Changing Dynamics of Human–Rickettsial Interactions

Fluctuations in the reported incidence of scrub typhus, Rocky Mountain spotted fever (RMSF), and Mediterranean spotted fever have been noted over the past century since their recognition as arthropod-borne infections, with decadelong periods between the peaks and troughs. In Japan, classic Leptotrombidium akamushi-transmitted scrub typhus occurred with a high incidence before the 1950s, and thereafter decreased dramatically, essentially disappearing by the early 1980s, at which time a tremendous rise in scrub typhus transmitted by Leptotrombidium pallidium and Leptotrombidium scutellare mites occurred. The report by Jeung and others in this issue addresses scrub typhus in South Korea, where the first case was diagnosed in 1985 and a rise to 10,365 cases was reported in 2013. By studying the times of peak incidence in provinces representing northern, central, and southern Korea over a 13-year-period during which the number of cases increased tremendously, they noted that the peak occurred progressively later in the year. Increase in the density of L. scutellare, the vector of Orientia tsutsugamushi, in northern and central Korea correlated with the increased incidence of disease. The possibility of global climate change as a factor contributing to these changes is supported by the effect of longer seasonal warm temperatures and L. scutellare abundance in temperate regions of Korea. Trombiculid mites feed particularly on rodent hosts such as Rattus species, and no longer remain active when the ground freezes. Because O. tsutsugamushi is apparently maintained solely by transovarian transmission in mites and is transmitted by larvae (the only stage of this arthropod that feeds on a host), the occurrence of scrub typhus depends on the abundance of infected chiggers and their contact with humans. The appearance of scrub typhus in recent years in areas where the illness was nearly forgotten, such as in India, Sri Lanka, the Maldives, and Micronesia, and in regions where it had not been known previously such as north of the Yangtze river in China and in Korea suggests that environmental changes including potential northward spread of infected mites may be occurring. Increased diagnosis of scrub typhus in Thailand, Taiwan, Japan, and Laos may represent truly increased incidence, greater awareness, or greater availability of diagnostic methods. Whatever the explanation for increasing incidence and geographic range, scrub typhus begs for greater medical, public health, and scientific attention. Diagnosis is difficult, frequently missed, and would benefit greatly from a low-cost point-of-care diagnostic tool that is effective early in the illness, when therapeutic decisions are being made. With an estimated 1 million cases annually and an average case-fatality rate of 10%, a vaccine that provides cross protection against 70 or more strains of O. tsutsugamushi is a true public health need. Research should begin with determination of protective immune mechanisms and with genome-wide bioinformatic analyses of potential protective antigens. Currently, excellent research on the pathobiology of O. tsutsugamushi–host interactions is being accomplished in Korea, but the development of an effective vaccine is far from near. Articles from the Centers for Disease Control and Prevention (CDC) in this issue describe a tremendous increase in reported cases of spotted fever group rickettsioses (SFGR) and the dramatic spread of Amblyomma americanum (the lone star tick) in the United States. At first impression, there appears to have been an enormous increase in cases of SFGR during the period 2008–2012. However, it should not be interpreted that these were all patients with RMSF, because the approach most widely used for laboratory confirmation of this diagnosis was detection of antibodies reactive with Rickettsia rickettsii, which also cross-react with other SFG rickettsiae includingRickettsia amblyommii,Rickettsia parkeri, Rickettsia strain 364D, Rickettsia akari, Rickettsia massiliae, and Rickettsia montanensis. As the authors acknowledge, the criteria for a “probable” case are problematic. Indeed, only 1% of cases reported on case report forms in 2008–2014 were confirmed by seroconversion, a 4-fold rise in antibody titer, immunohistochemical detection of SFG rickettsiae, polymerase chain reaction (PCR), or isolation of rickettsiae. Only the latter two methods are specific for a particular Rickettsia species; 23 cases of RMSF were identified by PCR and four by culture over the 5-year period. The diagnosis of the remainder of cases was based on a single, often low titer of antibodies. Moreover, the median day of collection of the single serum assayed was day 4 of illness, and in RMSF, antibodies to rickettsiae do not appear until days 7–10 of illness. It should be interpreted that seropositive patients commonly had antibodies preexisting during their acute illness, that infection with ehrlichiae or a virus was a more likely cause of acute illness than rickettsiae, and, thus, that these were unlikely to be SFGR cases. In fact, the clinical case definition for SFGR is a febrile patient who had one or more of the following: rash, eschar, headache, myalgia, anemia, thrombocytopenia, and elevated serum hepatic transaminases. Four of these are also characteristic of humanmonocytotropic ehrlichiosis. The case fatality rate of RMSF in the antibiotic era has been 4% or worse. The case fatality rate in this report of SFGR of 0.4% emphasizes the likelihood that most patients’ antibodies were stimulated by an agent other than R. rickettsii. Although human infections with R. parkeri and Rickettsia strain 364D are important discoveries, they are unlikely to account for a substantial portion of the reported cases, as only 3% of persons for whom eschar status is stated were reported to have the tickinoculation site lesions associated with these rickettsiae. The article by Dahlgren and others suggests the hypothesis that “less pathogenic rickettsiae are causing human infections,” and they document the geographic spread of the lone *Address correspondence to David H. Walker, 301 University Boulevard, Galveston, TX 77555-0609. E-mail: [email protected]