Coxiella Burnetii And Bartonella Biology
Blood culture negative endocarditis was recognized by Osler at the beginning of last century. Recently, many publications in European countries have demonstrated a significant involvement of Coxiella burnetti, Bartonella henselae, and B. quintana in patients with BCNE. C. burnetii is one of the most encountered fastidious agents in BCNE. Q fever is characterized by its clinical polymorphism and... the longest interval being 20 years after infection. Endocarditis is the main form of chronic Q fever (78% of all chronic Q fever cases). Some authors proposed that all patients with acute Q fever be investigated by a transthoracic echocardiography. The diagnosis of Q fever endocarditis requires both clinical endocarditis and isolation or serologic evidence of C burnetii. Because Q fever endocarditis is a chronic illness, a single serum specimen is sufficient for diagnosis. A phase I IgG titers of 800 or greater is one of the major modified Duke criteria. Previously studies showed that PCR with serum samples may be helpful in establishing an early diagnosis of chronic Q fever . Currently there is no data concerning the incidence of Q fever endocarditis cases among Romanian population. The first Q fever cases in Romania were registered in 1947 in Constanta County. The most recent data about Q fever in Romania were represented by urban sporadic cases reported in the period 1981-1987. All serum samples tested by serological methods for detection of IgG to C. burnetii, B. quintana and B. henselae originated from patients with clinical suspicion of BCNE. According to the modified Duke criteria a single positive blood culture for Coxiella burnetii or antiphase I IgG antibody titers >800 represents a major criterion for definite infective endocarditis. The results of serological testing showed that 9 out of 33 serum samples exhibited antiphase I C. burnetii IgG antibody titers >800, while none of samples has IgG for B. henselae or B. quintana. The modified Duke criteria used for definite infective endocarditis (IE) diagnosis of analyzed patients with clinical suspicions of BCNE are presented in Table 1. Diagnosis of IE is definite if there are 2 major criteria or 1 major and 3 minor criteria or 5 minor criteria. Eight out of nine investigated cases fulfilled 2 major criteria (antiphase I C. Burnetii IgG antibody titer >800 and when there is a vegetation or a new valvular regurgitation) for defining IE, while the remaining case fulfilled one major criterion (antiphase I C. burnetii IgG antibody titers >800) and one minor criterion (fever ï‚³ 38 °C), being classified as a possible case. It is well-known that endocarditis is the most common presentation of chronic Q fever. Initially thought to be a rare disorder, later it has been estimated to account for up to 5% of all endocarditis cases worldwide. Despite increasing awareness, recent studies show a mean delay of seven months from symptom onset to diagnosis. The diagnosis of Q fever endocarditis is hampered by the inability to culture C. burnetii using routine media. As a strict obligate intracellular bacterium, it can only be cultured in living cell lines, or embryonated chicken eggs, but the cultures cannot be easily performed in most laboratories, and the technique is restricted to biosafety level 3 laboratories. Thus, the diagnosis of chronic Q fever, therefore, relies on serological testing, being characterized by increased titres against the phase I antigen.
Detection of C. burnetii DNA by PCR is an important diagnostic method that could be used on
different types of clinical specimens (blood, serum, infected heart valves). The results of PCR assays performed on DNA from serum samples positive for antiphase I C. burnetii IgG showed that nested-PCR assay permitted the amplification of C. burnetii DNA. Thus, nested-PCR led to obtaining the amplification products of the repetitive element IS1111a associated to htpAB transposase gene in the second round of amplification for all analyzed DNAs. In this study we analyzed the role of C. burnetii as causative agent of blood culture negative infective endocarditis among patients with clinical diagnostic of infective endocarditis. The blood-cultures were performed for 102 patients hospitalized in three Institutes for Cardiovascular Diseases from Bucharest, Timisoara and Targu-Mures, and in Clinical Hospital for Infectious Diseases from Cluj. For each patient, a standardized questionnaire was filled by the physician in charge and logged into a database. The information filled in the questionnaire were consisted of: known preexisting valvular defect, type of valve involved (native/bioprosthetic/mechanical valve, and its position: aortic, mitral, tricuspid, pulmonary); previous antibiotic therapy; clinical symptoms; and laboratory results. Patients were considered to have possible or definite endocarditis according to the modified Duke criteria.
