train-asap ― training and research aimed at novel antibacterial solutions in animals and people
TRAIN-ASAP ― Training and Research AImed at Novel Antibacterial Solutions in Animals and People OPEN POSITIONS Initial Call RP1: New cyclic antimicrobial peptides from combinatorial libraries The aim of the project is to identify novel cyclic antimicrobial peptides from combinatorial libraries for treatment of multi-drug resistant bacterial infections in humans.
The candidate should have a second-level degree in Chemistry or closely
related area. Previous organic chemistry and microbiology laboratory
Further information on the requirements, application deadlines and
application procedures will be posted on Application deadline: 15 June 2012
RP2. Development of antimicrobial peptide-peptoid hybrids for veterinary use The aim of the project is to design new peptide-peptoid hybrids for veterinary topical applications in livestock and companion animals.
The candidate should have a second-level degree in Chemistry or closely
related area. Previous organic chemistry and microbiology laboratory
Further information on the requirements, application deadlines and
application procedures will be posted on Application deadline: 15 June 2012
RP3. Novel sources of antimicrobial diversity for new antibiotics The project involves identifying novel bacterial strains from their environment, screening for antibiotic activity and characterization of the bioactive compounds.
The candidate should have a second-level degree in chemical or biological
sciences. Previous lab experience with actinomycetes and/or natural
Please send a CV, a list of university classes attended, a motivation letter
and two letters of reference to train-asap@ktedogen.com Application deadline: 30 June 2012.
RP4. Expression systems for biosynthetic capacity of uncultured bacteria The aim is to exploit metagenomic libraries derived from cloning DNA
fragments extracted from interesting ecosystems. We will use heterologous
expression hosts and PCR primers to find interesting new natural product
Requirements: Master’s degree or good Bachelor’s degree in Life Sciences Application deadline: 31 May 2012.
Applications are strictly via FindAPhD project site:
RP5. Antivirulence therapy targeting S. aureus Antibiotic resistance in serious pathogens like Staphylococcus aureus is an increasing threat to human health. These challenges have lead to new therapeutic approaches including anti-virulence therapy that aims to reduce
the production or toxicity of virulence factors while allowing the host to
eliminate the infection. In this project we will search for anti-virulence
compounds targeting S. aureus and demonstrate the potential of this
approach either alone or in combination with antibiotics using various cell
based models and simple animal models. Also the identified compounds will be used as tools to dissect the complex control of virulence expression.
Further information on the requirements, application deadlines and application procedures will be posted on
RP6. Optimization of dosage and clinical efficacy of new macrolides New data indicates that macrolides belonging to the azalide class may have concentration-dependent killing activity in contrast to older macrolides, which are regarded as time-dependent antibiotics. Azalide products are currently administered in anticipation of time-dependent activity and may be used
inefficiently. This project will examine the kill rate of respiratory pathogens
after exposure to selected azalide in an in vitro model, study the distribution
of drugs in respiratory tract secretions and inflammatory cells using a porcine
infection model and perform a confirmative dose study in naturally infected
Requirements: DVM with interest in clinical microbiology and pharmacology. Further information on the requirements and application procedure will be posted onApplication deadline: 29 June 2012
RP7. Development of novel potentiated sulphonamides with enhanced antimicrobial activity Sulphonamide/trimethoprim (SXT) combinations have been widely used for the treatment of Gram-negative infections in both humans and animals but
resistance has widely developed over the years. In this project, novel
sulphonamide compounds against common SXT-resistant pathogens, alone
and in combination with trimethoprim analogues. Moreover, the candidate will
also be involved in the evaluation of novel SXT combinations in mouse in vivo models and target animal infection models.
