Volume 1, Number 1—January 1995
Unraveling Mysteries Associated with Cat-Scratch Disease, Bacillary Angiomatosis, and Related Syndromes
On This Page
- Clinical Features of CSD
- Enter Afipia felis
- Enter New Syndromes
- Enter Rochalimaea henselae
- The Cat-scratch Connection: A Synthesis
- Felis domesticus: A Reservoir for Rochalimaea henselae
- Changes in Nomenclature: Rochalimaea becomes Bartonella
- Remaining Questions for Ongoing and Future Research
- Cite This Article
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|EID||Regnery R, Tappero JW. Unraveling Mysteries Associated with Cat-Scratch Disease, Bacillary Angiomatosis, and Related Syndromes. Emerg Infect Dis. 1995;1(1):16-21. https://dx.doi.org/10.3201/eid0101.090103|
|AMA||Regnery R, Tappero JW. Unraveling Mysteries Associated with Cat-Scratch Disease, Bacillary Angiomatosis, and Related Syndromes. Emerging Infectious Diseases. 1995;1(1):16-21. doi:10.3201/eid0101.090103.|
|APA||Regnery, R., & Tappero, J. W. (1995). Unraveling Mysteries Associated with Cat-Scratch Disease, Bacillary Angiomatosis, and Related Syndromes. Emerging Infectious Diseases, 1(1), 16-21. https://dx.doi.org/10.3201/eid0101.090103.|
The search for the infectious agents responsible for cat-scratch disease, bacillary angiomatosis, and related syndromes has a long and often circuitous history. Recognition of the etiologic agents and a new understanding of the fundamental features of the epidemiology and natural history of modern day Bartonella (formerly Rochalimaea)-associated diseases culminate a multipartite story that combines clinical medicine, traditional microbiology, and novel technological approaches to solve a long-standing enigma.
The quest for the etiologic agent of cat-scratch disease (CSD) has frequently been described as a mystery (1,2). Indeed, the search has many qualities of a mystery novel; the pursuit has spanned several decades and recently taken several unexpected turns. During this period of important discovery, major microbial suspects have undergone name changes, novel microbial culprits have been introduced, new groups of affected patients have been recognized, and yet significant questions remain to be answered. Scientific and medical interest has been high; approximately 900 publications have dealt with CSD since the first good clinical description of the disease in 1950 (3).
Throughout the life of this evolving mystery, the clinical descriptions of classical CSD have remained remarkably consistent (Dalton MJ, et al. Rochalimaea antibody; a new era in the diagnosis of cat-scratch disease, submitted for publication; (4–6). CSD is typically a benign and self-limited illness lasting 6 to 12 weeks in the absence of antibiotic therapy. Regional lymphadenopathy (axillary, head and neck, inguinal) is the predominant clinical feature of CSD; affected nodes are often tender and occasionally suppurate (4–7). Between 25% and 60% of patients report a primary cutaneous inoculation lesion (0.5- to 1-cm papule or pustule) at the site of a cat scratch or bite (5,7). The skin lesions typically develop 3 to 10 days after injury and precede the onset of lymphadenopathy by 1 to 2 weeks. Low-grade fever and malaise accompany lymphadenopathy in up to 50% of patients; headache, anorexia, weight loss, nausea and vomiting, sore throat, and splenomegaly may develop. In addition, short-lived, non-specific maculopapular eruptions, erythema nodosum, figurate erythemas, and thrombocytopenic purpura have been observed (8).
Unusual manifestations of CSD, which occur in up to 14% of patients, include Perinaud's oculoglandular syndrome (6%), encephalopathy (2%), hepatic granulomas (0.3%), osteomyelitis (0.3%), and pulmonary disease (0.2%) (4,5,8). In general, these complications resolve without sequelae. Perinaud's oculoglandular syndrome is manifested by conjunctival granuloma, periauricular lymphadenopathy, and nonsuppurative conjunctivitis. Encephalopathy, manifested as fever and coma that progress to convulsions, may last for days to weeks; cerebrospinal fluid is unremarkable. Optic neuritis with transient blindness may also occur.
