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12th July 01:29
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National Library of Medicine
TITLE: Can protracted relapsing fever resemble Lyme disease? AUTHORS: Lange WR; Schwan TG; Frame JDAUTHOR AFFILIATION: Johns Hopkins Medical Institutions, Baltimore, MD 21205. SOURCE: Med Hypotheses 1991 Jun;35(2):77-9 CITATION IDS: PMID: 1890979 UI: 91367158 ABSTRACT: We report the case of a Protestant missionary who contracted tick-borne relapsing fever in 1979 while serving in the Sudan. Despite tetracycline treatment, his acute illness ran a protracted course, with migratory polyarthralgias lasting approximately 10 months. Symptoms recurred in 1984 and have persisted. At regular intervals, the patient has experienced recurrent episodes of fever, generalized fatigue, bilateral upper and lower extremity muscle weakness, and asymetric large joint polyarthralgia. Indirect fluorescent antibody testing of sera demonstrated titers of 1:16 for B. burgdorferi and 1:64 for B. hermsii, and immunoblotting confirmed past exposure to relapsing fever, but not Lyme disease. It is hypothesized that this individual's chronic symptoms have been related to relapsing fever, and that in certain situations or in select individuals, relapsing fever can be capable of producing a chronic clinical picture ****ogous to Lyme disease. LANGUAGES: Eng -------------------------------------------------- ".....4 ixodid tick species are known as vectors of B. theileri........" TITLE: Ticks and spirochetes. AUTHORS: Hoogstraal H SOURCE: Acta Trop 1979 Jun;36(2):133-6 CITATION IDS: PMID: 41420 UI: 80062108 ABSTRACT: The concept is expressed that Borrelia developed as symbionts of ticks (especially Argasidae) but act as parasites in mammals and birds ... borrelial reservoirs and amplifiers following bites by infected ticks. Certain tick borreliae may multiply in lice but one Borrelia has evolved into a n independent species (B. recurrentis) associated only with lice and humans. Seven**** argasid tick species are known as vectors of Borrelia species and 4 ixodid tick species are known as vectors of B. theileri. LANGUAGES: Eng TITLE: Neuroborreliosis during relapsing fever: review of the clinical manifestations, pathology, and treatment of infections in humans and experimental animals.AUTHORS: Cadavid D; Barbour AGAUTHOR AFFILIATION: Department of Neurology, Georgetown University School of Medicine, Washington, D.C. 20007, USA.SOURCE: Clin Infect Dis 1998 Jan;26(1):151-64CITATION IDS: PMID: 9455525 UI: 98116703ABSTRACT: The spirochetal disease relapsing fever is caused by different Borrelia species. Relapsing fever is well recognized as an infection of the blood, but little is known about its predilection for the nervous system and the eyes. To investigate neurological and ocular involvement during relapsing fever, we reviewed the clinical manifestations, pathology, and treatment of relapsing fever of humans and experimental animals. The results indicate that Borrelia turicatae and Borrelia duttonii, the agents of tick-borne relapsing fever in southwestern North America and sub-Saharan Africa, respectively, cause neurological involvement as often as Borrelia burgdorferi in Lyme disease. Evidence of this is the frequent occurrence of lymphocytic meningitis and peripheral facial palsy in human disease; the identification of spirochetes in the brain and other nervous tissues of humans, animals, and arthropod vectors; and the persistence of brain infection after treatment with antibiotics that do not readily penetrate the blood- brain barrier. Eng GRANT/CONTRACT ID: AI24424/AI/NIAID _______________________________________- TITLE: Ticks and Borrelia: model systems for investigating pathogen-arthropod interactions. AUTHORS: Schwan TG AUTHOR AFFILIATION: Laboratory of Microbial Structure and Function, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, MT 59840, USA. SOURCE: Infect Agents Dis 1996 Jun;5(3):167-81 CITATION IDS: PMID: 8805079 UI: 96398229 ABSTRACT: Blood-feeding arthropods transmit numerous types