eMedicine Specialties > Infectious Diseases > Bacterial Infections

Propionibacterium Infections: Treatment & Medication

Author: Sajeev Handa, MB, BCh, BAO, LRCSI, LRCPI, Director, Division of Hospital Medicine, Department of Medicine, Rhode Island Hospital
Contributor Information and Disclosures

Updated: Mar 30, 2009

Treatment

Medical Care

  • Acne vulgaris:12 Topical and oral agents act at various stages in the evolution of an acne lesion and may be used alone or in combination to enhance efficacy. Most cases of acne vulgaris are controlled with combinations of vitamin A acid, benzoyl peroxide, drying and peeling agents, and antibiotics. Topical agents should be applied to the entire affected area to treat existing lesions and to prevent the development of new ones. Potent topical steroid creams do not provide any short-term improvement in moderate acne. Laser therapy is being studied as a future treatment.
  • CNS shunt infections: Device removal is indicated for CNS shunt infections, and antibiotic treatment should be focused once results of Gram staining and culture are available.13 Empiric initial coverage with vancomycin plus ceftazidime, cefepime, or meropenem would be appropriate.
  • Other infections: Determination of the clinical significance of an isolate of Propionibacterium species must be made with caution because this will influence the need to direct therapy against that isolate.
  • Transfusion-transmitted bacterial infection: This requires stoppage of the blood transfusion, resuscitation of the patient, and, if suspicion is high, administration of empiric broad-spectrum antibiotics until results are available. A typical combination would be intravenous vancomycin and gentamicin.

Surgical Care

  • Acne vulgaris: Surgical care involves manual removal of comedones and drainage of pustules and cysts. When performed correctly, acne surgery speeds resolution and rapidly enhances cosmetic appearance. Scar revision via dermabrasion, excision, and gelatin matrix collagen implantation is performed in patients who are self-conscious about the pitted and craterlike scars that remain.
  • Cardiovascular device–related infections: Removal of the device is usually recommended.14 Bacteremia without a clear source may warrant an aggressive course of intravenous antibiotic therapy.
  • Chronic pseudophakic-related endophthalmitis: This may require vitrectomy,15 intravitreal vancomycin therapy, and replacement of the intraocular lens to ensure cure.16
  • CNS shunt infections: Device removal, external drainage, and subsequent shunt replacement should be performed once the CSF is sterile.13

Consultations

  • Acne vulgaris: Referral to a dermatologist may be appropriate for patients who do not respond to conventional treatment.
  • Other infections: Isolation of Propionibacterium species in the settings described above may require the assistance of an infectious diseases specialist for interpretation.

Diet

In cases of acne vulgaris, no evidence supports the elimination of various foods such as sweets, chocolate, milk, and fatty foods. However, many patients report that they notice flares after the consumption of certain foods, such as chocolate. In these scenarios, eliminating the implicated food item would be reasonable if the patient feels that it is aggravating the condition.

Medication

The following information primarily pertains to the treatment of Propionibacterium acne vulgaris.

Antibiotics used to treat anaerobic infections usually suffice for other types of Propionibacterium infections. These include the penicillins, carbapenems, and clindamycin. In addition, vancomycin and teicoplanin have been used. Some of these antibiotics are discussed after the treatment of acne vulgaris.

Keratolytics

These agents cause cornified epithelium to swell, soften, macerate, and then desquamate. Retinoids are now classified into 3 generations. The first comprises topical tretinoin and systemic isotretinoin. The second-generation retinoids are used to treat psoriasis. The third-generation retinoids include adapalene and tazarotene, which are topical agents.


Tretinoin (Retin-A, Avita)

Inhibits microcomedo formation and eliminates lesions present. Makes keratinocytes in sebaceous follicles less adherent and easier to remove. Available as 0.025%, 0.05%, and 0.1% creams. Available also as 0.01% and 0.025% gels.

Adult

Begin with lowest tretinoin formulation and increase as tolerated; apply hs or qod; reduce frequency of application if irritation develops

Pediatric

<12 years: Not established
>12 years: Apply as in adults

Toxicity increases with coadministration of benzoyl peroxide, salicylic acid, and resorcinol; avoid topical sulfur, resorcinol, salicylic acid, other keratolytics, abrasives, astringents, spices, and lime

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Photosensitivity may occur with excessive sunlight exposure; caution in eczema; not to be applied to mucous membranes, mouth, and angles of nose


Benzoyl peroxide (Benzac, Benoxyl)

Free-radical oxygen is released upon administration and oxidizes bacterial proteins in sebaceous follicles, decreasing the quantity of irritating free fatty acids and of anaerobic bacteria. It also has keratolytic and comedolytic effects. This agent is most effective for inflammatory acne. It is available OTC and by prescription.

