Colonisation of hospital surfaces from low- and middle-income countries by extended spectrum β-lactamase- and carbapenemase-producing bacteria.
Nieto-Rosado M., Sands K., Portal EAR., Thomson KM., Carvalho MJ., Mathias J., Milton R., Dyer C., Akpulu C., Boostrom I., Hogan P., Saif H., Sanches Ferreira AD., Hender T., Portal B., Andrews R., Watkins WJ., Zahra R., Shirazi H., Muhammad A., Ullah SN., Jan MH., Akif S., Iregbu KC., Modibbo F., Uwaezuoke S., Audu L., Edwin CP., Yusuf AH., Adeleye A., Mukkadas AS., Mazarati JB., Rucogoza A., Gaju L., Mehtar S., Bulabula ANH., Whitelaw A., Roberts L., Chan G., Bekele D., Solomon S., Abayneh M., Metaferia G., Group BARNARDS None., Walsh TR.
Hospital surfaces can harbour bacterial pathogens, which may disseminate and cause nosocomial infections, contributing towards mortality in low- and middle-income countries (LMICs). During the BARNARDS study, hospital surfaces from neonatal wards were sampled to assess the degree of environmental surface and patient care equipment colonisation by Gram-negative bacteria (GNB) carrying antibiotic resistance genes (ARGs). Here, we perform PCR screening for extended-spectrum β-lactamases (blaCTX-M-15) and carbapenemases (blaNDM, blaOXA-48-like and blaKPC), MALDI-TOF MS identification of GNB carrying ARGs, and further analysis by whole genome sequencing of bacterial isolates. We determine presence of consistently dominant clones and their relatedness to strains causing neonatal sepsis. Higher prevalence of carbapenemases is observed in Pakistan, Bangladesh, and Ethiopia, compared to other countries, and are mostly found in surfaces near the sink drain. Klebsiella pneumoniae, Enterobacter hormaechei, Acinetobacter baumannii, Serratia marcescens and Leclercia adecarboxylata are dominant; ST15 K. pneumoniae is identified from the same ward on multiple occasions suggesting clonal persistence within the same environment, and is found to be identical to isolates causing neonatal sepsis in Pakistan over similar time periods. Our data suggests persistence of dominant clones across multiple time points, highlighting the need for assessment of Infection Prevention and Control guidelines.