A molecular analysis of prokaryotic and viral DNA sequences in prostate tissue from patients with prostate cancer indicates the presence of multiple and diverse microorganisms

The Prostate ◽  
2008 ◽  
Vol 68 (3) ◽  
pp. 306-320 ◽  
Author(s):  
Karen S. Sfanos ◽  
Jurga Sauvageot ◽  
Helen L. Fedor ◽  
James D. Dick ◽  
Angelo M. De Marzo ◽  
...  
2000 ◽  
pp. 1221-1228 ◽  
Author(s):  
JOHN N. KRIEGER ◽  
DONALD E. RILEY ◽  
ROBERT L. VESELLA ◽  
DAVID C. MINER ◽  
SUSAN O. ROSS ◽  
...  

2000 ◽  
Vol 164 (4) ◽  
pp. 1221-1228 ◽  
Author(s):  
JOHN N. KRIEGER ◽  
DONALD E. RILEY ◽  
ROBERT L. VESELLA ◽  
DAVID C. MINER ◽  
SUSAN O. ROSS ◽  
...  

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7962 ◽  
Author(s):  
Sergio Ayala-Díaz ◽  
Roberto Jiménez-Lima ◽  
Katia M. Ramírez-Alcántara ◽  
Marcela Lizano ◽  
Leonardo J. Castro-Muñoz ◽  
...  

Background The canine transmissible venereal tumor (CTVT) or Sticker’s sarcoma is a neoplastic disease affecting dogs. This disease is presented as a tumoral mass in the genital organs of both, male and female individuals. Up to date, there is no clear evidence indicating a viral agent as the causative mediator for CTVT development. Purpose The present work aims to analyze 21 samples from canines with CTVT for molecular identification of Papillomavirus DNA sequences. In addition, microbiological analysis, cytologic and histopathologic evaluations were also performed. Results All patients showed no biochemical and microbiological alterations. Molecular analysis demonstrated the viral DNA presence in the samples using different primer sets. The MY primers amplified a 450 bp band in seven out of 21 samples (33%). The PVF and Fap64 primer set, targeting the L1 sequence of Canine Papillomavirus (CPV), showed positivity in 16 out of 21 samples (76%). Conclusion These results support the possible causative association between CPV and CTVT; nevertheless, additional studies are required to uphold such statement. This work presents evidence indicating that a viral agent might be involved in the pathogenesis of CTVT and set the bases for a better understanding of the CTVT pathobiology.


2020 ◽  
Vol 78 (7) ◽  
Author(s):  
Saman Saadat ◽  
Pezhman Karami ◽  
Mohammad Jafari ◽  
Mahdi Kholoujini ◽  
Zahra Rikhtegaran Tehrani ◽  
...  

ABSTRACT Background Mycoplasma hominis, an opportunistic pathogen in human genitourinary tract, can cause chronic infection in the prostate. Intracellular survival of M. hominis leads to a prolonged presence in the host cells that can affect the cell's biological cycle. In the present study, we aimed to evaluate the frequency of M. hominis DNA in prostate tissue of Iranian patients with prostate cancer (PCa) in comparison to a control group with benign prostatic hyperplasia (BPH). Methods This research was a retrospective case-control study using 61 archived formalin-fixed paraffin-embedded (FFPE) blocks of prostate tissue from patients with PCa and 70 FFPE blocks of patients with BPH. Real-time PCR, targeting two different genes, 16S rRNA and yidC, in the M. hominis genome was performed for all specimens. Results Out of 61 blocks of prostate biopsy from patients with PCa, eight samples (13%) were positive for M. hominis, while the bacterium was not detected in any of the 70 blocks of patients with BPH (P value, 0.002). Conclusions The high frequency of M. hominis in patients with PCa likely shows a hidden role of the organism in prostate cancer during its chronic, apparently silent and asymptomatic colonization in prostate.


1996 ◽  
Vol 12 (18) ◽  
pp. 1717-1724 ◽  
Author(s):  
EDUARDO N. ESTEBAN ◽  
MICHAEL P. SHERMAN ◽  
BERNARD L. POIESZ ◽  
ROBERT R. MARSHAK ◽  
DAVID J. WATERS ◽  
...  

1980 ◽  
Vol 210 (1180) ◽  
pp. 423-435 ◽  

We have cloned and propagated in prokaryotic vectors the viral DNA sequences that are integrated in a variety of cells transformed by adenovirus 2 or SV40. Analysis of the clones reveals that the viral DNA sequences sometimes are arranged in a simple fashion, collinear with the viral genome; in other cell lines there are complex arrangements of viral sequences in which tracts of the viral genome are inverted with respect to each other. In several cases the nucleotide sequences at the joints between cell and viral sequences have been determined: usually there is a sharp transition between cellular and viral DNAs. The viral sequences are integrated at different locations within the genomes of different cell lines; likewise there is no specific site on the viral genomes at which integration occurs. Sometimes the viral sequences are integrated within repetitive cellular DNA, and sometimes within unique sequences. In some cases there is evidence that the viral sequences along with the flanking cell DNA have been amplified after integration. The sequences that flank the viral insertion in the line of SV40-transformed rat cells known as 14B have been used as probes to isolate, from untransformed rat cells, clones that carry the region of the chromosome in which integration occurred. Analysis of the structure of these clones by restriction endonuclease digestion and heteroduplex formation shows that a rearrangement of cellular sequences has occurred, presumably as a consequence of integration.


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