Background: Bacterial DNA due to bacterial translocation has been identified in noninfectious ascitic fluid samples. Objective: This study investigated the possible presence of bacterial DNA in the pleural fluid of patients with pleural effusions of noninfectious origin, using a highly sensitive PCR-based method. Methods: Pleural fluid samples from 175 patients (average age ± SD: 69 ± 14 years) with noninfectious pleural effusion (62 transudates, 113 exudates) were analyzed. Bacterial DNA was detected using nested PCR with amplification of a fragment of the gene r16S, with 2 amplification protocols, i.e. low sensitivity (10 and 40 cycles) and high sensitivity (40 and 40 cycles). Results: With the less sensitive amplification process, only 1 sample was positive (Haemophilus parainfluenzae in a patient with hepatic hydrothorax). With the highly sensitive nested PCR method, bacterial DNA was identified in the pleural fluid, of both transudative and exudative origin, of 75 of the 175 patients (43%). In cases of isolation of a single bacterium, the more frequent were Escherichia coli, Salmonella enterica and Streptococcus pneumoniae.Conclusions: Regardless of its origin, bacterial DNA can be identified in almost half of noninfectious pleural effusions by using a highly sensitive PCR-based method. The possible clinical significance or prognostic value of these findings deserves to be evaluated.

1.
Rogers GB, Carroll MP, Bruce KD: Studying bacterial infections through culture-independent approaches. J Med Microbiol 2009;58:1401–1418.
2.
Utine GE, Pinar A, Ozcelik U, Sener B, Yalcin E, Dogru D, Menemenlioglu D, Gur D, Kiper N, Gocmen A: Pleural fluid PCR method for detection of Staphylococcus aureus, Streptococcus pneumoniae and Haemophilus influenzae in pediatric parapneumonic effusions. Respiration 2008;75:437–442.
3.
Berg RD, Garlington AW: Translocation of certain indigenous bacteria from the gastrointestinal tract to the mesenteric lymph nodes and other organs in a gnotobiotic mouse model. Infect Immun 1979;23:403–411.
4.
Berg RD: Bacterial translocation from the gastrointestinal tract. Adv Exp Med Biol 1999;473:11–30.
5.
Nayci A, Atis S, Talas DU, Ersoz G: Rigid bronchoscopy induces bacterial translocation: an experimental study in rats. Eur Respir J 2003;21:749–752.
6.
Rossi M, Sganga G, Mazzone M, Valenza V, Guarneri S, Portale G, Carbone L, Gatta L, Pioli C, Sanguinetti M, Montalto M, Glieca F, Fadda G, Schiavello R, Silveri NG: Cardiopulmonary bypass in man: role of the intestine in a self-limiting inflammatory response with demonstrable bacterial translocation. Ann Thorac Surg 2004;77:612–618.
7.
Ramirez P, Martí V, de la Plata AM, Salinas G, Bonastre J, Ruano M: Bacterial translocation in heat stroke. Am J Emerg Med 2009;27:1168.
8.
Cirera I, Bauer TM, Navasa Vila J, Grande L, Taura P, Fuster J, Garcia-Valdecasa J, Lacy A, Suarez MJ, Rimola A, Rodes J: Bacterial translocation of enteric organisms in patients with cirrhosis. J Hepatol 2001;34:32–37.
9.
Such J, Francés R, Muñoz C, Zapater P, Casellas JA, Cifuentes A, Rodríguez-Valera F, Pascual S, Sola-Vera J, Carnicer F, Uceda F, Palazón JM, Pérez-Mateo M: Detection and identification of bacterial DNA in patients with cirrhosis and culture-negative, nonneutrocytic ascites. Hepatology 2002;36:135–141.
10.
Albillos A, de la Hera A, González M, Moya JL, Calleja JL, Monserrat J, Ruiz-del-Arbol L, Alvarez-Mon M: Increased lipopolysaccharide binding protein in cirrhotic patients with marked immune and hemodynamic derangement. Hepatology 2003;37:208–217.
11.
Frances R, Benlloch S, Zapater P, González JM, Lozano B, Muñoz C, Pascual S, Casellas JA, Uceda F, Palazón JM, Carnicer F, Pérez-Mateo M, Such J: A sequential study of serum bacterial DNA in patients with advanced cirrhosis and ascites. Hepatology 2004;39:484–491.
12.
Vieira SM, Da Silveira TR, Matte U, Kieling CO, Ferreira CT, Taniguchi A, Oliveira Fdos S, Barth AL: Amplification of bacterial DNA does not distinguish patients with ascitic fluid infection from those colonized by bacteria. J Pediatr Gastroenterol Nutr 2007;44:603–607.
13.
El-Naggar MM, Khalil EAM, El-Daker MA, Salama MF: Bacterial DNA and its consequences in patients with cirrhosis and culture-negative, non-neutrocytic ascites. J Med Microbiol 2008;57:1533–1538.
14.
