377–1386CrossRef
9.
Zurück zum Zitat Tabassum I, Chaudhry R, Chourasia BK, Malhotra P (2010) Identification of an N-terminal 27 kDa fragment of Mycoplasma pneumoniae P116 protein as specific immunogen in M. pneumoniae infections. BMC Infect Dis. 10:350CrossRef Tabassum I, Chaudhry R, Chourasia BK, Malhotra P (2010) Identification of an N-terminal 27 kDa fragment of Mycoplasma pneumoniae P116 protein as specific immunogen in M. pneumoniae infections. BMC Infect Dis. 10:350CrossRef
10.
Zurück zum Zitat Dumke R, Strubel A, Cyncynatus C, Nuyttens H, Herrmann R, Lück C, Jacobs E (2012) Optimized serodiagnosis of Mycoplasma pneumoniae infections. Diagn Microbiol Infect Dis. 73(2):200–203CrossRef Dumke R, Strubel A, Cyncynatus C, Nuyttens H, Herrmann R, Lück C, Jacobs E (2012) Optimized serodiagnosis of Mycoplasma pneumoniae infections. Diagn Microbiol Infect Dis. 73(2):200–203CrossRef
11.
Zurück zum Zitat Xue G, Cao L, Wang L, Zhao H, Feng Y, Ma L, Sun H (2013) Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma pneumoniae infections. FEMS Microbiol Lett. 340(2):86–92CrossRef Xue G, Cao L, Wang L, Zhao H, Feng Y, Ma L, Sun H (2013) Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma pneumoniae infections. FEMS Microbiol Lett. 340(2):86–92CrossRef
12.
Zurück zum Zitat Nuyttens H, Cyncynatus C, Renaudin H, Pereyre S, Bébéar C (2010) Identification, expression and serological evaluation of the recombinant ATP synthase beta subunit of Mycoplasma pneumoniae. BMC Microbiol. 10:216CrossRef Nuyttens H, Cyncynatus C, Renaudin H, Pereyre S, Bébéar C (2010) Identification, expression and serological evaluation of the recombinant ATP synthase beta subunit of Mycoplasma pneumoniae. BMC Microbiol. 10:216CrossRef
13.
Zurück zum Zitat Kannan TR, Provenzano D, Wright JR, Baseman JB (2005) Identification and characterization of human surfactant protein A binding protein of Mycoplasma pneumoniae. Infect Immun 73(5):2828–2834CrossRef Kannan TR, Provenzano D, Wright JR, Baseman JB (2005) Identification and characterization of human surfactant protein A binding protein of Mycoplasma pneumoniae. Infect Immun 73(5):2828–2834CrossRef
14.
Zurück zum Zitat Kannan TR, Baseman JB (2006) ADP-ribosylating and vacuolating cytotoxin of Mycoplasma pneumoniae represents unique virulence determinant among bacterial pathogens. Proc Natl Acad Sci USA. 103(17):6724–6729CrossRef Kannan TR, Baseman JB (2006) ADP-ribosylating and vacuolating cytotoxin of Mycoplasma pneumoniae represents unique virulence determinant among bacterial pathogens. Proc Natl Acad Sci USA. 103(17):6724–6729CrossRef
15.
Zurück zum Zitat Medina JL, Brooks EG, Chaparro A, Dube PH (2017) Mycoplasma pneumoniae CARDS toxin elicits a functional IgE response in Balb/c mice. PLoS One. 12(2):e0172447CrossRef Medina JL, Brooks EG, Chaparro A, Dube PH (2017) Mycoplasma pneumoniae CARDS toxin elicits a functional IgE response in Balb/c mice. PLoS One. 12(2):e0172447CrossRef
16.
Zurück zum Zitat Maselli DJ, Medina JL, Brooks EG, Coalson JJ, Kannan TR, Winter VT, Principe M, Cagle MP, Baseman JB, Dube PH, Peters JI (2018) The Immunopathologic effects of mycoplasma pneumoniae and community-acquired respiratory distress syndrome toxin. A primate model. Am J Respir Cell Mol Biol. 58(2):253–260CrossRef Maselli DJ, Medina JL, Brooks EG, Coalson JJ, Kannan TR, Winter VT, Principe M, Cagle MP, Baseman JB, Dube PH, Peters JI (2018) The Immunopathologic effects of mycoplasma pneumoniae and community-acquired respiratory distress syndrome toxin. A primate model. Am J Respir Cell Mol Biol. 58(2):253–260CrossRef
17.
Zurück zum Zitat Kannan TR, Musatovova O, Balasubramanian S, Cagle M, Jordan JL, Krunkosky TM, Davis A, Hardy RD, Baseman JB (2010) Mycoplasma pneumoniae community acquired respiratory distress syndrome toxin expression reveals growth phase and infection-dependent regulation. Mol Microbiol. 76(5):1127–1141CrossRef Kannan TR, Musatovova O, Balasubramanian S, Cagle M, Jordan JL, Krunkosky TM, Davis A, Hardy RD, Baseman JB (2010) Mycoplasma pneumoniae community acquired respiratory distress syndrome toxin expression reveals growth phase and infection-dependent regulation. Mol Microbiol. 76(5):1127–1141CrossRef
