@phdthesis{Brado2020,
  author    = {Brado, Dominik Alexander},
  title     = {Genetic diversity and baseline drug resistance of South African HIV-1 Integrase sequences prior to the availability of Integrase strand-transfer inhibitors},
  doi       = {10.25972/OPUS-21656},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-216562},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2020},
  abstract  = {Background: Integrase strand transfer inhibitors (INSTIs) are the latest addition to the array of antiretroviral compounds used to treat an infection with Human Immunodeficiency Virus (HIV). Due to their high efficacy and increased tolerability, INSTIs have become an integral part of first-line therapy in most high-income countries over the past years. However, little is known about HIV-1's genetic inter- and intra-subtype diversity on the Integrase (IN)-gene and its impact on the emergence of INSTI-resistance. In the absence of a functional cure, long-term efficacy of first-line compounds remains paramount for reducing virological failure and curbing on-going HIV transmissions. South Africa, harbouring more than 20\% of the global HIV burden (7.7 / 37.9 million people), requires international attention in order to globally pursue UNAIDS' (Joint United Nations Programme on HIV/AIDS) 90-90-90 goals and the road to ending the HIV/AIDS (Acquired immunodeficiency syndrome) pandemic by 2030. Methods: In this study, the prevalence of INSTI-resistance associated mutations (RAM) was investigated in a cohort of 169 archived drug-na{\"i}ve blood samples from multiple collection sites around Cape Town, South Africa. Viral RNA was isolated from plasma samples, the integrase fragment amplified by RT-PCR and subsequently sequenced by Sanger-sequencing. Additionally, all publicly available drug-na{\"i}ve, South African IN sequences, isolated before the availability of the first INSTIs in 2007, were retrieved from the Los Alamos HIV sequence database (n=284). All sequences were analysed for RAMs using the Stanford HIV Drug resistance database. The identification of polymorphism in the South African subtype C IN consensus sequence allowed for comparative analyses with global subtype B, as well as subtype C sequences, from countries other than South Africa. Results: The IN gene could be amplified and sequenced in 95/169 samples (56\%). Phylogenetic inference revealed close homology between three sequence-pairs, warranting the exclusion of 3/95 sequences from further analyses. Of the 92 samples used for mutational analyses, 86/92 (93.5\%) belonged to subtype C, 5/92 (5.4\%) to subtype B and 1/92 (1.1\%) to subtype A. The prevalence of major and accessory INSTI RAMs was 0/92 (0\%) and 1/91 (1.1\%), respectively, similar to the observed rates of 8/284 (2.8\%) and 8/284 (2.8\%) in the database sequences (p = 0.2076 and p = 0.6944, Fisher's exact test). Compared to subtype B IN sequences, 15 polymorphisms were significantly enriched in South African subtype C sequences (corrected p<0.0015. Fisher's exact test, Bonferroni post-hoc procedure). Compared to subtype C IN sequences isolated outside South Africa, four polymorphisms were significantly enriched in this study cohort (corrected p<0.0014, Fisher's exact test, Bonferroni post-hoc procedure). The highest prevalence margin was observed for the polymorphism Met50Ile being present in 60.1\% of South African subtype C sequences, compared to 37\% in non-South African subtype C sequences. Conclusions: The low prevalence of major and minor RAMs in all South African Integrase sequences predicts a high susceptibility to INSTIs, however, the presence of natural polymorphisms, in particular Met50Ile, in the majority of sequences warrants further monitoring under therapeutic pressure, as their role in mutational pathways leading to INSTI- resistance is yet to be determined. Additionally, this study revealed the presence of substantial inter- and intra-subtype diversity within the HIV-1 Subtype C IN-gene. These results implicate the need for more research on a regional, potentially patient-specific level, as mutational insights from other diverse backgrounds may not accurately represent the South African context. The implementation of a national pre-treatment INSTI-resistance screening program may provide necessary insights into the development of mutational pathways leading to INSTI-resistance under therapeutic pressure for the South African context and thereby bring South Africa one step closer to achieving UNAIDS 90-90-90 goals and ending the AIDS epidemic by 2030.},
