Perspectives on the laboratory diagnosis of rickettsial diseases in the 21<span name="style_sup">st</span> century century

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Abstracts

Es necesario contar con métodos de laboratorio muy eficientes y específicos para poder distinguir las rickettiosis de otras enfermedades infecciosas y diferenciar con exactitud unas rickettsias de otras. Las categorías más importantes de métodos utilizados para diagnóstico de rickettsias son: Visualización directa por histología o tinciones inmunohistoquímicas, serología, cultivo y métodos moleculares, cada una de ellas posee sus fortalezas y debilidades. La presente revisión discute algunas de estas ventajas y desventajas inherentes a cada método y cómo estas técnicas pueden evolucionar colectivamente en el futuro. Históricamente, muchas enfermedades rickettsiales han sido pobremente estudiadas, generalmente porque estos patógenos se consideran difíciles de cultivar, difíciles de teñir y peligrosos de propagar en el laboratorio. Progresando hacia el siglo 21, un mayor uso de estos métodos de diagnóstico, especialmente en países tropicales y en vías de desarrollo podría beneficiar un reconocimiento global de las rickettsiosis y el impacto que estas tienen en un enorme segmento de la población mundial. Es cada vez más importante para los ricketsiólogos contemporáneos abstenerse de utilizar los métodos clásicos tales como cultivo, serología y hasta la visualización directa con la evolución de métodos moleculares más rápidos y sofisticados. Se pueden obtener resultados extraordinarios cuando se utilizan múltiples técnicas de manera concomitante.

Rickettsia; Ehrlichia; Orientia; Coxiella; diagnosis

Robust laboratory methods are necessary to distinguish rickettsioses from other infectious diseases and to accurately distinguish one rickettsiosis from another. The major categories of diagnostic techniques used for rickettsioses, i.e., direct visualization by histological or immunohistochemical stains, serology, culture, and molecular techniques, each have unique strengths and weaknesses. This review discusses some of the advantages and disadvantages inherent to each method and how these techniques might evolve collectively in the future. Many rickettsial diseases have been historically understudied, often because the pathogens were considered difficult to grow, difficult to stain, and dangerous to propagate. As we progress into the 21<span name="style_sup">st</span> century, the broader use of diagnostic assays, particularly in many tropical and developing countries, will better leverage the global recognition of rickettsioses, and the impact that these infections have on enormous segments of the world population. It will be increasingly important for contemporary rickettsiologists to refrain from replacing entirely classical methods such as culture, serology, or even direct visualization with more rapidly evolving and increasingly sophisticated molecular techniques. Extraordinary results can be achieved when multiple techniques are used in tandem. century, the broader use of diagnostic assays, particularly in many tropical and developing countries, will better leverage the global recognition of rickettsioses, and the impact that these infections have on enormous segments of the world population. It will be increasingly important for contemporary rickettsiologists to refrain from replacing entirely classical methods such as culture, serology, or even direct visualization with more rapidly evolving and increasingly sophisticated molecular techniques. Extraordinary results can be achieved when multiple techniques are used in tandem.

Rickettsia; Ehrlichia; Orientia; Coxiella; diagnosis

Conferencias

^st century

Rickettsia, Ehrlichia, Orientia, Coxiella, diagnóstico

^st century, the broader use of diagnostic assays, particularly in many tropical and developing countries, will better leverage the global recognition of rickettsioses, and the impact that these infections have on enormous segments of the world population. It will be increasingly important for contemporary rickettsiologists to refrain from replacing entirely classical methods such as culture, serology, or even direct visualization with more rapidly evolving and increasingly sophisticated molecular techniques. Extraordinary results can be achieved when multiple techniques are used in tandem.