of infectious agent\0 and parasite that have a tremendous impact on human health and mortality throughout the world. These vector-borne pathogens display a wide array of evolutionary patterns that allow them to infect and to be successfully transmitted by ticks, mites, and hematophagous insects. The vector's method of feeding, type of development, and host preference are also critical factors for the transfer of zoonotic agents from wild animal reservoirs to susceptible humans. Ticks are obligate blood-feeders in all life stages and biologically transmit many infectious agents. In North America, two ticks that are involved in the maintenance and transmission of pathogenic spirochetes include Ixodes scapularis (family Ixodidae) and Ornithodoros hermsi (family Argasidae). These ticks are the respective vectors of the Lyme disease spirochete Borrelia burgdorferi and a relapsing fever spirochete, Borrelia hermsii. Little is known concerning how these and related species of Borrelia adapt to successfully alternate between warm- blooded vertebrates and ticks; however, the possibility that borrelial surface proteins are differentially expressed in their different hosts is an exciting area of current research. LANGUAGES: Eng _______________________________- TITLE: Late relapse of tick-borne relapsing fever following treatment with doxycycline [letter] AUTHORS: Liles WC; Spach DH SOURCE: West J Med 1993 Feb;158(2):200 CITATION IDS: PMID: 8434483 UI: 93166786 ____________________________ TITLE: Identification of a protein in several Borrelia species which is related to OspC of the Lyme disease spirochetes. AUTHORS: Marconi RT; Samuels DS; Schwan TG; Garon CF AUTHOR AFFILIATION: Laboratory of Vectors and Pathogens, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840. SOURCE: J Clin Microbiol 1993 Oct;31(10):2577-83 CITATION IDS: PMID: 8253952 UI: 94075529 ABSTRACT: Using oligonucleotide probes which have previously been shown to be specific for the ospC gene found in the Lyme disease spirochete species Borrelia burgdorferi, B. garinii, and group VS461, we detected an ospC homolog in other Borrelia species including B. coriaceae, B. hermsii, B. anserina, B. turicatae, and B. parkeri. In contrast to the Lyme disease spirochetes, which carry the ospC gene on a 26-kb circular plasmid, we mapped the gene in other Borrelia species to linear plasmids which varied in size among the isolates tested. Some isolates carry multiple copies of the gene residing on linear plasmids of different sizes. The ****yses conducted here also demonstrate that these Borrelia species contain a linear chromosome. Northern (RNA) blot ****yses demonstrated that the gene is transcriptionally expressed in all species examined. High levels of transcriptional expression were observed in some B. hermsii isolates. Transcriptional start site ****yses revealed that the length of the untranslated leader sequence was identical to that observed in the Lyme disease spirochete species. By Western blotting (immunoblotting) with antiserum (polyclonal) raised against the OspC protein of B. burgdorferi, we detected an immunoreactive protein of the same molecular weight as the OspC found in Lyme disease spirochete species. The results presented here demonstrate the presence of a protein that is genetically and antigenically related to OspC which is expressed in all species of the genus Borrelia tested. LANGUAGES: Eng ________________________________________________ TITLE: Antigenic variation of surface proteins of Borrelia species. AUTHORS: Barbour AG AUTHOR AFFILIATION: Department of Microbiology, University of Texas Health Science Center, San Antonio 78284-7758. SOURCE: Rev Infect Dis 1988 Jul-Aug;10 Suppl 2:S399-402 CITATION IDS: PMID: 3055207 UI: 89043560 ABSTRACT: During relapsing fever, the etiologic spirochetes employ antigenic variation to avoid early immune clearance. In Borrelia hermsii, an agent of tick-borne relapsing fever, a switch in serotype is associated with a change in the predominant protein on the surface of the cells. The variable major proteins