Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie最新文献

{"title":"Ergebnisse der Lysotypie von Salmonella typhi und Salmonella paratyphi-B in den Jahren 1974–1978, erhoben in der Bundesrepublik Deutschland und Berlin (West)","authors":"H. Brandis ,&nbsp;V. Lenk,&nbsp;F. Würsching,&nbsp;U. Polanetzki,&nbsp;I. Böhlck","doi":"10.1016/S0172-5599(80)80051-4","DOIUrl":"10.1016/S0172-5599(80)80051-4","url":null,"abstract":"<div><p>In the period between 1.1.1974 and 31.12.1978 phage typing of 2058 strains of <em>S. typhi</em> and 1672 strains of <em>S. paratyphi-B</em> was carried out. <em>45 S. typhi</em> phage types were found, 11 of these occurred in a frequency of more than 1% (relevant to foci). These were E1a (21.6%), A (17.7%), F1 (5.8%), D1 (5.5%), C1 (4.6%), E1b (4.1%), D2 (2.5%), 40 (1.5%), 28 (1.3%), B2 (1.0%), 46 (1.0%). Among <em>S. paratyphi-B</em> strains 23 phage types or varieties were observed, 11 of these occurred in a frequency more than 1% (relevant to foci): Taunton (46.9%), 1 m.c. (7.8%), 3aI m.c. (7.7%), B.A.O.R. (6.5%), 3aI var. 1 (5.5%), Dundee (4.4%), 3a m.c. (3.0%), 3b m.c. (2.2%), Beccles m.c. (1.9%), Jersey (1.5%), 1 var. 1 (1.4%). In the year 1974 two epidemics of typhoid fever occurred, one with 417 cases (phage type A, subtype Tananarive) and the other with 41 cases (phage type E1a). In the year 1977 there was an outbreak of paratyphoid B fever with 53 cases (phage type 3aI var. 1). The increasing number of imported cases of typhoid and paratyphoid fever from other countries is remarkable. The age distribution of typhoid and paratyphoid bacilli carriers shows that persons who are older than 60 years represent the age group in which carriers occur most frequently.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 4","pages":"Pages 440-459"},"PeriodicalIF":0.0,"publicationDate":"1980-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80051-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88303712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Postoperative Herzinfektion mit M. fortuitum","authors":"K.H. Schröder ,&nbsp;H.H. Schassan","doi":"10.1016/S0172-5599(80)80062-9","DOIUrl":"10.1016/S0172-5599(80)80062-9","url":null,"abstract":"<div><p>Shortly after an open-heart operation a 5 year-old girl died of an infection caused by <em>M. fortuitum</em>. Strains of this species are often isolated from human specimens, but generally they are not correlated with pulmonary tuberculosis. Nevertheless <em>M. fortuitum</em> produces relatively often infections after transplantations of different kind. The diagnosis is difficult to find, especially because nobody thinks of the possibility that a rapid growing mycobacterium is able to cause such infections. — The therapy is very problematical. That is why these infections are not seldom fatal.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 4","pages":"Pages 557-562"},"PeriodicalIF":0.0,"publicationDate":"1980-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80062-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90470952","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Notable Aspergillus from a Mortal Aspergilloma of the Lung New Aspects of the Epidemiology, Serodiagnosis and Taxonomy of Aspergillus fumigatus","authors":"F. Staib ,&nbsp;S.K. Mishra ,&nbsp;C. Rajendran ,&nbsp;R. Voigt ,&nbsp;J. Steffen ,&nbsp;K.H. Neumann ,&nbsp;C.A. Hartmann ,&nbsp;G. Heins","doi":"10.1016/S0172-5599(80)80059-9","DOIUrl":"10.1016/S0172-5599(80)80059-9","url":null,"abstract":"<div><p>Different basic mycological observations were made in relation to a fatal case of aspergilloma of the lung in a 45-year-old male. Cultural examination of the sputum and autopsy material from the lung revealed the predominant presence of a white fungus along with a scarce growth of the typical <em>Aspergillus fumigatus</em>. The white isolate produced conidial heads almost similar to that of <em>A. fumigatus</em> but with apparent septation in the phialides.</p><p>With the help of the immunodiffusion test and use of the antigens from the typical <em>A. fumigatus</em> strain and from the white isolate, antibodies could be detected in the serum of this patient and an antigenetic relationship between these fungi could be observed.</p><p>It is assumed that this white isolate is a variant of <em>A. fumigatus</em> and its presence in the lung is an indication of chronic or progressed aspergillosis caused by <em>A. fumigatus</em></p><p>Cultural characteristics and developmental morphology of this fungus and the serodiagnostic value of the antigen derived from it will be described in detail in separate communications.