Rickettsia, Ehrlichia, Orientia, Coxiella, diagnosis

Ehrlichia chaffeensis ehrlichiosis can be life-threatening diseases that characteristically offer a relatively narrow window of time during when appropriate antibiotic therapy is most effective at minimizing morbidity and mortality. The term ‘acute doxycycline deficiency’ is used occasionally by clinicians in the United States during the spring and summer months to describe an acute febrile illness, presumably rickettsial in origin, that responds favorably to therapy with this antibiotic. The choice of appropriate therapy for these diseases is crucial, but must also be coupled with laboratory efforts that validate clinical suspicion. A response to doxycycline is not necessarily confirmatory evidence of a rickettsiosis, and not all febrile, rash-associated illnesses will necessarily respond to treatment with doxycycline. In this context, robust laboratory methods are needed to distinguish rickettsioses from other infectious diseases, and to accurately distinguish one rickettsiosis from another.

¹^-5 and the enormous downstream influence these assays have on epidemiological statistics for these diseases.^6,7 The following discussion is not intended to comprehensively evaluate each method, but rather to emphasize some general strengths and weaknesses of the 4 major classes of these techniques, and how these might evolve collectively in the future.

Rickettsia rickettsii. ^8,9 Ricketts was hesitant to state definitively that these structures were the etiologic agent of RMSF because he could not cultivate these bacteria by use of axenic media; nonetheless, his observations were soon corroborated by Simeon Burt Wolbach who used the same staining method to describe the characteristic appearance and distribution of rickettsiae in human tissues: …

¹⁰

Figure 1), and provided a foundation for the pathophysiology of all vasculotropic rickettsiosis;^11,12 nonetheless, the use of traditional histological stains as a diagnostic technique to detect rickettsiae in clinical samples is vanishingly rare in contemporary scientific and medical literature.^13-15

Figure 1

¹⁶ during the last 25 years, investigators have developed immunohistochemical (IHC) assays using monoclonal or polyclonal antibodies to identify various genera of rickettsial pathogens in formalin-fixed, paraffin-embedded biopsy or autopsy tissue specimens, including multiple SFG and typhus group (TG) Rickettsia species,^17-23 E. chaffeensis,^24-26 Anaplasma phagocytophilum²⁴ and Orientia tsutsugamushi.²⁷ Advantages of these methods include: (1) direct evidence of infection; (2) high sensitivity during the early stages of infection when other methods, particularly serology, are non-diagnostic; and, (3) excellent positive predictive value. The advantage provided by direct observation of the pathogen in the appropriate histopathological context is considerable and provides a second level of confirmation inherent only to this class of diagnostics.

²⁸ Application of immunohistochemical techniques identified O. tsutsugamushi in archival tissues >50 years old.²⁷ Finally, by identifying additional cellular targets of these pathogens, and by dissecting the specific inflammatory response of the vertebrate host, IHC techniques build on the foundation of rickettsial pathobiology established almost 100 years ago by conventional histological staining methods.¹⁹, ²¹, ^{26, 27} Disadvantages of IHC staining methods include: (1) the acquisition of the analyte, i.e., tissue, is typically more complex than collection of blood or serum; (2) the requirements of specimen processing and evaluation that often limit diagnostic capacity to specialized regional or national centers; and, (3) the use of immunologic reagents that are generally group-specific rather than species-specific.

E. chaffeensis and approximately 20%-80% of those infected with Anaplasma phagocytophilum.^29-31 The accuracy of these techniques is biased by the number of examined cells or blood smears, the level of immune compromise of the host, and the relative experience of the microscopist, who must distinguish morulae from other structures such as Döhle bodies, toxic granulations, or phagocytosed bacteria or fungi that may occur in the cytoplasm of white cells in other infectious conditions.²⁹ This technique is relatively insensitive and inconsistent; however, its simplicity and ubiquity provided the initial discoveries of human monocytic ehrlichiosis and human anaplasmosis in the United States during the late 1980s and early 1990s.²⁹, ³¹

^32,33

Orientia infection in a traveler to Dubai, hundreds of miles beyond the recognized range of classical scrub typhus, was initiated by a serologic result that indicated recent infection with a pathogen antigenically similar to O. tsustugamushi.³⁴

