Langbach Odd, Kristoffersen Anne Karin, Abesha-Belay Emnet, Enersen Morten, Røkke Ola, Olsen Ingar
Department of Gastroenterologic Surgery, Akershus University Hospital, University of Oslo, Lørenskog, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway;
J Oral Microbiol. 2016 Jul 29;8:31854. doi: 10.3402/jom.v8.31854. eCollection 2016.
In ventral hernia surgery, mesh implants are used to reduce recurrence. Infection after mesh implantation can be a problem and rates around 6-10% have been reported. Bacterial colonization of mesh implants in patients without clinical signs of infection has not been thoroughly investigated. Molecular techniques have proven effective in demonstrating bacterial diversity in various environments and are able to identify bacteria on a gene-specific level.
The purpose of this study was to detect bacterial biofilm in mesh implants, analyze its bacterial diversity, and look for possible resemblance with bacterial biofilm from the periodontal pocket.
Thirty patients referred to our hospital for recurrence after former ventral hernia mesh repair, were examined for periodontitis in advance of new surgical hernia repair. Oral examination included periapical radiographs, periodontal probing, and subgingival plaque collection. A piece of mesh (1×1 cm) from the abdominal wall was harvested during the new surgical hernia repair and analyzed for bacteria by PCR and 16S rRNA gene sequencing. From patients with positive PCR mesh samples, subgingival plaque samples were analyzed with the same techniques.
A great variety of taxa were detected in 20 (66.7%) mesh samples, including typical oral commensals and periodontopathogens, enterics, and skin bacteria. Mesh and periodontal bacteria were further analyzed for similarity in 16S rRNA gene sequences. In 17 sequences, the level of resemblance between mesh and subgingival bacterial colonization was 98-100% suggesting, but not proving, a transfer of oral bacteria to the mesh.
The results show great bacterial diversity on mesh implants from the anterior abdominal wall including oral commensals and periodontopathogens. Mesh can be reached by bacteria in several ways including hematogenous spread from an oral site. However, other sites such as gut and skin may also serve as sources for the mesh biofilm.
在腹疝手术中,使用补片植入物来降低复发率。补片植入后的感染可能是个问题,据报道感染率约为6 - 10%。对于没有感染临床症状的患者,补片植入物上的细菌定植尚未得到充分研究。分子技术已被证明在展示各种环境中的细菌多样性方面有效,并且能够在基因特异性水平上鉴定细菌。
本研究的目的是检测补片植入物中的细菌生物膜,分析其细菌多样性,并寻找与牙周袋细菌生物膜可能的相似性。
30例因既往腹疝补片修补术后复发而转诊至我院的患者,在进行新的疝修补手术前接受牙周炎检查。口腔检查包括根尖片、牙周探诊和龈下菌斑采集。在新的疝修补手术期间,从腹壁采集一块补片(1×1厘米),通过PCR和16S rRNA基因测序分析细菌。对PCR补片样本呈阳性的患者,用相同技术分析龈下菌斑样本。
在20个(66.7%)补片样本中检测到多种分类群,包括典型的口腔共生菌和牙周病原体、肠道菌和皮肤细菌。进一步分析补片和牙周细菌16S rRNA基因序列的相似性。在17个序列中,补片与龈下细菌定植之间的相似程度为98 - 100%,这表明但未证实口腔细菌转移至补片。
结果显示前腹壁补片植入物上存在高度的细菌多样性,包括口腔共生菌和牙周病原体。细菌可通过多种途径到达补片,包括从口腔部位的血行播散。然而,其他部位如肠道和皮肤也可能是补片生物膜的来源。