</p></div><div><p>Im Zusammenhang mit einem tödlich verlaufenen Lungenaspergillom bei einem 45 Jahre alt gewordenen Mann wurden verschiedenartige mykologische Beobachtungen gemacht. Bei der kulturellen Untersuchung von Sputumproben konnte überwiegend ein weiß wachsender Pilz neben nur vereinzelten Kolonien eines typischen <em>Aspergillus fumigatus</em> angezüchtet werden. Post mortem gelang vom Fungusball des Aspergilloms nur die Anzucht des weiß wachsenden Pilzes. Die Konidienköpfe dieses Pilzes ähnelten denen von <em>A. fumigatus</em>, zeigten aber eine auffällige Septierung der Phialiden.</p><p>Mit Hilfe des Immundiffusionstests konnten im Serum des Patienten unter Verwendung von Antigen des weißen Isolats und von Antigen eines typischen <em>A. fumigatus-Stammes</em> Antikörper nachgewiesen und eine Antigen-Verwandtschaft dieser beiden Pilze festgestellt werden. Es wird vermutet, daß dieses weiße Isolat ein Variant von <em>A. fumigatus</em> ist und sein Vorkommen als Hinweis auf eine chronische oder fortgeschrittene Aspergillose durch <em>A. fumigatus</em> zu werten ist.</p><p>Über die kulturellen und morphologischen Eigenschaften dieses Pilzes und den diagnostischen Wert seines Antigens soll an anderer Stelle ausführlich berichtet werden.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 4","pages":"Pages 530-536"},"PeriodicalIF":0.0,"publicationDate":"1980-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80059-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74432223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Reactivity of Isolated Lipopolysaccharides of Enterobacterial R Mutants with Complete or Incomplete Core Structures with Lectins","authors":"N. Mushtaq Ahamed ,&nbsp;Joanna Radziejewska-Lebrecht ,&nbsp;Christiane Widemann ,&nbsp;Hubert Mayer *","doi":"10.1016/S0172-5599(80)80053-8","DOIUrl":"10.1016/S0172-5599(80)80053-8","url":null,"abstract":"<div><p>Alkali-treated lipopolysaccharides of a range of enterobacterial R mutants with complete and incomplete core structures were investigated by agar gel and microcapillary precipitation onto their reactivity with three selected commerical lectins, namely Concanavalin A, Ricinus communis agglutinin and Wheat germ agglutinin.</p><p>R lipopolysaccharides with complete R cores of the six so far established core types were differentiable from each other by their characteristic lectin reactivity pattern. One core type showed no reaction with all the three lectins.</p><p>R lipopolysaccharides with incomplete core structures showed in general the reactivity pattern predictable from their individual chemical configuration. It was further shown that substitution of complete R cores by haptens (T1, T2 or ECA) or by a single repeating unit (SR mutant) did not change the reactivity pattern, although some interactions were less pronounced.</p><p>It will be demonstrated that lectin precipitation can be of help for structural studies in recognizing, for example, terminal sugar units and their anomeric linkages.</p></div><div><p>Alkali-behandelte Lipopolysaccharide einer Reihe enterobakterieller R-Mutanten mit kompletten oder inkompletten Core-Strukturen wurden mittels Agar- und Mikrokapillar- Präzipitation auf ihre Reaktivität mit drei ausgewählten käuflichen Lektinen untersucht, nämlich mit Concanavalin A, Ricinus communis- und Weizenkeim-Agglutinin.</p><p>R-Lipopolysaccharide mit kompletten Core-Strukturen aller sechs bis jetzt bekannten Core-Typen waren aufgrund ihrer charakteristischen Präzipitationsmuster voneinander differenzierbar, wobei ein Core-Typ mit keinem der Lektine reagierte.</p><p>R-Lipopolysaccharide mit inkompletten Core-Strukturen zeigten im allgemeinen die Präzipitationsmuster, die aus den vorgeschlagenen Strukturen zu erwarten waren. Eine Substitution kompletter Core-Strukturen mit Haptenen (T1, T2, ECA) oder mit einer einzelnen O-spezifischen Wiederholungseinheit (SR-Mutante) ändert das Reaktionsmuster nicht, einige Präzipitationen sind jedoch weniger stark ausgeprägt.</p><p>Es wird gezeigt, daß die Reaktivität mit Lektinen für Struktur-chemische Fragen herangezogen werden kann, beispielsweise zur Ermittlung terminal-ständiger Zucker und deren anomerer Bindung.