Dentre os contaminantes de água subterrânea de maior importância está o tetracloroeteno (PCE), o qual é altamente tóxico e potencialmente carcinógeno. As comunidades bacterianas de águas subterrâneas contaminadas com PCE e a diversidade de bactérias capazes de degradar esses organoclorados são pouco conhecidas. O objetivo deste trabalho é comparar a estrutura das comunidades de bactérias de amostras de água subterrânea em uma área contaminada com PCE e selecionar um consórcio microbiano capaz de degradar eficientemente o PCE em reator horizontal de leito fixo (RHLF). Amostras de água subterrânea de oito poços de monitoramento, instalados em uma área contaminada com PCE foram coletadas e analisadas para determinação de oxigênio dissolvido, potencial redox, condutividade elétrica, pH e concentração de tetracloroeteno, tricloroeteno, cis-dicloroeteno e cloreto de vinila (COVs). As amostras foram analisadas também para a determinação da estrutura das comunidades de bactéria por PCRDGGE e seqüenciamento de clones do gene rRNA 16S. Os parâmetros físico-químicos oscilaram consideravelmente ao longo do tempo em todos os poços de monitoramento (PM). Tetracloroeteno e tricloroeteno foram detectados apenas no PM6. As estruturas das comunidades bacterianas dos PMs analisados mostraram tanto variação temporal quanto espacial. As análises das comunidades bacterianas nos PM6 e PM8, contaminado e não-contaminado com PCE, revelaram resultados semelhantes aos obtidos por DGGE. Uma maior riqueza estimada de espécies bacterianas foi observada nas amostras do PM8, pelo menos em duas épocas de amostragem, sugerindo que a contaminação com PCE está associada com a redução da diversidade bacteriana em água subterrânea. Cultivos de enriquecimento e ensaios de degradação do PCE foram realizados utilizando-se um RHLF, o qual foi preenchido com sedimento do PM6 imobilizado em espuma de poliuretano e enriquecido com meio mineral básico suplementado com PCE. A análise das alterações nas comunidades de bactérias nos reatores foi feita por PCRDGGE e seqüenciamento parcial do gene rRNA 16S. No ensaio de degradação do PCE no RHLF foi utilizado meio com PCE suplementado ou não com lactato e acetato. Tanto pelo DGGE quanto pelo seqüenciamento, foi observada a seleção de bactérias específicas no reator. A partir das análises de seqüenciamento, essas bactérias foram identificadas como Alphaproteobacteria e Sphingobacteria. No ensaio de degradação do PCE, os parâmetros físico-químicos do meio não mostraram variações ao longo do comprimento dos reatores. As análises de COVs mostraram uma grande eficiência na degradação do PCE (98%), com um tempo de retenção de 12 horas, não havendo diferença significativa na percentagem de degradação em meio com lactato ou acetato, com relação ao controle sem fonte de carbono. No processo de degradação nenhum dos produtos da via de degradação do PCE foi detectado, o que sugere uma via alternativa de degradação do PCE, a qual ocorre em aerobiose. / Tetrachloroethene (PCE) is one of the most important contaminants of groundwater, since it is highly toxic and potentially carcinogenic. The bacterial communities of PCE contaminated groundwater and the diversity of bacteria capable of degrading this contaminant are barely known. The objective of this work is to compare the structure of bacterial communities from groundwater samples from a PCE contaminated site and select a microbial consortium capable to degrading efficiently PCE in a horizontal fixed bed reactor (HFBR). Groundwater samples from eight monitoring wells, installed in a PCE contaminated site were collected and analyzed for determination of dissolved oxygen, redox potential, electrical conductivity, pH, and concentrations of tetrachloroethene, trichloroethene (TCE), cis- and trans-dichloroethene, vinyl chloride (VOCs). The structure of the bacterial communities was determined by PCR-DGGE and 16S rRNA gene clone sequencing. The physical-chemical parameters oscillated considerately throughout time in all the monitoring wells (MW). PCE and TCE were detected only in MW6. The bacterial community structures in the groundwater from the MWs analyzed showed temporal and spatial variation. The analysis of the bacterial communities in MW6 and MW8, contaminated and non-contaminated with PCE, respectively, based on sequencing of 16S rRNA gene clones revealed results to the ones observed by DGGE. Estimated richness of bacterial species was higher in samples from MW8, at least in two sampling times, suggesting