Adult

Apply sparingly qd; gradually increase to bid/tid prn; reduce dose, frequency, or concentration if excessive dryness or peeling occurs

Pediatric

Not established

Potentiates adverse effects of tretinoin

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Avoid contact with lips, eyelids, mucous membranes, and eyes; for external use only; discontinue if swelling, burning, or excessive dryness occurs


Azelaic acid (Azelex, Finevin)

Has been shown to help normalize keratinization and to reduce proliferation of P acnes and has proven to be effective against both noninflammatory and inflammatory lesions. This medication may decrease microcomedo formation in acne vulgaris and may have a bleaching effect on skin. May also have antimicrobial effect. Efficacy may be enhanced when used in combination with other topical medications (eg, benzoyl peroxide, clindamycin, tretinoin). Hands should be washed following application. Duration of treatment can vary from person to person and varies depending on severity. Improvement occurs in the majority of patients with inflammatory lesions within 4 wk.

Adult

Wash area and apply sparingly bid; duration of use can vary from person to person and depends on severity of acne

Pediatric

Not established

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Avoid contact with eyes; discontinue use if severe irritation develops; adverse reactions generally are mild and transient; most common adverse reactions (occurring in approximately 1-5% of patients) are pruritus, burning, stinging, and tingling


Tazarotene (Tazorac, Avage)

Retinoid prodrug whose active metabolite modulates differentiation and proliferation of epithelial tissue; may also have anti-inflammatory and immunomodulatory properties. This agent is strictly contraindicated in pregnancy.

Adult

Apply thin film (ie, 2 mg/cm2) hs to clean, dry skin where acne appears

Pediatric

Children: Not established
Adolescents: Apply as in adults

Do not use concomitantly with dermatologic drugs or cosmetics that have a strong drying effect on the skin (eg, salicylic acid, benzoyl peroxide, astringents)

Pregnancy

X - Contraindicated; benefit does not outweigh risk

Precautions

May cause burning or stinging; discontinue upon excessive irritation; rinse thoroughly upon contact with eyes, eyelids, or mouth; may cause severe irritation in eczematous skin; photosensitivity may occur

Antibiotics

These agents are useful in papular, pustular, and cystic acne and must be taken for weeks to be effective. They are typically used for many weeks or months to achieve maximum benefit.

Long-term antibiotics may be required and necessitate monitoring for adverse drug events. Females should be warned about the development of Candida albicans vaginitis.

Topical antibiotics are useful in mild pustular and comedone acne. These preparations include clindamycin, erythromycin, and Benzamycin (erythromycin 3%-benzoyl peroxide 5% gel).

P acnes has been developing increasing resistance to erythromycin, so the oral formulation is of less benefit than it once was.


Oxytetracycline (Terramycin)

Treats gram-positive and gram-negative organisms as well as mycoplasmal, chlamydial, and rickettsial infections. Inhibits bacterial protein synthesis by binding with 30S and possibly 50S ribosomal subunit(s).

Adult

500 mg PO bid

Pediatric

<8 years: Not recommended
>8 years: 25-50 mg/kg/d PO qid

Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy; can increase hypoprothrombinemic effects of anticoagulants

Documented hypersensitivity; severe hepatic dysfunction

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last half of pregnancy through 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines


Tetracycline (Sumycin)

Inhibits bacterial protein synthesis by binding with 30S and, possibly, 50S ribosomal subunit(s). Tetracycline has anti-inflammatory activity.

Adult

250-500 mg PO q6h
Mild-to-moderate infections: 500 mg PO bid or 250 mg PO qid for 7-14 d

Pediatric

<8 years: Not recommended
>8 years: 25-50 mg/kg/d (10-20 mg/lb) PO qid

Bioavailability decreases with antacids that contain aluminum, calcium, magnesium, iron, or bismuth subsalicylate; can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy; tetracyclines can increase hypoprothrombinemic effects of anticoagulants

Documented hypersensitivity; severe hepatic dysfunction

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (second half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines


Minocycline (Minocin)

Treats infections caused by susceptible gram-negative and gram-positive organisms, in addition to infections caused by susceptible Chlamydia, Rickettsia, and Mycoplasma species.

Adult

100 mg PO bid for 5-7 d or longer for acne

Pediatric

<8 years: Not recommended
>8 years: 4 mg/kg PO initially, followed with 2 mg/kg q12h

Bioavailability decreases with antacids that contain aluminum, calcium, magnesium, iron, or bismuth subsalicylate; can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy; tetracyclines can increase hypoprothrombinemic effects of anticoagulants

Documented hypersensitivity; severe hepatic dysfunction

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (second half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines; hepatitis or lupuslike syndromes may occur


Clindamycin (Cleocin)

Lincosamide for treatment of serious skin and soft tissue staphylococcal infections. Also effective against aerobic and anaerobic streptococci (except enterococci). Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest.

