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Updated: May 17, 2026

A Non-invasive and Technically Non-intensive Method for Induction and Phenotyping of Experimental Bacterial Pneumonia in Mice
Published on: September 28, 2016
Diagnostic usefulness of ribosomal protein l7/l12 for pneumococcal pneumonia in a mouse model
Tomoka Sawa1, Soichiro Kimura, Natsue Hosono Honda
1Department of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan.
Abstract:
The capsular antigen detection (CAD) kit is widely used in clinics to detect Streptococcus pneumoniae infection from urine, because it is rapid, convenient, and effective. However, there are several disadvantages, including false-positive results in children colonized with S. pneumoniae and prolonged positive readings even after the bacteria have been cleared. RP-L7/L12 is a component of the 50S ribosome that is abundant in all bacteria and is specific for each bacterial species. We investigated whether RP-L7/L12 could be used to accurately diagnose pneumococcal pneumonia infection in mouse models of pneumonia and colonization generated by infecting CBA/JN or CBA/N mice, respectively, with S. pneumoniae strain 741. RP-L7/L12 detection by enzyme-linked immunosorbent assay accurately assessed active lung infection, as RP-L7/L12 levels decreased simultaneously with the bacterial lung burden after imipenem administration in the pneumonia mouse model. Based on the data, antibodies detecting RP-L7/L12 were applied to rapid immunochromatographic strips (ICS) for urine sample testing. When we compared the ICS test with the CAD kit in the pneumonia model, the results correlated well. Interestingly, however, when the lung bacterial burden became undetectable after antibiotic treatment, the ICS test was correspondingly negative, even though the same samples tested by the CAD kit remained positive. Similarly, while the ICS test exhibited negative results in the nasal colonization model, the CAD kit demonstrated positive results. Bacterial RP-L7/L12 may be a promising target for the development of new methods to diagnose infectious disease. Further studies are warranted to determine whether such a test could be useful in children.
Insights
RP-L7/L12, a bacterial ribosome component, shows promise for diagnosing Streptococcus pneumoniae infections. This new method accurately detects active infections and avoids false positives from colonization, unlike current urinary antigen tests.
Area of Science:
- Microbiology
- Immunology
- Diagnostic Development
Background:
- The capsular antigen detection (CAD) kit is a common clinical tool for detecting Streptococcus pneumoniae infections in urine.
- However, the CAD kit has limitations, including false positives in colonized children and prolonged positive results after bacterial clearance.
Purpose of the Study:
- To evaluate the potential of bacterial ribosomal protein RP-L7/L12 as a specific biomarker for diagnosing pneumococcal pneumonia.
- To develop and assess a rapid immunochromatographic strip (ICS) test using RP-L7/L12 for urine sample analysis.
Main Methods:
- Mouse models of S. pneumoniae pneumonia and nasal colonization were established.
- RP-L7/L12 levels were measured using enzyme-linked immunosorbent assay (ELISA) in pneumonia models.
- Antibodies against RP-L7/L12 were used to create ICS tests for urine, compared against the CAD kit.
Main Results:
- ELISA detection of RP-L7/L12 accurately reflected active lung infection, decreasing with bacterial load after antibiotic treatment.
- The RP-L7/L12-based ICS test showed negative results when lung bacteria were cleared, unlike the persistent positive CAD test.
- The ICS test was negative in nasal colonization models, whereas the CAD kit remained positive.
Conclusions:
- Bacterial RP-L7/L12 is a promising target for developing new diagnostic methods for infectious diseases.
- The RP-L7/L12 ICS test offers improved specificity compared to the CAD kit, distinguishing active infection from colonization or cleared infection.
- Further research is needed to validate the utility of RP-L7/L12-based tests in pediatric populations.

