Dual-species biofilm formation between Gardnerella vaginalis strains isolated from women with or without bacterial vaginosis (BV) and other 24 BV-associated microorganisms support that the key difference in virulence potential between BV-negative and BV-positive G. vaginalis strains seems not to be related with biofilm maturation.FCT Strategic Project of UID/BIO/04469/2013 unit and the project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462

Castro, J.

Cerca, Nuno

Anaerobe

Joana Castro

Nuno Cerca

Crossref

BV and non-BV associated Gardnerella vaginalis establish similar synergistic interactions with other BV-associated microorganisms in dual-species biofilms

Universidade do Minho: RepositoriUM

lable at ScienceDirectAnaerobe 36 (2015) 56e59Contents lists avaiAnaerobejournal homepage: www.elsevier .com/locate/anaerobeBV and non-BV associated Gardnerella vaginalis establish similarsynergistic interactions with other BV-associated microorganisms indual-species bioﬁlmsJoana Castro a, b, Nuno Cerca a, *a Centre of Biological Engineering (CEB), Laboratory of Research in Bioﬁlms Rosario Oliveira (LIBRO), University of Minho, Campus de Gualtar,4710-057 Braga, Portugalb Instituto de Cie^ncias Biomedicas Abel Salazar (ICBAS), University of Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugala r t i c l e i n f oArticle history:Received 5 October 2015Received in revised form19 October 2015Accepted 21 October 2015Available online 24 October 2015Keywords:Polymicrobial bioﬁlmsBacterial vaginosisGardnerella vaginalis virulence* Corresponding author.E-mail address: nunocerca@ceb.uminho.pt (N. Cerhttp://dx.doi.org/10.1016/j.anaerobe.2015.10.0081075-9964/© 2015 Elsevier Ltd. All rights reserved.a b s t r a c tDual-species bioﬁlm formation between Gardnerella vaginalis strains isolated from women with orwithout bacterial vaginosis (BV) and other 24 BV-associated microorganisms support that the key dif-ference in virulence potential between BV-negative and BV-positive G. vaginalis strains seems not to berelated with bioﬁlm maturation.© 2015 Elsevier Ltd. All rights reserved.Bacterial vaginosis (BV) is often characterized by a shift of thevaginal microbiota from a Lactobacillus-dominated community to adense bioﬁlm containing a complex mixture of microorganisms [1].Gardnerella vaginalis is the dominant pathogen colonising BVwomen, often adopting the bioﬁlm mode of growth as a survivalstrategy [2]. During BV, there is a complex interplay betweenpathogenic species, endogenous vaginal microbiota and the vaginalepithelium [1,3,4]. These interactions become more complex whenmicrobes are adhered to the epithelium, forming bioﬁlms, andcommunicate via “quorum-sensing”, a cell-density dependentbacterial intercellular signalling mechanism [5]. However,G. vaginalis can also be a part of the vaginal microbiota in healthywomen [6]. This raised the question whether there are pathogenicand commensal lineages within this species. Jayaprakash and col-leagues provided genomic evidence that all G. vaginalis strains hadthe potential to form bioﬁlm but not all strains had the potential tocause BV symptoms, namely due to absence of sialidase gene [7].We recently also provided in vitro evidence that supports Jayapra-kash hypothesis [8]. However, only the BV isolates demonstratedhigher cytotoxicity and were able to adhere in high density clustersto a HeLa cell line [9], a condition necessary to foster in vivo bioﬁlmca).development [5]. Another important insight providing evidencethat not all G. vaginalis have the same virulence potential wasderived from recent in vivo observations by Swidsinski and col-leagues. They demonstrated the presence of adherent bacterialbioﬁlms in 90% of biopsies fromwomen with BV, while only 10% ofhealthy women exhibited a similar bioﬁlms [10]. Subsequently,they proposed that the mere presence of loosely adherentG. vaginalis on the vaginal epithelium was of lesser clinical signiﬁ-cance than the presence of high density clusters of G. vaginalis [2].In effort to better understand the differences between virulent andnon-virulent G. vaginalis strains, the aim of the present studywas toanalyze the interactions between non-BV (n ¼ 3) or BV (n ¼ 3)G. vaginalis isolates and other BV-associated pathogens (n ¼ 24)using a dual-species bioﬁlm assembly, consisting in