For many years, CSD has been clinically diagnosed when three of the following four criteria are met in a patient: 1) history of traumatic cat contact; 2) positive skin-test response to CSD skin-test antigen; 3) characteristic lymph node lesions; and 4) negative laboratory investigation for unexplained lymphadenopathy (8). Although biopsy confirmation of CSD has been rarely required (especially in lieu of a reliable serologic test see below), a constant pathologic hallmark of CSD-affected tissues has been granuloma formation. With hematoxylin and eosin stains, the primary inoculation lesion of CSD reveals small areas of frank necrosis surrounded by concentric layers of histiocytes, lymphocytes, and nucleated giant cells (9). Affected lymph nodes are characterized by necrotizing granulomas ringed by lymphocytic infiltrates and multinucleated giant cells.
During the past 44 years, a variety of microbial agents, including herpes viruses and bacteria of the genera Chlamydia and Pasteurella, have been suspected as the causes of CSD (3). A major chapter of the CSD saga unfolded with the 1988 announcement by the Armed Forces Institute of Pathology that a bacterial agent had been visualized within CSD-involved lymph nodes by using the Warthin-Starry silver stain (10), and a novel bacterial agent had been isolated from a CSD patient's lymph node (11). By 1992, this agent was characterized fully, given the name Afipia felis (Afipia being a latinized acronym for the source of the original isolate, the Armed Forces Institute of Pathology, and felis referring to the presumed vertebrate vector of the human infection), and proclaimed the agent of CSD (12).
Although A. felis was declared the putative CSD bacillus, evidence of convincing patient humoral or cellular immune responses to laboratory cultured A. felis antigen was not forthcoming. Despite numerous attempts, other laboratories were unable to recover additional isolates of A. felis from CSD patients. In addition, although the majority of patients with CSD reported exposure to a cat(s), no clear link between cats and A. felis was demonstrated.
The story of CSD took a significantly divergent path with the recognition that opportunistic infections were an important consideration for patients infected with human immunodeficiency virus (HIV). Bacillary angiomatosis (BA), a newly recognized disease characterized by cutaneous and subcutaneous vascular lesions containing bacillary organisms visualized by Warthin-Starry silver staining, was described predominantly among HIV-infected patients; however, bacterial isolates were not made or identified (13–15). Over the ensuing decade, the clinical spectrum of BA was expanded to include patients with single or multiple vascular lesions affecting virtually every organ system, including lymph node, bone, brain, liver (peliosis hepatis), and spleen (14–17). Independently, an unidentified gram-negative pathogen was isolated predominantly from HIV-infected patients with fever and bacteremia, however, these patients lacked cutaneous or parenchymal vascular lesions and were not recognized as BA patients (18).
Because silver staining and electron microscopy of both BA and CSD tissue sections revealed bacillary organisms indistinguishable from one another, several authors suggested that BA might represent disseminated CSD in the immunocompromised host (17,19-21). In addition, several anecdotal reports of BA described a history of cat contact preceding the onset of disease (22).
Ultimately, the relationships between possible environmental exposures and BA or CSD were systematically investigated. The first case-control study conducted among patients with BA found traumatic contact with a cat (bite or scratch) to be significantly associated with BA disease (22). BA patients were also more likely than controls to have a household kitten (a cat <1 year of age). A subsequent case-control study of CSD patients found that these patients were more likely than controls to have traumatic contact with a cat, to own at least one kitten, and to have kittens with fleas (7).
Despite the similarities in histochemical staining properties and epidemiology, serious reservations remained concerning a possible link between the causative agents of CSD and BA. The pathologic features of classical CSD (granuloma) and BA (proliferative vascular lesions without granuloma) were distinctly different, and the two diseases seemed to respond differently to antibiotic therapy. Although antimicrobial therapy for BA and CSD have not been systematically evaluated, the majority of BA patients evaluated responded quickly to single-agent therapy with either erythromycin or doxycycline (14,23), whereas the symptoms and signs of patients with CSD failed to show consistent rapid resolution following antibiotic therapy (5). In addition, clinicians' first choices of antibiotics for treating BA and CSD vary (5,6,14,23).
