Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80026-5
Dorothee Imhoff, Gisela Schallehn
Four bacteriophages of Clostridum novyi type A (PFö, P5771, PA1350e and P19402) were examined. The phages were spontaneously released to the culture medium in titers of 106 to 108 pfu/ml at the end of the bacterial growth of the donor strain. The phage titer could be increased to 109 to 1012 pfu/ml by growing the phages in the culture of the indicator strain C. novyi 5771/HS10. These high titered phage suspensions were used for morphological studies and for the production of anti-phage-sera. The phages of C. novyi were unstable and lost most of their infectivity within 24 h. Lyophilizing the phages in glutamate medium seemed to be one possible way of partially stabilizing these phages. Phages PFö, P5771, PA1350e and P19402 were similar in morphology and size, in antigenic pattern and in plaque morphology. Phage PA1350e was stabile only at pH 7 and below 40 °C for a short time. It was inactivated at 50 °C within 20 min, at 55 °C and at 60 °C in 4 min.
{"title":"Zur Charakterisierung von Bakteriophagen von Clostridium novyi Typ A","authors":"Dorothee Imhoff, Gisela Schallehn","doi":"10.1016/S0172-5599(80)80026-5","DOIUrl":"10.1016/S0172-5599(80)80026-5","url":null,"abstract":"<div><p>Four bacteriophages of <em>Clostridum novyi</em> type A (PFö, P5771, PA1350e and P19402) were examined. The phages were spontaneously released to the culture medium in titers of 10<sup>6</sup> to 10<sup>8</sup> pfu/ml at the end of the bacterial growth of the donor strain. The phage titer could be increased to 10<sup>9</sup> to 10<sup>12</sup> pfu/ml by growing the phages in the culture of the indicator strain <em>C. novyi</em> 5771/HS10. These high titered phage suspensions were used for morphological studies and for the production of anti-phage-sera. The phages of <em>C. novyi</em> were unstable and lost most of their infectivity within 24 h. Lyophilizing the phages in glutamate medium seemed to be one possible way of partially stabilizing these phages. Phages PFö, P5771, PA1350e and P19402 were similar in morphology and size, in antigenic pattern and in plaque morphology. Phage PA1350e was stabile only at pH 7 and below 40 °C for a short time. It was inactivated at 50 °C within 20 min, at 55 °C and at 60 °C in 4 min.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 101-113"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80026-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82862595","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80014-9
Gabriele Döller , Josef Jakubik
A direct solid-phase radioimmunoassay (dRIA) was developed in order to demonstrate antibodies against Aujeszky's disease virus (ADV) in sera obtained from pigs and rabbits. In the presence of guinea-pig complement the above test is 160-fold to 1500-fold more sensitive than the neutralization test (NT) and 320-fold to 150000-fold more sensitive than NT without complement. By means of dRIA ADV antibodies could be detected in swine sera obtained from an ADV-infected farm, which were found to be negative in the complement assisted NT. It is possible to test a single dilution of unknown serum by dRIA by comparing same with a standard curve and to make a statement regarding its ADV-specific binding capacity to 125I-labelled ADV antigen.
The advantages of dRIA in comparison to the indirect RIA and the advantages and disadvantages with regard to ELISA were discussed.
{"title":"Direkter Festphasen-Radioimmunoassay zum Nachweis von Aujeszkyvirus-Antikörpern","authors":"Gabriele Döller , Josef Jakubik","doi":"10.1016/S0172-5599(80)80014-9","DOIUrl":"10.1016/S0172-5599(80)80014-9","url":null,"abstract":"<div><p>A direct solid-phase radioimmunoassay (dRIA) was developed in order to demonstrate antibodies against Aujeszky's disease virus (ADV) in sera obtained from pigs and rabbits. In the presence of guinea-pig complement the above test is 160-fold to 1500-fold more sensitive than the neutralization test (NT) and 320-fold to 150000-fold more sensitive than NT without complement. By means of dRIA ADV antibodies could be detected in swine sera obtained from an ADV-infected farm, which were found to be negative in the complement assisted NT. It is possible to test a single dilution of unknown serum by dRIA by comparing same with a standard curve and to make a statement regarding its ADV-specific binding capacity to <sup>125</sup>I-labelled ADV antigen.</p><p>The advantages of dRIA in comparison to the indirect RIA and the advantages and disadvantages with regard to ELISA were discussed.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 1-7"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80014-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91437489","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80021-6
D. Veljanov , Al. Rutkov , T. Radoutcheva , D. Harbov , E. Golovinsky
The changes induced in strains of Pseudomonas pseudomallei and Salmonella typhimuriumunder the action of D.L-ureidosuccinic acid dihydrazide were characterized. A decrease of the speed of multiplication in vitro and of the oxygen consumption was established.The virulence of the strains was reduced and their susceptibility to phagocytosis in vitro was increased.