the combina-tion of G. vaginalis and secondary BV-associated species. All speciesused are listed in Table 1.The dual-species bioﬁlm formation model used was the same asdescribed by Machado and colleagues [11], with some minormodiﬁcations. Brieﬂy, G. vaginalis cultures were adjusted to1  107 colony-forming units (cfu)/mL by optical density (OD) at600 nm (Model Sunrise, Tecan). After homogenization, 100 mL ofeach bacterial suspension of G. vaginalis isolates was dispensed intoeach well of 96-well ﬂat-bottom tissue culture plate (Orange Sci-entiﬁc). The tissue cultured plates were then placed in an incubatorTable 1GenBank accession numbers of strains used in this study.Bacteriaa,b Genes Accession numberscActinomyces neuii UM067An 16S rRNA KT805271Actinomyces turicensis UM066At 16S rRNA KT805270Aerococcus christensenii UM137Ac 16S rRNA KT805273Bacillus ﬁrmus UM034Bf 16S rRNA KT805263Brevibacterium ravenspurgense UM066Br 16S rRNA KT805269Corynebacterium amycolatum UM065Ca 16S rRNA/rpoB KT805275/KT923481Corynebacterium tuberculostearicum UM137Ct2 16S rRNA/rpoB KT805279/KT923486Corynebacterium tuscaniense UM137Ct 16S rRNA/rpoB KT805278/KT923485Enterococcus faecalis UM035 16S rRNA KT614045Escherichia coli UM056 16S rRNA KT614048Gardnerella vaginalis UM085 16S rRNA KP996679Gardnerella vaginalis UM121 16S rRNA KP996681Gardnerella vaginalis UM131 16S rRNA KP996676Gardnerella vaginalis UM137 16S rRNA KP996682Gardnerella vaginalis UM241 16S rRNA KP996683Gardnerella vaginalis UM246 16S rRNA KP996677Gemella haemolysans UM034Gh 16S rRNA KT805264Lactobacillus vaginalis UM062Lv 16S rRNA KT805268Mobiluncus mulieris ATCC 35239 whole genome NZ_GL405260.1Nosocomiicoccus ampullae UM121Na 16S rRNA KT805272Prevotella bivia ATCC 29303 16S rRNA L16475.1Propionibacterium acnes UM034Pa 16S rRNA KT805265Streptococcus agalactiae UM035Sa 16S rRNA KT805266Staphylococcus epidermidis UM066Se 16S rRNA/rpoB KT805277/KT923483Staphylococcus haemolyticus UM066Sh 16S rRNA/rpoB KT805276/KT923482Staphylococcus hominis UM224Sh rpoB KT923487Staphylococcus saprophyticus UM121Ss rpoB KT923484Staphylococcus simulans UM059Ss 16S rRNA KT805267Staphylococcus warnerii UM224Sw rpoB KT923488Streptococcus anginosus UM241b 16S rRNA KT805274a Due to NCBI sequence deposition regulations, the designation of the strains previously used in Alves et al. [8], were updated (highlighted inbold).b Strains were grown in supplemented brain heart infusion (sBHI) and incubated at 37 C in 10% CO2 for 24 h, as described by Alves et al. [8]. Theexceptions were M. mulieris and P. bivia that were grown in sBHI and incubated at 37 C, under anaerobic conditions (AnaeroGen AtmosphereGeneration system; Oxoid, United Kingdom) for 48 h.c The accession numbers of partial 16S ribosomal RNA or rpoB gene sequence of vaginal isolates are downloadable from NCBI.J. Castro, N. Cerca / Anaerobe 36 (2015) 56e59 57at 37 C in 10% CO2. Following 24 h, the culture medium coveringthe bioﬁlmwas carefully removed and replaced by freshmedium. Asecond inoculationwith 1 107 cfu/mL of each BV-associated strainwas performed and bioﬁlms were allowed to growth for another24 h. Quantiﬁcation of bioﬁlm was performed by the crystal violetstaining, as previously described [12]. All assays were repeated atleast 3 times with 8 technical replicates. The data were analyzedusing the non-parametric KruskaleWallis test, since the data didnot follow a normal distribution according Kolmogorov-Smirvon'stest, with the statistical software package SPSS 17.0 (SPSS Inc.Chicago, IL). P-values of less than 0.05 were considered signiﬁcant.As described in Fig. 1, our results revealed that 54% (n ¼ 13) ofthe BV-associated species tested had a synergistic effect in most ofG. vaginalis strains. However, only 6 species caused an increase inbioﬁlm formation in all tested conditions: Actinomyces neuii, Bre-vibacterium ravenspurgense, Corynebacterium amycolatum, Coryne-bacterium tuscaniense, Staphylococcus hominis and Staphylococcussaprohyticus. Conversely, we observed that 42% of the tested speciesshowed variable interactions dependent of the speciﬁc G. vaginalisstrain used. However, no link (P ¼ 0.131; KruskaleWallis) wasfound between non-BV and BV G. vaginalis strains, with theexception of Mobiluncus mulieris, which showed an antagonisticeffect when added to the bioﬁlm formed by BV