³⁵ however, when this protocol is not followed, the opportunities for misinterpreting data generated by serological assays are considerable, particularly when no other laboratory methods are included in the diagnostic evaluation of the patient. Paradoxically, serological methods are particularly insensitive during the acute stage of rickettsial infections, when most patients seek medical attention and when the majority of specimens are collected for subsequent evaluation by these techniques. As an example, initial serum samples collected from 11 of 22 patients with laboratory-confirmed rickettsialpox failed to demonstrate IgG antibody levels reactive with Rickettsia akari antigens at or above the conventionally recognized cutoff dilution when tested by using an IFA assay; confirmatory evidence of infection with R. akari in these 11 patients was obtained only because diligent clinicians collected additional specimens, including convalescent-phase serums and skin biopsy specimens for IHC, culture, and PCR.²⁰Approximately 50% of patients with RMSF lack a diagnostically relevant IFA titer (i.e., > 64) during the first week of illness; however, at least half of all deaths attributed to R. rickettsii occur within 7-9 days after illness onset, explaining the large percentage of persons who die of RMSF without serological confirmation.¹⁸ In these circumstances, IFA methods have an exceptionally low negative predictive value and molecular methods (see below) can greatly enhance a diagnosis in cases of fatal disease, particularly if a serum sample collected during the acute illness is the only diagnostic specimen obtained by clinicians.³⁶

Rickettsia, Ehrlichia, Anaplasma, Coxiella or Orientia species characteristically generate antibodies that are genus- or group-specific rather than species-specific. An important limitation of serological methods occurs when antibody titers are over-interpreted to ascribe a species-specific etiology based entirely on reactivity to a particular rickettsial antigen. In 2003, cases of Brazilian spotted fever (BSF) were reported for the first time in the state of Santa Catarina in southern Brazil. Because serological testing revealed antibodies reactive with R. rickettsii in these patients, their illnesses were categorized officially as BSF. However, observant clinicians recognized that the clinical composite of “BSF” in Santa Catarina differed significantly from that of historically recognized disease in the state of São Paulo, particularly with respect to life-threatening manifestations and death (Table 1).³⁷ Indeed, no deaths were reported among the 139 cases of “BSF” identified in Santa Catarina during 2003-2009; in contrast, the case-fatality rate of BSF in São Paulo during this same interval was approximately 30% (www.cve.saude.sp.gov.br/htm/zoo/fm_i8503.htm). Because many of the severe cases in São Paulo were confirmed infections with R. rickettsii ³⁸ investigators suggested that a Rickettsia species other than R. rickettsii was responsible for the mild cases of “BSF” in Santa Catarina.³⁶ Indeed, subsequent entomological surveys for SFG rickettsiae in ticks in Santa Catarina detected a strain of Rickettsia parkeri,³⁹ recognized previously in other parts of Brazil as the cause of a rickettsiosis far milder than BSF.^40,41

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Table 1

R. rickettsii occur at “diagnostic” levels in as many as 5% to 10% of the general population.^42-46 There are several possible explanations for the serological noise created by diagnostically relevant antibody titers to pathogenic rickettsiae among otherwise healthy persons. These include serum reactivity with antigenically related but minimally or non-pathogenic species, and persistence of antibody levels among persons previously infected with or exposed to rickettsial antigens weeks, months, or perhaps years earlier (Figure 2).⁴⁷