differ from one another in primary structure along their lengths. Genes encoding the different variable major proteins can be found in both "silent" and "active" environments. At the active site the gene is expressed; at the silent site the gene appears to be in storage. In variant cells, which express the new serotype-specific surface protein in a population, a gene from a silent site has replaced the previously sitting gene at the active site through transposition. LANGUAGES: Eng GRANT/CONTRACT ID: AI 24424/AI/NIAID __________________________________________________ ___ TITLE: Identification of an uncultivable Borrelia species in the hard tick Amblyomma americanum: possible agent of a Lyme disease-like illness.A AUTHORS: Barbour AG; Maupin GO; Teltow GJ; Carter CJ; Piesman J AUTHOR AFFILIATION: Department of Microbiology, University of Texas Health Science Center, San Antonio 78284, USA. SOURCE: J Infect Dis 1996 Feb;173(2):403-9 CITATION IDS: PMID: 8568302 UI: 96162099 ABSTRACT: Bites from the hard tick Amblyomma americanum are associated with a Lyme disease-like illness in the southern United States. To identify possible etiologic agents for this disorder, A. americanum ticks were collected in Missouri, Texas, New Jersey, and New York and examined microscopically. Uncultivable spirochetes were present in approximately 2% of the ticks. Borrelia genus-specific oligonucleotides for the flagellin and 16S rRNA genes were used for amplification of DNA. Products were obtained from ticks containing spirochetes by microscopy but not from spirochete-negative ticks. Sequences of partial genes from spirochetes in Texas and New Jersey ticks differed by only 2 of 641 nucleotides for flagellin and 2 of 1336 nucleotides for 16S rRNA. Phylogenetic ****ysis showed that the spirochete was a Borrelia species distinct from previously characterized members of this genus, including Borrelia burgdorferi. Gene amplification could be used to detect these spirochetes in ticks and possible mammalian hosts. LANGUAGES: Eng __________________________________________________ ________ TITLE: Isolation of Borrelia spirochetes from patients in Texas. AUTHORS: Rawlings JA; Fournier PV; Teltow GJ SOURCE: J Clin Microbiol 1987 Jul;25(7):1148-50 CITATION IDS: PMID: 3611307 UI: 87280609 ABSTRACT: The Texas Department of Health Laboratory began culturing the Lyme disease spirochete Borrelia burgdorferi in 1985. This organism was subsequently isolated from blood, cerebrospinal fluid, joint fluid, skin, bone, and autopsy tissues from humans. Fluorescent-antibody tests with murine monoclonal antibodies confirmed that seven of these isolates were B. burgdorferi and that two others belonged to the genus Borrelia. LANGUAGES: Eng ____________________________________________- _________________________________________________- TITLE: Experimental infection of the mouse brain by a relapsing fever Borrelia species: a molecular ****ysis. AUTHORS: Cadavid D; Bundoc V; Barbour AG AUTHOR AFFILIATION: Department of Microbiology, University of Texas Health Science Center, San Antonio 78284-7758. SOURCE: J Infect Dis 1993 Jul;168(1):143-51 CITATION IDS: PMID: 8515101 UI: 93294348 ABSTRACT: The spirochetal disease relapsing fever is notable not only for multiphasic antigenic variation but also for central neurologic manifestations. To further characterize involvement of the brain in this disorder, immunocompetent and -deficient mice were infected with Borrelia hermsii. Immunodeficient mice were treated while spirochetemic with neutralizing IgM monoclonal antibodies to the infecting serotype. Blood, cerebrospinal fluid, and brain tissue were examined by culture and polymerase chain reaction. In immunocompetent mice, antigenic variation occurred in the brain as well as in the blood. In immunodeficient mice, the infecting serotype was still present in the brain after it had been eliminated from the blood by the administered antibodies. These latter results cannot be accounted for by contamination of brain tissue and cerebrospinal fluid by blood and, hence, establish the