Journal of Clinical Microbiology, April 2002, p. 1129-1133, Vol. 40, No. 4
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.4.1129-1133.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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Department of Pathology and Clinical Microbiology Laboratories, Massachusetts General Hospital, Boston, Massachusetts 02114, and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115
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From James M. Sherman's classic 1937 treatise on the genus Streptococcus (20)
Clinical microbiologists who contemplate the current bewildering assortment of catalase-negative gram-positive cocci that grow aerobically are likely to feel bombarded by what appear to be facts in isolation. They may find themselves longing for the days when laboratory identification of this group of bacteria was simple and straightforward. They no doubt abhor, in Sherman's (20) words, "...the hair-splitting divisions which have been set up by some taxonomically-minded bacteriologists."
Until the mid-1980s clinical microbiologists viewed catalase-negative gram-positive coccal isolates in essentially the same way Sherman and his colleagues did. All such isolates were streptococci, unless, of course, their cells were arranged in clusters, indicating a probable Aerococcus viridans strain (usually considered a contaminant). The streptococcal isolates could be divided into beta-hemolytic strains, enterococcal strains, pneumococci, and the puzzling "Streptococcus viridans" group, an unruly collection that defied classification by Lancefield's serological methods. This simplistic view of catalase-negative gram-positive cocci fell by the wayside as molecular taxonomic studies of these bacteria gave rise to an ever-expanding list of new genera and species. Taxonomic hair-splitting was, however, not the only factor contributing to the increasing number of recognized catalase-negative gram-positive cocci.
Concomitant medical progress in the treatment of serious diseases created a growing population of patients with compromised defenses against infection and altered normal flora. We began to see more frequent opportunistic infections in this patient group, and catalase-negative, gram-positive cocci, some familiar and some not previously described in human clinical specimens, emerged as new agents of infection. Today we recognize at least 15 genera (in addition to Streptococcus and Enterococcus) and numerous new species of catalase-negative gram-positive cocci that have been isolated from human clinical specimens. This review examines their basic characteristics and clinical significance and offers a philosophy (based on facts in relation) on dealing with these bacteria in the clinical microbiology laboratory.
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TABLE 1. Some characteristics of the viridans streptococcal species groupsa
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Salivarius group. Streptococcus salivarius and Streptococcus vestibularis are the salivarius group species usually found as part of the normal human oral flora. On blood agar, these strains form non-hemolytic or alpha-hemolytic colonies, and S. salivarius produces distinctive mucoid colonies on sucrose agar due to the production of extracellular polysaccharides. S. vestibularis is polysaccharide production negative and, along with some S. salivarius isolates, urease positive. S. salivarius has been noted as an infrequently isolated opportunistic pathogen, producing septicemia in neutropenic patients.
Bovis group. Formerly set apart from other streptococci as nonenterococcal group D streptococci, bovis group species are now considered as part of the viridans streptococcal division. S. bovis is the most well characterized human isolate in this species group, and can be divided into a number of biotypes based on phenotypic characteristics. A strong association between the presence of the extracellular polysaccharide-forming biotype of S. bovis in the bloodstream and endocarditis and colonic cancer has been demonstrated (18).
Mitis group. The mitis group includes species we think of as viridans streptococci along with Streptococcus pneumoniae. As suggested in Table 1, the predominantly alpha-hemoytic viridans species in this complex group can be divided phenotypically into two subgroups on the basis of their ability to hydrolyze arginine. Among the arginine hydrolysis-positive strains, Streptococcus sanguis and Streptococcus gordonii are both common isolates from cases of endocarditis, with the majority of strains producing extracellular polysaccharides. Of the arginine hydrolysis-negative species, S. mitis and Streptococcus oralis, S. oralis is found more commonly in cases of endocarditis and is variable for extracellular polysaccharide production. The polysaccharide production-negative S. mitis has been noted as an agent of infection in neutropenic patient and as a species that displays penicillin resistance (7).