A breakthrough occurred when a novel approach was used to identify possible prokaryotic ribosomal DNA extracted from BA skin lesions. When prokaryotic ribosomal gene DNA extracted from BA lesions and amplified by polymerase chain reaction (PCR) was compared with sequenced ribosomal genes from other organisms, it become apparent that the agent associated with BA in this study was related to, but not necessarily identical to, the agent of trench fever, Rochalimaea quintana (24).
At nearly the same time in Oklahoma, Rochalimaea-like organisms were being isolated on blood agar from bacteremic patients (18). Independently in Houston, Texas, fastidious, slow-growing Rochalimaea-like isolates were recovered on several occasions from the blood of an HIV-infected patient with relapsing fever of unknown origin; like the isolates from the Oklahoma patients, the Houston isolate was recovered from a patient in the absence of BA or CSD lesions (25). The Houston isolate (Houston-1) was identified as the prototype isolate of a novel species of Rochalimaea by using traditional as well as genotypic methods, including ribosomal RNA gene analysis similar to that used to identify the nucleic acid found in BA patients' lesions (25). Almost simultaneously, the group from Oklahoma had come to a similar conclusion by using DNA relatedness data (26); most of their isolates also consisted of the novel species, R. henselae. The new species designation, first officially used to describe the Houston-1 isolate, was coined in recognition of the contribution of Diane Hensel, a microbiologist who had isolated several of the initial organisms in Oklahoma (18,25,26). Subsequently, Koehler et al. isolated bacilli directly from cutaneous lesions of persons with BA (27); surprisingly, either R. henselae or R. quintana was isolated from BA lesions from different HIV-infected patients.
At this juncture, R. henselae infections had been described predominantly among immunocompromised patients with either BA or fever with bacteremia. The availability of isolates made it possible to develop a test for serologic evidence of Rochalimaea infection and to refine PCR methods for identification of Rochalimaea organisms in tissues and other samples. These methods, together with new techniques for recovering Rochalimaea species isolates, were crucial to obtaining a more detailed account not only of BA but also of CSD.
A Rochalimaea genus-specific, indirect fluorescence antibody (IFA) test using irradiated whole cell antigen from the Houston-1 isolate of R. henselae was developed by the Centers for Disease Control and Prevention (CDC) to help identify risk factors for Rochalimaea-associated disease. Several blinded serum samples from both HIV-infected BA patients and HIV-infected controls residing in San Francisco were sent to CDC for serologic testing. High-titered antibodies were identified in serum samples from several of the BA patients (28). Similar high-titered antibodies were not detected for any of non-BA control patients with one exception; a serum sample from an HIV-infected patient with CSD also demonstrated strong serologic reactivity to R. henselae antigen.
Shortly thereafter, single sera collected from patients with suspected CSD to look for A. felis antibodies were evaluated with the new R. henselae serologic test; 36 (88%) of 41 sera were positive (29). None of the sera had significantly elevated titers to A. felis antigen. The same set of sera were coded and resubmitted along with sera taken from other well-characterized bacterial and viral diseases and tested again in a blinded manner. The IFA test accurately identified sera of case-patients with suspected CSD. In addition, 6 (6%) of 107 sera from ostensibly healthy persons, obtained from a commercial vendor, showed antibody by IFA testing (29). These serologic data were the first laboratory evidence suggesting that R. henselae was associated with CSD.
Data further substantiating the role of R. henselae in the etiology of CSD soon followed. The newly developed serologic test was used to help investigate a possible cluster of CSD cases in Connecticut; 38 (84%) of 45 suspected CSD cases had elevated Rochalimaea antibody titers, whereas 4 (3.6%) of 112 age-matched controls had detectable antibody titers (7). In another investigation, serum samples obtained from 600 prospectively evaluated patients with well-characterized CSD (i.e., persons with history of cat scratch, papule at site of inoculation, and enlarged regional lymph node) had a 95% correlation with positive Rochalimaea serology.