Adult

75-300 mg PO bid/qid
Alternatively, 600 mg IV q8h

Pediatric

Not established; 20-40 mg/kg/d IV divided tid/qid suggested

Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects of clindamycin; antidiarrheals may delay effect

Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis by allowing overgrowth of Clostridium difficile


Erythromycin (E.E.S., E-Mycin, Eryc)

Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. For treatment of staphylococcal and streptococcal infections. Age, weight, and severity of infection determine proper dosage in children. When bid dosing is desired, half the total daily dose may be taken q12h. For more severe infections, double the dose.

Adult

250 mg erythromycin stearate/base (or 400 mg ethylsuccinate) PO q6h 1 h ac, or 500 mg q12h
Alternatively, 333 mg PO q8h; increase to 4 g/d depending on severity of infection

Pediatric

30-50 mg/kg/d (15-25 mg/lb/d) PO divided q6-8h; double dose for severe infection

Coadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis

Documented hypersensitivity; hepatic impairment

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in liver disease; estolate formulation may cause cholestatic jaundice; GI adverse effects are common (administer doses pc); discontinue use upon nausea, vomiting, malaise, abdominal colic, or fever


Vancomycin (Vancocin, Vancoled, Lyphocin)

Potent antibiotic directed against gram-positive organisms and active against Enterococcus species. Useful in the treatment of septicemia and skin structure infections. Indicated for patients who cannot receive, or who have failed to respond to, penicillins and cephalosporins or have infections with resistant staphylococci.
To avoid toxicity, current recommendation is to assay vancomycin trough levels after third dose drawn 0.5 h prior to next dosing. Use creatinine clearance to adjust dose in patients diagnosed with renal impairment.

Adult

1 g IV q12h (normal renal function)

Pediatric

40 mg/kg/d IV divided tid/qid for 7-10 d

Erythema, histaminelike flushing, and anaphylactic reactions may occur when administered with anesthetic agents; when taken concurrently with aminoglycosides, risk of nephrotoxicity may increase above that with aminoglycoside monotherapy; effects in neuromuscular blockade may be enhanced when coadministered with nondepolarizing muscle relaxants

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in renal failure, neutropenia; red man syndrome is caused by too rapid IV infusion (dose administered over a few min) but rarely happens when dose is administered IV over 2 h or as PO or IP administration; red man syndrome is not an allergic reaction

Antiandrogen therapies

These agents are reserved for patients with acne who have clinical signs of androgen excess and for those in whom other treatments have failed. It is used in women with treatment-resistant, late-onset, or persistent acne. Some of these women have signs suggestive of hyperandrogenism (eg, hirsutism, irregular menses, menstrual dysfunction), but others are without abnormalities. Serum androgen levels may or may not be elevated.

Three options are available. Estrogen suppresses ovarian androgens (oral contraceptives), glucocorticoids suppress adrenal androgen, and antiandrogens (eg, spironolactone, cyproterone acetate) act at the peripheral level.


Spironolactone (Aldactone)

Aldosterone antagonist inhibits ovarian and adrenal production of androgens. Competes with dihydrotestosterone, binding at hormone receptor sites on hair follicle cells. Also reduces 17-alpha-hydroxylase activity, lowering plasma levels of testosterone and androstenedione.

Adult

200 mg PO qd

Pediatric

Not established

May decrease effect of anticoagulants; potassium and potassium-sparing diuretics may increase toxicity of spironolactone

Documented hypersensitivity; anuria; renal failure; hyperkalemia

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in renal and hepatic impairment


Cyproterone (Androcur)

Not available in the United States. This is an oral contraceptive that is highly effective in improving acne. An androgen receptor antagonist and weak gonadal androgen production inhibitor. Also a weak progestin.

Adult

2 mg PO qd with either 0.035 or 0.050 mg ethynyl estradiol; clinical benefit can be enhanced by administering 50 or 100 mg PO qd from the 5th to the 14th day of cycle

Pediatric

Not established

Documented hypersensitivity; pregnancy and breastfeeding; Dubin-Johnson syndrome; hepatic disease; blood-clotting disorder; Rotor syndrome

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in chronic depression, diabetes with vascular changes, and sickle cell anemia

Oral retinoids

Isotretinoin is related to vitamin A and is very effective in controlling acne and inducing long-term remissions.


Isotretinoin (Accutane)

Oral agent that treats serious dermatologic conditions. Synthetic 13-cis isomer of the naturally occurring tretinoin (trans -retinoic acid). Both agents are structurally related to vitamin A. Isotretinoin decreases sebaceous gland size and sebum production and may inhibit sebaceous gland differentiation and abnormal keratinization. Treatment is weight-based, and the standard course of treatment usually is from 16-20 wk.

