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Vibrio cholerae O1 Ogawa, classical biotype is a specific strain of the Gram-negative bacterium responsible for the first six cholera pandemics [1, 3]. The O1 designation refers to the major cell wall lipopolysaccharide (LPS) antigen, while Ogawa denotes a specific serotype within that group, and classical refers to the biotype characterized by specific phenotypic traits such as sensitivity to polymyxin B and phage IV [1, 10]. This organism is the primary target of cholera vaccines, which utilize inactivated or attenuated forms of the bacteria to induce mucosal immunity against the O-antigen and the cholera toxin [11, 13]. In clinical settings, the pathogen is targeted by antibiotics like doxycycline and azithromycin, which aim to reduce the duration of diarrhea and bacterial shedding [8, 12]. Understanding this specific biotype is crucial for epidemiological tracking and for the development of broad-spectrum vaccines that cover both classical and the currently dominant El Tor biotypes [5, 9]. Although the classical biotype has largely been replaced by the El Tor biotype in the current seventh pandemic, it remains a significant reference for vaccine efficacy and virulence studies [1, 6].
Antibiotics target bacterial protein synthesis (e.g., doxycycline) or DNA replication (e.g., ciprofloxacin), while vaccines induce active mucosal immunity against the O1 antigen and cholera toxin.
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