Anginosus group. At one time anginosus group strains were considered to constitute a single species, but they are currently divided into three species named S. anginosus, Streptococcus constellatus, and Streptococcus intermedius. These organisms have undergone repeated revisions in taxonomy and nomenclature during the past 50 years. Previous epithets for streptococci in this group include "Streptococcus milleri," "Streptococcus MG-intermedius," and "Streptococcus anginosus-constellatus." S. anginosus group strains may be alpha-, non-, or beta-hemolytic, and may produce Lancefield group A, C, F, or G antigen or no detectable antigen. Beta-hemolytic strains produce small colonies that, along with physiological traits, differentiate them from large colony-forming pyogenic, beta-hemolytic group A, C, or G streptococci. Anginosus group strains are PYR-negative (unlike Streptococcus pyogenes) and beta-glucuronidase-negative (unlike large colony-forming human isolates of group C and G streptococci). Anginosus group species do not produce extracellular polysaccharides and are, unlike other viridans streptococci, noted for their association with serious purulent infections.
Leuconostoc and Pediococcus. Leuconostoc and Pediococcus were among the first new genera of catalase-negative, gram-positive cocci to be described as clinical isolates in the mid-1980s. These genera display intrinsic high-level vancomycin resistance that is unrelated to the acquired vancomycin resistance observed in enterococci and staphylococci. Leuconostoc and Pediococcus had previously been well known to food microbiologists, since they occur in various foods and on vegetation, but they were not recognized in human infection until an optimal combination of compromised hosts and antibiotic usage patterns most likely created the conditions for their emergence as opportunists. Members of both genera are PYR-negative and produce alpha- or non-hemolytic viridans streptococcal-like colonies on blood agar. Leuconostoc strains form cocci in pairs and chains but, unlike viridans streptococci, produce gas as an end product of glucose metabolism and are LAP negative. Pediococcus strains form cocci in clusters, are negative for gas production from glucose, and are LAP positive (Table 2 and references 1, 9, and 17). Members of both genera have been implicated in bloodstream and other types of infections in compromised hosts.
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TABLE 2. Reactions of miscellaneous catalase-negative gram-positive cocci in basic phenotypic testsa
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Gemella. Although the Gemella genus has recently grown to include a total of four species (Gemella haemolysans, Gemella morbillorum, Gemella bergeriae, and Gemella sanguinis), G. haemolysans and G. morbillorum are the two most well described species of the genus. Most strains of these species are PYR and LAP positive and produce colonies on blood agar that resemble those of viridans streptococci. While the cellular morphology of G. morbillorum resembles that of streptococci, G. haemolysans forms Neisseria-like diplococci that may also be arranged in tetrads and clusters and may appear to be gram variable. Part of the normal flora of the oral cavity (G. haemolysans) and the gastrointestinal tract (G. morbillorum), Gemella strains have been isolated from cases of endocarditis, meningitis, and other infections (8).
Rothia mucilaginosa (formerly Stomatococcus mucilaginosus). R. mucilaginosa strains, members of normal oral flora, form cocci in clusters and display variable catalase reactions ranging from negative to weakly positive to strongly positive. Their white to grayish non-hemolytic colonies may be mucoid, rubbery, or sticky in consistency and adherent to agar. The inability to grow in the presence of 5% NaCl distinguishes R. mucilaginosa from members of the genera Staphylococcus and Micrococcus. Stomatococci have been described as opportunistic agents of infection in cases of endocarditis, meningitis, peritonitis, and other infections (15, 17).
Aerococcus. Aerococcus viridans, the most well known species of this genus of cluster-forming cocci has been noted as an infrequent cause of infection in compromised hosts. A number of newer species have been described more recently, and of these, Aerococcus urinae has been well documented as an agent of urinary tract infection and endocarditis in compromised patients (2, 11). Aerococci form alpha-hemolytic colonies on blood agar, and A. viridans colonies are larger than those of A. urinae. The two species also differ in other phenotypic traits (A. viridans is PYR positive and LAP negative, while A. urinae is PYR negative and LAP positive).
Lactococcus and Vagococcus. The genus Lactococcus was created to accommodate non-beta-hemolytic Lancefield group N streptococci normally isolated from dairy products. Eventually, organisms identified as motile strains of lactococci were reclassified in a new genus, Vagococcus. Members of these genera resemble either streptococci or enterococci in terms of phenotypic traits and are infrequently isolated opportunistic pathogens. Lactococci have been isolated from cases of endocarditis and a variety of other infections, and while vagococci have been isolated from clinical specimens, little is currently known about the extent of their role in human disease (8).