Es werden die unter dem Einfluß von D,L-Ureidobernsteinsäuredihydrazin aufgetretenen Veränderungen in Pseudomonas pseudomallei- und Salmonella typhimurium-Stämmen charakterisiert, wobei eine verringerte Vermehrungsrate in vitro und ein Rückgang des Sauerstoffverbrauches festgestellt wurde. Die Virulenz der Stämme nahm ab, während sich ihre Phagozytoseempfindlichkeit in vitro verstärkte.
{"title":"Influence of D,L-Ureidosuccinic Acid Dihydrazide on Some Biological Properties of Pseudomonas pseudomallei and of Salmonella typhimurium","authors":"D. Veljanov , Al. Rutkov , T. Radoutcheva , D. Harbov , E. Golovinsky","doi":"10.1016/S0172-5599(80)80021-6","DOIUrl":"10.1016/S0172-5599(80)80021-6","url":null,"abstract":"<div><p>The changes induced in strains of <em>Pseudomonas pseudomallei</em> and <em>Salmonella typhimurium</em>under the action of D.L-ureidosuccinic acid dihydrazide were characterized. A decrease of the speed of multiplication in vitro and of the oxygen consumption was established.The virulence of the strains was reduced and their susceptibility to phagocytosis in vitro was increased.</p></div><div><p>Es werden die unter dem Einfluß von D,L-Ureidobernsteinsäuredihydrazin aufgetretenen Veränderungen in <em>Pseudomonas pseudomallei</em>- und <em>Salmonella typhimurium</em>-Stämmen charakterisiert, wobei eine verringerte Vermehrungsrate <em>in vitro</em> und ein Rückgang des Sauerstoffverbrauches festgestellt wurde. Die Virulenz der Stämme nahm ab, während sich ihre Phagozytoseempfindlichkeit <em>in vitro</em> verstärkte.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 64-70"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80021-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18049759","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80022-8
K. Özsan , F. MercangÖz
The new media are recommended for the isolation of cholera vibrios. The medium for Vibrio El Tor contains only starch, gelatin polymyxin B and natrium chloride and has no nutrient or inhibitor substances such as peptone, meat extract, yeast extract, blood, natrium taurocholate and bile salts. The medium for Vibrio cholerae contains starch, gelatin, natrium taurocholate and potassium tellurite, but has no peptone, meat extract, yeast extract or polymyxin B.
{"title":"New Media for the Isolation of Vibrio cholerae","authors":"K. Özsan , F. MercangÖz","doi":"10.1016/S0172-5599(80)80022-8","DOIUrl":"10.1016/S0172-5599(80)80022-8","url":null,"abstract":"<div><p>The new media are recommended for the isolation of cholera vibrios. The medium for <em>Vibrio El Tor</em> contains only starch, gelatin polymyxin B and natrium chloride and has no nutrient or inhibitor substances such as peptone, meat extract, yeast extract, blood, natrium taurocholate and bile salts. The medium for <em>Vibrio cholerae</em> contains starch, gelatin, natrium taurocholate and potassium tellurite, but has no peptone, meat extract, yeast extract or polymyxin B.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 71-73"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80022-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18444112","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80015-0
Doris StüNzner , Werner Thiel, Franz Pötsch, Wolf Sixl
In the course of a study which was made in order to contribute to the knowledge about influenza viruses in birds, 18 strains of avian Influenza-A-subtypes were isolated from cloaca swabs.