Figure 2

R. rickettsii at titers > 64 by using a well-validated IFA assay,⁴⁸ while in Caldas Province, a staggering 490 (72%) of 682 sampled volunteers demonstrated IgG antibody titers > 64 to antigens of Rickettsia felis, Rickettsi typhi or both rickettsiae.⁴⁹ In the Department of Loreto in the Amazon basin of Peru, a serosurvey of 1,195 persons during 2006 revealed antibodies reactive with SFG and TG Rickettsia species in 521 (43.6%) and 123 (10.3%) participants, respectively.⁵⁰ Diagnostically relevant titers (i.e., > 64) to antigens of E. chaffeensis were identified among 15 (14%) of 105 healthy persons in a rural area of Jujuy Province, Argentina, despite the absence of any recently reported illnesses compatible with ehrlichiosis among the persons sampled.⁵¹

O. tsutsugamushi used as antigen, the targeted antibody isotype, and the selection of cutoff titers that defined a positive result. In the majority of these studies no clear justification for the cutoff titer was provided. These authors concluded that no single antibody titer can reliably be considered diagnostic unless prior studies have been performed to determine the seroprevalence levels in the normal population of that locality.⁵² Important serological discrepancies occur even when identical specimens are evaluated by different laboratories. When a panel of serum specimens, collected from 52 persons 6 years after a point source outbreak of Q fever in Australia, were evaluated by IFA methods at 3 different international reference centers for serological evidence infection with Coxiella burnetii, the concordance status of IgG and IgM titers used to determine acute and chronic infections, past exposures, and serologically negative persons was only 35% among these highly respected laboratories.⁵³

Figure 3). The impact of diagnostic inaccuracy upon epidemiologic observations may be considerable. During 2000-2007, the reported case-fatality rate for RMSF in the United States was 0.5%, based on CRF denominator data comprising 7,796 cases, or approximately 1000 cases each year.⁶ One explanation for this estimate lies in the composition of the denominator, which is likely populated with patients with milder infections, caused by SFG Rickettsia species other than R. rickettsii.⁷

Figure 3

³ In theory, cross-adsorption is the best serological method of identifying the specific rickettsial agent responsible for the infection and is based on the principle that homologous and heterologous antibodies will be removed entirely when the patient serum is incubated with the antigens of the specific pathogen responsible for the disease. When incubated with a heterologous antigen, only the group-specific antibodies responsible for the cross-reaction will be removed, whereas species-specific antibodies are retained. This technique has been used successfully to discriminate serologic responses to R. typhi from those to R. prowazekii.⁵⁴ Nonetheless, the rationale for this technique can unravel when applied to SFG rickettsioses because: (1) the inherent pretest bias, i.e., an assumption that one of the antigens used in the assay is the pathogen responsible for the infection; and (2) the absence of appropriate positive and negative controls to validate the technique. In practice, most applications of the cross-adsorption technique assume only 2 possible pathogens, and the panel consists of 4 reactions; however, if correctly applied, adsorption panels must become considerably larger and more complex as additional SFG Rickettsia species are discovered and considered as potential pathogens. For example, if 3 sympatric SFG rickettsioses exist in a region, a panel should require 9 separate cross-adsorptions. If there are 4 possible agents, a correctly designed panel becomes prohibitively large with 16 separate reactions, which in practice is never observed. In this context, the utility of cross-adsorption is diminished in regions where there are multiple co-circulating and antigenically similar pathogens that cause similar clinical syndromes.

Rickettsia species will proliferate in many commonly used cell lines such as Vero E6 cells and human embryonic lung fibroblasts. The recent discovery of an axenic media for C. burnetii suggests that culture of other rickettsiae might also be achieved in carefully defined, cell-free mediums.⁵⁵ Historically, rickettsiologists have been adept at culture techniques and these skills have resulted serendipitously in the isolation of several other important and novel non-rickettsial pathogens, including Legionella pneumophila, Tropheryma whipplei, and Heartland virus.^56-58 Nonetheless, diagnostic laboratories are often reluctant to attempt isolation of rickettsial agents, founded largely on the perception of the dangers associated with this task. For much of the 20^th century, cultivation of rickettsiae was inextricably linked with the unfortunate and surprisingly frequent occurrence of laboratory-acquired rickettsioses, often resulting in the death of the investigator. Rickettsioses accounted for approximately 15% of 3921 laboratory-associated infections and 14% of the infection-related deaths tabulated through 1974.⁵⁹