direct involvement of the central nervous system in this experimental infection. LANGUAGES: Eng GENE SYMBOL: vmp GRANT/CONTRACT ID: AI 24424/AI/NIAID ------------------------------------------------------------------------ TITLE: Tick-borne relapsing fever: an interstate outbreak originating at Grand Canyon National Park. AUTHORS: Boyer KM; Munford RS; Maupin GO; Pattison CP; Fox MD; Barnes AM; Jones WL; Maynard JE SOURCE: Am J Epidemiol 1977 May;105(5):469-79 CITATION IDS: PMID: 871120 UI: 77179213 ABSTRACT: During the 1973 summer season, 27 employees and 35 overnight guests at the North Rim, Grand Canyon National Park, Arizona, acquired febrile illnesses compatibel with relapsing fever. Six**** cases were confirmed by finding Borrelia spirochetes in peripheral blood smears or inoculated Swiss mice. Retrospective surveys of 278 employees and 7247 guests at the park revealed that acquisition of illness was significantly associated with the persons sleeping in rustic log cabins and acquiring bites of "unknown" insects. From rodent nesting materials found in the walls and attics of cabins where cases had occurred, infective Ornithodoros hermsi ticks were recovered. Exceptional activity of ticks in human populations appeared to have resulted from a decreased population of the ticks' usual rodent hosts. Vector control activities consisted of spraying the cabins with residual insecticide, removing nesting materials, and "rodent proofing." This outbreak, the largest yet identified in North America, extends the known range of a principal vector and establishes the North Rim as an endemic source of tick-borne relapsing fever. LANGUAGES: Eng TITLE: Tick-borne relapsing fever in the Eastern United States. AUTHORS: Linnemann CC Jr; Barber LC; Dine MS; Body AE SOURCE: Am J Dis Child 1978 Jan;132(1):40-2 CITATION IDS: PMID: 623062 UI: 78100491 ABSTRACT: Tick-borne relapsing fever is endemic in the western part of the United States, but it has not been reported east of the Mississippi River. Sporadic cases have been reported in the eastern part of the United States, but travel to the West during the inubation period appeared to provide the source of infection. In the fall of 1975, a case of relapsing fever was diagnosed in Cincinnati in a child who had not traveled outside of Ohio, indicating the presence of Borrelia in this area. Serial serological studies indicated that B turicatae was the species involved. The occurrence of this case suggests that relapsing fever may exist in the eastern part of the United States, but its presence may not be appreciated because of the rarity of the disease and the difficulty in confirming the diagnosis. LANGUAGES: Eng TITLE: Tick-borne relapsing fever in British Columbia, Canada: first isolation of Borrelia hermsii.A AUTHORS: Banerjee SN; Banerjee M; Fernando K; Burgdorfer W; Schwan TG AUTHOR AFFILIATION: B.C. Centre for Disease Control Society, Vector-Borne Diseases Laboratory, Vancouver, British Columbia V5Z 4R4, Canada. SOURCE: J Clin Microbiol 1998 Dec;36(12):3505-8CITATION IDS: PMID: 9817862 UI: 99036748 ABSTRACT: The spirochete that causes tick-borne relapsing fever, Borrelia hermsii, was isolated in pure culture during 1995 and 1996 from three acutely ill human patients infected in southern British Columbia, Canada. The geographic area of exposure is a known focus of this disease dating back to 1930 when the first case was recognized in a human. ****yses of plasmid DNA, protein profiles, and reactivity with a species-specific monoclonal antibody identified the new isolates of spirochetes as B. hermsii, all of which were most similar to an isolate of this spirochete from northern California described previously. These are the first reported isolates of B. hermsii from Canada.MAIN MESH HEADINGS: Borrelia/*isolation & purification Relapsing Fever/*microbiology ADDITIONAL MESH HEADINGS: Adult Antibodies, Bacterial/blood British Columbia Female Human Male Relapsing Fever/diagnosis PUBLICATION TYPES: JOURNAL ARTICLE CAS REGISTRY NUMBERS: 0 (Antibodies, Bacterial) LANGUAGES: Eng TITLE: Tick-borne