Came across this recently. Any thoughts?

~Hanan


http://www.healthsci.tufts.edu/apua/Newsletter/17_3a.html

Silver cations as an antimicrobial agent: clinical uses and bacterial 
resistance
Simon Silver, Jeng-Fan Lo and Amit Gupta
Department of Microbiology and Immunology, University of Illinois, Chicago, 
Illinois, USA

Silver cations (Ag+) are important, often misunderstood compounds that play a 
significant role as effective and legitimate antimicrobial agents, used 
particularly in the treatment of burns. Their spectrum of uses is broad and 
generally unfamiliar, ranging from beneficial clinical applications, to 
commercial- and folk-practices that are of questionable value but of little 
harm, to "snake oil" products and frauds found through the internet and in 
health food stores.
In an effort to better understand and anticipate the uses of these compounds, 
we recently studied plasmid-mediated resistance to silver.1 Advances in 
molecular genetics have allowed us to use epidemiological tools to establish 
the range and diversity of resistance systems. Past difficulties in measuring 
Ag+ resistance have been overcome.2 The importance of the halide 
concentration and initial cell number in such measurements has been shown, 
and after the sequence of the first silver resistance gene cluster was 
complete,1 we found closely homologous genetic determinants surprisingly 
abundant in hospital collections of enteric bacteria, both from 
silver-exposed and not-knowingly silver-exposed sources (A. Gupta et al., in 
prep.).
Clinical Uses of Silver Products
Silver cations are microcidal at low concentrations, and are without serious 
side effects for humans. Argyria (irreversible discoloration of the skin 
resulting from subepithelial silver deposits) is rare and mostly of cosmetic 
concern. The widest and best-known medicinal use of silver preparations is as 
preferred antimicrobial agents for the treatment of serious burns.3 Silver 
sulfadiazine cream that contains 1% silver sulfadiazine plus 0.2% 
chlorhexidine digluconate is the mostly widely used product, marketed as 
Silvazine in the United States for human and veterinary use. Flamazine is the 
same product in other countries, largely in the United Kingdom, Canada and 
continental Europe. Ag-coated nylon is increasingly being used to cover burn 
wounds and traumatic injuries to humans4 and large animals.5 Silver 
sulfadiazine-coated methacrylate sheet material that provides a stable base 
for sustained release of Ag+ over days is also being investigated.6 These 
silver-containing fabrics are easier to apply and remove from large burns 
than is the residue of a cream. Sometimes a low voltage DC current is applied 
across a sheet to accelerate release of Ag+ from the cloth.4,7 Additional 
clinical uses include aseptic coverings for plastic surgery, traumatic 
wounds, leg ulcers, skin grafts, incisions, abrasions and minor cuts. Plastic 
indwelling catheters coated with silver compounds8 are being developed to 
retard the formation of biofilms and stem the incidence of nosocomial 
infection. The use of Ag-coated nylon threads in electroretinograms has 
allowed the detection of tissue damage without fear of infection.9 Silver 
salts have traditionally been administered to the eyes of newborn infants to 
prevent neonatal eye infections. Dental amalgam, so-called "silver fillings," 
contain about 35% Ag(0) and 50% Hg(0), but we do not know if sufficient Ag+ 
is released to have an antimicrobial effect. It is known, however, that the 
release of Hg2+ from dental amalgams selects for metal-resistant bacteria.10
Bacterial Resistance and Genetics
Bacterial resistance to silver sulfadiazine, with its sometimes tragic 
consequences, has been periodically reported. An Ag+-resistant Salmonella 
strain killed three patients and required the closing of the burn ward at 
Massachusetts General Hospital (MGH).11 Although silver 
sulfadiazine-resistant bacteria have occasionally been observed in burn ward 
infections, and while chromosomal mutations of clinical strains to Ag+ 
resistance may also cause a problem in infection,12 resistance rates have not 
been followed.
The plasmid-determined gene cluster for silver resistance from the MGH 
Salmonella11 contained a total of nine genes, seven of which we have named 
with the two less recognized open reading frames still called ORFs: in order 
silP(ORF105)silAB(ORF96)C silRS silE.1 The system encodes a periplasmic 
Ag+-binding protein (SilE) plus two membrane Ag+ efflux pumps (SilCBA and 
SilP). The central six genes (silA through silS) produce products that are 
homologous to an unstudied gene cluster on the Escherichia coli genome 
(currently called ybdE, ylcD, ylcC, ylcB, ylcA and ybcZ, in order) and less 
closely to other metal resistance systems. In Southern blotting DNA/DNA 
hybridization analysis of clinical isolates with homologous DNA, the central 
six genes appear to always be present together, but homologs of the outer two 
genes, silP and silE, are occasionally missing (A. Gupta et al., in prep.). 
