Sharklet (material)

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Sharklet, manufactured by Sharklet Technologies, is a bio-inspired plastic sheet product structured to impede microorganism growth, particularly bacterial growth. It is marketed for use in hospitals and other places with a relatively high potential for bacteria to spread and cause infections. [1] Coating surfaces with Sharklet works due to the micro-scale of the product's surface. [2]

Contents

The inspiration for Sharklet's texture came through analysis of the texture of shark skin, which does not attract barnacles or other biofouling, unlike ship hulls and other smooth surfaces. The texture was later found to also repel microbial activity. [3]

History

Sharklet is a bio-inspired material that was invented by Dr. Anthony Brennan, a materials science and engineering professor at the University of Florida, while working to improve antifouling technology for ships and submarines at Pearl Harbor. [4]

Brennan noticed that sharks do not get fouled. He discovered that shark skin denticles are structured in a characteristic diamond repeating micro-pattern with millions of small ribs [4] at the micrometer scale. His mathematical model for the texture of a substance that would deter microorganisms from settling corresponds to the width-to-height ratio of shark denticle riblets. When compared to smooth surfaces, [5] the first test revealed an 85% reduction in green algae settlement.

Texture

Sharklet's texture is a combination of “ridge” and “ravine” on a micrometer scale.

Resistance to bacterial attachment

Adherence prevention and translocation restriction have been demonstrated, and are believed to contribute significantly to restrict the risk of device-associated infections.

Sharklet's topography creates mechanical stress on settling bacteria, a phenomenon known as mechanotransduction. Nanoforce gradients caused by surface variations induces stress gradients within the lateral plane of the surface membrane of a settling microorganism during initial contact. This stress gradient disrupts normal cell functions, forcing the microorganism to provide energy to adjust its contact area on each topographical feature to equalize the stresses. This expenditure of energy is thermodynamically unfavorable for the settler, inducing it to search for a different surface to attach to. [6] Sharklet is made, however, with the same material as other plastics.

The physical arrangement enhances the hydrophobicity of the device surface such that the bacteria attachment energy is insufficient for adherence and/or colonization[ citation needed ].

Environmental surface contamination provides a potential reservoir for pathogens to persist and cause infection in susceptible patients. Microorganisms colonize biomedical implants by developing biofilms, structured communities of microbial cells embedded in an extracellular polymeric matrix that are adherent to the implant or the host tissues. Biofilms are an important threat to human health as they may harbor large numbers of pathogenic bacteria. Up to 80% of bacterial infections in humans involve microorganisms from biofilms, and biofilm formation on medical devices can lead to nosocomial infections and potentially higher mortality rate. [7] Indwelling of medical devices is associated with high risk of infection, given the abundance of bacterial flora on human skin and the risk of contamination from other sources. The fact that many of the pathogens responsible for these infections are multi-drug-resistant, or even panresistant, has become particularly problematic because few treatment options are available to healthcare workers. The industry is seeking safe and effective means to prevent device-associated infections. [8]

Sharklet micro-patterns can be incorporated onto the surfaces of a variety of medical devices during the manufacturing process. This micro-pattern is effective against bio-fouling and microbial attachment and is non-toxic. It therefore has potential to help infection control on medical devices such as per-cutaneous devices. Sharklet micro-patterns have been shown to control the bio-adhesion of a wide range of marine microorganisms, pathogenic bacteria, and eukaryotic cells. They reduce S. aureus and S. epidermidis colonization after exposure to a simulated vascular environment by 70% or greater when compared to smooth controls. This micro-pattern similarly reduces platelet adhesion and fibrin sheath formation by approximately 80%. [9] An in vitro study demonstrated that it reduced the colonization of S. aureus and P. aeruginosa bacterial pathogens effectively. [8] Importantly, this infection control was achieved without the aid of antimicrobial agents.

