{"doi":"10.4269/ajtmh.2005.73.1083","title":"A HIGHLY SENSITIVE AND SPECIFIC REAL-TIME PCR ASSAY FOR THE DETECTION OF SPOTTED FEVER AND TYPHUS GROUP RICKETTSIAE","abstract":"<jats:p>A highly specific real-time polymerase chain reaction (PCR) assay was developed to detect spotted fever and typhus group rickettsiae using the citrate synthase gene as the target. The assay amplified rickettsial members of the spotted fever and typhus group including <jats:italic>Rickettsia akari</jats:italic>, <jats:italic>R. australis</jats:italic>, <jats:italic>R. conorii, R. honei</jats:italic>, <jats:italic>“R. marmionii,” R. sibirica</jats:italic>, <jats:italic>R. rickettsii</jats:italic>, <jats:italic>R. typhi</jats:italic>, and <jats:italic>R. prowazekii</jats:italic>. The ancestral group rickettsia, <jats:italic>R. bellii</jats:italic>, did not produce a positive reaction, nor did other members of the order <jats:italic>Rickettsiales</jats:italic> or any non-rickettsial bacteria. The assay had a sensitivity of one target copy number per reaction as determined by serial dilutions of a plasmid containing a spotted fever group target sequence. This quantitative assay is useful for the enumeration of rickettsiae in clinical specimens and the diagnosis of rickettsial illnesses, when rickettsial numbers are very low.</jats:p>","journal":"The American Journal of Tropical Medicine and Hygiene","year":2005,"id":667149,"datarank":0.8570599208264055,"base_score":5.713732805509369,"endowment":5.713732805509369,"self_citation_contribution":0.8570599208264055,"citation_network_contribution":0.0,"self_endowment_contribution":0.8570599208264055,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":302,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1742251,"name":"STEPHEN R. GRAVES","orcid":null,"position":1,"is_corresponding":false},{"id":1742252,"name":"NATHAN B. UNSWORTH","orcid":null,"position":2,"is_corresponding":false},{"id":1742250,"name":"JOHN STENOS","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"A HIGHLY SENSITIVE AND SPECIFIC REAL-TIME PCR ASSAY FOR THE DETECTION OF SPOTTED FEVER AND TYPHUS GROUP RICKETTSIAE","abstract":"<jats:p>A highly specific real-time polymerase chain reaction (PCR) assay was developed to detect spotted fever and typhus group rickettsiae using the citrate synthase gene as the target. The assay amplified rickettsial members of the spotted fever and typhus group including <jats:italic>Rickettsia akari</jats:italic>, <jats:italic>R. australis</jats:italic>, <jats:italic>R. conorii, R. honei</jats:italic>, <jats:italic>“R. marmionii,” R. sibirica</jats:italic>, <jats:italic>R. rickettsii</jats:italic>, <jats:italic>R. typhi</jats:italic>, and <jats:italic>R. prowazekii</jats:italic>. The ancestral group rickettsia, <jats:italic>R. bellii</jats:italic>, did not produce a positive reaction, nor did other members of the order <jats:italic>Rickettsiales</jats:italic> or any non-rickettsial bacteria. The assay had a sensitivity of one target copy number per reaction as determined by serial dilutions of a plasmid containing a spotted fever group target sequence. This quantitative assay is useful for the enumeration of rickettsiae in clinical specimens and the diagnosis of rickettsial illnesses, when rickettsial numbers are very low.</jats:p>","is_dataset_classified":null,"base_score":0.0,"endowment":0.0,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"16354816","pmcid":null,"openalex_id":null,"authors":[],"funders":[],"total_grants":0,"fwci":null,"citation_percentile":null,"influential_citations":0,"citation_trend":[],"oa_status":"closed","license":null,"oa_locations":[{"url":"https://www.ajtmh.org/view/journals/tpmd/73/6/article-p1083.xml","host_type":"publisher"},{"url":"https://www.ajtmh.org/downloadpdf/journals/tpmd/73/6/article-p1083.xml","host_type":"publisher"}],"fields_of_study":[],"mesh_terms":["Humans","Rickettsia","Rickettsia Infections","Rocky Mountain Spotted Fever","Citrate (si)-Synthase","DNA, Bacterial","DNA Primers","Reagent Kits, Diagnostic","Sensitivity and Specificity","Predictive Value of Tests","Polymerase Chain Reaction","Victoria"],"keywords":[],"sdg_mappings":[],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-08-13T16:49:43.666840Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}