Bruns T, Sachse S, Straube E, Assefa S, Hermann A, Hagel S, Lehmann M, Stallmach A: Identification of bacterial DNA in neutrocytic and non-neutrocytic cirrhotic ascites by means of a multiplex polymerase chain reaction. Liver Int 2009;29:1206–1214.
15.
Guarner C, González-Navajas JM, Sánchez E, Soriando G, Francés R, Chiva M, Zapater P, Benlloch S, Muñoz C, Pascual S, Balanzó J, Pérez-Mateo M, Such J: The detection of bacterial DNA in blood of rats with CCl4-induced cirrhosis with ascites represents episodes of bacterial translocation. Hepatology 2006;44:633–639.
16.
Shuurman T, De Boer RF, Kooistra-Smid AMD, Van Zwet AA: Prospective study of use of PCR amplification and sequencing of 16S ribosomal DNA from cerebrospinal fluid for diagnosis of bacterial meningitis in a clinical setting. J Clin Microbiol 2004;42:734–740.
17.
Rodriguez JC, Fuentes E, Royo G: Comparison of two different PCR detection methods. Application to the diagnosis of pulmonary tuberculosis. APMIS 1997;105:612–616.
18.
Maskell NA, Batt S, Hedley EL, Davies CW, Gillespie SH, Davies RJ: The bacteriology of pleural infection by genetic and standard methods and its mortality significance. Am J Respir Crit Care Med 2006;174:817–823.
19.
Nagesh BS, Sehgal S, Jindal SK, Arora SA: Evaluation of polymerase chain reaction for detection of Mycobacterium tuberculosis in pleural fluid. Chest 2001;119:1737–1741.
20.
Falguera M, Lopez A, Nogues A, Porcel JM, Rubio-Caballero M: Evaluation of the polymerase chain reaction method for detection of Streptococcus pneumoniae DNA in pleural fluid samples. Chest 2002;122:2212–2216.
21.
Neugebauer H, Hartmann P, Krenn S, Glück T, Schölmerich J, Straub R, Wiest R: Bacterial translocation increases phagocytic activity of polymorphonuclear leucocytes in portal hypertension: priming independent of liver cirrhosis. Liver Int 2008;28:1149–1157.
22.
Openshaw PJ: Crossing barriers: infections of the lung and the gut. Mucosal Immunol 2009;2:100–102.
23.
Keely S, Glover LE, Weissmueller T, MacManus CF, Fillon S, Fennimore B, Colgan SPl: HIF-dependent regulation of platelet activating factor receptor as a route for gram positive bacterial translocation across epithelia. Mol Biol Cell 2010;21:538–546.
24.
Lachmann RA, Van Kaam AH, Haitsma JJ, Lachmann B: High positive end-expiratory pressure levels promote bacterial translocation in experimental pneumonia. Intensive Care Med 2007;33:1800–1804.
25.
Croswell A, Amir E, Teggatz P, Barman M, Salzman NH: Prolonged impact of antibiotics on intestinal microbial ecology and susceptibility to enteric Salmonella infection. Infect Immun 2009;77:2741–2753.
26.
Frances R, Muñoz C, Zapater P, Uceda F, Gascón I, Pascual S, Pérez-Mateo M, Such J: Bacterial DNA activates cell mediated immune response and nitric oxide overproduction in peritoneal macrophages from patients with cirrhosis and ascites. Gut 2004;53:860–864.
27.
Frances R, Gonzalez-Navajas JM, Zapater P, Muñoz C, Caño R, Pascual S, Santana F, Márquez D, Pérez-Mateo M, Such J: Translocation of bacterial DNA from gram-positive microorganisms is associated with a species-specific inflammatory response in serum and ascitic fluid of patients with cirrhosis. Clin Exp Immunol 2007;150:230–237.
28.
Frances R, Gonzalez-Navajas JM, Zapater P, Muñoz C, Caño R, Pascual S, Márquez D, Santana F, Pérez-Mateo M, Such J: Bacterial DNA induces the complement system activation in serum and ascitic fluid from patients with advanced cirrhosis. J Clin Immunol 2007;27:438–444.
29.
Zapater P, Francés R, González-Navajas JM, de la Hoz MA, Moreu R, Pascual S, Monfort D, Montoliu S, Vila C, Escudero A, Torras X, Cirera I, Llanos L, Guarner-Argente C, Palazón JM, Carnicer F, Bellot P, Guarner C, Planas R, Solá R, Serra MA, Muñoz C, Pérez-Mateo M, Such J: Serum and ascitic fluid bacterial DNA: a new independent prognostic factor in noninfected patients with cirrhosis. Hepatology 2008;48:1924–1931.
30.
Appenrodt B, Grünhage F, Gentemann MG, Thyssen L, Sauerbruch T, Lammert F: Nucleotide-binding oligomerization domain containing 2 (NOD2) variants are genetic risk factors for death and spontaneous bacterial peritonitis in liver cirrhosis. Hepatology 2010;51:1327–1333.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.