  subject      = {HIV},
  language  = {en}
}
@phdthesis{Dostal2001,
  author    = {Dostal, Stefan},
  title     = {Molekulare Differenzierung von Mykobakterien},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-3348},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2001},
  abstract  = {Die Differenzierung von Mykobakterien auf Speziesebene mithilfe von herk{\"o}mmlichen biochemischen Testverfahren ist langwierig, was zu signifikanten Verz{\"o}gerungen in der Diagnostik f{\"u}hrt. Molekulare Identifizierung hingegen weist, verglichen mit der ph{\"a}notypischen Identifizierung, zwei entscheidende Vorteile auf: es kommt dabei zu einem Geschwindigkeitszuwachs und zu einer h{\"o}heren Genauigkeit des Diagnoseerfahrens. Der Informationsgehalt des 5'-Endes des 16S-rRNA-Gens ist ausreichend f{\"u}r die Identifizierung der meisten bakteriellen Spezies. Wegen der vielen fehlerhaften Datenbest{\"a}nde k{\"o}nnen {\"o}ffentliche Sequenzdatenbanken die ben{\"o}tigten Referenzsequenzen jedoch nicht zur Verf{\"u}gung stellen. Es wurde deshalb eigens eine Datenbank mit qualitativ hochwertigen Sequenzen geschaffen. Die Sequenzen beinhalten beide Str{\"a}nge der 5'-16S-rDNA (E. coli-Position 54-510) von 125 Stammsammlungisolaten. Dabei wurden alle bis zum 31.03.2000 valide beschriebenen Arten (n=89) und einige weitere, bereits ver{\"o}ffentlichte Sequevare-Varianten eingeschlossen. Konnten St{\"a}mme anhand der 16S-Sequenzen nicht unterschieden werden, wurde zus{\"a}tzlich die Sequenz der „Internal Transcribed Spacer Region" bestimmt (n=45). Insgesamt existierten von den St{\"a}mmen, die anhand ihrer 16S-rDNA-Sequenz nicht eindeutig zu identifizieren waren, 77 Isolate in der {\"o}ffentlichen Datenbank Genbank. Den neu analysierten Sequenzen gegen{\"u}bergestellt weisen diese im paarweisen Vergleich eine durchschnittliche Diskrepanz von 4,31 Basen auf. Durch die vergleichende 5'-16S-rDNA-Sequenzanalyse war es m{\"o}glich 64 der 89 validen Spezies zu identifizieren (71.9\%). Nach Hinzunahme der ITS-Sequenz war es m{\"o}glich, weitere 15 Spezies zu differenzieren. Nur die Arten des M. tuberculosis complex, M. marinum und M. ulcerans und die M. avium Subspezies konnten weder durch 5'16S-rDNA-Sequenzanalyse noch anhand der ITS-Sequenz differenziert werden. Die Sequenzen aller St{\"a}mme sind abrufbar in der Datenbank des RIDOM-Projekts ("Ribosomal Differentiation of Medical Microorganisms"). Weiterf{\"u}hrende Informationen (z.B. taxonomischer oder medizinischer Art) vervollst{\"a}ndigen zusammen mit einem Algorithmus zur genotypischen Identifizierung aller valide beschriebenen Mykobakterien dieses Angebot. Nach ausf{\"u}hrlicher Analyse verschiedener Mykobakterien Spezies ist es nun in der Tat m{\"o}glich, die meisten Mykobakterien Arten anhand der vergleichenden Seqenzanalyse der 16S-rDNA und ITS zu unterscheiden. Voraussetzung hierf{\"u}r ist eine Datenbank mit qualitativ hochwertigen Referenzsequenzen. Bereits in naher Zukunft ist die Anwendung dieses Verfahrens im Routinebetrieb, v.a. in Referenzlaboratorien, denkbar.},
  language  = {de}
}
@phdthesis{Friedrich2009,
  author    = {Friedrich, Torben},
  title     = {New statistical Methods of Genome-Scale Data Analysis in Life Science - Applications to enterobacterial Diagnostics, Meta-Analysis of Arabidopsis thaliana Gene Expression and functional Sequence Annotation},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-39858},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2009},