From the Central European bird species, one strain of Influenza A/England/62 was isolated from a mallard.
All other species of birds obtained from three different biotopes from Austria and Hungary showed negative results.
The other 17 influenza strains were isolated from imported birds from Senegal.
Nine of these strains corresponded to subtype A/duck/England/62, five to subtype duck/ England/56. One isolated strain showed a relation to A/duck/England/56 in terms of the hemagglutinin and to chicken/Brescia/1902 in terms of the neuraminidase. Two other strains reacted best with antisera against duck/England/62 in the hemagglutination inhibition test; the neuraminidase inhibition test showed a relation to subtype quail/Italy/65. The Newcastle disease-Virus was not isolated in any sample.
In einem Beitrag zum Studium der aviären Influenza-Viren wurden Vögel aus Österreich (Biotop Schützen am Gebirge, Mörbisch und Apetlon am Neusiedlersee, den Murauen bei Graz) und Jagdwild aus Ungarn untersucht. Die Virusisolierung von einem Stamm Influenza A/duck/England/62 gelang von einer Stockente (Anas platyrhynchos).
Weiters wurden Importe von exotischen Vögeln aus Senegal und Argentinien auf die Anwesenheit von Influenzaviren untersucht. Dabei konnten 17 Stämme isoliert werden. Es handelt sich dabei um 10 Stämme verwandt mit Influenza A/duck/England/62, viermal wurden Stämme gefunden, die verwandt sind mit Influenza A/duck/England/56. Ein Isolat war hinsichtlich des Hämagglutinins verwandt mit duck/England/56 und bezüglich der Neuraminidase reagierte es am besten mit Antisera gegen chicken/Brescia/1902.
Zwei weitere Stämme reagierten im Hämagglutinationshemmtest am besten mit Antisera gegen duck/England/62 aber die Neuraminidase reagierte am besten mit Antisera gegen quail/Italy/65.
Insgesamt wurden also 18 aviäre Influenzastämme aus 700 Vögeln isoliert: New castle disease konnte in keinem Fall isoliert werden.
在一项旨在增进对鸟类流感病毒的认识的研究中,从泄殖腔拭子中分离出18种禽流感a亚型毒株。从中欧鸟类中,从一只野鸭中分离出一株甲型流感病毒/英格兰/62。从奥地利和匈牙利三个不同的生物群落中获得的所有其他鸟类都显示阴性结果。另外17个流感毒株是从塞内加尔输入的禽鸟中分离出来的。其中9株属于A/duck/England/62亚型,5株属于鸭/England/ 56亚型。一株分离菌株在血凝素方面与a/ duck/England/56有关,在神经氨酸酶方面与鸡/Brescia/1902有关。另外2株对鸭/英格兰/62抗血清的血凝抑制效果最好;神经氨酸酶抑制试验显示与鹌鹑/Italy/65亚型有关。新城疫病毒未从任何样本中分离出来。In einem Beitrag zum Studium der aviären Influenza-Viren wurden Vögel aus Österreich (Biotop sch, Mörbisch und Apetlon am Neusiedlersee, den Murauen bei Graz)和Jagdwild aus Ungarn untersucht。Die Virusisolierung von einem Stamm Influenza A/duck/England/62 gelang von einer Stockente (Anas platyrhynchos)。weites wurden import von exotischen Vögeln aus塞内加尔和阿根廷的auites auweden Anwesenheit von Influenzaviren untersut。大北康宁17 Stämme isoliert werden。Es handelt sich dabei um 10 Stämme verwandt mit Influenza A/duck/England/62, vimal wurden Stämme gefunden, die verwandt sind mit Influenza A/duck/England/56。Ein Isolat war hinsichtlich des Hämagglutinins verwandt mit duck/England/56 und bez glich der Neuraminidase reagerte es am besten mit Antisera gegen chicken/布雷西亚/1902。Zwei weitere Stämme reagierten im Hämagglutinationshemmtest am besten mit Antisera gegen duck/英国/62 aber die Neuraminidase reagierte am besten mit Antisera gegen鹌鹑/意大利/65。Insgesamt wurden也18 aviäre Influenzastämme aus 700 Vögeln isoliert: New castle disease konte in keinem Fall isoliert werden。