that the contamination with PCE is associated with reduction of bacterial diversity in groundwater. Enrichment cultures and PCE biodegradation assays were performed in a HFBR, which was filled with sediment from MW6 immobilized onto polyurethane foam and enriched with basic mineral medium supplemented with PCE. Shifts in bacterial community structure were analyzed using PCRDGGE and partial sequencing of 16S rRNA gene clones. In the PCE biodegradation assays in the HFBR, were performed in medium containing lactate or acetate. DGGE and 16S rRNA gene clone sequencing data suggest selection of specific bacteria in the reactor. Sequencing data showed that these bacteria belong to Alphaproteobacteria and Sphingobacteria. In the PCE biodegradation assays, media physical-chemical parameters did not show variation along the reactor length. VOC analyses showed a great efficiency in the degradation of PCE (98%) with a residence time of 12 hours in the reactor, and no significant differences were observed in the presence of lactate or acetate, as compared to the medium without a carbon source. During the biodegradation process, none of the products from the anaerobic pathway of PCE reductive dechlorination was detected, suggesting that an alternative PCE biodegradation pathway is occurring in aerobiosis.

Staphylococcus aureus has been extensively studied, yet it remains unclear why certain individuals continually carry the bacteria while others do not. Livestock workers are known to be at an increased risk of S. aureus colonization, but have not been as studied as other high risk groups, including hospitalized patients, have been. Culture based studies have shown other bacteria may decrease the likelihood of S. aureus colonization. Here, we utilize 16s rRNA sequencing to better characterize the ecologic relationships between S. aureus and the other microbes in the nares and oropharynx in a population of livestock workers. A cross-sectional, epidemiological study was conducted enrolling 59 participants (26 of which had livestock contact) in Iowa. Participants were enrolled in one of four ways: from an existing prospective cohort study (n=38), from the Iowa Department of Natural Resources Animal Feeding Operations database (n=17), through Iowa county fairs (n=3), and through snowball sampling (n=1). We collected two sets of swabs from the nares and oropharynx of each participant. The first set of swabs was used to assess the microbiome via 16s rRNA sequencing and the second was used to culture S. aureus. We observed livestock workers to have greater diversity in their microbiomes compared to those with no livestock contact. In the nares, there were 26 operational taxonomic units found to be different between livestock workers and non-livestock workers with the greatest difference seen with Streptococcus and Proteobacteria. In the oropharynx, livestock workers with swine exposure were more likely to carry several pathogenic organisms. We also observed colonized livestock workers to be more likely to carry P. gingivalis which may act as a bridge allowing S. aureus to adhere to Streptococcus in the oral cavity. While we observed no significant differences when comparing colonized persons to non-colonized persons in either the nares or oropharynx, Corynebacterium was more abundant in the colonized persons. Colonized individuals also had greater diversity in their nasal microbiome compared to non-colonized individuals. However, when comparing persistently colonized persons to intermittently colonized persons, we found Corynebacterium argentorantense to be more abundant in the persistently colonized individuals. We hypothesized the genera present in the nares and oropharynx of S. aureus carriers would be different from that of non-carriers and there would be differences in the nasal and oropharyngeal microbiomes based on livestock contact and carrier state (persistent, intermittent, and non-carrier). While there were no significant differences between carriers and non-carriers, we were able to identify several operational taxonomic units that were different between livestock worker carrier and non-carriers as well as differences by carrier state. The results of this study are the first to characterize the livestock worker nasal and oropharyngeal microbiomes. Additionally, the results shed light onto several organisms that may be influential in S. aureus carriage. However, further studies are needed to better understand these relationships and determine causality.