18.
Zurück zum Zitat Techasaensiri C, Tagliabue C, Cagle M, Iranpour P, Katz K, Kannan TR, Coalson JJ, Baseman JB, Hardy RD (2010) Variation in colonization, ADP-ribosylating and vacuolating cytotoxin, and pulmonary disease severity among mycoplasma pneumoniae strains. Am J Respir Crit Care Med. 182(6):797–804CrossRef Techasaensiri C, Tagliabue C, Cagle M, Iranpour P, Katz K, Kannan TR, Coalson JJ, Baseman JB, Hardy RD (2010) Variation in colonization, ADP-ribosylating and vacuolating cytotoxin, and pulmonary disease severity among mycoplasma pneumoniae strains. Am J Respir Crit Care Med. 182(6):797–804CrossRef
19.
Zurück zum Zitat Kannan TR, Coalson JJ, Cagle M, Musatovova O, Hardy RD, Baseman JB (2011) Synthesis and distribution of CARDS toxin during Mycoplasma pneumoniae infection in a murine model. J Infect Dis 204(10):1596–1604CrossRef Kannan TR, Coalson JJ, Cagle M, Musatovova O, Hardy RD, Baseman JB (2011) Synthesis and distribution of CARDS toxin during Mycoplasma pneumoniae infection in a murine model. J Infect Dis 204(10):1596–1604CrossRef
20.
Zurück zum Zitat Kannan TR, Krishnan M, Ramasamy K, Becker A, Pakhomova ON, Hart PJ, Baseman JB (2014) Functional mapping of community-acquired respiratory distress syndrome (CARDS) toxin of Mycoplasma pneumoniae defines regions with ADP-ribosyltransferase, vacuolating and receptor-binding activities. Mol Microbiol. 93(3):568–581CrossRef Kannan TR, Krishnan M, Ramasamy K, Becker A, Pakhomova ON, Hart PJ, Baseman JB (2014) Functional mapping of community-acquired respiratory distress syndrome (CARDS) toxin of Mycoplasma pneumoniae defines regions with ADP-ribosyltransferase, vacuolating and receptor-binding activities. Mol Microbiol. 93(3):568–581CrossRef
21.
Zurück zum Zitat Becker A, Kannan TR, Taylor AB, Pakhomova ON, Zhang Y, Somarajan SR, Galaleldeen A, Holloway SP, Baseman JB, Hart PJ (2015) Structure of CARDS toxin, a unique ADP-ribosylating and vacuolating cytotoxin from Mycoplasma pneumoniae. Proc Natl Acad Sci USA. 112(16):5165–5170CrossRef Becker A, Kannan TR, Taylor AB, Pakhomova ON, Zhang Y, Somarajan SR, Galaleldeen A, Holloway SP, Baseman JB, Hart PJ (2015) Structure of CARDS toxin, a unique ADP-ribosylating and vacuolating cytotoxin from Mycoplasma pneumoniae. Proc Natl Acad Sci USA. 112(16):5165–5170CrossRef
22.
Zurück zum Zitat Somarajan SR, Al-Asadi F, Ramasamy K, Pandranki L, Baseman JB, Kannan TR (2014) Annexin A2 mediates Mycoplasma pneumoniae community-acquired respiratory distress syndrome toxin binding to eukaryotic cells. mBio 5(4):e01497–e01e14CrossRef Somarajan SR, Al-Asadi F, Ramasamy K, Pandranki L, Baseman JB, Kannan TR (2014) Annexin A2 mediates Mycoplasma pneumoniae community-acquired respiratory distress syndrome toxin binding to eukaryotic cells. mBio 5(4):e01497–e01e14CrossRef
23.
Zurück zum Zitat Dumke R, Jacobs E (2016) Antibody response to mycoplasma pneumoniae: protection of host and influence on outbreaks? Front Microbiol 7:39CrossRef Dumke R, Jacobs E (2016) Antibody response to mycoplasma pneumoniae: protection of host and influence on outbreaks? Front Microbiol 7:39CrossRef
24.
Zurück zum Zitat Wood PR, Hill VL, Burks ML, Peters JI, Singh H, Kannan TR, Vale S, Cagle MP, Principe MF, Baseman JB, Brooks EG (2013) Mycoplasma pneumoniae in children with acute and refractory asthma. Ann Allergy Asthma Immunol. 110(5):328–334CrossRef Wood PR, Hill VL, Burks ML, Peters JI, Singh H, Kannan TR, Vale S, Cagle MP, Principe MF, Baseman JB, Brooks EG (2013) Mycoplasma pneumoniae in children with acute and refractory asthma. Ann Allergy Asthma Immunol. 110(5):328–334CrossRef
Metadaten
Titel
Evaluation of the CARDS toxin and its fragment for the serodiagnosis of Mycoplasma pneumoniae infections
verfasst von
Guanhua Xue
Hanqing Zhao
Chao Yan
Shaoli Li
Jinghua Cui
Yanling Feng
Xianghui Xie
Jing Yuan
Publikationsdatum
18.03.2021
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Clinical Microbiology & Infectious Diseases / Ausgabe 8/2021
Print ISSN: 0934-9723
Elektronische ISSN: 1435-4373
DOI
https://doi.org/10.1007/s10096-021-04209-2

