Open Access Research article

Invasion of Ureaplasma diversum in Hep-2 cells

Lucas M Marques1,2, Priscilla M Ueno1, Melissa Buzinhani1, Beatriz A Cortez3, Renata L Neto1, Maurício Yamaguti1, Rosângela C Oliveira1, Ana MS Guimarães1, Telma A Monezi1, Antonio CR Braga2, Gláucia M Machado-Santelli3 and Jorge Timenetsky1*

Author Affiliations

1 Departamento de Microbiologia, Instituto de Ciências Biomédicas, Universidade de São Paulo. Av. Professor Lineu Prestes, 1374. 05508-900, São Paulo, SP, Brazil

2 Núcleo de Tecnologia em Saúde, Instituto Multidisciplinar em Saúde, Universidade Federal da Bahia. Av. Olívia Flores, 3000. 45055-090, Vitória da Conquista, BA, Brazil

3 Departamento de Biologia Celular e do Desenvolvimento, Instituto de Ciências Biomédicas, Universidade de São Paulo. Av. Professor Lineu Prestes, 1374. CEP 05508 900, São Paulo, SP, Brazil

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BMC Microbiology 2010, 10:83 doi:10.1186/1471-2180-10-83

Published: 17 March 2010

Abstract

Background

Understanding mollicutes is challenging due to their variety and relationship with host cells. Invasion has explained issues related to their opportunistic role. Few studies have been done on the Ureaplasma diversum mollicute, which is detected in healthy or diseased bovine. The invasion in Hep-2 cells of four clinical isolates and two reference strains of their ureaplasma was studied by Confocal Laser Scanning Microscopy and gentamicin invasion assay.

Results

The isolates and strains used were detected inside the cells after infection of one minute without difference in the arrangement for adhesion and invasion. The adhesion was scattered throughout the cells, and after three hours, the invasion of the ureaplasmas surrounded the nuclear region but were not observed inside the nuclei. The gentamicin invasion assay detected that 1% of the ATCC strains were inside the infected Hep-2 cells in contrast to 10% to the clinical isolates. A high level of phospholipase C activity was also detected in all studied ureaplasma.

Conclusions

The results presented herein will help better understand U. diversum infections, aswell as cellular attachment and virulence.