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Journal of Clinical Microbiology, November 2002, p. 4180-4184, Vol. 40, No. 11
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.11.4180-4184.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Clinical Microbiology Laboratory, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel
Received 26 April 2002/ Returned for modification 17 June 2002/ Accepted 31 July 2002
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Despite the enlarging body of information on the clinical and diagnostic aspects of K. kingae infections, the epidemiology of the organism remains largely unknown. A study was performed to investigate the sex, age, and seasonal distributions of invasive K. kingae infections and to correlate these data with the respiratory carriage of the organism.
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Bacteriological methods. Patients referred to the emergency department or hospitalized at SUMC with a febrile illness undergo routine blood cultures with the BACTEC system (Becton Dickinson Diagnostic Instrument Systems, Towson, Md.), which are processed according to established bacteriologic procedures (16). Bone exudates and synovial fluid specimens are routinely inoculated into blood culture bottles in addition to routine plating onto solid media, because this procedure has been shown to improve the recovery of K. kingae (22).
Throat cultures obtained from hospital and community patients for isolation of Streptococcus pyogenes are sent to the CML of SUMC in transport medium (MW 173 Amies medium; Transwab; Medical Wire and Equipment, Potley, United Kingdom) and arrive within 4 h. For isolation of K. kingae from the respiratory tract, swabs are seeded onto a selective vancomycin-containing medium especially designed to improve detection of the organism (23) and examined once a day for 2 days. K. kingae is identified by the typical morphological and biochemical characteristics of this species (short, gram-negative bacilli with tapered ends often in pairs or forming short chains; beta-hemolysis; production of acid from glucose and maltose but not from other sugars; positive oxidase reaction; and negative catalase, urease, indole, and motility tests [16]) and confirmed with the API NH kit (bioMerieux, Marcy-l'Etoile, France).
Invasive K. kingae infections. Medical records of all patients in whom an invasive K. kingae infection, defined as isolation of the organism from normally sterile body fluids, was diagnosed from 1 January 1988 through 31 December 2001 were reviewed, and relevant demographic data were collected. The fact that all children in southern Israel are born in and receive inpatient medical services at SUMC allowed us to calculate the annual incidence of invasive K. kingae infections in this population.
Respiratory prevalence study. A fraction of all pharyngeal swabs sent to the CML of SUMC for detection of S. pyogenes during two time periods in 2001 were cultured for isolation of K. kingae on selective medium (23). The first period (February to May) was chosen to comprise the time of the year when only a small fraction of patients with invasive K. kingae infections are usually diagnosed. The second period (October to December) coincides with the season in which the vast majority of these infections are detected. Information regarding clinical symptoms or recent antibiotic exposure of the population from which these respiratory specimens derived was not available.
Throat swabs were stratified according to patients' ages before the data were examined, as follows: 0 to 3 years, 4 to 17 years, and
18 years. These intervals were chosen to represent children at the age at which invasive diseases are especially common, older children, and adults, respectively. For each period and age group, samples of swabs of approximately similar sizes were randomly chosen for K. kingae isolation.
Statistical methods.
The significance of the differences between two means was assayed by using Student's t test. Assuming that there is no gender predisposition or seasonal preference for infection, episodes of invasive disease were expected to be evenly distributed between the sexes and the two study periods. The comparison of observed distribution to expected distribution was assessed by using the
2 test. A P value of <0.05 was considered statistically significant for all calculations.
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FIG. 1. Monthly distribution of cases of invasive K. kingae infections diagnosed at SUMC between 1 January 1988 and 31 December 2002.
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TABLE 1. Prevalence of K. kingae in the respiratory tract and annual incidence of invasive disease in children younger than 48 months
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Respiratory prevalence study. A total of 2,044 of 11,202 throat specimens (18.2%) sent to the CML were cultured for K. kingae (1,020 of 6,205 [16.4%] in the February-to-May period and 1,024 of 4,997 [20.5%] in the October-to-December period). Demographic characteristics of the patients from whom the pharyngeal cultures were screened for K. kingae are shown in Table 2. The populations studied in the February-to-May and October-to-December periods were similar in terms of age and sex distribution. Thirty-seven specimens were positive for K. kingae (21 in the February-to-May period and 16 in the October-to-December period; P > 0.4). Overall, 978 specimens (47.8%) were obtained from males, of which 17 (1.7%) were positive for K. kingae, and 1,066 (52.2%) were obtained from females, of which 20 (1.9%) grew the organism (P > 0.9). The prevalence of the organism did not significantly differ between sexes in any of the age groups studied (P > 0.05 for all calculations; results not shown). The prevalence of the organism by season and age group is shown in Table 3. In the February-to-May period, the prevalence of K. kingae was higher among 0- to 3-year-old children than among the two older population groups and showed a significant decrease with increasing age. In the October-to-December period, the prevalence of K. kingae was also higher among the youngest population and gradually decreased in older individuals, but this trend did not reach statistical significance. The rate of carriage of the organism among children younger than 48 months is shown in Table 1. Because throat cultures are infrequently obtained in infants, the 0- to 11-month age group was underrepresented in the population (fewer than 5% of the children screened). The carriage rate did not differ significantly between the population age groups, and the trend towards higher prevalence of K. kingae in the February-to-May period did not reach statistical significance.
