Arcanobacterium Haemolyticum 

Updated: Mar 14, 2022
Author: Nicole Ufkes; Chief Editor: William D James, MD 


Practice Essentials

The bacterium now named Arcanobacterium haemolyticum was first described in 1946 as the pathogenic agent causing pharyngitis and cutaneous infections among US service members and indigenous peoples of the South Pacific.[1, 2]  As a result of its close resemblance to Corynebacterium pyogenes, some investigators believed the bacterium to be a mutant of this species and appended a subspecies name, C pyogenes subsp hominis.

Based on its peptidoglycan, fatty acid, and DNA characteristics, the bacterium was renamed and reclassified as the first member of the genus Arcanobacterium, which means "secretive bacteria.[3]  " Since its original description, the spectrum of diseases caused by A. haemolyticum has been expanded to include invasive infections, including sepsis and osteomyelitis. The importance of A. haemolyticum to dermatology lies in the characteristic rash associated with pharyngeal infection. Interestingly, the cutaneous manifestations of A. haemolyticum infection apparently were not reported in the dermatologic literature until 1996.[4]

Also see Bacterial Pharyngitis.


The most common symptoms include the following[5, 6] :

  • Sore throat (97-100%)

  • Pruritus (33%)

  • Nonproductive cough (33%)

In a systematic review of 191 patients with A. haemolyticum infections, 93.7% of patients reported throat pain. Greater than 50% of cases also presented with tonsillar exudates, fever, and rash.[7]


No risk factors are known for A. haemolyticum infection. Although purely speculative, Parija et al[8]  suggested in 2005 that close contact with animals such as cows and buffaloes and handling or consumption of unpasteurized milk might put patients at risk. A 2006 investigation did isolate a strain of A. haemolyticum (DSM 20595T) from preputial swabs of European bison (Bison bonasus) bulls with balanoposthitis.[9]


Peritonsillar abscess has been reported in 5 patients. The patients presented with severe sore throat and fever (37.3-40.1°C). After drainage, resolution occurred in all patients.[5, 10, 11]

Sepsis, with isolation of A. haemolyticum from blood cultures, has occurred in patients with pharyngitis.[12, 13, 14, 15, 16]


Skin biopsy specimens of the exanthem typically reveal edema in the superficial dermis with a mixed perivascular infiltrate consisting of lymphocytes and smaller numbers of neutrophils, eosinophils, and plasma cells. The infiltrate is without antibody or fibrin deposition. Organisms are not observed in skin biopsy specimens.[5] ​[17]

No imaging studies are recommended. Radiography, computed tomography scanning, or magnetic resonance imaging can be used in special circumstances when A. haemolyticum is suspected in peritonsillar abscesses, osteomyelitis, sinusitis, pulmonary infections, or central nervous system lesions.


Without antibiotic therapy, symptoms from Arcanobacterium haemolyticum pharyngeal infection last from a few days to 2 weeks. With antibiotic therapy, patients have symptoms for an average of 3 days.[18]  Whether antimicrobial therapy prevents late sequelae of infection is not known. However, due to the fact that the organism's prevalence may be increasing and because some of infections may be serious, antibiotic therapy is recommended.[19]  A 2015 study of isolates from soft-tissue infections revealed susceptibility to minocycline, vancomycin, and beta-lactam antibiotics, but several strains are resistant to gentamicin and levofloxacin.[20]

In an in vitro trial, antiseptic lozenges containing amylmetacresol and 2,4-dichlorobenzyl alcohol eliminated at least 99.9% of all colony-forming units of 7 bacterial species associated with pharyngitis, including A. haemolyticum.[21]

Occasionally, a patient who appears very ill with pharyngitis caused by Arcanobacterium haemolyticum (ie, unable to swallow, illness is severe) may require admission for administration of parenteral antibiotics.

Admit patients with systemic infections caused by A. haemolyticum to administer parenteral antibiotics and manage their infection in a way similar to that of a patient with bacteremia or focal abscess.


Consult an otolaryngologist to drain any suspected peritonsillar abscesses.


Although epidemiologic contact studies suggest that the disease is spread from human to human, the exact mechanism of spread has not been determined. However, it is not unreasonable to suggest that judicious handwashing and avoiding shared utensils and food may help to prevent the spread of the disease.