Information about applicant requirements and application deadlines will be posted at a later time
RP8. Blocking 16S RNA methyltransferases
Recently, a new family of plasmid-mediated aminoglycoside resistance
determinants, the 16S rRNA methyltransferases, has emerged in Gram-
negative bacteria. In this project, “helper drugs” blocking binding of the 16S
rRNA methyltransferase to the ribosome and/or inhibiting methyltransferase
activity will be designed to enable development of new aminoglycoside
formulations active against this emerging resistance mechanism.
Information about applicant requirements and application deadlines will be
RP9. Bacteriocins against S. suis in pigs
The aim is to develop a novel approach to prevent carriage of S. suis, a
major porcine pathogen of high zoonotic potential. A high- throughput
screening effort will be used to isolate bacteriocin-producing commensals
from the porcine nasopharyngeal cavity that inhibit S. suis. The commensals
will be tested in pigs to determine whether they can confer protection against
infection in piglets or prevent carriage in adult pigs. Additionally, transposon mutant libraries of S. suis will be screened to identify virulence determinants
required for colonization of pigs. These will be investigated as potential targets for novel vaccines or anti-infectives. The candidate should have Batchelors degree/Masters in the life sciences preferably with laboratory experience in microbiology and molecular biology. Please send a CV, a list of University Courses and a motivation letter to Application deadline: 11th June 2012.
RP10. Phage against avian pathogenic E. coli in poultry
As a PhD student you will perform research on Phage therapy in poultry. The
focus will be on Avian Pathogenic Escherichia coli (APEC) causing systemic
infections. You will isolate new phages and characterize them as well as
perform their therapeutic efficacy and transmission studies.
Requirements: A master diploma in biological sciences or a DVM. Interest in
microbiology and working with animals Applications, together with a motivation letter and CV, which includes studies
and grades should be sent to: Further information can be found on the website of CODA
RP11. Phages against S. pseudintermedius in dogs
The aim is to isolate a wide range of bacteriophages for phage therapy with
phage cocktails. We have demonstrated that lysogenic bacteriophages can
be modified to be effective agents for phage therapy.
Requirements: Masters degree or a good Bachelors degree in Life Sciences. Application deadline: 31 May 2012.
Applications are strictly via FindAPhD project site:
RP12. A novel strategy to reduce selection of resistance
Take an active part in the stimulating development of a unique product
aiming to reduce the emergence of resistant bacteria in animals during antibiotic treatments. Within Da Volterra, a Paris-based biotech company,
you will collaborate with the teams of one of the leading European group in bacterial resistance at the Veterinary School of Toulouse. You will work on
the product formulation, in vivo pharmacological studies, in vitro and in vivo microbiological assays and consequent analysis of the outcomes towards
market access. The project includes stays in Toulouse and Copenhagen for in-animal studies and metagenomics developments on the animal commensal flora. A great training opportunity in an industrial environment, in
one of the most pleasant cities in the world.
The candidate will have preferentially a veterinary or pharmacological background with experience in bacteriology, and looking to gain a strong expertise in veterinary drug research and development. Send your resume and a motivation letter to jobs@davolterra.com with the reference DVTA-2012.03.128 Application deadline: 15 June 2012
Applicants for the PhD positions must not yet been awarded a PhD degree and must be in the first 4 years (full-time equivalent) of their research careers prior to the recruitment. All applicants must not have resided or carried out their main activity (work, studies, etc.) in the country of the organization they are applying to for more than 12 months in the 3 years immediately prior to the recruitment. Positions include interdisciplinary training, summer schools and yearly international meetings. Please apply to the organization of interest by providing the appropriate information and by the individual project application deadline.
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J Microbiol Immunol Infect2004;37:382-384 Guidelines for chemotherapy of tuberculosis in Taiwan Infectious Diseases Society of the Republic of China; The Society of Tuberculosis, Taiwan; Medical Foundation in Memory of Dr. Deh-Lin Cheng; Foundation of Professor Wei-Chuan Hsieh for Infectious Diseases Research and Education; and CY Lee’s Research Foundation for Pediatric Infectious Tuber