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Mycoplasma hyopneumoniae

Molecular classification
Other (Bacterium; class Mollicutes, phylum Firmicutes)
01

Overview

Mycoplasma hyopneumoniae is a small, wall-less, gram-negative bacterium and the primary causative agent of porcine enzootic pneumonia, a chronic, economically significant respiratory disease of pigs[1][3][5][6][7]. It specifically colonizes the ciliated epithelium of the swine respiratory tract, adhering via major surface adhesins such as P97 and P102[1]. The pathogen damages the mucociliary apparatus, impairs ciliary function, and induces both local inflammation and susceptibility to secondary infections[1][3][5]. It is classified as a prokaryotic microorganism, not as a canonical drug target such as a receptor, enzyme, or transporter. Control strategies include vaccination (which limits severity but does not prevent infection) and antimicrobial therapy, though complete eradication in commercial swine herds is rare[3][4][7]. **Note:** - This entry is marked **is_incorrect: true** because “Mycoplasma hyopneumoniae” is a whole organism (prokaryotic pathogen), not a canonical drug target molecule (e.g., protein, receptor, enzyme). Thus, it does not fit standard target molecule database schemas. - The information above is structured for clarity but does not denote a singular molecular target. Preferred targets would be molecular components of M. hyopneumoniae (such as the P97 adhesin) rather than the organism as a whole.

Other names
M. hyopneumoniae
02

Mechanism of action

Inhibition of bacterial protein synthesis (by antimicrobials such as macrolides and tetracyclines)[4]

03

Biological functions

Pathogenesis of respiratory disease (in pigs)Adherence to respiratory epithelial cellsDisruption of mucociliary clearanceInduction of host inflammation
04

Disease associations

Infection (porcine enzootic pneumonia)
05

Safety considerations

Antimicrobial resistance developmentSuboptimal vaccine protectionPersistence of infection even after treatment/vaccination[3]
06

Interacting drugs

Antimicrobial agents (e.g., tulathromycin, tiamulin, tilmicosin, doxycycline, enrofloxacin)[4]
07

Biomarkers

PCR detection of M. hyopneumoniae DNA in respiratory tissues[7]Serological assays (ELISA for antibodies)[7]Histopathological lung lesions (e.g., peribronchiolar lymphoid hyperplasia)[8]

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