The bacterium Vibrio vulnificus is an autochthonous inhabitant of estuarine waters and also found in shellfish such as oysters. It is a human pathogen of importance in the seafood industry, and can also infect recreational water users. Currently, recognized methods of detection rely upon isolation of pure cultures which requires at least 24 hours. To reduce the time needed for identification of the pathogen and simultaneously ascertain the virulence potential of the strains present, real-time PCR assays and sample processing procedures were developed (Chapter 1). These assays discriminate between type A (environmental, generally lower virulence) and type B (clinical, higher virulence) isolates. The genetic relationships between environmental V. vulnificus strains isolated from permitted and prohibited shellfish harvesting areas was determined using BOX-PCR genomic fingerprinting coupled with sequence analysis of three proposed virulence markers: (1) the virulence correlated gene (vcg), (2) 16S rRNA type and (3) presence/absence of the vulnibactin gene (viuB) (Chapter 2). The real-time PCR assays were able to detect the presence of seeded V. vulnificus in environmental water at a concentration of 160 cells 100·ml-1. In seeded oyster homogenates, the assays were able to detect a minimum of 10³ cells and 10² cells per reaction of type A and type B respectively. The phylogenetic analysis separated the majority of type A/ vcgE strains isolated from permitted shellfish harvesting areas from those isolated from prohibited harvesting areas. The genomic (BOX-PCR) fingerprints of type A and type AB isolates were more similar to one another than to type B isolates. Only one type A/ vcgE isolate contained the viuB gene; however, eight type B/ vcgC isolates had that gene. No obvious grouping was discerned between type B/ vcgC isolates from permitted versus prohibited shellfish harvesting areas or between those possessing the viuB gene versus those lacking viuB. These data provide insight into the ecology and correlation between population biology and general water quality, as gauged by the classification of the shellfish growing area waters. The 16S typing assays can be used for routine rapid typing to aid in risk assessment and reduce infection frequency through consumption of contaminated seafood.

Cyanobacteria are an ancient lineage of gram-negative photosynthetic prokaryotes that play an important role in the nitrogen cycle in terrestrial and aquatic systems. Widespread cyanobacterial blooms have prompted numerous studies on the classification of this group, however defining species is problematic due to lack of clarity as to which characters best define the various taxonomic levels. The genera Anabaena, Aphanizomenon and Nostoc form one of the most controversial groups and are typically paraphyletic within phylogenetic trees and share similar morphological characters. This study’s purpose was to determine the taxonomic and phylogenetic relationships among isolates from these three genera using 16S rRNA and bacterial elongation factor P (efp) gene sequences as well as morphological analyses. These data confirmed the non-monophyly of Anabaena and Aphanizomenon and demonstrated that many of the isolates were intermixed among various clades in both gene phylogenies. In addition, the genus Nostoc was clearly not monophyletic and this finding differed from previous studies. The genetic divergence of the genus Nostoc was confirmed based on 16S rRNA gene sequence similarities (≥85.1%), and the isolates of Anabaena were genetically differentiated, contrary to previous studies (16S rRNA gene sequence similarities ≥89.4%). The morphological diversity was larger than the molecular diversity, since the statistical analysis ANOSIM showed that the isolates were morphologically well differentiated; however, the 16S rRNA gene sequence similarities showed some isolates as being related at the species level. Planktonic and benthic strains were not distinguished phylogenetically, although some well-supported clusters were noted. Cellular measurements (length and width of vegetative cells, end cells, heterocysts and akinetes) were noted to be the morphological characters that best supported the differentiation among isolates, more than qualitative characterization. Among the metric parameters, the length of akinetes resulted in better differentiation among isolates. The efp gene sequence analyses did not appear to be useful for the taxonomic differentiation at lower taxonomic levels, but gave well-supported clusters for Aphanizomenon that was supported by the morphological analyses. Both gene regions gave similar trees with the exception of the Aphanizomenon isolates which clustered together in phylogenetic trees based on the efp gene. This differed from the 16S rRNA gene in which this genus was paraphyletic with Anabaena species that were similar in morphology to Aphanizomenon. Hence, the application of multiple taxonomic criteria is required for the successful delineation of cyanobacterial species.