See also

Related Research Articles

<span class="mw-page-title-main">Biofilm</span> Aggregation of bacteria or cells on a surface

A biofilm is a syntrophic community of microorganisms in which cells stick to each other and often also to a surface. These adherent cells become embedded within a slimy extracellular matrix that is composed of extracellular polymeric substances (EPSs). The cells within the biofilm produce the EPS components, which are typically a polymeric combination of extracellular polysaccharides, proteins, lipids and DNA. Because they have a three-dimensional structure and represent a community lifestyle for microorganisms, they have been metaphorically described as "cities for microbes".

<i>Staphylococcus aureus</i> Species of Gram-positive bacterium

Staphylococcus aureus is a Gram-positive spherically shaped bacterium, a member of the Bacillota, and is a usual member of the microbiota of the body, frequently found in the upper respiratory tract and on the skin. It is often positive for catalase and nitrate reduction and is a facultative anaerobe that can grow without the need for oxygen. Although S. aureus usually acts as a commensal of the human microbiota, it can also become an opportunistic pathogen, being a common cause of skin infections including abscesses, respiratory infections such as sinusitis, and food poisoning. Pathogenic strains often promote infections by producing virulence factors such as potent protein toxins, and the expression of a cell-surface protein that binds and inactivates antibodies. S. aureus is one of the leading pathogens for deaths associated with antimicrobial resistance and the emergence of antibiotic-resistant strains, such as methicillin-resistant S. aureus (MRSA), is a worldwide problem in clinical medicine. Despite much research and development, no vaccine for S. aureus has been approved.

<span class="mw-page-title-main">Human microbiome</span> Microorganisms in or on human skin and biofluids

The human microbiome is the aggregate of all microbiota that reside on or within human tissues and biofluids along with the corresponding anatomical sites in which they reside, including the gastrointestinal tract, skin, mammary glands, seminal fluid, uterus, ovarian follicles, lung, saliva, oral mucosa, conjunctiva, and the biliary tract. Types of human microbiota include bacteria, archaea, fungi, protists, and viruses. Though micro-animals can also live on the human body, they are typically excluded from this definition. In the context of genomics, the term human microbiome is sometimes used to refer to the collective genomes of resident microorganisms; however, the term human metagenome has the same meaning.

Virulence is a pathogen's or microorganism's ability to cause damage to a host.

<span class="mw-page-title-main">Keratitis</span> Medical condition

Keratitis is a condition in which the eye's cornea, the clear dome on the front surface of the eye, becomes inflamed. The condition is often marked by moderate to intense pain and usually involves any of the following symptoms: pain, impaired eyesight, photophobia, red eye and a 'gritty' sensation. Diagnosis of infectious keratitis is usually made clinically based on the signs and symptoms as well as eye examination, but corneal scrapings may be obtained and evaluated using microbiological culture or other testing to identify the causative pathogen.

An antimicrobial is an agent that kills microorganisms (microbicide) or stops their growth. Antimicrobial medicines can be grouped according to the microorganisms they act primarily against. For example, antibiotics are used against bacteria, and antifungals are used against fungi. They can also be classified according to their function. The use of antimicrobial medicines to treat infection is known as antimicrobial chemotherapy, while the use of antimicrobial medicines to prevent infection is known as antimicrobial prophylaxis.

<span class="mw-page-title-main">Biofouling</span> Growth of marine organisms on surfaces

Biofouling or biological fouling is the accumulation of microorganisms, plants, algae, or small animals where it is not wanted on surfaces such as ship and submarine hulls, devices such as water inlets, pipework, grates, ponds, and rivers that cause degradation to the primary purpose of that item. Such accumulation is referred to as epibiosis when the host surface is another organism and the relationship is not parasitic. Since biofouling can occur almost anywhere water is present, biofouling poses risks to a wide variety of objects such as boat hulls and equipment, medical devices and membranes, as well as to entire industries, such as paper manufacturing, food processing, underwater construction, and desalination plants.

<i>Staphylococcus epidermidis</i> Species of bacterium

Staphylococcus epidermidis is a Gram-positive bacterium, and one of over 40 species belonging to the genus Staphylococcus. It is part of the normal human microbiota, typically the skin microbiota, and less commonly the mucosal microbiota and also found in marine sponges. It is a facultative anaerobic bacteria. Although S. epidermidis is not usually pathogenic, patients with compromised immune systems are at risk of developing infection. These infections are generally hospital-acquired. S. epidermidis is a particular concern for people with catheters or other surgical implants because it is known to form biofilms that grow on these devices. Being part of the normal skin microbiota, S. epidermidis is a frequent contaminant of specimens sent to the diagnostic laboratory.

