Related Experiment Video
Updated: Nov 9, 2025

Antigen-Capture Enzyme-Linked Immunosorbent Assay for Specific Detection of Mycoplasma pneumoniae
Published on: February 24, 2023
Mycoplasma pneumoniae Genotypes and Clinical Outcome in Children
Patrick M Meyer Sauteur1, Elena Pánisová1, Michelle Seiler2
1Division of Infectious Diseases and Hospital Epidemiology, University Children's Hospital Zurich, Zurich, Switzerland.
Abstract:
Factors leading to the wide range of manifestations associated with Mycoplasma pneumoniae infection are unclear. We investigated whether M. pneumoniae genotypes are associated with specific clinical outcomes. We compared M. pneumoniae loads and genotypes of children with mucocutaneous disease to those of children with pneumonia, family members with upper respiratory tract infection (URTI), and carriers from a prospective cohort study (n = 47; 2016 to 2017) and to those of other children with mucocutaneous disease from a case series (n = 7; 2017 to 2020). Genotyping was performed using macrolide resistance determination, P1 subtyping, multilocus variable-number tandem-repeat analysis (MLVA), and multilocus sequence typing (MLST). Comparisons were performed with a pairwise Wilcoxon rank sum test and a Fisher exact test with corrections for multiple testing, as appropriate. M. pneumoniae loads did not statistically differ between patients with mucocutaneous disease and those with pneumonia or carriers. Macrolide resistance was detected in 1 (1.9%) patient with mucocutaneous disease. MLVA types from 2016 to 2017 included 3-5-6-2 (n = 21 [46.7%]), 3-6-6-2 (n = 2 [4.4%]), 4-5-7-2 (n = 14 [31.1%]), and 4-5-7-3 (n = 8 [17.8%]), and they correlated with P1 subtypes and MLST types. MLVA types were not associated with specific outcomes such as mucocutaneous disease, pneumonia, URTI, or carriage. They were almost identical within families but varied over geographic location. MLVA types in patients with mucocutaneous disease differed between 2016 to 2017 (3-5-6-2, n = 5 [62.5%]) and 2017 to 2020 (4-5-7-2, n = 5 [71.4%]) (P = 0.02). Our results suggest that M. pneumoniae genotypes may not determine specific clinical outcomes.
Insights
Mycoplasma pneumoniae genotypes do not appear to determine specific clinical outcomes in infections. This study found no direct link between M. pneumoniae strains and diseases like pneumonia or mucocutaneous conditions.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Mycoplasma pneumoniae infections present with diverse clinical manifestations, but the underlying factors remain unclear.
- Understanding the relationship between M. pneumoniae genotypes and clinical outcomes is crucial for diagnosis and treatment.
Purpose of the Study:
- To investigate the association between Mycoplasma pneumoniae genotypes and specific clinical outcomes in infected children.
- To compare M. pneumoniae loads and genotypes across different clinical presentations, including mucocutaneous disease, pneumonia, and upper respiratory tract infections (URTI).
Main Methods:
- Genotyping of M. pneumoniae using macrolide resistance determination, P1 subtyping, multilocus variable-number tandem-repeat analysis (MLVA), and multilocus sequence typing (MLST).
- Comparison of M. pneumoniae loads and genotypes between patients with mucocutaneous disease and other groups (pneumonia, URTI, carriers).
- Statistical analysis using pairwise Wilcoxon rank sum test and Fisher exact test with corrections for multiple testing.
Main Results:
- M. pneumoniae loads did not significantly differ between mucocutaneous disease patients, pneumonia patients, or carriers.
- Macrolide resistance was rare (1.9%) in patients with mucocutaneous disease.
- MLVA types correlated with P1 subtypes and MLST types but were not associated with specific clinical outcomes. However, MLVA types in mucocutaneous disease patients showed a significant difference between 2016-2017 and 2017-2020 (P=0.02).
Conclusions:
- Mycoplasma pneumoniae genotypes may not be the primary determinant of specific clinical outcomes observed in infections.
- While MLVA types showed temporal variation in mucocutaneous disease cases, overall genotype did not correlate with disease presentation.
- Further research is needed to elucidate the factors contributing to the varied clinical spectrum of M. pneumoniae infections.
Related Concept Videos
Pneumonia II: Pathophysiology
Pneumonia I: Introduction
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
Pneumonia III: Complications and Assessment
COPD: Pathogenesis and Clinical Features
The primary cause for the onset of COPD is cigarette smoking and exposure to air pollution. These hazardous factors initiate a chain reaction within the lungs, resulting in chronic inflammation, damage to the airways, and a...
Acute Pyelonephritis II: Diagnostic Studies and Management
Pharmacokinetics in Pediatric Patients: Drug Excretion

