Isolation, Characterization, Genome Analysis and Host Resistance Development of Two Novel Lastavirus Phages Active against Pandrug-Resistant Klebsiella pneumoniae

Author:

Obradović Mina1ORCID,Malešević Milka1,Di Luca Mariagrazia2ORCID,Kekić Dušan3ORCID,Gajić Ina3ORCID,McAuliffe Olivia4ORCID,Neve Horst5ORCID,Stanisavljević Nemanja1,Vukotić Goran16ORCID,Kojić Milan1ORCID

Affiliation:

1. Laboratory for Molecular Microbiology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, 11000 Belgrade, Serbia

2. Department of Biology, University of Pisa, 56127 Pisa, Italy

3. Institute of Microbiology and Immunology, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia

4. Department of Food Biosciences, Teagasc Food Research Centre, P61 C996 Fermoy, Ireland

5. Department of Microbiology and Biotechnology, Max Rubner-Institut, 24103 Kiel, Germany

6. Faculty of Biology, University of Belgrade, 11000 Belgrade, Serbia

Abstract

Klebsiella pneumoniae is a global health threat and bacteriophages are a potential solution in combating pandrug-resistant K. pneumoniae infections. Two lytic phages, LASTA and SJM3, active against several pandrug-resistant, nosocomial strains of K. pneumoniae were isolated and characterized. Their host range is narrow and latent period is particularly long; however, their lysogenic nature was refuted using both bioinformatic and experimental approaches. Genome sequence analysis clustered them with only two other phages into the new genus Lastavirus. Genomes of LASTA and SJM3 differ in only 13 base pairs, mainly located in tail fiber genes. Individual phages, as well as their cocktail, demonstrated significant bacterial reduction capacity in a time-dependent manner, yielding up to 4 log reduction against planktonic, and up to 2.59 log on biofilm-embedded, cells. Bacteria emerging from the contact with the phages developed resistance and achieved numbers comparable to the growth control after 24 h. The resistance to the phage seems to be of a transient nature and varies significantly between the two phages, as resistance to LASTA remained constant while resensitization to SJM3 was more prominent. Albeit with very few differences, SJM3 performed better than LASTA overall; however, more investigation is needed in order to consider them for therapeutic application.

Funder

Ministry of Education, Science and Technological Development, Serbia

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference56 articles.

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