Rickettsia typhi, R. prowazekii, O. tsutsugamushi,R. akari, R. africae, R. australis, and especially C. burnetii, have been associated with laboratory-acquired infections;^59-67 however, it is the notoriety of R. rickettsii that instills the greatest fear among clinical microbiologists. During 1912-1942, 12 investigators in the United States, Brazil, Colombia, and Japan who worked with R. rickettsii died from laboratory-associated RMSF.⁶⁸ The deaths of a custodian and glassware worker at the Centers for Disease Control and Prevention in 1977 represent the only laboratory-associated fatal illnesses in the history of this agency. Although neither employee worked directly with R. rickettsii, both worked in the building and had access to laboratories where infected embryonated chicken eggs were processed and where discard pans containing rickettsiae were autoclaved.⁶⁹ During 1955-1965, 5 cases of laboratory-acquired RMSF occurred at Ft. Detrick, Maryland via tick bite, needle inoculation and respiratory transmission,⁷⁰ and 9 laboratorians engaged in research into the pathogenesis and immunology of rickettsioses at the United States Army Medical Research Institute of Infectious Diseases developed RMSF during 1971-1976, following inhalation of infectious aerosols containing R. rickettsii.⁷¹

⁵⁹ before the availability of effective antibiotic therapy for these infections, and typically in circumstances lacking biological safety cabinets. Many of these deaths resulted from failure to use simple barrier precautions, such as disposable latex gloves, eye protection, or filtering facepieces. Finally, almost all laboratory-acquired rickettsioses have occurred in research facilities where: (1) large numbers of infected arthropods were housed for study or vaccine development;⁶⁸ (2) massively infected cell cultures, embryonated chicken eggs, or animal tissues were manipulated by using unsafe techniques that generated infectious aerosols,^60-62,^64,65,^70,71 or; (3) routine safety precautions and reporting of laboratory accidents were not followed.⁶³,⁶⁶,⁶⁹ These facilities and circumstances are far different than those reasonably expected in a routine diagnostic laboratory. Finally, it is should also be noted that through 1974, there were 439 cases and 40 deaths attributable to laboratory-associated typhoid, leptospirosis, and psittacosis,⁵⁹ to underscore the fact that cultivation of any pathogenic agent posed far greater risks to microbiologists before the implementation of the safeguards and guidelines that are now used in diagnostic laboratories around the world.

Rickettsia, Orientia, or Coxiella species.⁷² For exquisitely infectious agents such as C. burnetii, and highly virulent rickettsiae such as R. prowazekii and R. rickettsii, this level of containment seems justified. However, different species of Rickettsia vary greatly in pathogenicity, and a rational application of species-specific rather than genus-wide recommendations for cultivating rickettsial agents deserves some consideration in the future, particularly if more clinical laboratories are ever expected to pursue culture isolation as a contemporary diagnostic technique. Microbiologists are confronted continuously with pathogens that pose some level of occupational risk. As an example, Neisseria meningitidis is classified as a biosafety level 2 pathogen;⁷² nonetheless, 18 cases of laboratory-acquired meningococcal disease, including 8 deaths, were identified in laboratories around the world during 1985-2002, predominantly among laboratorians who worked with isolates on an open benchtop.⁷³ An argument might be made that the hazards associated with some rickettsial pathogens are no greater, and quite possibly less, than those associated with N. meningitidis, particularly if all work is performed using a biological safety cabinet. One additional level of complexity was alleviated in December 2012, when R. rickettsii was removed from the list of select agents, so that possession, storage, or transfer of cultures infected with this pathogen no longer require registration with and oversight by the Centers for Disease Control and Prevention.⁷⁴

⁷⁵

Rickettsia, Orientia, Ehrlichia, and Anaplasma spp. recognized as pathogens of humans has more than doubled since 1985.