Adult

0.5-1.5 mg/kg/d (usually 1 mg/kg/d) PO for 20 wk

Pediatric

Not established

Toxicity may occur with vitamin A coadministration; pseudotumor cerebri or papilledema may occur when coadministered with tetracyclines; isotretinoin may reduce plasma levels of carbamazepine

Pregnancy

X - Contraindicated; benefit does not outweigh risk

Precautions

Severity of adverse effects proportional to daily dose; monitor triglyceride levels, LFTs, and CBC counts prior to and during treatment; if triglyceride levels >700-800 mg/dL, discontinue medication to diminish risk of pancreatitis; perform pregnancy test prior to commencing treatment; additional adverse effects include hyperostoses, cheilitis, headache, and amenorrhea

Acne products

These agents may modify or inhibit the inflammatory process.


Erythromycin and benzoyl peroxide (Benzamycin)

Contains erythromycin, which is a macrolide antibiotic, as well as benzoyl peroxide. Benzoyl peroxide, in addition to being an antibacterial agent, is a keratolytic and desquamative agent. With benzoyl peroxide, free-radical oxygen is released upon administration, oxidizing bacterial proteins in sebaceous follicles and decreasing the number of anaerobic, bacterial, and irritating free fatty acids. Has keratolytic and comedolytic effects.
Erythromycin is indicated for infections caused by susceptible strains of microorganisms.

Adult

Apply bid qam and qpm to affected areas after skin is washed thoroughly, rinsed with warm water, and gently patted dry

Pediatric

<12 years: Not established
>12 years: Administer as in adults

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

For external use only; avoid contact with lips, eyelids, mucous membranes, and eyes; discontinue upon swelling, burning, or excessive dryness


Adapalene (Differin)

Modulates cellular differentiation, inflammation, and keratinization. May be tolerated by individuals who cannot tolerate tretinoin creams. A therapeutic response can be expected following 8-12 wk of therapy. Available as 0.1% gel or solution.

Adult

Apply hs, some patients may tolerate bid dosing

Pediatric

Not established

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Avoid contact with mucous membranes, eyes, mouth, and nostrils; avoid exposure to sunlight and sunlamps; dryness of skin, scaling, erythema, burning, and pruritus may occur

More on Propionibacterium Infections

Overview: Propionibacterium Infections
Differential Diagnoses & Workup: Propionibacterium Infections
Treatment & Medication: Propionibacterium Infections
Follow-up: Propionibacterium Infections
Multimedia: Propionibacterium Infections
References

References

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  2. Mandell GL, Bennett JE, Dolin R. Principles and Practice of Infectious Diseases. 6th ed. New York, NY: Churchill Livingstone; 2005.

  3. Delyle LG, Vittecoq O, Bourdel A, et al. Chronic destructive oligoarthritis associated with Propionibacterium acnes in a female patient with acne vulgaris: septic-reactive arthritis?. Arthritis Rheum. Dec 2000;43(12):2843-7. [Medline].

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Further Reading

Keywords

Propionibacterium infection, Propionibacterium acnes, P acnes, Propionibacterium granulosum, P granulosum, Propionibacterium avidum, P avidum, Propionibacterium propionicus, P propionicus pustular acne, acne vulgaris, cystic acne, nodular acne, acneiform drug eruptions, Propionibacterium acne, inflammatory acne, Propionibacterium acne vulgaris

Contributor Information and Disclosures

Author

Sajeev Handa, MB, BCh, BAO, LRCSI, LRCPI, Director, Division of Hospital Medicine, Department of Medicine, Rhode Island Hospital
Sajeev Handa, MB, BCh, BAO, LRCSI, LRCPI is a member of the following medical societies: Infectious Diseases Society of America and Society of Hospital Medicine
Disclosure: Nothing to disclose.

Medical Editor

Douglas A Drevets, MD, Assistant Professor, Department of Medicine, Section of Infectious Disease, Oklahoma University Health Sciences Center
Douglas A Drevets, MD is a member of the following medical societies: American Association of Immunologists, American Society for Microbiology, Central Society for Clinical Research, and Christian Medical & Dental Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Aaron Glatt, MD, Professor of Clinical Medicine, New York Medical College; President and CEO, Former Chief Medical Officer, Departments of Medicine and Infectious Diseases, New Island Hospital
Aaron Glatt, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physician Executives, American College of Physicians, American College of Physicians-American Society of Internal Medicine, American Medical Association, American Society for Microbiology, American Thoracic Society, American Venereal Disease Association, Infectious Diseases Society of America, International AIDS Society, and Society for Healthcare Epidemiology of America
Disclosure: Nothing to disclose.

CME Editor

Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

 
 
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