  abstract  = {Recent progresses and developments in molecular biology provide a wealth of new but insufficiently characterised data. This fund comprises amongst others biological data of genomic DNA, protein sequences, 3-dimensional protein structures as well as profiles of gene expression. In the present work, this information is used to develop new methods for the characterisation and classification of organisms and whole groups of organisms as well as to enhance the automated gain and transfer of information. The first two presented approaches (chapters 4 und 5) focus on the medically and scientifically important enterobacteria. Its impact in medicine and molecular biology is founded in versatile mechanisms of infection, their fundamental function as a commensal inhabitant of the intestinal tract and their use as model organisms as they are easy to cultivate. Despite many studies on single pathogroups with clinical distinguishable pathologies, the genotypic factors that contribute to their diversity are still partially unknown. The comprehensive genome comparison described in Chapter 4 was conducted with numerous enterobacterial strains, which cover nearly the whole range of clinically relevant diversity. The genome comparison constitutes the basis of a characterisation of the enterobacterial gene pool, of a reconstruction of evolutionary processes and of comprehensive analysis of specific protein families in enterobacterial subgroups. Correspondence analysis, which is applied for the first time in this context, yields qualitative statements to bacterial subgroups and the respective, exclusively present protein families. Specific protein families were identified for the three major subgroups of enterobacteria namely the genera Yersinia and Salmonella as well as to the group of Shigella and E. coli by applying statistical tests. In conclusion, the genome comparison-based methods provide new starting points to infer specific genotypic traits of bacterial groups from the transfer of functional annotation. Due to the high medical importance of enterobacterial isolates their classification according to pathogenicity has been in focus of many studies. The microarray technology offers a fast, reproducible and standardisable means of bacterial typing and has been proved in bacterial diagnostics, risk assessment and surveillance. The design of the diagnostic microarray of enterobacteria described in chapter 5 is based on the availability of numerous enterobacterial genome sequences. A novel probe selection strategy based on the highly efficient algorithm of string search, which considers both coding and non-coding regions of genomic DNA, enhances pathogroup detection. This principle reduces the risk of incorrect typing due to restrictions to virulence-associated capture probes. Additional capture probes extend the spectrum of applications of the microarray to simultaneous diagnostic or surveillance of antimicrobial resistance. Comprehensive test hybridisations largely confirm the reliability of the selected capture probes and its ability to robustly classify enterobacterial strains according to pathogenicity. Moreover, the tests constitute the basis of the training of a regression model for the classification of pathogroups and hybridised amounts of DNA. The regression model features a continuous learning capacity leading to an enhancement of the prediction accuracy in the process of its application. A fraction of the capture probes represents intergenic DNA and hence confirms the relevance of the underlying strategy. Interestingly, a large part of the capture probes represents poorly annotated genes suggesting the existence of yet unconsidered factors with importance to the formation of respective virulence phenotypes. Another major field of microarray applications is gene expression analysis. The size of gene expression databases rapidly increased in recent years. Although they provide a wealth of expression data, it remains challenging to integrate results from different studies. In chapter 6 the methodology of an unsupervised meta-analysis of genome-wide A. thaliana gene expression data sets is presented, which yields novel insights in function and regulation of genes. The application of kernel-based principal component analysis in combination with hierarchical clustering identified three major groups of contrasts each sharing overlapping expression profiles. Genes associated