2009 in Mexicali, Mexico,⁷⁶ shared several epidemiological and entomological features with a large cluster of cases that occurred several years earlier in a rural community in Navajo County in eastern Arizona.⁷⁷ Both events were triggered by an abundance of free-roaming and stray dogs and massive populations of Rhipicephalus sanguineus ticks in the peridomestic environments. Because of the similarities between these outbreaks, recognized 5 years apart and separated by a distance of approximately 450 km, molecular typing assays were used to evaluate DNA samples of R. rickettsii obtained from ticks and ill patients at both locations. A detailed analysis of 3 variable intergenic regions, used previously to characterize all known isolates of R. rickettsii,⁷⁸ provided investigators the data needed to determine that the outbreaks of RMSF in Arizona and Mexicali were independent events involving genetically different strains of R. rickettsii.⁷⁹

R. conorii that was more frequently associated with severe disease in this patient population.⁸⁰Molecular methods can be used to examine the natural history and disease dynamics of rickettsioses. The first description of confirmed reinfection of a human host with E. chaffeensis was identified by using molecular techniques.⁸¹ A 56-year-old liver transplant reciepient from a rural area of Missouri developed laboratory confirmed ehrlichiosis in 1997 and 1999. Whole blood specimens collected during each episode were evaluated separately by using PCR and sequence analysis to determine the nucleotide pattern of the variable-length PCR target (VLPT) and 120-kDa genes of E. chaffeensis present in each sample. Because the VLPT and 120-kDa antigen genes demonstrate a variety of strain-specific patterns, it could be determined conclusively that the 2 episodes resulted from infections with separate and distinct strains of E. chaffeensis, rather than recrudescence of a persistent infection (Table 2).⁸¹

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Table 2

^82-86It has been proposed that these types of diagnostic tests can be implemented easily in laboratories with basic molecular capacity and developed as acute point-of-care assays.^84,85 Highly specific molecular assays have great utility in regions where particular rickettsial pathogens are known to be endemic; however, broad-range molecular methods can be extremely useful in some circumstances, particularly when multiple, genetically distinct agents occur sympatrically, or in regions where the existence of a novel rickettsiosis is unrecognized. In Missouri, investigators used molecular methods to discriminate infections caused by Ehrlichia ewingii from those caused by E. chaffeensis. Their discovery unveiled a second, clinically and ecologically similar illness, the identity of which was previously obscured because of sufficient overlap of disease manifestations and a shared tick vector.⁸⁷ The initial report of a scrub typhus-like illness in Chile in 2011, caused by a pathogen with highest molecular similarity to O. tsutsugamushi, represents the first identification of an Orientia species infection in the Western Hemisphere and resulted from the use of a broad-range PCR assay designed to amplify a large segment of the prokaryotic 16S rRNA gene.⁸⁸

⁹ today, cellular sediments obtained from serum represent just one of many non-conventional specimens used increasingly as successful sources of template for molecular assays. This technique has been used effectively to provide diagnostic material for PCR-confirmation of various rickettsioses, including RMSF,³⁶,⁷⁷,⁷⁹ Israeli spotted fever,⁸⁹ Thai tick typhus,^90,91 Rickettsia felis rickettsiosis,^92,93 and scrub typhus.⁸³ Improvements in nucleic acid extraction technology permit better recovery of rickettsial DNA from formalin-fixed, paraffin-embedded skin biopsy or autopsy tissues to allow species-specific PCR assays. Included among infections confirmed recently by using this technique are those caused by R. rickettsii,^94,95 R. parkeri⁹⁶ and Rickettsia 364D.⁹⁷