The six genes, silPORF105ABORF96silC, are co-transcribed in a very long 
mRNA.1 The regulatory gene pair silRS is co-transcribed separately, and silE 
is transcribed by itself as a third mRNA.1
Mechanism of Resistance 
The functions of silver-resistance gene products can be recognized by 
homology to other gene products that have been studied. SilP is a membrane 
P-type ATPase that pumps Ag+ from the cell1,13,14 and is most similar to Cu+ 
and Cd2+ efflux ATPases. SilCBA (probably together with the ORF96 product) 
form a second Ag+ efflux pump driven by the membrane potential and not ATP. 
This pump consists of three proteins, one in the inner membrane (SilA), 
another in the outer membrane (SilC), and the third bridging the periplasmic 
space (SilB). Three-protein membrane potential-driven cation/proton 
exchangers were initially recognized in our laboratory with a bacterial 
Cd2+/Zn2+/Co2+ system.14
This silver resistance system is the first time we have seen three different 
mechanisms in a single toxic metal cation resistance determinant. It appears 
to be transcriptionally controlled by the products of two genes, SilS (a 
histidine-containing membrane auto-kinase "sensor") and SilR (a cytoplasmic 
DNA-binding activator "responder" that contains an aspartate residue that is 
trans-phosphorylated from SilS). SilRS is homologous in sequence to members 
of the large family of two-component sensor/responder transcriptional 
regulators that respond to extracellular signals.1,14
SilE is a small periplasmic Ag+-binding protein that binds Ag+ ions 
specifically at the cell surface, presenting the first line of resistance 
against Ag+ toxicity. The SilE protein has been purified to homogeneity and 
extensively studied by J-F Lo et al. (in prep.). The SilE protein contains 
ten histidine residues that bind five Ag+ cations1 (J-F Lo et al., in prep.). 
In contrast to other metal-binding proteins, SilE has no cysteine residues. 
Binding of Ag+ to the SilE protein brings about an unusually large change in 
protein folding, from essentially disordered, to a predominantly alpha 
helical structure. At this early stage, we do not know whether silE, which 
confers some Ag+ resistance by itself, will ever be found alone or how the 
various sil gene products interact for full resistance.
Non-Clinical Uses of Silver
Our primary concern remains Ag+ usage in the clinic and the selection for Ag+ 
resistance. The wide spread, often unchecked application of silver products 
as biocides is adding to the problem. Silver-containing products are used in 
hospital and hotel water distribution systems to control infectious agents 
(e.g., Legionella). Silver has been used to sterilize recycled water aboard 
the MIR space station and on the NASA space shuttle.15 Home-water 
purification units sold in the US supermarkets contain silverized activated 
carbon filters and ion-exchange resins (Fig. 1). Silver is a health additive 
in traditional Chinese and Indian Ayurvedic medicine.16 In Mexico, 
supermarkets sell Microdyn, colloidal silver in gelatin, to disinfect salad 
vegetables and drinking water (Fig. 2). Johnson Matthey Chemicals (UK) uses 
an inorganic composite with immobilized slow-release silver as a preservative 
in cosmetics and toiletries.17 In Japan, a new compound is mixed into 
plastics for lasting antimicrobial protection of telephone receivers, 
calculators, toilet seats, and children's toys.18 Metallic silver-copper 
containing ceramic disks, marketed as "Clean Power Plus," are sold as an 
alternative to laundry detergents.19 Silver addition to fabrics (similar to 
clinical use of Ag-nylon) is proposed to reduce buildup of microbial 
populations and therefore offensive smells in camping gear and clothing. 
While folk remedies and "snake oil" preparations are not the same, they are 
coupled here as representative of applications with suspect benefit.9 
Over-the-counter Ag+ health food supplements are probably not effective20 and 
are frequently mislabeled.21 The non-clinical uses of silver appear endless, 
with one possible, detrimental side-effect being the lessening of its 
usefulness as an antimicrobial agent.
What is Needed
The identification of the genes for silver resistance, and the determination 
of closely related genes in bacteria from environmental and clinical 
environments, and from diverse geographical locations (A. Gupta et al., in 
prep.) should eliminate recent skepticism about the existence of 
silver-resistant bacteria. Now that the means for identifying silver 
resistance determinants in Enterobacteriaceae is available, similar efforts 
should be made with respect to other common pathogens, particularly those 
associated with large burns (i.e., pseudomonads and staphylococci). The wide 
and rather uncontrolled use of silver products may result in increased 
resistance, analogous to the emergence of antibiotic- and other 
biocide-resistant bacteria. Undermining the benefits of these compounds would 
be unfortunate to the clinical and hygienic uses that depend on the 
microcidal properties of silver. 

