Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Mar 8:7:232.
doi: 10.3389/fmicb.2016.00232. eCollection 2016.

The Evolution of Advanced Molecular Diagnostics for the Detection and Characterization of Mycoplasma pneumoniae

Affiliations
Review

The Evolution of Advanced Molecular Diagnostics for the Detection and Characterization of Mycoplasma pneumoniae

Maureen H Diaz et al. Front Microbiol. .

Abstract

Over the past decade there have been significant advancements in the methods used for detecting and characterizing Mycoplasma pneumoniae, a common cause of respiratory illness and community-acquired pneumonia worldwide. The repertoire of available molecular diagnostics has greatly expanded from nucleic acid amplification techniques (NAATs) that encompass a variety of chemistries used for detection, to more sophisticated characterizing methods such as multi-locus variable-number tandem-repeat analysis (MLVA), Multi-locus sequence typing (MLST), matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS), single nucleotide polymorphism typing, and numerous macrolide susceptibility profiling methods, among others. These many molecular-based approaches have been developed and employed to continually increase the level of discrimination and characterization in order to better understand the epidemiology and biology of M. pneumoniae. This review will summarize recent molecular techniques and procedures and lend perspective to how each has enhanced the current understanding of this organism and will emphasize how Next Generation Sequencing may serve as a resource for researchers to gain a more comprehensive understanding of the genomic complexities of this insidious pathogen.

Keywords: Mycoplasma pneumoniae; molecular characteristics; molecular diagnostics; molecular epidemiology; whole genome sequencing.

PubMed Disclaimer

Figures

FIGURE 1
FIGURE 1
Timeline of milestones in whole genome sequencing of Mycoplasma pneumoniae.

References

    1. Atkinson T. P., Balish M. F., Waites K. B. (2008). Epidemiology, clinical manifestations, pathogenesis and laboratory detection of Mycoplasma pneumoniae infections. FEMS Microbiol. Rev. 32 956–973. 10.1111/j.1574-6976.2008.00129.x - DOI - PubMed
    1. Baseman J. B., Reddy S. P., Dallo S. F. (1996). Interplay between mycoplasma surface proteins, airway cells, and the protean manifestations of mycoplasma-mediated human infections. Am. J. Respir. Crit. Care Med. 154 S137–144. 10.1164/ajrccm/154.4_pt_2.s137 - DOI - PubMed
    1. Baseman J. B., Tully J. G. (1997). Mycoplasmas: sophisticated, reemerging, and burdened by their notoriety. Emerg. Infect. Dis. 3 21–32. 10.3201/eid0301.970103 - DOI - PMC - PubMed
    1. Bebear C., Pereyre S., Peuchant O. (2011). Mycoplasma pneumoniae: susceptibility and resistance to antibiotics. Future Microbiol. 6 423–431. 10.2217/fmb.11.18 - DOI - PubMed
    1. Beersma M. F., Dirven K., Van Dam A. P., Templeton K. E., Claas E. C., Goossens H. (2005). Evaluation of 12 commercial tests and the complement fixation test for Mycoplasma pneumoniae-specific immunoglobulin G (IgG) and IgM antibodies, with PCR used as the “gold standard.” J. Clin. Microbiol. 43 2277–2285. 10.1128/JCM.43.5.2277-2285.2005 - DOI - PMC - PubMed

LinkOut - more resources