⁹⁸ Subsequent reports described successful application of this simple and minimally invasive method to confirm cases of Queensland tick typhus,⁶⁷ African tick bite fever,⁶⁷,⁹⁹ Mediterranean spotted fever,¹⁰⁰ R. parkeri rickettsiosis,¹⁰¹ and Rickettsia 364D rickettsiosis.¹⁰² Eschar swabs represent highly versatile specimens that can provide confirmatory results retrospectively from healing lesions, in some cases as long as 2 weeks after initiation of antibiotic therapy.⁹⁸,¹⁰¹ Because the technique is more rapid, easier to perform, and generally less painful than biopsy techniques, there is greater patient and physician acceptance, particularly in areas with limited medical resources;⁶⁷,¹⁰⁰ Scab material from the eschar surface may also provide a source of rickettsial DNA suitable for molecular confirmation.¹⁰³ Despite these important advantages, eschar swabs should not be considered categorically as a replacement for cutaneous biopsy methods, for unlike swab material, tissue specimens provide histological context that may assist in an alternate diagnosis if the skin lesion is caused by something other than a Rickettsia species.¹⁰⁴ Skin biopsy techniques also allow for cultivation of rickettsiae from the clinical specimen and are more likely than swabs to provide confirmatory results by molecular evaluation.²²,⁶⁷,¹⁰⁴

E. chaffeensis.¹⁰⁵ During a serological study in the states of Jalisco and Yucatan in Mexico, an astounding 20 (40%) of 50 of patients with a clinical diagnosis of dengue had robust antibody titers reactive with SFG Rickettsia species, yet no demonstrable antibodies reactive with dengue virus.¹⁰⁶ In a similar manner, serological evidence of recent infections with SFG Rickettsia species was identified in 22% of 96 serum samples collected during 2000-2001 as part of regional surveillance for dengue in Cundinamarca, Colombia. ¹⁰⁷ Two confirmed and 7 probable cases of R. parkeri rickettsiosis in Argentina were identified by careful laboratory evaluation of patients presenting to one hospital with fever, myalgias and rash, several of whom were diagnosed initially with leptospirosis or dengue.¹⁰⁸

¹⁰⁹ The rigorous and routine use of rickettsial diagnostics in several prospective studies of febrile patients in these understudied regions has unveiled a surprisingly high prevalence of rickettsioses in these areas and signals an interesting and important period of discovery (Table 3). The frequency of undetected rickettsioses may be even greater when diseases associated with fever and cutaneous eruptions are investigated by these methods. During a prospective study at 2 hospitals in eastern Algeria, 108 adults who presented with fever and rash during 2000-2006 were evaluated for laboratory evidence of a rickettsiosis; acute infection with a SFG or TG Rickettsia species was confirmed in 14 (13%) of 108 enrolled patients during this interval.¹¹⁴ Confirmatory evidence of SFG rickettsioses was obtained from PCR analysis of skin biopsy specimens obtained from 24 (58.6%) of 58 consecutive patients with fever and rash who presented for care at a hospital in Tamil Nadu State, India, during 2006-2008.¹¹⁵

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Table 3

^st century, the diagnostic techniques outlined above will leverage the global recognition of rickettsial diseases and the impact that these have infections on enormous segments of the world population. Each method has unique strengths, and it is important for rickettsiologists to refrain from replacing entirely classical methods with rapidly evolving and increasingly sophisticated molecular techniques. The pitfall of routinely relying on a single diagnostic method was recognized by Pijper and Crockett in 1938,¹¹⁶ when they stated,

E. chaffeensis were detected among a cohort of ill patients in Wisconsin and Minnesota, who presented with classical signs and symptoms of ehrlichiosis but who resided hundreds of miles beyond the established range of the recognized tick vector of E. chaffeensis, the application of cell culture and molecular techniques subsequently revealed a newly recognized ehrlichial pathogen in the United States.¹¹⁷ Laboratories that develop expertise in and routinely apply multiple combinations of these methods provide the highest level of diagnostic accuracy and are positioned characteristically at the leading edge of discovery.

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Publication Dates

Publication in this collection
09 Nov 2015
Date of issue
July 2013

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