with two groups are known to play important roles in Indol-3 acetic acid (IAA) mediated plant growth and development as well as in pathogen defence. Yet uncharacterised serine-threonine kinases could be assigned to novel functions in pathogen defence by meta-analysis. In general, hidden interrelation between genes regulated under different conditions could be unravelled by the described approach. HMMs are applied to the functional characterisation of proteins or the detection of genes in genome sequences. Although HMMs are technically mature and widely applied in computational biology, I demonstrate the methodical optimisation with respect to the modelling accuracy on biological data with various distributions of sequence lengths. The subunits of these models, the states, are associated with a certain holding time being the link to length distributions of represented sequences. An adaptation of simple HMM topologies to bell-shaped length distributions described in chapter 7 was achieved by serial chain-linking of single states, while residing in the class of conventional HMMs. The impact of an optimisation of HMM topologies was underlined by performance evaluations with differently adjusted HMM topologies. In summary, a general methodology was introduced to improve the modelling behaviour of HMMs by topological optimisation with maximum likelihood and a fast and easily implementable moment estimator. Chapter 8 describes the application of HMMs to the prediction of interaction sites in protein domains. As previously demonstrated, these sites are not trivial to predict because of varying degree in conservation of their location and type within the domain family. The prediction of interaction sites in protein domains is achieved by a newly defined HMM topology, which incorporates both sequence and structure information. Posterior decoding is applied to the prediction of interaction sites providing additional information of the probability of an interaction for all sequence positions. The implementation of interaction profile HMMs (ipHMMs) is based on the well established profile HMMs and inherits its known efficiency and sensitivity. The large-scale prediction of interaction sites by ipHMMs explained protein dysfunctions caused by mutations that are associated to inheritable diseases like different types of cancer or muscular dystrophy. As already demonstrated by profile HMMs, the ipHMMs are suitable for large-scale applications. Overall, the HMM-based method enhances the prediction quality of interaction sites and improves the understanding of the molecular background of inheritable diseases. With respect to current and future requirements I provide large-scale solutions for the characterisation of biological data in this work. All described methods feature a highly portable character, which allows for the transfer to related topics or organisms, respectively. Special emphasis was put on the knowledge transfer facilitated by a steadily increasing wealth of biological information. The applied and developed statistical methods largely provide learning capacities and hence benefit from the gain of knowledge resulting in increased prediction accuracies and reliability.},
  subject      = {Genomik},
  language  = {en}
}
@phdthesis{Singer2005,
  author    = {Singer, Christian J.},
  title     = {Molekulare Identifizierung von Neisseriaceae und Moraxellaceae mittels ribosomaler DNA-Sequenzierung},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-16823},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2005},