Not many of the abundant freshwater bacterial groups have a representative cultured isolate. In this master thesis project, some abundant bacterioplankton from two lakes (Lake Ekoln and Lake Erken) could be isolated by a dilution-to-extinction approach. Sterilized lake water which was obtained through an ultrafiltration system was used resembling a natural medium. Specific fragments of 16s rRNA of the isolates were amplified by universal bacterial primers (27f and 1492r, 341f and 805r.) for genotyping against a freshwater sequence database and RDP training set (Version 7). A total of 33 isolates from the two lakes were taxonomically classified and revealed the isolation of typical and abundant freshwater bacteria. Original bacterial community of Lake Ekoln was also analyzed by 16S rRNA clone library construction for diversity study. Phylogenetic trees were built through neighbor-joining method by Mega (Version 5) to reveal the evolutionary relationships among database entries, obtained isolates and clones.

Cyanobacteria are an ancient lineage of gram-negative photosynthetic prokaryotes that play an important role in the nitrogen cycle in terrestrial and aquatic systems. Widespread cyanobacterial blooms have prompted numerous studies on the classification of this group, however defining species is problematic due to lack of clarity as to which characters best define the various taxonomic levels. The genera Anabaena, Aphanizomenon and Nostoc form one of the most controversial groups and are typically paraphyletic within phylogenetic trees and share similar morphological characters. This study’s purpose was to determine the taxonomic and phylogenetic relationships among isolates from these three genera using 16S rRNA and bacterial elongation factor P (efp) gene sequences as well as morphological analyses. These data confirmed the non-monophyly of Anabaena and Aphanizomenon and demonstrated that many of the isolates were intermixed among various clades in both gene phylogenies. In addition, the genus Nostoc was clearly not monophyletic and this finding differed from previous studies. The genetic divergence of the genus Nostoc was confirmed based on 16S rRNA gene sequence similarities (≥85.1%), and the isolates of Anabaena were genetically differentiated, contrary to previous studies (16S rRNA gene sequence similarities ≥89.4%). The morphological diversity was larger than the molecular diversity, since the statistical analysis ANOSIM showed that the isolates were morphologically well differentiated; however, the 16S rRNA gene sequence similarities showed some isolates as being related at the species level. Planktonic and benthic strains were not distinguished phylogenetically, although some well-supported clusters were noted. Cellular measurements (length and width of vegetative cells, end cells, heterocysts and akinetes) were noted to be the morphological characters that best supported the differentiation among isolates, more than qualitative characterization. Among the metric parameters, the length of akinetes resulted in better differentiation among isolates. The efp gene sequence analyses did not appear to be useful for the taxonomic differentiation at lower taxonomic levels, but gave well-supported clusters for Aphanizomenon that was supported by the morphological analyses. Both gene regions gave similar trees with the exception of the Aphanizomenon isolates which clustered together in phylogenetic trees based on the efp gene. This differed from the 16S rRNA gene in which this genus was paraphyletic with Anabaena species that were similar in morphology to Aphanizomenon. Hence, the application of multiple taxonomic criteria is required for the successful delineation of cyanobacterial species.