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 4","pages":"Pages 468-482"},"PeriodicalIF":0.0,"publicationDate":"1980-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80053-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82240901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Humoral and Cellular Immune Response in Mice After Infection with Salmonella typhimurium","authors":"Andreas Sziegoleit","doi":"10.1016/S0172-5599(80)80052-6","DOIUrl":"10.1016/S0172-5599(80)80052-6","url":null,"abstract":"<div><p>NMRI mice were infected orally with <em>S. typhimurium</em>. Specific antibody titers determined by indirect hemagglutination, and cellular immune response tested by blastogenesis transformation of lymphocytes and enhanced bactericidal action on <em>Listeria monocytogenes</em> were studied in relation to persistence of bacteria up to one year after the infection. About three weeks after the infection cell mediated immune reactions were no longer detected and in the course of a year detection of serum antibodies often failed despite persistence of <em>Salmonella</em>.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 4","pages":"Pages 460-467"},"PeriodicalIF":0.0,"publicationDate":"1980-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80052-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79399924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Adherence of Group A Streptococci to Epithelial Cells in Tissue Culture","authors":"Kornelia B. Grabovskaya ,&nbsp;A.A. Totoljan ,&nbsp;M. Rýc ,&nbsp;J. Havlíček ,&nbsp;Larissa A. Bürova ,&nbsp;Ruth Bícová","doi":"10.1016/S0172-5599(80)80034-4","DOIUrl":"10.1016/S0172-5599(80)80034-4","url":null,"abstract":"<div><p>Using the HEp-2 cell line system the factors and mechanisms of group A Streptococcus adherence had been studied.</p><p>It was shown that high adherence was chiefly found in strains showing attributes of virulence (presence of M protein, growth in human blood, lethality for mice). The data supplied by experiments with pepsin and LTA suggest that there exist at least two mechanisms of adherence.</p></div><div><p>Streptokokken der Gruppe A heften sich an HEp-2 Zellkulturen an. Diese Epithelzellen können zwischen virulenten (M⁺) und avirulenten (M^-) Streptokokkenstämmen unterscheiden. Nach 30 min Inkubation sind an 24–51% der HEp-2 Zellen M⁺-Streptokokken adhärent (mit 3 bis 6 Kokken je Zelle). Die Verlängerung der Inkubationszeit führt zur Erhöhung der Zahl infizierter Zellen auf 90–100%, teilweise mit Mikrokoloniebildung in disen Zellen. Unter gleichen Versuchsbedingungen infizieren M^--Stämme weniger als 28% der HEp-2 Zellen und der Adhärenzindex liegt bei 1–2 Kokken je Zelle. Mit steigender Suspensionsdichte der Bakterien nehmen die Adhärenzparameter zu und die Unterschiede zwischen M⁺ und M^--Varianten werden früher nachweisbar.</p><p>Eine Vorbebrütung der M⁺-Streptokokkenstämme mit EDTA führt — im Gegensatz zu den M^--Stämmen — zu einer deutlichen Verminderung der Adhärenz. Die Adhärenz der M⁺-Stämme wird auch durch Trypsin vermindert, wobei das Enzym die Zellwände vollkommen von den filamentösen Protrusionen befreit. Eine Vorbehandlung der Zellen mit Pepsin, wobei das M-Protein entfernt wird, nicht aber die Filamente, führt dagegen nur bei einigen Stämmen zu einer verminderten Adhärenz. Die Behandlung der HEp-2 Zellen mit Lipoteichonsäure blockiert gleichfalls die Adhärenz mit quantitativen stammabhängigen Unterschieden. Die Analyse der Unterschiede in den Adhärenzparametern mehrerer Streptokokkenstämme läßt den Schluß zu, daß wenigstens zwei Zellwandkomponenten an der Adhärenz der Streptokokkenzellen an HEp-2 Zellen beteiligt sind: das M-Protein und Lipoteichonsäure.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 3","pages":"Pages 303-314"},"PeriodicalIF":0.0,"publicationDate":"1980-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80034-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79482333","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Identifizierung von Enterobakterien mit MICRO-ID®, einem nicht automatisierten Vier-Stunden-System","authors":"Wolfgang Peuckert ,&nbsp;Klaus Pelz","doi":"10.1016/S0172-5599(80)80036-8","DOIUrl":"10.1016/S0172-5599(80)80036-8","url":null,"abstract":"<div><p>Micro-ID®, a new kit system for rapid identification of Enterobacteriaceae, was compared with a conventional media-system, the extended Enterotube® system (completed with arabinose, rhamnose and the Voges-Proskauer reaction), and partially with the API-20E® system. When the computer generated Identification Manual for Micro-ID was consulted the system showed complete agreement at the genus level, but differed in 5% at the species level. Problems arose from misidentifications by nonfermenting organisms. 