In 1993, R. henselae was isolated directly from the lymph nodes of two CSD patients and was identified by genotypic means; both patients had strong serologic responses to Rochalimaea antigen (30). Evidence of R. henselae-specific nucleic acid sequences were found in 21 (84%) of 25 CSD lymph node tissues submitted to CDC for evaluation (31).
Additional supporting evidence for a Rochalimaea as the cause of CSD came from archival sources. Skin-test antigen, used rather extensively in the past to help diagnose examples of CSD (4,8), consisted of pasteurized exudate collected from suppurative CSD lymph nodes. Among a cohort of CSD patients who were skin-test positive, 52 (93%) of 56 had positive IFA antibody titers to the defined Rochalimaea reagents (32). Furthermore, various lots of skin-test antigen were shown by PCR analysis to contain Rochalimaea nucleic acid sequences (33), and R. henselae sequences in particular (34). No A. felis DNA sequences could be detected by PCR. These data strongly indicated that microbiologically undefined skin-test reagents, which had been used for many years for the diagnosis and clinical characterization of CSD, were in fact R. henselae reagents.
Collectively, these data supported a Rochalimaea species etiology for both CSD and BA. Despite numerous attempts, recent efforts to implicate A. felis as a cause of either of these two clinical entities have repeatedly failed.
In addition to epidemiologic data, serologic evidence also implicated domestic cats with Rochalimaea-associated disease. Rochalimaea-specific IFA antibodies were demonstrated in 6 (46%) of 13 pet cats not associated with human disease and among 39 (81%) of 48 cats living in households reporting human CSD in Connecticut (7). Microbiologic evidence for the domestic cat as a reservoir for R. henselae soon followed. R. henselae was isolated over a 3-week period from the blood of a single cat not linked to human illness (35). Investigations by Koehler et al. established the cat as a reservoir for R. henselae infection (36). R. henselae was established as the cause of cutaneous BA in three or four patients with the disease. R. henselae was isolated from the blood of all seven asymptomatic pet cats with which these four BA patients had prolonged contact. The prevalence of infection among cats in the greater San Francisco Bay region was also studied; 25 (41%) of 61 pet or impounded cats had asymptomatic R. henselae bacteremia (36). R. henselae was also detected by both direct culture and PCR from several cat fleas combed from these bacteremic cats (36).
The human body louse (Pediculus humanus) was established as a vector for human-to-human trench fever R. quintana transmission during the First World War (37). Likewise, B. bacilliformis, a closely related organism (see below) found in the mountains of South America, can be transmitted by another arthropod, the Phlebotomus sand fly (38). The observation that related microbes are vectored between humans by arthropods adds credence to the proposed role of arthropod vectors of CSD. Despite several suggestions that fleas or possibly ticks (7,36,39) are associated with R. henselae disease, no experimental data exist to clearly demonstrate that arthropods act as direct vectors.
Genotypic evaluation of members of the genus Rochalimaea has led to the conclusion that members of the genus are closely related to Bartonella bacilliformis, the agent of Carri¢n disease, Oroya fever, and verruga peruana (40). Because of historical precedence, the genus designation Bartonella is now applied to all species of the old genus Rochalimaea and replaces the Rochalimaea designation (species names remain unchanged).
Physicians and researchers need to exercise care in using the term bartonellosis. This term has classically been used to describe the frequently fatal syndromes caused by B. bacilliformis. To date, B. bacilliformis and its associated syndrome (bartonellosis) have been identified exclusively in South America (38,41).