relapsing fever in the northwestern United States and southwestern Canada. AUTHORS: Dworkin MS; Anderson DE Jr; Schwan TG; Shoemaker PC; Banerjee SN; Kassen BO; Burgdorfer W AUTHOR AFFILIATION: Section of Communicable Disease Epidemiology, Washington State Department of Health, Seattle, USA. SOURCE: Clin Infect Dis 1998 Jan;26(1):122-31 CITATION IDS: PMID: 9455520 UI: 98116698 ABSTRACT: Records from 182 cases of tick-borne relapsing fever (TBRF) were reviewed. In confirmed cases, there was febrile illness, and spirochetes were identified on peripheral blood preparations. In probable cases, there were clinical features of TBRF and either the same exposure as a confirmed case or serological (indirect fluorescent antibody test and western blotting [WB]) evidence of infection with Borrelia hermisii. Sera also were tested for antibody to Borrelia burgdorferi. We identified 133 confirmed and 49 probable cases of TBRF. A Jarisch-Herxheimer reaction was reported in 33 (54.1%) of 61 cases for which this information was available. Most patients who had antibodies to B. hermsii were serologically positive for B. burgdorferi, and WB demonstrated false positivity of testing for B. burgdorferi. Thirty-five (21%) of 166 cases were unreported to public health authorities. In 52 cases, there were more than two relapses before the diagnosis. This study demonstrates that TBRF is underrecognized and underreported and may be falsely identified as Lyme disease. Lang: Eng. TITLE: Population structure of the relapsing fever spirochete Borrelia hermsii as indicated by polymorphism of two multigene families that encode immunogenic outer surface lipoproteins. AUTHORS: Hinnebusch BJ; Barbour AG; Restrepo BI; Schwan TG AUTHOR AFFILIATION: Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 59840, USA. joe_hinnebusch@nih.gov SOURCE: Infect Immun 1998 Feb;66(2):432-40CITATION IDS: PMID: 9453591 UI: 98114336 ABSTRACT: The tick-borne relapsing fever spirochete Borrelia hermsii evades the mammalian immune system by periodically switching expression among members of two multigene families that encode immunogenic, antigenically distinct outer surface proteins. The type strain, B. hermsii HS1, has at least 40 complete genes and pseudogenes that participate in this multiphasic antigenic variation. Originally termed vmp (for variable major protein) genes, they have been reclassified as vsp (for variable small protein) and vlp (for variable large protein) genes, based on size and amino acid sequence similarities. To date, antigenic variation in B. hermsii has been studied only in the type strain, HS1. Nucleotide sequence comparisons of 23 B. hermsii HS1 genes revealed five distinct groups, the vsp gene family and four subfamilies of vlp genes. We used PCR with family- and subfamily-specific primers, followed by restriction fragment length polymorphism ****ysis, to compare the vsp and vlp repertoires of HS1 and seven other B. hermsii isolates from Washington, Idaho, and California. This ****ysis, together with pulsed-field gel electrophoresis genome profiles, revealed that the eight isolates formed three distinct groups, which likely represent clonal lineages. Members of the three groups coexisted in the same geographic area, but they could also be isolated across large geographical distances. This population structure may result from immune selection by the host, as has been proposed for other pathogens with polymorphic antigens. LANGUAGES: Eng GRANT/CONTRACT ID: AI24424/AI/NIAID TITLE: GlpQ: an antigen for serological discrimination between relapsing fever and Lyme borreliosis. AUTHORS: Schwan TG; Schrumpf ME; Hinnebusch BJ; Anderson DE Jr; Konkel ME AUTHOR AFFILIATION: Laboratory of Microbial Structure and Function, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 59840, USA. SOURCE: J Clin Microbiol 1996 Oct;34(10):2483-92CITATION IDS: PMID: 8880505 UI: 97034849 ABSTRACT: Tick-borne relapsing fever is caused by numerous Borrelia species maintained in nature by Ornithodoros tick-mammal cycles. Serological confirmation is based on either an