Host tropism is the infection specificity of certain pathogens to particular hosts and host tissues. This explains why most pathogens are only capable of infecting a limited range of host organisms.

<span class="mw-page-title-main">Bacteria</span> Domain of microorganisms

Bacteria are ubiquitous, mostly free-living organisms often consisting of one biological cell. They constitute a large domain of prokaryotic microorganisms. Typically a few micrometres in length, bacteria were among the first life forms to appear on Earth, and are present in most of its habitats. Bacteria inhabit soil, water, acidic hot springs, radioactive waste, and the deep biosphere of Earth's crust. Bacteria play a vital role in many stages of the nutrient cycle by recycling nutrients and the fixation of nitrogen from the atmosphere. The nutrient cycle includes the decomposition of dead bodies; bacteria are responsible for the putrefaction stage in this process. In the biological communities surrounding hydrothermal vents and cold seeps, extremophile bacteria provide the nutrients needed to sustain life by converting dissolved compounds, such as hydrogen sulphide and methane, to energy. Bacteria also live in mutualistic, commensal and parasitic relationships with plants and animals. Most bacteria have not been characterised and there are many species that cannot be grown in the laboratory. The study of bacteria is known as bacteriology, a branch of microbiology.

<i>Xanthomonas campestris</i> Species of bacterium

Xanthomonas campestris is a gram-negative, obligate aerobic bacterium that is a member of the Xanthomonas genus, which is a group of bacteria that are commonly known for their association with plant disease. This species includes Xanthomonas campestris pv. campestris the cause of black rot of brassicas, one of the most important diseases of brasicas worldwide.

<span class="mw-page-title-main">Medical microbiology</span> Branch of medical science

Medical microbiology, the large subset of microbiology that is applied to medicine, is a branch of medical science concerned with the prevention, diagnosis and treatment of infectious diseases. In addition, this field of science studies various clinical applications of microbes for the improvement of health. There are four kinds of microorganisms that cause infectious disease: bacteria, fungi, parasites and viruses, and one type of infectious protein called prion.

<span class="mw-page-title-main">Skin flora</span> Microbiota that reside on the skin

Skin flora, also called skin microbiota, refers to microbiota that reside on the skin, typically human skin.

<span class="mw-page-title-main">Extracellular polymeric substance</span> Gluey polymers secreted by microorganisms to form biofilms

Extracellular polymeric substances (EPSs) are natural polymers of high molecular weight secreted by microorganisms into their environment. EPSs establish the functional and structural integrity of biofilms, and are considered the fundamental component that determines the physicochemical properties of a biofilm. EPS in the matrix of biofilms provides compositional support and protection of microbial communities from the harsh environments. Components of EPS can be of different classes of polysaccharides, lipids, nucleic acids, proteins, lipopolysaccharides, and minerals. This chemical formula is (C135H217N15Na2O74P10).

<span class="mw-page-title-main">Oral microbiology</span>

Oral microbiology is the study of the microorganisms (microbiota) of the oral cavity and their interactions between oral microorganisms or with the host. The environment present in the human mouth is suited to the growth of characteristic microorganisms found there. It provides a source of water and nutrients, as well as a moderate temperature. Resident microbes of the mouth adhere to the teeth and gums to resist mechanical flushing from the mouth to stomach where acid-sensitive microbes are destroyed by hydrochloric acid.

Oral ecology is the microbial ecology of the microorganisms found in mouths. Oral ecology, like all forms of ecology, involves the study of the living things found in oral cavities as well as their interactions with each other and with their environment. Oral ecology is frequently investigated from the perspective of oral disease prevention, often focusing on conditions such as dental caries, candidiasis ("thrush"), gingivitis, periodontal disease, and others. However, many of the interactions between the microbiota and oral environment protect from disease and support a healthy oral cavity. Interactions between microbes and their environment can result in the stabilization or destabilization of the oral microbiome, with destabilization believed to result in disease states. Destabilization of the microbiome can be influenced by several factors, including diet changes, drugs or immune system disorders.