References 

1.  Gupta A, Matsui K, Lo JF, Silver S. 1999. Nature Medicine 5:183-188. 
2.  Gupta A, Maynes M, Silver S. 1998. Applied Environmental Microbiol 64: 
5042-5045. 
3.  Rosenkranz HS, Carr HS. 1972. Antimicrob Agents Chemother 2: 367-372; 
Monafo WW, West MA. 1990. Drugs 40:364-373; Fox CL Jr, Rao TN, Azmeth R, 
Gandhi SS, Modak S. 1990. J Burn Care Rehabilitation 11:112-117. 
4.  Deitch EA, Marino AA, Malakanok V, Albright JA. 1987. J Trauma 27: 
301-304. 
5.  Adams, AP, Santschi EM, Mellencamp MA. 1999. Veterinary Surgery 28: 
219-225. 
6.  Miller L, Hansbrough J, Slater H, Goldfarb IW , Kealey P, Saffle J, 
Kravitz M, Silverstein P. 1990. J Burn Care Rehabilitation 11:35-41. 
7.  Modak S, Fox P, Stanford J, Sampath L, Fox CL Jr. 1986. J Burn Care 
Rehabilitation 7: 422-425. 
8.  Gabriel MM, Mayo MS, May LL,Simmons RB, Ahearn DG. 1996. Current 
Microbiol 33:1-5. 
9.  The Silver Institute. Washington, DC, USA. 
10. Lorscheider FL, Vimy MJ, Summers AO. 1995. FASEB J 9:504-508, 1499-1500. 
11. McHugh SL, Moellering RC, Hopkins CC, Swartz MN. 1975. Lancet i: 235-240. 
12. Li XZ, Nikaido H, Williams KE. 1997. J Bacteriol 179:6127-6132. 
13. Silver S, Gupta A, Matsui K, Lo J-F. 1999. Metal-Based Drugs 6 (in press).
 
14. Silver S, Phung LT. 1996 Annual Review Microbiol 50: 753-789. 
15. Adachi K (editor). Colloidal Silver. Educate-Yourself. Costa Mesa, CA, 
USA. 
16. Reach for Life Enterprises. Fresno, CA, USA. 
17. Johnson Matthey. London, England, UK. 
18. Amenitop, silica gel microspheres containing a silver-thiosulfate 
complex. Washington Post, February 5, 1993. 
19. Mass Appeal Marketing. Torrance, CA, USA. 
20. Fung MC, Weintraub M, Bowen DL. 1995. JAMA 274:1196-1197. 
21. US Food and Drug Administration. 1996. Over-the-counter drug products 
containing colloidal silver ingredients or silver salts. Federal Register, 
October 15, 61(200): 53685-53688; US Food and Drug Administration. 1994. FDA 
Health Fraud Bulletin #19, Colloidal Silver, October 7.


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