immunofluorescence assay or an enzyme-linked immunosorbent assay using whole cells or sonicated Borrelia hermsii as the antigen. However, antigenic variability of this bacterium's outer surface proteins and antigens shared with the Lyme disease spirochete (B. burgdorferi), may cause both false-negative and false-positive results when testing sera of patients suspected to have either relapsing fever or Lyme disease. To develop a specific serological test for relapsing fever, we created a genomic DNA library of B. hermsii, screened transformed Escherichia coli cells for immunoreactivity with high-titered (> or = 1:2,048) human anti-B. hermsii antiserum, and selected an immunoreactive clone (pSPR75) expressing a 39-kDa protein. DNA sequencing, subcloning, and serum adsorption experiments identified the immunoreactive protein as a homolog of GlpQ, a glycerophosphodiester phosphodiesterase identified previously in E. coli, Haemophilus influenzae, and Bacillus subtilis. Serum samples from humans and mice infected with B. hermsii or other species of relapsing fever spirochetes contained antibodies recognizing GlpQ, whereas serum samples from Lyme disease and syphilis patients were nonreactive. Serologic tests based on this antigen will identify people exposed previously to relapsing fever spirochetes and help clarify the distribution of relapsing fever and Lyme disease in situations in which the occurrence of their causative agents is uncertain. LANGUAGES: Eng SECONDARY SOURCE ID: GENBANK/U40762 National Library of Medicine: IGM Full Record Screen <Picture: Help><Picture: Log off IGM> <Picture: Next Record><Picture: Return to Results><Picture: Return to Search Screen><Picture: Previous Record> ------------------------------------------------------------------------ ------------------------------------------------------------------------ ------------------------------------------------------------------------ ------------------------------------------------------------------------ TITLE: A new Borrelia species isolated from patients with relapsing fever in Spain [see comments] AUTHORS: Anda P; Sanchez-Yebra W; del Mar Vitutia M; Perez Pastrana E; Rodriguez I; Miller NS; Backenson PB; Benach JL AUTHOR AFFILIATION: Centro Nacional de Microbiologia, Virologia e Inmunologia Sanitarias, Instituto de Salud Carlos III, Madrid, Spain. SOURCE: Lancet 1996 Jul 20;348(9021):162-5 CITATION IDS: PMID: 8684157 UI: 96295298 COMMENT: Comment in: Lancet 1996 Jul 20;348(9021):141-2 Comment in: Lancet 1996 Nov 2;348(9036):1251 ABSTRACT: BACKGROUND: Lyme disease and tick-borne relapsing fever are worldwide systemic borrelioses caused by several Borrelia species transmitted by hard ticks (family Ixodidae) and soft ticks (family Argasidae), respectively. A previous seroepidemiological study of Lyme borreliosis showed several serologically reactive patients with clinically atypical presentations, and this discovery led to the hypothesis that some of the cases of Lyme borreliosis had been caused by another borrelia organism. METHODS: Blood from patients in southern Spain who had suspected Lyme disease or relapsing-fever borreliosis was cultured before treatment began. Isolates of Borrelia spp were inoculated into several strains of mice of different ages. The 16S rRNA and flagellin in genes of Borrelia spp were sequenced by PCR and assessed by phylogenetic ****yses. FINDINGS: We isolated a species of Borrelia from three patients with relapsing fever and from Ornithodorus spp ticks in southern Spain. This organism (refractory to in-vitro cultivation) caused a relapsing spirochaetaemia with multiple organ involvement in laboratory mice that recreated the human disease. Phylogenetic ****ysis showed that this organism is a previously unrecognised species. INTERPRETATION: We have discovered a new borrelia pathogen that is closely related to the other tick-borne agents of relapsing fever in Europe and Africa, and which causes a relapsing systemic disease with serological similarities to Lyme borreliosis. LANGUAGES: Eng GRANT/CONTRACT ID: TITLE: The spirochete