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TABLE 2. Demographic data for the population studied
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TABLE 3. Prevalence of K. kingae in the respiratory tract by age group and study period
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In previous studies it was demonstrated that K. kingae is frequently isolated from the upper respiratory tracts of young children. In a prospective study, the oropharynges and nasopharynges of 48 children age 6 to 42 months attending a local DCC were cultured separately (24). K. kingae was isolated from 109 of 624 oropharyngeal cultures (17.5%), and 34 children (70.8%) carried the organism at least once during an 11-month study period. The organism was not isolated from any of the nasopharyngeal cultures, suggesting that K. kingae occupies a narrow respiratory niche (24).
The results of the present investigation demonstrate that when blood cultures are routinely obtained from young febrile children and synovial fluid specimens are inoculated into blood culture bottles, K. kingae appears as a not-uncommon cause of invasive infection. Examination of our extensive experience over a 14-year period shows three remarkable epidemiological features: invasive K. kingae is a pediatric disease especially affecting populations below 4 years of age, the disease is significantly more common in males, and cases tend to cluster between July and December.
It was expected, then, that the respiratory carriage of the organism would have similar characteristics of age, sex, and seasonal predilection. The results of the carriage study confirmed that the prevalence of the organism in the pharynges of children younger than 4 years (3.2%) was significantly higher than that in older individuals (Table 3). However, this phenomenon was observed only during the early months of the year, whereas in the later cross-sectional survey, the rate of carriage of K. kingae in the segment of the population younger than 4 years decreased and was comparable to that observed in older individuals.
We could not demonstrate a correlation between the pattern of carriage of the organism and the seasonal occurrence of cases of invasive disease. In general terms, the period of the year when there was maximal prevalence of the organism in the respiratory tract did not overlap with that when the attack rate of invasive infection was highest. Whereas almost three-quarters of the patients with invasive K. kingae disease were diagnosed between July and December, the carriage rate showed an opposite, albeit not significant, trend. It might be postulated that exposure of patients with suspected streptococcal pharyngitis to antimicrobial drugs accounted for the overall low prevalence of K. kingae as well as for the unexpected low carriage rate found in the October-to-December period. Because the occurrence of respiratory infections follows a seasonal pattern, the population in general, and especially young children, is more commonly given antimicrobial drugs during the winter (1). Therefore, the prevalence of K. kingae could have been reduced by previous exposure to drugs such as ß-lactams, trimethoprim-sulfamethoxazole, or macrolides, which are commonly given to patients with respiratory infections and to which the organism is exquisitely susceptible (26). Although no actual data on antibiotic exposure were collected in the present study, it should be pointed out that throat cultures are usually obtained before the onset of antimicrobial therapy. In addition, the four colder months of the year (November to March) were equally distributed between the two study periods, neutralizing the possible effect of antibiotic exposure on the rate of recovery of the organism.
The results of the present study show that there are not significant sex differences in the rate of carriage of K. kingae, whereas invasive diseases show a clear male predominance. The explanation for this observation is not obvious, although increased male-to-female ratios have been described for other infectious conditions such as those caused by S. pneumoniae and N. meningitidis (10, 12). Clearly, because most cases of K. kingae invasive infection occur among infants and toddlers, this striking feature cannot be explained by different behavioral patterns of male and female children resulting in different degrees of exposure.
The overall prevalence of K. kingae in the 0- to 4-year-old group found in this investigation is substantially lower than that detected a few years ago among children attending a DCC in the city of Beer-Sheva (24). It should be pointed out that the fraction of children attending DCCs in the present study population could not be determined. It is possible that the high rate of carriage of K. kingae found in the previous study was the result of increased transmission of the organism among susceptible young children exposed to crowded conditions prevalent in the DCC. Increased rates of carriage of other respiratory pathogens such as S. pneumoniae or H. influenzae type b have also been demonstrated among DCC attendees compared to children cared for at home (11).
It appears, then, that the striking epidemiological features of invasive K. kingae infections cannot be explained solely on the basis of the characteristics of the respiratory carriage of the organism, and, therefore, additional factors should be proposed. It is remarkable that signs of upper respiratory tract infection, stomatitis, or diarrhea were found on admission in more than half of the children who later grew K. kingae from a normally sterile body site. These findings, which were recorded in the patients' charts by physicians who were unaware of the etiology of the infection, are highly suggestive of a concomitant viral infection. The important role played by viruses in the causation of pneumococcal or meningococcal infections has been firmly established (16, 17). Respiratory viruses are frequent precipitating factors of otitis media, pneumonia, bacteremia, or meningitis among persons already colonized by these respiratory pathogens (15, 17). Recent reports have shown that specific viral infections may also predispose individuals to acquisition of invasive K. kingae infections. In a study by Amir and Yagupsky, K. kingae bacteremia was documented in 4 of 29 young children with culture-proven herpetic gingivostomatitis (2). In addition, occurrence of K. kingae endocarditis following chicken pox was also described in another report (21). These reports suggest that viral infections causing damage to the respiratory mucosa or buccal aftae facilitate local invasion by K. kingae organisms residing in the pharynx, followed by penetration of the bacterium into the bloodstream and seeding to remote sites. It is suggested that the peculiar epidemiological features of invasive K. kingae infections result from the interplay of the respiratory carriage of the organism with viral infections and possibly other, still-unidentified factors.
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