57 serum samples were tested by indirect immunofluorescence assay (IFA) for detection of IgG
antibodies to C. burnetii, B. henselae and B. quintana. From these samples 33 originated from patients
with BCNE, and the rest of samples were tested before obtaining the blood cultures results, which
finally were positive. We used IFA kits (Vircell, Spain) for detection of IgG antiphase I and antiphase
II C. burnetii, and for IgG to B. quintana and IgG to B. henseale. The presence of IgG titers >800
to C. burnetii or B. quintana or B. henselae were considered positive for endocarditis diagnosis.
Furthermore, we analyzed the positive serum samples for C. burnetii with antiphase I IgG antibody
titers >800 using molecular methods for the confirmation of serological results. The serum samples from nine patients with antiphase I C. burnetii IgG antibody titer >800, were used for DNA extraction. Total genomic DNA was extracted from 200 microliters of serum using the QIAamp blood kit (Qiagen, Hilden, Germany) according to the manufacturer instructions. DNA was resuspended in fifty microliters of elution buffer. Genomic DNAs were stored at 4 °C until their use as templates in PCR assays and subsequently at −20 °C. DNA samples have been handled carefully to avoid the risk of cross-contamination. DNA extraction, mix preparation, and PCR were performed in different rooms to prevent PCR carryover contamination. No positive control was used to prevent lateral contamination (i.e., contamination caused by PCR products amplified in other tubes in the same assay). DNA extracted from serum specimens of blood donors was used every 4 specimens as a negative control. We used a nested-PCR assay for detection of the repetitive element IS1111 associated to htpAB transposase gene (GenBank accession number M80806). This repetitive element is present in multiple copies in the genome of C. burnetii strains (e.g., there are 20 copies of this element in the C. Burnetii Nine Mile I genome), which increase the detection sensitivity of this pathogen in serum samples. In the first round of amplification we used IS111F1 and IS111R1 primers, which were designed to amplify a 485-bp fragment of the repetitive element IS1111, while the second round of amplification was performed using the IS111F2 and IS111R2 primers, which amplify an internal 260-bp fragment from the same target. The sequence of specific primers used in nested-PCR reactions, and the molecular size of the amplicons are presented in Table 2. In the nested-PCR assay, each gene fragment amplified separately on 2700 Applied Biosystems instrument using necessary components provided by Promega. The components used in each type of PCR reaction are described in Table 3. The parameters for the amplification cycles used in each PCR experiment are presented in Table 4. PCR products from nested-PCR assay were separated in a 1.5% agarose gel for 1 h at 100 V, stained with ethidium bromide and detected by UV transillumination. 3. The sequencing of the amplicons from nested-PCR has been used to confirm the PCR results. The
amplicons from the second round of nested-PCR were sequenced in both directions using the BigDye
V3.1 kit as described by the manufacturer. Sequencing products have been resolved using an ABI 3100
automated Avant Genetic Analyzer (Applied Biosystems). Sequence analysis was performed with
BioEdit program, which permitted obtaining of the consensus sequences that were compared with
similar sequences from BLAST. The sequences obtained showed a sequence similarity of 100% with
that of the GenBank prototype strain sequence. Thus, sequencing of the amplicons from the second
round of PCR reaction has permitted to confirm that amplification products belong to C. burnetii.
These two molecular tests were used together for the first time to investigate the BCNE cases with
C. burnetii in Romania. We propose that all patients with clinical suspicion of IE be tested serologically for evidence of infection with other agents such as C. burnetii in parallel with performing blood cultures. This is the first report in this country for using the molecular methods to confirm Q fever endocarditis cases on the serum samples from eight confirmed cases and from one possible case of Q fever endocarditis tested by nested-PCR, based on repetitive element IS1111a of the transposase gene. This assay exhibited high sensitivity and specificity and led us to obtain specific amplification products, which were subsequently confirmed by direct sequencing to belong to C. burnetii, confirming previous studies showing that this nested-PCR assay presents a specificity of 100% and a sensitivity of one C. burnetii DNA copy . In conclusion, our results have demonstrated that nested-PCR amplification, followed by direct sequencing, is a reliable and accurate method when applied to serum samples and can be used as a supplementary diagnosis tool for BCNE cases. 9809
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