A. haemolyticum is a pleomorphic, facultatively anaerobic, nonmotile, nonsporulating, non–acid-fast, catalase-negative, hemolytic gram-positive rod. However, the organism can demonstrate a variable response to Gram staining if examined after 24 hours of growth.[1, 22, 23] The 70 known strains are divided into smooth and rough biotypes.[24] The smooth biotype predominates in wound infections, and the rough biotype predominates in respiratory tract infections.[25]

The composition of the cell wall is based on lysine, and its fatty acids are primarily straight and monounsaturated.[26]  A. haemolyticum ferments dextrose, maltose, lactose, galactose, and glycerol. It coagulates milk and causes liquefaction of gelatin. The bacterium does not reduce nitrates or produce indole.[1]

A. haemolyticum infection has rarely been reported in animals, and its pathogenicity in animals has not been well documented.[27, 28] Humans are believed to be its main environmental reservoir, although A. haemolyticum is not usually a respiratory colonizer.

Since its original description, A. haemolyticum has been occasionally isolated in patients with sepsis, osteomyelitis, septic arthritis, cellulitis, wound infections, necrotizing fasciitis, venous ulcers, skin abscesses, peritonsillar abscesses, cavitary pneumonia, pyothorax, paronychia, omphalitis, otitis media, endocarditis, sinusitis, orbital cellulitis, canaliculitis, meningitis, brain abscesses, diabetic soft-tissue infections, spontaneous bacterial peritonitis, liver abscesses, and chorioamnionitis.[29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 8, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54]

Many of the patients are immunocompromised (eg, from cancer, diabetes). In a 2016 case study, A. haemolyticum was found in not only the wound but also the blood of a diabetic patient presenting with a deep ulcer.[55] Diabetic patients are more vulnerable to infection by A. haemolyticum, and wound and blood cultures are appropriate if the patient appears septic. Multiple wound cultures may be required before A. haemolyticum is identified. A. haemolyticum is sometimes a copathogen with other bacteria, including with Fusobacterium necrophorum in 1 case of Lemierre disease.[56]

Although A. haemolyticum has been implicated in a wide spectrum of diseases, it has been most commonly associated with pharyngitis. Several investigators reported A. haemolyticum as the sole or dominant pathogen in patients presenting with pharyngitis. These studies are limited because the investigators did not look for concomitant infection by viruses or atypical bacteria.

Patients from whom A. haemolyticum is cultured develop specific antibody responses to the bacteria.[18] Furthermore, the bacteria gradually disappear from the oropharynx as the symptoms subside.[1] These studies suggest that A. haemolyticum is a pathogenic organism in some adults with pharyngitis. However, in experimental studies conducted on humans, 325,000 A. haemolyticum organisms were inoculated into each tonsil of 7 healthy volunteers. No organisms could be recovered 1 hour later, but cultures performed 24-48 hours after inoculation showed a predominant growth of A. haemolyticum, which persisted for 4-6 weeks.[1] None of these patients developed symptomatic disease.

Pharyngitis caused by A. haemolyticum must be differentiated from the more prevalent pharyngitis caused by streptococcal organisms. Group A β-hemolytic streptococcus (GABHS) is often the primary cause of bacterial pharyngitis.[57]  A. haemolyticum may be missed on routine throat cultures because of the use of rapid group A streptococcal antigen assays and the use of special culture media for optimal isolation of group A streptococcal species. Most cultures for pharyngitis are evaluated at 24 hours, at which point A. haemolyticum colonies are very small and demonstrate minimal hemolysis, and the cultures may be discarded.[20]

Epidemiologic contact studies indicate that the infection is likely spread through an unknown route by human contact with people who are infected.[5]  A. haemolyticum is rarely recovered in healthy individuals.[6, 58]

The mechanism responsible for adherence of A. haemolyticum to the pharyngeal mucosa is not known. In vitro experiments have shown that A. haemolyticum does have the ability to invade HEp-2 cells (immortalized upper respiratory tract epithelial cells) and survive there for 4 days, thus creating an intracellular reservoir of bacteria.[59]  Gellings and McGee report that the cytolytic action of A. haemolyticum is cholesterol-dependent. A. haemolyticum produces phospholipase D and arcanolysin. Phospholipase D increased the accessibility of cholesterol in the host membrane, and arcanolysin then interacts with that cholesterol, allowing the bacterium to form pores in the host cell.[60, 61]  

The pathophysiology of the rash is also unknown; however, the hypothesis that the rash is caused by a bacterial exotoxin is reasonable. Phospholipase D, neuraminidase, and a hemolysin have been identified as extracellular toxins secreted by A. haemolyticum.[62, 63]