Persister cells are subpopulations of cells that resist treatment, and become antimicrobial tolerant by changing to a state of dormancy or quiescence. Persister cells in their dormancy do not divide. The tolerance shown in persister cells differs from antimicrobial resistance in that the tolerance is not inherited and is reversible. When treatment has stopped the state of dormancy can be reversed and the cells can reactivate and multiply. Most persister cells are bacterial, and there are also fungal persister cells, yeast persister cells, and cancer persister cells that show tolerance for cancer drugs.

<i>Staphylococcus capitis</i> Species of bacterium

Staphylococcus capitis is a coagulase-negative species (CoNS) of Staphylococcus. It is part of the normal flora of the skin of the human scalp, face, neck, scrotum, and ears and has been associated with prosthetic valve endocarditis, but is rarely associated with native valve infection.

Biofilm formation occurs when free floating microorganisms attach themselves to a surface. Although there are some beneficial uses of biofilms, they are generally considered undesirable, and means of biofilm prevention have been developed. Biofilms secrete extracellular polymeric substance that provides a structural matrix and facilitates adhesion for the microorganisms; the means of prevention have thus concentrated largely on two areas: killing the microbes that form the film, or preventing the adhesion of the microbes to a surface. Because biofilms protect the bacteria, they are often more resistant to traditional antimicrobial treatments, making them a serious health risk. For example, there are more than one million cases of catheter-associated urinary tract infections (CAUTI) reported each year, many of which can be attributed to bacterial biofilms. There is much research into the prevention of biofilms.

Antivirulence is the concept of blocking virulence factors. In regards to bacteria, the idea is to design agents that block virulence rather than kill bacteria en masse, as the current regime results in much more selective pressure.

References

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  2. "Imitation shark skin could prevent infections". seed.nih.gov. 14 Apr 2020. Retrieved 2 April 2024.
  3. Rostami S and Garipcan B (2022)Surface Innovations 10(3): 165–190,https://doi.org/10.1680/jsuin.21.00055
  4. 1 2 "'Inspired by Nature'". Sharklet Technologies Inc. 2010. Retrieved 6 June 2014.
  5. Alsever, Jennifer (2013-05-31). "Sharklet: A biotech startup fights germs with sharks". CNN.com Money.
  6. Schumacher, J. F.; Long, C. J.; Callow, M. E.; Finlay, J. A.; Callow, J. A.; Brennan, A. B. (2008). "Engineered Nanoforce Gradients for Inhibition of Settlement (Attachment) of Swimming Algal Spores". Langmuir. 24 (9): 4931–7. doi:10.1021/la703421v. PMID   18361532.
  7. Kim, Eun; Kinney, William H.; Ovrutsky, Alida R.; Vo, Danthy; Bai, Xiyuan; Honda, Jennifer R.; Marx, Grace; Peck, Emily; Lindberg, Leslie; Falkinham, Joseph O.; May, Rhea M.; Chan, Edward D. (2014-09-09). "A surface with a biomimetic micropattern reduces colonization ofMycobacterium abscessus". FEMS Microbiology Letters. 360 (1). Oxford University Press (OUP): 17–22. doi: 10.1111/1574-6968.12587 . ISSN   0378-1097. PMID   25155501.
  8. 1 2 Xu, Binjie; Wei, Qiuhua; Mettetal, M. Ryan; Han, Jie; Rau, Lindsey; Tie, Jinfeng; May, Rhea M.; Pathe, Eric T.; Reddy, Shravanthi T.; Sullivan, Lauren; Parker, Albert E.; Maul, Donald H.; Brennan, Anthony B.; Mann, Ethan E. (2017-11-01). "Surface micropattern reduces colonization and medical device-associated infections". Journal of Medical Microbiology. 66 (11). Microbiology Society: 1692–1698. doi: 10.1099/jmm.0.000600 . ISSN   0022-2615. PMC   5903250 . PMID   28984233.
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