{"title":"Isolation of Influenza Viruses from Exotic and Central European Birds","authors":"Doris StüNzner , Werner Thiel, Franz Pötsch, Wolf Sixl","doi":"10.1016/S0172-5599(80)80015-0","DOIUrl":"10.1016/S0172-5599(80)80015-0","url":null,"abstract":"<div><p>In the course of a study which was made in order to contribute to the knowledge about influenza viruses in birds, 18 strains of avian Influenza-A-subtypes were isolated from cloaca swabs.</p><p>From the Central European bird species, one strain of Influenza A/England/62 was isolated from a mallard.</p><p>All other species of birds obtained from three different biotopes from Austria and Hungary showed negative results.</p><p>The other 17 influenza strains were isolated from imported birds from Senegal.</p><p>Nine of these strains corresponded to subtype A/duck/England/62, five to subtype duck/ England/56. One isolated strain showed a relation to A/duck/England/56 in terms of the hemagglutinin and to chicken/Brescia/1902 in terms of the neuraminidase. Two other strains reacted best with antisera against duck/England/62 in the hemagglutination inhibition test; the neuraminidase inhibition test showed a relation to subtype quail/Italy/65. The Newcastle disease-Virus was not isolated in any sample.</p></div><div><p>In einem Beitrag zum Studium der aviären Influenza-Viren wurden Vögel aus Österreich (Biotop Schützen am Gebirge, Mörbisch und Apetlon am Neusiedlersee, den Murauen bei Graz) und Jagdwild aus Ungarn untersucht. Die Virusisolierung von einem Stamm Influenza A/duck/England/62 gelang von einer Stockente (<em>Anas platyrhynchos</em>).</p><p>Weiters wurden Importe von exotischen Vögeln aus Senegal und Argentinien auf die Anwesenheit von Influenzaviren untersucht. Dabei konnten 17 Stämme isoliert werden. Es handelt sich dabei um 10 Stämme verwandt mit Influenza A/duck/England/62, viermal wurden Stämme gefunden, die verwandt sind mit Influenza A/duck/England/56. Ein Isolat war hinsichtlich des Hämagglutinins verwandt mit duck/England/56 und bezüglich der Neuraminidase reagierte es am besten mit Antisera gegen chicken/Brescia/1902.</p><p>Zwei weitere Stämme reagierten im Hämagglutinationshemmtest am besten mit Antisera gegen duck/England/62 aber die Neuraminidase reagierte am besten mit Antisera gegen quail/Italy/65.</p><p>Insgesamt wurden also 18 aviäre Influenzastämme aus 700 Vögeln isoliert: New castle disease konnte in keinem Fall isoliert werden.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 8-17"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80015-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18444113","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80019-8
D.N. Garg , D.N. Bhargava, V.K. Sharma
A biotyping scheme has been described which is based on the biochemical behaviour of S. weltevreden strains towards 5 substrates (sorbitol, dextrin, malonate, rhamnose, starch). The 228 S. weltevreden strains examined were grouped into 25 of the 32 theoretical biotypes. Frequently occurring biotypes were: biotype 10 (16.2%), biotype 5 (13.4%) and biotype 11 (11.4%). No substantial correlation could be established between biotypes and source or geographic distribution of S. weltevreden. Sero-fermentative-phage types were computed for 145 strains, phage-types of which has been described earlier and five predominant sero-fermentative-phage types emerged. The sero-fermentative-phage type 3,10:r: z6;5;1 (serotype = 3, 10:r:z6; biotype = 5; phagetype = 1) occurred most commonly with a frequency of 10.3%. The strains belonging to this pattern were from lizard, guinea-pig and humans in India, Netherlands and United States of America.