Helcococcus. Helcococcus kunzii is currently the only species in this genus of PYR-positive, LAP-negative cluster-forming cocci that has been isolated from human clinical specimens. H. kunzii forms small, non-hemolytic, slowly growing colonies on blood agar and has been described as an agent of wound infections (3, 17).
Globicatella and related genera (Facklamia, Ignavigranum, and Dolosicoccus). The description of the alpha-hemolytic, PYR-positive, LAP-negative, salt-tolerant species Globicatella sanguinis (originally named Globicatella sanguis) in the early 1990s was followed by descriptions of the additional related genera, Facklamia, Ignavigranum, and Dolosicoccus (5, 6, 13, 14). Dolosicoccus is, like G. sanguinis, alpha-hemolytic, PYR positive, and LAP negative, while Facklamia and Ignavigranum isolates are positive for both of these enzyme activities and non-hemolytic. All organisms in this group form cocci in chains, except for the cluster-forming Facklamia languida (13). Isolates of Ignavigranum may, like Abiotrophia and Granulicatella, display satelliting behavior. Strains of these genera have been isolated from blood cultures and cultures of other specimen types, but more information is needed concerning their role in infection.
Dolosigranulum. Dolosigranulum pigrum, the sole species in the genus, has been isolated from blood, ocular fluid, and other body site cultures. The organism forms cocci arranged in pairs, tetrads, and clusters, and produces colonies on blood agar that resemble those of viridans streptococci. D. pigrum is PYR and LAP positive (12).
Many of the miscellaneous catalase-negative, gram-positive cocci can only be accurately identified by reference laboratories. Clinical microbiologists should be aware of the plethora of genera and species of catalase-negative, gram-positive cocci and realize that they may encounter strains that do not fit into the categories of routinely isolated organisms. On the other hand, some of the miscellaneous catalase-negative, gram-positive cocci may be misidentified as more frequently isolated organisms. Clinical microbiologists should be aware of the possibilities when examining isolates in this group of bacteria. Armed with knowledge of the basic traits of the infrequently encountered catalase-negative, gram-positive cocci, the clinical microbiologist should be able to make an educated guess as to the nature of the isolate and send the strain to a reference lab if complete identification is desired. A somewhat vague preliminary report (e.g., gram-positive coccus, probable Gemella, sent to reference lab for confirmation) is preferable to an authoritative but incorrect identification.
Identification methods. Although a number of commercially available products are capable of identifying some species of viridans streptococci and a number of the other organisms mentioned here, the accuracy of these products with newer genera and species is not established. Rapidly changing taxonomy within this group has made it difficult to keep the databases of identification products up-to-date. Tests for some of the phenotypic characteristics used to differentiate new genera and species may not be included in some of the commercially available products.
A few basic phenotypic tests (Table 2 and references 8, 17, and 19) can aid in the preliminary characterization or presumptive identification of the miscellaneous catalase-negative gram-positive cocci. Table 2 displays the possible reactions of the genera discussed in this review in tests for PYR and LAP production and growth in 6.5% salt broth. Additional phenotypic characteristics of these organisms and methods for performing the tests can be found in references 8, 17, and 19. If, as mentioned above, a complete identification seems warranted, a reference laboratory should be consulted.
Susceptibility studies. Standardized susceptibility testing methods have been established for the viridans streptococci (16), but no methods have been validated for other miscellaneous catalase-negative, gram-positive cocci. Results of susceptibility testing performed by various methods can be found in the literature, and these studies suggest that, with the exception of Leuconostoc and Pediococcus, these organisms are uniformly susceptible to vancomycin. Many of the miscellaneous catalase-negative, gram-positive cocci appear to be susceptible to beta-lactam agents and a variety of other antimicrobial agents. Organisms in which elevated MICs for beta-lactams have been observed include some strains of R. mucilaginosa, Abiotrophia species, and Granulicatella species (17). Most viridans streptococci remain susceptible to penicillin, but a survey of U.S. isolates revealed penicillin resistance among strains belonging to the mitis species group (7).
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