Anchialine blue holes found in the interior of the Bahama Islands have distinct fresh and salt water layers, with vertical mixing, and dysoxic to anoxic conditions below the halocline. Scientific cave diving exploration and microbiological investigations of Cherokee Road Extension Blue Hole on Abaco Island have provided detailed information about the water chemistry of the vertically stratified water column. Hydrologic parameters measured suggest that circulation of seawater is occurring deep within the platform. Dense microbial assemblages which occurred as mats on the cave walls below the halocline were investigated through construction of 16S rRNA clone libraries, finding representatives across several bacterial lineages including Chlorobium and OP8. In many blue holes, microbial metabolism of organic matter in the presence of seawater sulfate leads to anoxic and sulfidic conditions at or below halocline. Sunlight penetrating this sulfidic layer allows for in situ primary production to be dominated by bacterial anoxygenic phototrophs. Although water column chemistry and molecular genetic diversity of microbial mats in Cherokee Road Extension Blue Hole were investigated in this study, the full scope of the biogeochemistry of inland blue holes throughout the Bahamas Archipelago is complex and poorly understood. However, these microbial communities are clearly influenced by several factors including solar insolation, terrestrial and marine inputs of oxygen, carbon, and nutrients, water residence times, depth to the halo/chemocline, and cave passage geometry. The biogeochemistry of inland blue holes throughout the Bahamas is so distinctive which makes Abaco Island and the rest of the archipelago valuable as natural experiments, repositories of microbial diversity, and analogs for stratified and sulfidic oceans present early in Earth's history.

Probiotics are viable microorganisms that show beneficial effects on the health of the host by improving their intestinal microflora. The microorganisms applied as probiotics mainly include Lactobacillus and Bifidobacterium species. Probiotics can inhibit the bacterial pathogens, reduce serum cholesterol levels, improve lactose tolerance and stimulate the immune response. They also have other properties such as / tolerance to acid and bile salts, adherence to gastrointestinal cells for colonization, resistance to antibiotics and &beta / -galactosidase acitivity. The properties of probiotic products are determined by the characteristics of the microorganisms they contain. For that reason, isolation and characterization of new strains having probiotic properties is an important issue. New strains are generally isolated from their natural habitats which are fermented dairy products such as kefir. In order to exert beneficial health affects in the digestive system, commercial probiotic products should contain adequate numbers of viable cells. Probiotic microorganisms should protect their viability during their shelf storage. Therefore, the viability of probiotics is especially important for food manufacturers that search for new probiotic strains with good survival and stability properties upon storage. In this study, probiotic microorganisms were isolated from traditional kefir grains known as a &lsquo / complex probiotic&rsquo / . The isolates were firstly identified using biochemical tests, then the putative species belonging to &lsquo / Lactobacillus acidophilus group&rsquo / were identified with 16S rRNA gene sequencing. Analysis of sequencing resulted in differentiation of &ldquo / L. acidophilus group&rdquo / organisms, namely L. amylovorus and L. acidophilus. Moreover, typing of commercial and traditional L. acidophilus strains and L. amylovorus strains were performed with RAPD-PCR by using primer M13. While several L. acidophilus strains showed different RAPD fingerprints most of the L. acidophilus and L. amylovorus strains could not be differentiated due to high similarity of their RAPD fingerprints. Following identification, survival of these isolates in probiotic yogurt preparations were investigated and compared to the survival of commercial probiotics. Consequently, although the survival of kefir grain isolates were less than commercial probiotics, they sustained the minimum recommended level for probiotics (106 cfu/ml) during cold storage. Such level of survival makes them considerably good candidates to be used as commercial probiotic cultures.