Es wird ein Schema zur Ermittlung des Biotyps beschrieben, das auf dem biochemischen Verhalten von S. weltevreden-Stämmen gegenüber 5 Substraten (Sorbit, Dextrin, Malonat, Rhamnose, Stärke) basiert. Die 228 untersuchten Stämme von S. weltevreden wurden 25 von 32 theoretisch möglichen Biotypen zugeordnet. Die häufig auftretenden Biotypen waren 10 (16,2%), 5 (13,4%) und 11 (11,4%). Es ließ sich keine substantielle Korrelation zwischen den Biotypen und der Herkunft oder geographischen Verteilung von S. weltevreden herstellen. Die Sero-, Gärungs- und Lysotypen wurden bei 145 Stämmen berechnet, deren Lysotypen bereits vorher beschrieben worden waren; dabei stellte sich heraus, daß 5 Sero-, Gärungs- und Lysotypen vorherrschten. Der Sero-, Gärungs- und Lysotyp 3,10:r:z6;5;l (Serotyp = 3, 10:r:z6; Biotyp = 5; Lysotyp = 1) war mit einer Häufigkeit von 10,3% am weitesten verbeitet. Die diesem Schema entsprechenden Stämme stammten von Eidechsen, Meerschweinchen und vom Menschen in Indien, den Niederlanden und den USA.
根据S. weltevreden菌株对5种底物(山梨醇、糊精、丙二酸盐、鼠李糖、淀粉)的生化行为,描述了一种生物分型方案。228株weltevreden菌株被分为32种理论生物型中的25种。常见的生物型为生物10型(16.2%)、生物5型(13.4%)和生物11型(11.4%)。该菌的生物型与来源或地理分布没有明显的相关性。计算了145株菌株的血清发酵噬菌体类型,这些噬菌体类型已经被描述过,并出现了5种主要的血清发酵噬菌体类型。血清型为3,10:r: z6;5;1(血清型= 3,10:r: z6;生物型= 5;Phagetype = 1)最常见,发生率为10.3%。属于这一模式的菌株来自印度、荷兰和美利坚合众国的蜥蜴、豚鼠和人类。[endnoter.com] [endnoter.com] [endnoter.com] [endnoter.com] [endnoter.com] [endnoter.com] [endnoter.com] [endnoter.com]。]Die 228 untersuchten Stämme von S. weltevreden wurden 25 von 32 theortisch möglichen Biotypen zugeordnet。Die häufig auftretenden Biotypen waren 10(16.2%), 5(13.4%)和11(11.4%)。[2][1][2][2][1][2][1][2][1][2][1][2][1][3]。Die Sero-, Gärungs- and Lysotypen wurden bei 145 Stämmen berechnet, deren Lysotypen bereits vorher beschrieben worden waren;大北星型星型星型星型星型星型星型星型星型星型星型星型星型星型星型星型星型星型星型。Der Sero-, Gärungs-和lysotype 3,10:r:z6;5; 1 (serotype = 3,10:r:z6;biotype = 5;lysotype = 1) war mit iner Häufigkeit von 10.3% am weitesten verbetet。Die diesem Schema entsprechenden Stämme stammten von Eidechsen, Meerschweinchen和vom Menschen在印度,荷兰和美国。
{"title":"The Sero-fermentative-phage Types of Salmonella weltevreden","authors":"D.N. Garg , D.N. Bhargava, V.K. Sharma","doi":"10.1016/S0172-5599(80)80019-8","DOIUrl":"10.1016/S0172-5599(80)80019-8","url":null,"abstract":"<div><p>A biotyping scheme has been described which is based on the biochemical behaviour of <em>S. weltevreden</em> strains towards 5 substrates (sorbitol, dextrin, malonate, rhamnose, starch). The 228 <em>S. weltevreden</em> strains examined were grouped into 25 of the 32 theoretical biotypes. Frequently occurring biotypes were: biotype 10 (16.2%), biotype 5 (13.4%) and biotype 11 (11.4%). No substantial correlation could be established between biotypes and source or geographic distribution of <em>S. weltevreden</em>. Sero-fermentative-phage types were computed for 145 strains, phage-types of which has been described earlier and five predominant sero-fermentative-phage types emerged. The sero-fermentative-phage type 3,10:r: z6;5;1 (serotype = 3, 10:r:z6; biotype = 5; phagetype = 1) occurred most commonly with a frequency of 10.3%. The strains belonging to this pattern were from lizard, guinea-pig and humans in India, Netherlands and United States of America.