strains, whereas asynergistic interaction was veriﬁed in presence bioﬁlms formed bynon-BV G. vaginalis isolates. Finally, our data also revealed anantagonistic interaction between all G. vaginalis strains tested andLactobacillus vaginalis.The most recent model for the pathogenesis of BV suggests thatG. vaginalis adhered to vaginal epithelium might be acting as ascaffold for the attachment of a subsequent species [1,13]. However,the role of BV-associated bacteria in multi-species bioﬁlms is stillpoorly understood. An early study by Machado and colleaguesdemonstrated that a few secondary BV-associated anaerobes, suchas Prevotella bivia, were able to increment the concentration of cellswithin the bioﬁlm, when added to a pre-formed G. vaginalis bio-ﬁlms [11].Herein, we were interested to determine if similar synergisticinteractions occurredwhen using BV or non-BVG. vaginalis isolates.Surprisingly, with the exception of one species (M. mulieris), nodifferences were found between BV and non-BV associatedG. vaginalis mediated dual-species bioﬁlm augmentation. Theseresults suggests that the key difference in BV or non-BV G. vaginalisvirulence potential seems not to be related with bioﬁlm matura-tion, at least in a dual-species model. We propose that once speciﬁcstrains of G. vaginalis are able to outcompete the resident Lacto-bacillus species and start to growth in clusters, secondary anaerobeswill easily incorporate the bioﬁlm. This might be the key differencein virulence potential of G. vaginalis [9].A particular example of synergistic interaction in dual-speciesbioﬁlms is the case of G. vaginalis and P. bivia. It has been previ-ously shown that G. vaginalis produces amino acids through itsmetabolism and P. bivia, a strict anaerobe, uses amino acids as itsfuel source and as a result produces ammonia, which in turn is usedby G. vaginalis [14]. Nevertheless, our data also showed thatL. vaginalis had an antagonistic effect in the presence of all testedG. vaginalis bioﬁlms. Boskey and colleagues have showed that theFig. 1. Synergistic, antagonistic or neutral interactions detected in dual-species bioﬁlms in relation to a single bioﬁlms of non-BV or BV G. vaginalis isolates. The data are presented asfold change relative to the single G. vaginalis bioﬁlm (fold change ¼ 1, control). Interactions were classiﬁed as antagonistic (cut-off < 0.75-fold changes), neutral (0.75  foldchanges < 1.25) and synergistic (cut-off  1.25 e fold changes). Results represents at least 3 independent experiments performed with 8 technical replicates. No signiﬁcant dif-ferences between non-BV and BV G. vaginalis strains were found in a dual-species bioﬁlm formation (P ¼ 0.131; KruskaleWallis), with exception to M. mulieris (P ¼ 0.05;KruskaleWallis).J. Castro, N. Cerca / Anaerobe 36 (2015) 56e5958growth limiting factor for L. vaginalis was a depletion of a metab-olite or the buildup of an unspeciﬁed toxic waste product [15], thatmight also be toxic to G. vaginalis causing a disruption of the bio-ﬁlm. Curiously, our ﬁndings revealed that M. mulieris was the onlybacterial speciewith opposing interactions in the presence of eithernon-BV or BV pre-formed G. vaginalis bioﬁlms. Nevertheless,further work is required to explore the bacterial interactions be-tween these bacterial species.The results from our study should be interpreted in light ofseveral limitations. First, initial adhesion by G. vaginalis was per-formed in polystyrene microtiter plate wells rather than vaginalepithelium, where the presence of host-derived factors (e.g. mucusproduction, speciﬁc receptors on the epithelial surface) can inﬂu-ence bacterial adherence and bioﬁlm formation. This technicallimitation is not easy to overcome since, as we shown before,G. vaginalis quickly induces cytotoxic changes and detachment ofpre-adhered epithelial cultures [9]. Furthermore, the growth me-dium did not contain all of the factors found in vivo, and somein vivo cues may turn on expression of bioﬁlm-related genes.However, these limitations aside, in vitro models can be veryinformative and are key to furthering our understanding on multi-species bioﬁlms and the development of BV.In conclusion, this study provides direct evidence that conﬁrmssynergistic roles of many secondary or late colonizers in BV multi-species bioﬁlm development, but reveals