United States

A. haemolyticum has been isolated from the pharynx in 0.4% of adult patients with pharyngitis in the United States.[5] When specifically sought in throat swab cultures, A. haemolyticum is found responsible for 0.5-2.5% of bacterial pharyngitis cases, especially among adolescents.[64]


In Canada and Finland, A. haemolyticum pharyngitis has a similar incidence to that found in the United States. In Israel, Czechia, and Sweden, A. haemolyticum was cultured from the pharynx of people with pharyngitis with frequencies of 0.2%, 0.75%, and 2% of patients, respectively.[58, 65, 66, 67, 68]

No known racial susceptibility to the disease has been reported. In 1 study, a higher rate of pharyngitis caused by A. haemolyticum was reported in females than in males, in which the male-to-female ratio was 1:1.6, while another study reported a higher rate in males compared with females, in which the male-to-female ratio was 1.3:1.[6, 69]  Pharyngitis caused by A. haemolyticum most commonly affects adolescents and young adults aged 10-30 years, with the maximum incidence occurring among those aged 15-18 years.[65]


The natural course of pharyngitis caused by A. haemolyticum is resolution within a few days to 2 weeks. Antibiotics have been shown to eradicate A. haemolyticum from the oropharynx and to resolve symptoms within 3 days.[5] Whether antibiotic therapy prevents complications in patients with pharyngitis is not known.

Rarely, a patient with pharyngitis caused by A. haemolyticum is hospitalized because of an inability to swallow. Cases of peritonsillar abscess have been reported, requiring drainage in 5 patients.[5, 10, 11] Sepsis developed in 4 patients with pharyngitis; A. haemolyticum was isolated from blood cultures of these patients.[12, 13, 14, 15] Sepsis and pulmonary abscess with tonsillitis developed in 1 patient.[12] No deaths have been reported resulting from pharyngitis caused by A. haemolyticum, although A. haemolyticum caused the death of 2 patients with endocarditis.[33, 44]



Physical Examination

Physical examination findings include fever (40-64%), pharyngeal erythema (97-100%), tonsillar exudate (70%), lymphadenopathy (41-48%), and rash (0-75%). The fever ranges from 37.6-40°C.[5, 68]


The pharyngeal exudate is patchy and gray-to-white. It is difficult to scrape off. Although the appearance of the posterior aspect of the pharynx is similar to that of scarlet fever, no associated hemorrhagic macules on the palate or findings on the tongue are present.[5]


The exanthem has been described only in patients with pharyngitis, not in patients with infection of other sites. It usually develops 1-4 days after the pharyngitis, although occasionally, it is the initial manifestation of the infection.

It has been described as erythematous (see the image below), pruritic, urticarial, scarlatiniform, and maculopapular.

Rash associated with pharyngitis caused by Arcanob Rash associated with pharyngitis caused by Arcanobacterium haemolyticum. Note the erythematous nature of the rash.

It usually begins on the extensor surfaces of the extremities, where it is most severe (see the images below). Over the next 2-3 days, it spreads centrally to the neck and the trunk.

The rash associated with pharyngitis caused by Arc The rash associated with pharyngitis caused by Arcanobacterium haemolyticum is most prominent on the extremities. Note the rash on the upper limbs.
The rash associated with pharyngitis caused by Arc The rash associated with pharyngitis caused by Arcanobacterium haemolyticum is most prominent on the extremities. Note the rash on the lower limbs.

It almost always spares the face (see the image below), the palms, and the soles, and the abdomen and the buttocks are relatively spared.

Rash associated with pharyngitis caused by Arcanob Rash associated with pharyngitis caused by Arcanobacterium haemolyticum. Note the significant involvement of the extremities and the relative sparing of the face.

It usually persists longer than 48 hours, and mild desquamation may occur during resolution.[5] No long-term sequelae have been noted.

Although the onset of rash and the constitutional symptoms are similar to those of scarlet fever, the rash in scarlet fever is centrifugal and has prominent Pastia lines. In both conditions, desquamation may occur during resolution of the rash.


Patients may develop anterior cervical or submandibular lymphadenopathy that is bilateral, tender, and 1-1.5 cm in size.



Diagnostic Considerations

Also consider the following:

Differential Diagnoses



Laboratory Studies

A complete blood cell count can show a white blood cell count of 7,100-23,000 cells/µL, with polymorphonuclear leukocytosis and a mean level of 13,000 cells/µL.[5, 6]

Monospot and antistreptolysin O titers are negative (unless concomitant infection is present), and help to distinguish A. haemolyticum infection from infectious mononucleosis and scarlet fever.