Borrelia crocidurae causes erythrocyte rosetting during relapsing fever.A AUTHORS: Burman N; Shamaei-Tousi A; Bergstrom S AUTHOR AFFILIATION: Department of Microbiology, Umea University, Sweden. SOURCE: Infect Immun 1998 Feb;66(2):815-9 CITATION IDS: PMID: 9453646 UI: 98114391 ABSTRACT: Several species of the genus Borrelia exhibit antigenic variation of variable major proteins on their surface during relapsing fever. We have investigated the African relapsing fever species Borrelia crocidurae during infections in mice and compared it with the thoroughly studied North American species Borrelia hermsii. A major difference between the two species is that B. crocidurae can bind and become completely covered with erythrocytes. In addition, B. crocidurae causes a prolonged spirochetemia which coincides with a delayed appearance of antiborrelial antibodies. We show that the antibody response against an unrelated antigen is not delayed and that antibiotic treatment, which dissociates rosettes and inhibits the spirochetes, also leads to an early antibody response. Taken together, the erythrocyte aggregation and prolonged spirochetemia hint at a new mode of immune evasion where erythrocyte-covered spirochetes may avoid contact with the phagocytic cells and B cells of the immune system, thereby delaying the onset of a specific immune response. LANGUAGES: Eng TITLE: Tick-borne relapsing fever in a premature infant. AUTHORS: Brasseur D SOURCE: Ann Trop Paediatr 1985 Sep;5(3):161-2 CITATION IDS: PMID: 2415056 UI: 86049284 ABSTRACT: Relapsing fever is caused by the Borrelia species of spirochetes. Louse- born epidemics of the disease may occur but the endemic disease is usually transmitted to humans by the bite of an infected tick (Ornithodorus). Transplacental infection was suggested more than 75 years ago (1) but has been rarely do***ented (2). We describe a case of neonatal relapsing fever where maternal infection was the probable cause of the premature delivery and infection in the infant. LANGUAGES: Eng National Library of Medicine: IGM Full Record Screen <Picture: Help><Picture: Log off IGM> <Picture: Next Record><Picture: Return to Results><Picture: Return to Search Screen><Picture: Previous Record> ------------------------------------------------------------------------ ------------------------------------------------------------------------ ------------------------------------------------------------------------ ------------------------------------------------------------------------ TITLE: Relapsing fever and its serological discrimination from Lyme borreliosis.AUTHORS: Rath PM; Rogler G; Schonberg A; Pohle HD; Fehrenbach FJAUTHOR AFFILIATION: Abt. fur Medizinische Mikrobiologie, Universitatsklinikum Rudolf Virchow, Germany.SOURCE: Infection 1992 Sep-Oct;20(5):283-6CITATION IDS: PMID: 1385332 UI: 93052805ABSTRACT: Patients with Borrelia-caused relapsing fever produce cross-reacting antibodies to Borrelia burgdorferi, the anti-genetically related causative agent of Lyme borreliosis. The antibody response of the serum of a patient (acute and convalescent) with relapsing fever was ****ysed by the immunoblot technique using Borrelia hermsii and B. burgdorferi as antigens. The diagnosis was established by microscopic detection of spirochetes in the patient's blood. The patient's serum showed significantly elevated titers of IgG and IgM in a B. burgdorferi indirect immunofluorescence assay. Immunoblot ****ysis indicated the presence of cross-reacting antibodies directed to B. burgdorferi antigens with apparent molecular weights of 60, 41, 40, 36, 30 and 20 kDa. LANGUAGES: Eng TITLE: Tick-borne relapsing fever in the Pacific Northwest: an underdiagnosed illness? AUTHORS: Fihn S; Larson EB SOURCE: West J Med 1980 Sep;133(3):203-9 CITATION IDS: PMID: 7415171 UI: 81017090 TITLE: Outbreak of tick-borne relapsing fever in Spokane County, Washington. AUTHORS: Thompson RS, et al. SOURCE: JAMA. 1969 Nov 10;210(6):1045-50. No abstract available. CIT. IDS: PMID: 5394422 UI: 70004012 |
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