Kompaktes Leitlinien-Wissen Innere Medizin (Link öffnet in neuem Fenster)

Mit medbee Pocketcards schnell und sicher entscheiden.
Leitlinien-Wissen kostenlos und immer griffbereit auf ihrem Desktop, Handy oder Tablet.

Neu im Fachgebiet Innere Medizin

Verbände und Cremes gegen Dekubitus: „Wir wissen nicht, was sie bringen!“

Die Datenlage zur Wirksamkeit von Verbänden oder topischen Mitteln zur Prävention von Druckgeschwüren sei schlecht, so die Verfasser einer aktuellen Cochrane-Studie. Letztlich bleibe es unsicher, ob solche Maßnahmen den Betroffenen nutzen oder schaden.

Schützt das tägliche Glas Milch vor Darmkrebs?

Die Milch machts – sie bietet Frauen nach Daten einer großen Ernährungsanalyse den besten Darmkrebsschutz aller Lebensmittel, was am hohen Kalziumgehalt liegen dürfte. Am anderen Ende des Spektrums steht der Alkoholkonsum: Das Glas Wein am Abend ist eher ungünstig.

Vorsicht mit Glukokortikoiden bei Glomerulopathie

Auch niedrig dosierte Glukokortikoide zur Behandlung einer primären Glomerulopathie lassen offenbar die Infektionsgefahr steigen. In einer US-Studie hing das Risiko vor allem mit der kombinierten Anwendung von Immunsuppressiva zusammen.

KI-gestütztes Mammografiescreening überzeugt im Praxistest

Mit dem Einsatz künstlicher Intelligenz lässt sich die Detektionsrate im Mammografiescreening offenbar deutlich steigern. Mehr unnötige Zusatzuntersuchungen sind laut der Studie aus Deutschland nicht zu befürchten.

EKG Essentials: EKG befunden mit System (Link öffnet in neuem Fenster)

In diesem CME-Kurs können Sie Ihr Wissen zur EKG-Befundung anhand von zwölf Video-Tutorials auffrischen und 10 CME-Punkte sammeln.
Praxisnah, relevant und mit vielen Tipps & Tricks vom Profi.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.