</p></div><div><p>Es wird ein Schema zur Ermittlung des Biotyps beschrieben, das auf dem biochemischen Verhalten von <em>S. weltevreden</em>-Stämmen gegenüber 5 Substraten (Sorbit, Dextrin, Malonat, Rhamnose, Stärke) basiert. Die 228 untersuchten Stämme von <em>S. weltevreden</em> wurden 25 von 32 theoretisch möglichen Biotypen zugeordnet. Die häufig auftretenden Biotypen waren 10 (16,2%), 5 (13,4%) und 11 (11,4%). Es ließ sich keine substantielle Korrelation zwischen den Biotypen und der Herkunft oder geographischen Verteilung von <em>S. weltevreden</em> herstellen. Die Sero-, Gärungs- und Lysotypen wurden bei 145 Stämmen berechnet, deren Lysotypen bereits vorher beschrieben worden waren; dabei stellte sich heraus, daß 5 Sero-, Gärungs- und Lysotypen vorherrschten. Der Sero-, Gärungs- und Lysotyp 3,10:r:z6;5;l (Serotyp = 3, 10:r:z6; Biotyp = 5; Lysotyp = 1) war mit einer Häufigkeit von 10,3% am weitesten verbeitet. Die diesem Schema entsprechenden Stämme stammten von Eidechsen, Meerschweinchen und vom Menschen in Indien, den Niederlanden und den USA.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 43-49"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80019-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18444111","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80029-0
N. Dickgiesser , E. Pieringer
In a clinical routine study 304 yeasts were examined with the aid of API 20 C Auxanogram (Analytab Products Inc.), Mycotube (Roche) and Bacto-Candida-albicans-Antiserum (Difco) (=CAA). API (in parenthesis the result of the Mycotube test) identified 99% (92.4%) correctly; without considering C. albicans, the result was correct in 96.5% (75.8%). The CAA indicated a high specificity against C. albicans.
For the Routine Laboratory we recommend screening of all yeasts with the CAA; an additional morphological examination is also recommended as cross-reactions with C. tropicalis and Torulopsis species are found. The non-agglutinating yeasts can then be further examined with the API 20 C.
In einer Studie wurden im Routinelabor 304 Sproßpilze mit dem neuen API 20 C Auxanogramm (Analytab Products Inc.), dem Mycotube (Roche) und dem Bacto-Candida-albicans-Antiserum ( = CAA) (Difco) untersucht. API 20 C (in Klammern Ergebnisse des Mycotube) differenzierte 99% (92,4%) der Sproßpilze korrekt, wenn man C. albicans nicht berücksichtigt, traf das Ergebnis in 96,5% (75,8%) der Fälle zu. Das CAA zeichnete sich durch hohe Spezifität gegenüber C. albicans aus.
Für das Routinelabor wird empfohlen, ein Screening aller Hefen und hefeähnlichen Pilze mit dem CAA vorzunehmen; man muß dabei berücksichtigen, daß Kreuzreaktionen mit C. tropicalis und T. glabrata möglich sind, so daß auch eine morphologische Beurteilung zu empfehlen ist. Die mit dem CAA nicht agglutinierenden Pilze sollten mit dem API 20 C untersucht werden.