The ecological niche of the vagina contains a large number of different microbes that are constantly interacting with each other and the host. Culture methods have not been sufficient in order to resolve the complexity of the normal vaginal flora. Further, the methods for delineating normal flora from not normal flora are not easily handled and are traditionally not based on culture but on microscopy of elements of the vaginal fluid. In the work presented in this thesis, an international collaboration was established that pin-pointed some of the difficulties in classifying vaginal floras, including staining, sampling, and discordance when lactobacilli are few in number, and that emphasized the importance of the size of the vision field in microscopes. As lactobacilli are prominent members of the normal vaginal flora they need to be carefully classified if further work towards more robust scoring tools is to be achieved. Phenotypic methods have not been able to separate the closely related Lactobacillus species of the vagina. Progress in molecular biology has provided possibilities to characterize these lactobacilli, which are mainly from the Lactobacillus acidophilus group. In this work a large number of strains collected by true random sampling were subjected to RAPD-PCR, TTGE and multiplex PCR for species identification. The major species found were L. crispatus, L. gasseri and L. jensenii and the recently described L. iners. The presence of L. iners has not been detected in previous studies due to its special nutrient requirements. Development of pyrosequencing technology also made it possible to match signatures of the two variable regions V1 and V3 of the 16S rRNA gene of the vaginal lactobacilli and identify them to the species level in a high throughput manner. The study confirmed that the dominating flora in women with normal vaginal flora comprises the four species mentioned previously. Repetitive sampling during IVF-treatment with highly varying oestrogen levels demonstrates changes that possibly occur during changes in the natural life cycle. Furthermore, L. iners was found to be the first species to be established after spontaneously resolved or treated Bacterial Vaginosis. These findings can be of help in developing new strategies for regaining and retaining the normal vaginal flora.

Τα ισόποδα αποτελούν τη μοναδική τάξη οργανισμών ανάμεσα σε όλα τα Καρκινοειδή που πέτυχε να εποικήσει όλους τους τύπους ενδιαιτημάτων, από τα βάθη των ωκεανών μέχρι τα βουνά, τις έρημους και τις τροπικές περιοχές. Παρόλα αυτά, οι φυλογενετικές σχέσεις εντός της τάξης των ισοπόδων παραμένουν σε πολλά σημεία ασαφείς. Η οικογένεια Tylidae, που περιλαμβάνει 27 αμφίβια είδη, ανήκει σύμφωνα με τη σημερινή συστηματική κατάταξη στην υπόταξη Oniscidea, τη μοναδική που περιλαμβάνει αντιπροσώπους με χερσαίο ή ημι-χερσαίο τύπο διαβίωσης. Αν και υπάρχουν αμφιβολίες ως προς τη μονοφυλετική προέλευση αρκετών από τις 9 υποτάξεις που περιλαμβάνουν θαλάσσιους αντιπροσώπους, η προέλευση των Oniscidea θεωρείται αδιαμφισβήτητα μονοφυλετική. Εντούτοις, δεν υπάρχει ακόμη συμφωνία ως προς την ακριβή τοποθέτηση του κλάδου των Tylidae στο φυλογενετικό δέντρο των Oniscidea. Ο βασικός στόχος της παρούσας εργασίας ήταν ο προσδιορισμός των φυλογενετικών σχέσεων των αμφιβίων ισοπόδων της οικογένειας Tylidae με τα υπόλοιπα ισόποδα, με έμφαση στις σχέσεις με τα υπόλοιπα Oniscidea. Για το σκοπό αυτό χρησιμοποιήθηκαν μοριακοί δείκτες από 14 γένη ισοπόδων, τα οποία αντιπροσωπεύουν όλους τους τύπους διαβίωσης, από τον αποκλειστικά θαλάσσιο έως τον αποκλειστικά χερσαίο. Η πειραματική προσέγγιση περιλάμβανε τον πολλαπλασιασμό αλληλουχιών του πυρηνικού γονίδιου 18s rDNA και των μιτοχονδριακών 16s rDNA και COI με τη μέθοδο της αλυσιδωτής αντίδρασης πολυμέρασης (PCR), τον προσδιορισμό της αλληλουχίας τους και τη φυλογενετική ανάλυσή τους με μεθόδους μέγιστης