Although B. henselae is now regarded as the etiologic agent of CSD, as well as a cause of BA, endocarditis (42), and fever with bacteremia, many questions remain unanswered. For example, why did it take so long to isolate and identify B. henselae? Part of the answer probably stems from the requirements necessary for growth in vitro, including enriched, non-selective blood agar incubated over a prolonged period in a CO2 atmosphere. Most hospital laboratories discard their bacteriological plates before primary isolates of B. henselae would be expected to appear (9-40 days). Extreme sensitivity to a wide variety of antibiotics, at least in vitro, suggests that residual levels of antibiotics in patients' blood or other tissues (such as lymph node biopsy) might inhibit Bartonella growth during primary isolation attempts in vitro. Selective medium has yet to be developed. Novel genotypic methods were crucial for identification of B. henselae; thus, isolates may well have been made in the past but remained unidentified.
As mentioned above, it has become apparent that in addition to B. henselae, B. quintana can also be another significant cause of BA disease, at least among immunocompromised patients in San Francisco (27). Another focus of B. quintana infections ( urban trench fever ) has been identified among homeless alcoholics in Seattle (43,44). How common are B. quintana infections; are they louseborne and vectored strictly between humans, as was believed during World War I (37)? B. quintana-associated disease has no known link with an alternative vertebrate vector (such as cats).
Bartonella elizabethae is known only from a single isolate from a man surviving endocarditis following aortic valve-replacement surgery (45). Is there further public health significance to this organism? What additional Bartonella species have yet to be identified and what diseases may they cause?
Members of the genus Bartonella are exquisitely sensitive to antibiotics in vitro (30,46). Why then do CSD patients not respond as rapidly and consistently to antibiotic therapy as BA patients do? One hypothesis is that immunocompetent patients somehow sequester infectious organisms beyond the reach of antibiotics, whereas immunocompromised patients do not. An alternative hypothesis regarding differential antibiotic responsiveness recognizes that many of the signs of CSD are immune mediated; antibiotics, even if effective in neutralizing or killing bacteria, may not immediately alleviate long-duration immunologic tissue manifestations of antigen stimulation. Conversely, in the absence of the immunologic capability to react to bacterial infection by forming granulomas, as in the case of severely immunocompromised persons with BA, antibiotics are generally effective in alleviating the symptoms and signs of infection. Does this suggest that possible non-granulomatous manifestations of CSD (for example, neuroretinitis and encephalopathy) should respond well to the appropriate antibiotic therapy?
Although BA has been described in immunocompetent patients (15), the vast majority of BA patients are immunocompromised (14). What are the factors explaining why B. henselae and B. quintana induce vascular proliferative lesions, such as BA and parenchymal bacillary peliosis, almost exclusively in severely immunocompromised patients?
What percentage of the relatively large numbers of undiagnosed febrile disease among HIV-infected persons is in fact due to Bartonella species infections? The answer to this important question may help alleviate significant morbidity among HIV-infected patients. The potential for selection for drug-resistance during long-term antimicrobial therapy deserves scrutiny.
Does the 4%-6% of IFA antibody-positive, ostensibly healthy control study populations suggest a relatively common undercurrent of undiagnosed, subclinical Bartonella-associated disease?
Is it possible to immunize cats and thereby interrupt B. henselae transmission to humans? Preliminary data suggest that asymptomatic bacteremia in cats can be successfully treated with antimicrobial therapy (36). Once cleared of bacteremia, are these cats routinely susceptible to reinfection?
Are the complications occasionally associated with CSD and BA associated with different strains of Bartonella species or are the variations in clinical presentation strictly functions of dose, route of inoculation, and immune status?
And finally, in what role, if any, will A. felis reappear as an agent of human disease? Is A. felis responsible for the relatively small number of cases of CSD-like lymphadenopathy that have no evidence of antibody to B. henselae? Or is there another explanation for the originally proposed association between A. felis and CSD that has not yet come to light?
The new recognition of the importance of Bartonella-associated diseases will continue to spawn a host of unanswered related questions. Whereas novel subplots will continue to unfold, the new puzzles are no longer totally shapeless, and answers to questions of natural history and epidemiology, enhanced diagnosis and treatment, and methods for disease intervention should now begin to unfold rapidly.
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