  abstract  = {Die schnelle und verl{\"a}ssliche Identifizierung mikrobiologischer Isolate ist ein fundamentales Ziel der klinischen Mikrobiologie. Bei einigen gram-negativen Spezies ist die klassische ph{\"a}notypische Identifizierung, basierend auf metabolischen, enzymatischen oder serologischen Methoden erschwert, zeitraubend oder nicht suffizient. Durch die Sequenzierung partieller Abschnitte der 16S- oder 23S-rDNA k{\"o}nnen Bakterien meist exakt spezifiziert werden. Hauptziel der vorliegenden Arbeit war es, hypervariable rDNA Abschnitte zu finden, die von stark konservierten Regionen flankiert werden, um auf molekularer Ebene Mitglieder der Familie Neisseriaceae und Moraxellaceae zu diskriminieren. Die inter- und intragenetischen Beziehungen von insgesamt 94 St{\"a}mmen wurden untersucht. Im Vergleich zu den Referenzst{\"a}mmen der Genera waren bei der partiellen 16S-rDNA (E. coli Position 54 - 510) je Spezies durchschnittlich 30 polymorphe Positionen vorhanden. Die partiellen 23S-rDNA Abschnitte (E. coli Position 1400 - 1600) zeigten durchschnittlich 11 polymorphe Positionen. Neisseria macacae und N. mucosa subsp. mucosa (ATCC 19696) zeigten identische 16S- und 23S-rDNA Sequenzen. Die Gruppierung verschiedener Isolate war bei Acinetobacter lwoffii, Moraxella lacunata und Neisseria mucosa an beiden untersuchten Genabschnitten heterogen. Im Fall von N. meningitidis konnte mit Hilfe der 23S-rDNA Daten nicht suffizient gruppiert werden. Die Ergebnisse zeigen eine {\"U}berlegenheit der untersuchten partiellen 16S-rDNA zur Diagnostik der Neisseriaceae und Moraxellaceae. Eine Referenzdatenbank zur Diagnostik von Mikroorganismen sollte mehr als ein Isolat einer Spezies enthalten und zudem einen polyphasischen Ansatz verfolgen. Die Sequenz-Chromatogramme und weitere diagnostisch relevante Informationen wurden mit der „offline"-Datenbank RIDOM_Tool gesammelt und sind ein Teil des Internet-basierenden Service von RIDOM (www.ridom-rdna.de). Eine eingegebene Sequenzfolge kann online eingef{\"u}gt und damit ein direkter Vergleich mit den in der RIDOM Referenzdatenbank existierenden Datens{\"a}tzen initiiert werden.},
  language  = {de}
}
@phdthesis{Wohlleben2004,
  author    = {Wohlleben, Michael},
  title     = {Sequenzanalyse des humanen 5´-Deiodase (Typ I) -Gens bei Patienten mit Schilddr{\"u}senfunktionsst{\"o}rungen},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-7621},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2004},
  abstract  = {Durch ihre Aufgaben im Metabolismus der Schilddr{\"u}senhormone kommt der Enzymfamilie der Deiodasen im feinregulierten Zusammenspiel der Aktivierung und Inaktivierung dieser signalgebenden Stoffe eine zentrale Rolle zu. St{\"o}rungen in diesem System ziehen weitreichende Folgen auf der Ebene der Entwicklung und Steuerung des gesamten Organismus nach sich. Verminderte Aktivit{\"a}t der 5´DI, sei sie durch unzureichende Expression des Gens oder posttranskriptionelle Fehlsteuerung bedingt, geht dabei mit einer sogenannten „Konversionshemmung" einher, die sich in erh{\"o}hten T4- und rT3-Spiegeln bei vermindertem Plasma-T3-Gehalt {\"a}ußert. Diese Konstellation wird in Tiermodellen, bei denen ein 5´DI-Defekt auf molekularer Ebene bekannt ist, beobachtet. Ein derartiger Defekt ist jedoch beim Menschen bislang nicht festgestellt worden. Eine routinem{\"a}ßige Untersuchung des 5´DI-Gens von Patienten, bei denen ein Enzymdefekt die Ursache ihrer Symptomatik sein k{\"o}nnte, ist mit Hilfe des hier aufgef{\"u}hrten Verfahrens unter einfachen Bedingungen m{\"o}glich. In dieser Arbeit wird neben der Beschreibung eines stummen Polymorphismus im Exon 1 erstmals eine potentiell relevante Ver{\"a}nderung im translatierten Bereich des 5´DI-Gens beschrieben. Ausgew{\"a}hlte Patienten, deren Symptome den Verdacht auf eine Konversionshemmung aufkommen lassen, sind (bei sonst unver{\"a}nderter Exonstruktur) heterozygot f{\"u}r eine Punktmutation im Codon 108 im Exon 1. Durch den Austausch von G durch A ergibt sich bei ihnen aus dem Codon UGG f{\"u}r die Aminos{\"a}ure Tryptophan das Stop- beziehungsweise SeCys-Codon UGA. Im ersten Fall entsteht dadurch ein etwa um die H{\"a}lfte verk{\"u}rztes und damit wohl funktionsunf{\"a}higes Protein, im zweiten ein in Konformation und Aktivit{\"a}t sicherlich beeintr{\"a}chtigtes Enzym, vorausgesetzt, das im 3'-untranslatierten Bereich der mRNA befindliche SECIS-Element ist f{\"u}r dieses UGA-Codon wirksam. Bei beiden Varianten ist jedoch zu kl{\"a}ren, ob der Defekt durch das zweite wildtypische Allel teilweise oder v{\"o}llig kompensiert werden kann, wozu Untersuchungen von Gewebeproben aus Leber und Niere beziehungsweise die Expression des ver{\"a}nderten Gens in Zellkultur erforderlich w{\"a}ren.},
  language  = {de}
}