φειδωλότητας, μέγιστης πιθανοφάνειας και μπεϊεσιανής συμπερασματολογίας. Οι μιτοχονδριακές αλληλουχίες εμφανίζουν πολύ υψηλά ποσοστά νουκλεοτιδικών υποκαταστάσεων, και σε συνδυασμό με τη χαμηλή αξιοπιστία των δέντρων που παράγονται φαίνεται πως έχουν απωλέσει εντελώς το φυλογενετικό τους σήμα. Η αλληλουχία του 18s rDNA έχει μήκος 2400-3400 bp και αποτελείται από 4 συντηρημένες περιοχές και 3 υπερ-μεταβλητές. Για τις φυλογενετικές αναλύσεις χρησιμοποιήθηκαν μόνο οι συντηρημένες περιοχές, που συνιστούν ένα σύνολο 1597 διακριτών χαρακτήρων. Στα αποτελέσματα από όλες τις υπολογιστικές μεθόδους η οικογένεια Tylidae τοποθετείται στο τελικό δέντρο σε αδελφό κλάδο του τάξου Crinochaeta της υπόταξης Oniscidea. Εντούτοις, παρατηρήθηκε πως η οικογένεια Ligiidae τοποθετείται σε κλάδο μη-συγγενικό προς τα υπόλοιπα χερσαία ισόποδα, υπονοώντας πως η υπόταξη Oniscidea δεν είναι μονοφυλετική. Για να ελέγξουμε αυτήν την υπόθεση, χωρίσαμε τα δεδομένα μας σε αλληλουχίες από θαλάσσιους και σε αλληλουχίες από χερσαίους αντιπροσώπους, πραγματοποιώντας ένα σύνολο από πρόσθετες αναλύσεις. Από τα αποτελέσματα φαίνεται πως η υπόταξη Oniscidea είναι μονοφυλετική και η αντίθετη αρχική υπόθεση οφείλεται σε ‘θόρυβο’ στο φυλογενετικό σήμα των συντηρητικών περιοχών του 18s rDNA. Τέλος, από τις πρόσθετες αναλύσεις προκύπτουν, με ισχυρή στατιστική στήριξη, φυλογενετικά δέντρα που υποστηρίζουν τη συστηματική κατάταξη που είχε προτείνει ο Erhard από τις μορφολογικές του μελέτες, τοποθετώντας τα Tylidae εντός του τάξου ‘Holoverticata’. / Isopods comprise a unique order among the Crustaceans that has settled effectively all possible habitats on the planet. The phylogenetic relationships, though, between the 10 suborders remain unresolved, as many of them might prove to be non-monophyletic taxa. The family Tylidae consists of 27 amphibian species and is traditionally classified in the suborder Oniscidea, which includes all the terrestrial and semi-terrestrial isopods and that is thought to be unambiguously monophyletic. However, the previous phylogenetic studies have proposed many hypotheses concerning the relations between the Tylidae and the other Oniscidea, lacking any plausible consensus. In order to resolve those phylogenetic relations, we used two mitochondrial sequences (16s, COI) and one nuclear (18s) from 14 genera of isopods. Our experimental approach included PCR amplification, sequencing and computational phylogenetic analyses by means of maximum parsimony, maximum likelihood and Bayesian inference. The mitochondrial sequences present extreme values of nucleotide substitutions and evident saturation, a fact that prohibits their use in further analyses. The 18s sequences vary significantly in size (2400-3400 bp) and consist of 4 conserved and 3 hyper-variable regions. Only the conserved regions were used for analysis, resulting to a dataset of 1597 discrete nucleotide characters. Regardless of the method used, the family Tylidae appeared as a sister-clade of the taxon Crinochaeta (suborder Oniscidea) in the cladograms. We noticed, though, that the taxon Diplochaeta (Oniscidea: Ligiidae) appeared (with low bootstrap values) in a distant clade of all the other Oniscidea, a result that does not support the monophyletic origin of the Oniscidea. In order to test the validity of this result, we splitted our dataset and conducted additional, separate analyses for the sequences of the marine isopods and those of the terrestrial isopods. Our results indicate that the suborder Oniscidea is monophyletic, so the initial opposite hypothesis was due to weak phylogenetic signal. Finally, our cladograms support, with significant confidence, the systematic classification that Erhard (1998) had proposed through his studies on morphological characters of the Oniscidea, placing together the family Tylidae and the taxon Crinochaeta under the name ‘Holoverticata’.