@article{NeidhoeferSibBenhsainetal.2023,
  author    = {Claudio Neidh{\"o}fer and Esther Sib and Al-Harith Benhsain and Christina Mutschnik-Raab and Anna Schwabe and Alexander Wollkopf and Nina Wetzig and Martin A. Sieber and Ralf Thiele and Manuel D{\"o}hla and Steffen Engelhart and Nico T. Mutters and Marijo Parčina},
  title     = {Examining Different Analysis Protocols Targeting Hospital Sanitary Facility Microbiomes},
  series   = {Microorganisms},
  volume    = {11},
  number    = {1},
  publisher = {MDPI},
  address   = {Basel},
  issn      = {2076-2607},
  doi       = {10.3390/microorganisms11010185},
  url       = {https://nbn-resolving.org/urn:nbn:de:hbz:1044-opus-65910},
  year      = {2023},
  abstract  = {Indoor spaces exhibit microbial compositions that are distinctly dissimilar from one another and from outdoor spaces. Unique in this regard, and a topic that has only recently come into focus, is the microbiome of hospitals. While the benefits of knowing exactly which microorganisms propagate how and where in hospitals are undoubtedly beneficial for preventing hospital-acquired infections, there are, to date, no standardized procedures on how to best study the hospital microbiome. Our study aimed to investigate the microbiome of hospital sanitary facilities, outlining the extent to which hospital microbiome analyses differ according to sample-preparation protocol. For this purpose, fifty samples were collected from two separate hospitals—from three wards and one hospital laboratory—using two different storage media from which DNA was extracted using two different extraction kits and sequenced with two different primer pairs (V1–V2 and V3–V4). There were no observable differences between the sample-preservation media, small differences in detected taxa between the DNA extraction kits (mainly concerning Propionibacteriaceae), and large differences in detected taxa between the two primer pairs V1–V2 and V3–V4. This analysis also showed that microbial occurrences and compositions can vary greatly from toilets to sinks to showers and across wards and hospitals. In surgical wards, patient toilets appeared to be characterized by lower species richness and diversity than staff toilets. Which sampling sites are the best for which assessments should be analyzed in more depth. The fact that the sample processing methods we investigated (apart from the choice of primers) seem to have changed the results only slightly suggests that comparing hospital microbiome studies is a realistic option. The observed differences in species richness and diversity between patient and staff toilets should be further investigated, as these, if confirmed, could be a result of excreted antimicrobials.},
  language  = {en}
}