15 turbid blood cultures with gramnegative rods were tested additionally. In 11 cases the Micro-ID provided correct identification of the species and in further 3 cases of the genus.</p><p>In summary Micro-ID is easy to handle and an accurate, convenient kit for the short-term identification of Enterobacteriaceae.</p><p>Zusammenfassung</p><p>Micro-ID® ist ein Vier-Stunden-System zur schnellen Identifizierung von Enterobakterien. 215 Enterobakterienstämme, isoliert aus klinischem Untersuchungsmaterial, wurden mit dem Micro-ID-System (MID), der konventionellen „Bunten Reihe“, dem um drei Reaktionen erweiterten Enterotube® und zum Teil mit API-20E® identifiziert. Zusätzlich wurden 15 positive Blutkulturen nach Anfertigen eines Grampräparates und ohne Subkultur direkt mit Micro-ID untersucht. Bei den 215 Stämmen ergaben sich für MID hinsichtlich der Gattungsdiagnose eine vollständige Übereinstimmung mit den konventionellen Systemen und bei der Speziesdiagnose eine Abweichung von 5%, wenn das computererstellte Identifizierungs-Handbuch benutzt wurde. Die Direktbeimpfung aus den Blutkulturen ergab 14 mal Übereinstimmung in der Gattungs- und 11 mal in der Speziesdiagnose.</p><p>Auf Fehlbestimmungen durch nichtfermentierende gramnegative Stäbchen mußte geachtet werden. MID erwies sich als leicht zu handhabendes, mit konventionellen Verfahren gut vergleichbares und zeitlich ausgesprochen günstiges Identifizierungs-System für Enterobakterien.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 3","pages":"Pages 323-332"},"PeriodicalIF":0.0,"publicationDate":"1980-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80036-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77089257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Serodiagnosis of Human Leptospirosis by Enzyme-Linked-Immunosorbent-Assay (ELISA)","authors":"Wiepko J. Terpstra ,&nbsp;Geertruida S. Ligthart,&nbsp;Gerard J. Schoone","doi":"10.1016/S0172-5599(80)80045-9","DOIUrl":"https://doi.org/10.1016/S0172-5599(80)80045-9","url":null,"abstract":"<div><p>An enzyme-linked-immunosorbent-assay (ELISA) is described for the serodiagnosis of leptospirosis. Using an antigen prepared from a heated culture of a single leptospira strain (Wijnberg) the ELISA is a genusspecific test. The microscopic agglutination test (MAT) served as a reference. ELISA and MAT results agreed in 95% of the sera from 96 leptospirosis patients. One false positive was found in 217 controls. The ELISA is sensitive, specific and relatively easy to perform.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 3","pages":"Pages 400-405"},"PeriodicalIF":0.0,"publicationDate":"1980-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80045-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91765080","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Response of Developing Branched Bacteria to Adverse Environments","authors":"Romano Locci (Director:Prof.Dr.)","doi":"10.1016/S0172-5599(80)80042-3","DOIUrl":"10.1016/S0172-5599(80)80042-3","url":null,"abstract":"<div><p>An early symptom of lysozyme treatment of developing actinomycete microcolonies is hyphal tip swelling, illustrating the plasticity of this region in relation to filament extension. The reaction is not limited to true mycelia of <em>Streptomyces, Streptoverticillium</em> and <em>Rhodococcus</em> but is also characteristic of unbranched filaments of actinomycetes exposed during their elongation stage. On the other hand rods whose extension has ceased and which are undergoing fragmentation do not show any localized weakness but a generalized lysis. Results are discussed with reference to polarity of growth in actinomycetes.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 3","pages":"Pages 374-382"},"PeriodicalIF":0.0,"publicationDate":"1980-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80042-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87415617","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ein einwandfreier Nachweis der urogenitalen Myiasis in Mitteleuropa, verursacht von der Fleischfliege Thyrsocnema incisilobata (Pandellé, 1896) (Diptera, Sarcophagidae)","authors":"L. Pospíšil, D. Povolný","doi":"10.1016/S0172-5599(80)80048-4","DOIUrl":"https://doi.org/10.1016/S0172-5599(80)80048-4","url":null,"abstract":"","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"3 1","pages":"418-423"},"PeriodicalIF":0.0,"publicationDate":"1980-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91059210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}