Diagnosing and Treating Biofilm Infections
Credit: CDC/ Rodney M. Donlan, Ph.D.; Janice Haney Carr
Planktonic vs. biofilm phenotypes
All microorganisms can exist in both the planktonic (fee-living) and biofilm phenotypic states, but tend to gravitate towards a biofilm phenotype due to their preference for attaching to each other and to surfaces. Biofilm formation is now recognized as causing or exacerbating a majority of chronic infections.
Culture can’t adequately detect biofilm bacteria, but MicroGenDX Next-generation sequencing (NGS) can
A biofilm can have multiple gradients of anoxic and acidic zones in the interior of biofilm clusters, requiring differentiated media, growth conditions, and varying lengths of time to cultivate — all of which are not supported by standard culture.
A biofilm-mediated adaptation also produces trade-offs that could limit the ability of bacteria to transition between biofilm growth and the free-living state, and thereby generate a specimen that may escape detection by culture-based sampling.
Next-generation sequencing (NGS) can identify the multiple bacteria and fungi that make up a biofilm, along with the clinically relevant distributions of each in the sample, which is a critical starting point in understanding a biofilm’s involvement in a given infection.
Biofilms are more resistant to antimicrobials than planktonic cells
Bacteria within a biofilm activate many genes that alter the cell envelope and molecular targets, as well as altering the susceptibility to antimicrobial agents (intrinsic resistance). Current opinion is that phenotypic changes brought on by a genetic switch, where 65–80 proteins change, play a hugely important role in protection from antimicrobial agents.
In addition, biofilms can achieve greater antimicrobial resistance through one or more of the following conditions:
- Transmission of resistance genes within the bacterial community
- Reduced metabolic and growth rates from a nutrient-limited environment
- The presence of metabolically inactive cells known as persisters, where bacteria enter a spore-like, non-dividing state that is more tolerant to antimicrobials
- The induction of a biofilm phenotype (i.e the expression of active mechanisms to combat the detrimental effects of antimicrobial agents)
References
- Hall-Stoodley L, Stoodley P. Evolving concepts in biofilm infections. Cell Microbiol. 2009;11(7):1034‐1043. doi:10.1111/j.1462-5822.2009.01323.x
- Vuotto C, Longo F, et al. Antibiotic Resistance Related to Biofilm Formation in Klebsiella pneumoniae. Pathogens. 2014;3(3):743-758. Published 2014 Sep 5. doi:10.3390/pathogens3030743
- Penterman J, Nguyen D, et al. Rapid evolution of culture-impaired bacteria during adaptation to biofilm growth. Cell Rep. 2014;6(2):293‐300. doi:10.1016/j.celrep.2013.12.019
- Høiby N, Bjarnsholt T, et al. Antibiotic resistance of bacterial biofilms. Int J Antimicrob Agents. 2010;35(4):322‐332. doi:10.1016/j.ijantimicag.2009.12.011
- Ehrlich G D et al. Culture Negative Orthopedic Biofilm Infections, Springer Series on Biofilms 7. 2012. doi.org/10.1007/978-3-642-29554-6_1
- Jamal M, Ahmad W, Andleeb S, et al. (2018). Bacterial biofilm and associated infections. J. Chin. Med. Assoc.81, 7–11. doi: 10.1016/j.jcma.2017.07.012
Biofilm research papers and videos
Explore a selection of biofilm research papers and videos below.
Biofilm research videos
What Are Bacterial Biofilms?
Dr. Bill Costerton: Diagnosing and Treating Biofilm Infections
Randy Wolcott, MD - Diagnosing & Treating Bacterial Biofilm Infections
Why Am I Still Sick?
Rodney Donlan on Biofilm Infections
Biofilm: A New (Gross) Thing to Worry About
Next-gen DNA sequencing (NGS) can identify the multiple bacteria and fungi that make up a biofilm, which is a first step in addressing this challenge
- Microorganisms in free-living planktonic state.
- In seconds – Planktonic cells initiation attachment to each other.
- Within 24 hours – Microbes build a protective community with an extracellular matrix (EPS) of polysaccharides, proteins, and glycoproteins. Horizontal gene transfer strengthens antimicrobial resistance for the community.
- Within 72 hours – Biofilm matures. Aerobic and anaerobic bacteria occupy spaces with differed O2 levels, and nutrient limitations of the biofilm’s interior induce slow-growth or no-growth states.
- Bacteria will continually detach individually – or in clumps that can retain antimicrobial resistance – and establish other biofilm colonies.