Kits are available to identify Arcanobacterium haemolyticum, such as the bioMérieux ANI card and the bioMérieux Coryne strip (a miniaturized test strip format), but are infrequently used in clinical laboratories.[56]

The diagnosis is most often made by culturing the pharyngeal swab on 5% blood agar plates (preferably rabbit or human blood agar, although sheep blood agar works if read at 48 h) at 37°C with 5% carbon dioxide for 24-48 hours. One study suggests that a 48-hour incubation on trypticase soy agar with 5% horse blood in 5% carbon dioxide may be the best medium.[19] Because most throat cultures are plated on sheep blood agar and read at 24 hours, the slow-growing colonies of A. haemolyticum may be missed.[70] At 48 hours, the bacteria produce nonpigmented 1-mm diameter colonies surrounded by a 3- to 5-mm diameter zone of hemolysis. Transmitted light may reveal a small, dark dot at the center of each colony.[8] A 2016 study suggests that hemolytic differential identification using the cyclic adenosine monophosphate (cAMP) inhibition and reverse cAMP tests may be effective in differentiating A. haemolyticum from other gram-positive coryneform bacillus and β-hemolytic streptococci.[23] These tests should used in conjunction with biochemical property test kits, colony size, and morphology.

If the clinician suspects this diagnosis, the laboratory should be notified because special media, longer incubation times, and further investigations are required for isolation and identification.



Medication Summary

No controlled trials of antimicrobial therapy have been conducted for pharyngitis caused by A. haemolyticum. Many patients with pharyngitis have been treated with 1 dose of intramuscular penicillin or 7-10 days of erythromycin or oral penicillin.[5] Antibiotic sensitivity testing reveals that most strains are resistant to trimethoprim-sulfamethoxazole; tetracycline resistance has been observed in 30% of strains tested.[22, 71] An isolate reported in 2006 was also resistant to ciprofloxacin.[45] Virtually all strains of A. haemolyticum studied so far are sensitive to erythromycin, azithromycin, gentamicin, and clindamycin.[22, 72] The majority of isolates are susceptible to penicillin, although tolerance has been reported. Accordingly, macrolides are now considered the drugs of choice.[5, 6, 58]

Penicillin treatment failures also may be related to the ability of A. haemolyticum to invade HEp-2 cells (immortalized upper respiratory epithelial cells) and survive there for 4 days, thus creating an intracellular reservoir of bacteria.[59] Macrolides achieve much higher intracellular concentrations than penicillin.[59, 73, 74]

More serious systemic infections have been treated successfully with high-dose intravenous beta-lactams (eg, penicillin, ampicillin, amoxicillin, cefuroxime, cefotaxime). Vancomycin is also an acceptable choice for serious infections; however, 1 strain carries the vanA gene, which is resistant to vancomycin.[75] Antibiotic selection should be based on antibiotic sensitivity testing because no clinical trials of treatment of systemic infections have been conducted.


Class Summary

Although antibiotic therapy decreases the duration of symptoms, whether it prevents sequelae of pharyngeal infection is not known.

Erythromycin ethylsuccinate (E.E.S., EryPed)

Erythromycin inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, arresting RNA-dependent protein synthesis. It is for the treatment of staphylococcal and streptococcal infections.

In children, age, weight, and severity of infection determine proper dosage. When twice-daily dosing is desired, half of the total daily dose may be taken every 12 hours. For more severe infections, double the dose. While no controlled studies have been performed, erythromycin has been effective in case series and most strains are susceptible.

Azithromycin (Zithromax)

Azithromycin acts by binding to the 50S ribosomal subunit of susceptible microorganisms and blocks dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Nucleic acid synthesis is not affected. It concentrates in phagocytes and fibroblasts as demonstrated by in vitro incubation techniques. In vivo studies suggest that concentration in phagocytes may contribute to drug distribution to inflamed tissues. Azithromycin treats mild-to-moderate microbial infections. A shorter course and daily dosing make this a good alternative for patients who are sensitive to penicillin.

Clindamycin (Cleocin)

Clindamycin is a semisynthetic antibiotic produced by the 7(S)-chloro-substitution of 7(R)-hydroxyl group of the parent compound lincomycin. It inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. It widely distributes in the body without penetration of the CNS. Clindamycin is protein bound and is excreted by the liver and kidneys.

It is an oral or parenteral antibiotic for anaerobic or susceptible streptococcal, pneumococcal, or staphylococcal species. It is considered to have good absorption into the bloodstream in both oral and parental forms.