The Presence of Adhesion Factors NOX, α-enolase, TrmFO, P27, and VpmaX in Wild Isolates in Japan
Overview
Affiliations
Background: causes various diseases such as bronchopneumonia, otitis media, arthritis, and mastitis in cattle. is often isolated from the deep pharynges of healthy cattle and is generally considered not to cause clinical symptoms while in the upper respiratory tract. In mycoplasma infections, adhesion to the host cells is a crucial step. In recent years, five new adhesins, NOX, α-enolase, TrmFO, P27, and VpmaX, have been reported in strains from pneumonia cases. However, the presence of these adhesins in wild isolates has not been established.
Aim: This study aimed to investigate the presence of these adhesin genes in wild isolates isolated from cattle nasal cavities and lesion sites (pneumonia, otitis media, arthritis, and mastitis) in various regions in Japan and clarify the relationship between adhesion and the symptoms caused by infection.
Methods: A total of 141 wild isolates isolated from nasal cavities (healthy or sick cattle), lungs with pneumonia, ears with otitis media, joint fluids of arthritic animals, and milk of mastitic animals. type strain PG45 was also used. Specific polymerase chain reaction reactions were performed to detect , , , , and , which are adhesins of .
Results: This study reports 139 wild isolates were positive for , , , , and , while two isolates each lacked or genes. PG45 also had all five adherens genes.
Conclusion: Almost all wild isolates possessed all , , , , and genes regardless of the lesion site or region of origin. This means no relationship was found between the presence of the five adhesins and lesion sites in and isolated from the nasal cavities of asymptomatic cattle have the same numbers and types of adhesins as isolates from symptomatic lesion sites (pneumonia, otitis media, arthritis, and mastitis). This suggests that not only isolates from pulmonary lesions, but also existing in the nasal cavity has the potential to causes symptoms in the host.
Gelgie A, Desai S, Gelalcha B, Kerro Dego O Front Vet Sci. 2024; 11:1322267.
PMID: 38515536 PMC: 10956102. DOI: 10.3389/fvets.2024.1322267.