that those interactions arenot speciﬁc for more virulent BV-associated G. vaginalis.AcknowledgementsThe authors thank the FCT Strategic Project of UID/BIO/04469/2013 unit and the project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462). The funders had no role in study design, datacollection and analysis, decision to publish, or preparation of themanuscript. JC was funded by the FCT individual fellowship SFRH/BD/93963/2013. NC is an Investigador FCT.References[1] J.R. Schwebke, C.A. Muzny, W.E. Josey, Role of Gardnerella vaginalis in thepathogenesis of bacterial vaginosis: a conceptual model, J. Infect. Dis. 210(2014) 338e343. http://dx.doi.org/10.1093/infdis/jiu089.[2] A. Swidsinski, V. Loening-Baucke, W. Mendling, Y. D€orffel, J. Schilling,Z. Halwani, et al., Infection through structured polymicrobial Gardnerellabioﬁlms (StPM-GB), Histol. Histopathol. 29 (2013) 567e587, http://dx.doi.org/10.14670/HH-29.10.567.[3] J.M. Marrazzo, Interpreting the epidemiology and natural history of bacterialvaginosis: are we still confused? Anaerobe 17 (2011) 186e190, http://dx.doi.org/10.1016/j.anaerobe.2011.03.016.[4] M.J. Redelinghuys, M.M. Ehlers, A.W. Dreyer, M.M. Kock, Normal ﬂora andbacterial vaginosis in pregnancy: an overview, Crit. Rev. Microbiol. (2015)1e12, http://dx.doi.org/10.3109/1040841X.2014.954522.J. Castro, N. Cerca / Anaerobe 36 (2015) 56e59 59[5] B.M. Peters, M.A. Jabra-Rizk, G.A. O'May, J.W. Costerton, M.E. Shirtliff, Poly-microbial interactions: impact on pathogenesis and human disease, Clin.Microbiol. Rev. 25 (2012) 193e213, http://dx.doi.org/10.1128/CMR.00013-11.[6] J.M. Marrazzo, L.A. Koutsky, D.A. Eschenbach, K. Agnew, K. Stine, S.L. Hillier,Characterization of vaginal ﬂora and bacterial vaginosis in women who havesex with women, J. Infect. Dis. 185 (2002) 1307e1313, http://dx.doi.org/10.1086/339884.[7] T.P. Jayaprakash, J.J. Schellenberg, J.E. Hill, Resolution and characterization ofdistinct cpn60-based subgroups of Gardnerella vaginalis in the vaginalmicrobiota, PLoS One 7 (2012) e43009. http://dx.doi.org/10.1371/journal.pone.0043009.[8] P. Alves, J. Castro, C. Sousa, T.B. Cereija, N. Cerca, Gardnerella vaginalis out-competes 29 other bacterial species isolated from patients with bacterialvaginosis, using in an in vitro bioﬁlm formation model, J. Infect. Dis. 210(2014) 593e596. http://dx.doi.org/10.1093/infdis/jiu131.[9] J. Castro, P. Alves, C. Sousa, T. Cereija, A^. França, K.K. Jefferson, et al., Using anin-vitro bioﬁlm model to assess the virulence potential of bacterial vaginosisor non-Bacterial vaginosis Gardnerella vaginalis isolates, Sci. Rep. 5 (2015)11640. http://dx.doi.org/10.1038/srep11640.[10] A. Swidsinski, W. Mendling, V. Loening-Baucke, A. Ladhoff, S. Swidsinski,L.P. Hale, et al., Adherent bioﬁlms in bacterial vaginosis, Obstet. Gynecol. 106(2005) 1013e1123. http://dx.doi.org/10.1097/01.AOG.0000183594.45524.d2.[11] A. Machado, K.K. Jefferson, N. Cerca, Interactions between Lactobacilluscrispatus and bacterial vaginosis (BV)-Associated bacterial species in initialattachment and bioﬁlm formation, Int. J. Mol. Sci. 14 (2013) 12004e12012,http://dx.doi.org/10.3390/ijms140612004.[12] D. Machado, A. Palmeira-de-Oliveira, N. Cerca, Optimization of culture con-ditions for Gardnerella vaginalis bioﬁlms formation, J. Microbiol. Methods 14(118) (2015) 143e146, http://dx.doi.org/10.1016/j.mimet.2015.09.007.[13] A. Machado, N. Cerca, Inﬂuence of bioﬁlm formation by Gardnerella vaginalisand other anaerobes on bacterial vaginosis, J. Infect. Dis. (2015), http://dx.doi.org/10.1093/infdis/jiv338 (in press).[14] V. Pybus, A.B. Onderdonk, Evidence for a commensal, symbiotic relationshipbetween Gardnerella vaginalis and Prevotella bivia involving ammonia: po-tential signiﬁcance for bacterial vaginosis, J. Infect. Dis. 175 (1997) 406e413.http://dx.doi.org/10.1093/infdis/175.2.406.[15] E.R. Boskey, K.M. Telsch, K.J. Whaley, T.R. Moench, R.A. Cone, Acid productionby vaginal ﬂora in vitro is consistent with the rate and extent of vaginalacidiﬁcation, Infect. Immun. 67 (1999) 5170e5175. PMID: 10496892.

BV and non-BV associated Gardnerella vaginalis establish similar synergistic interactions with other BV-associated microorganisms in dual-species biofilms

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Universidade do Minho: RepositoriUM