在一项临床常规研究中,用API 20c Auxanogram (Analytab Products Inc.)、Mycotube (Roche)和bact - candida -albicans- anti - serum (Difco) (=CAA)对304株酵母菌进行了检测。API(括号中为Mycotube检测结果)正确率99% (92.4%);不考虑白色念珠菌的结果正确率为96.5%(75.8%)。CAA对白色念珠菌具有高特异性。对于常规实验室,我们建议用CAA筛选所有酵母;当发现与热带C.和Torulopsis种交叉反应时,还建议进行额外的形态学检查。非凝集酵母可用API 20c进一步检测。在iner study wurden in routinelabine 304 spproß pilze mitdem neuen API 20c auxanogram (Analytab Products Inc.)、dem Mycotube (Roche)和dem Bacto-Candida-albicans-Antiserum (= CAA) (Difco)等实验中,使用API 20c auxanogram (Analytab Products Inc.)检测。API 20 C(在Klammern Ergebnisse des Mycotube中)与sppros ßpilze korrekt差异99%(92,4%),与白色念珠菌nicht (cksichtigt)差异95,5%(75,8%)与Fälle zu差异。Das CAA zeichnete sich ch hoh Spezifität gegene ber白色念珠菌。作者:dr . das routinelabichen, in Screening aller Hefen and hefeähnlichen Pilze mit of CAA vorzunmen;man musß dabei bercksictigen, dasß Kreuzreaktionen mit C. tropical alis and T. glabrata möglich sind, so dasß auch eine morphologche Beurteilung zu empenlen ist。在此基础上,研究了聚乳酸乳酸酶(CAA)夜间凝集剂和聚乳酸乳酸酶(API) 20c固化剂。
{"title":"Suitability of the Modified API 20 C, Mycotube and Bacto-Candida-albicans-Antiserum for the Identification of Yeasts in the Routine Laboratory","authors":"N. Dickgiesser , E. Pieringer","doi":"10.1016/S0172-5599(80)80029-0","DOIUrl":"10.1016/S0172-5599(80)80029-0","url":null,"abstract":"<div><p>In a clinical routine study 304 yeasts were examined with the aid of API 20 C Auxanogram (Analytab Products Inc.), Mycotube (Roche) and Bacto-Candida-albicans-Antiserum (Difco) (=CAA). API (in parenthesis the result of the Mycotube test) identified 99% (92.4%) correctly; without considering <em>C. albicans</em>, the result was correct in 96.5% (75.8%). The CAA indicated a high specificity against <em>C. albicans</em>.</p><p>For the Routine Laboratory we recommend screening of all yeasts with the CAA; an additional morphological examination is also recommended as cross-reactions with <em>C. tropicalis</em> and Torulopsis species are found. The non-agglutinating yeasts can then be further examined with the API 20 C.</p></div><div><p>In einer Studie wurden im Routinelabor 304 Sproßpilze mit dem neuen API 20 C Auxanogramm (Analytab Products Inc.), dem Mycotube (Roche) und dem Bacto-Candida-albicans-Antiserum ( = CAA) (Difco) untersucht. API 20 C (in Klammern Ergebnisse des Mycotube) differenzierte 99% (92,4%) der Sproßpilze korrekt, wenn man <em>C. albicans</em> nicht berücksichtigt, traf das Ergebnis in 96,5% (75,8%) der Fälle zu. Das CAA zeichnete sich durch hohe Spezifität gegenüber <em>C. albicans</em> aus.</p><p>Für das Routinelabor wird empfohlen, ein Screening aller Hefen und hefeähnlichen Pilze mit dem CAA vorzunehmen; man muß dabei berücksichtigen, daß Kreuzreaktionen mit <em>C. tropicalis</em> und <em>T. glabrata</em> möglich sind, so daß auch eine morphologische Beurteilung zu empfehlen ist. Die mit dem CAA nicht agglutinierenden Pilze sollten mit dem API 20 C untersucht werden.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 132-137"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80029-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18049754","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80027-7
Arno SchÖnberg , Eulógio Moreira Caldas , Marilena B. Sampaio , Everáldo Costa , Stephen J. Plank
In the State of Bahia (Brazil) the leptospirin produced in Germany for experimental use by the Institute for Veterinary Medicine, Federal Health Office, Berlin, was administered to humans and animals in order to diagnose leptospirosis in collaboration with this Institute. The results were compared with the microscopic agglutination reaction. The total number of test persons or animals was 268; this group included 81 human patients, 60 heads of cattle, 50 goats, 40 pigs, 25 horses, and 12 dogs. All were tested serologically and simultaneously the intracutaneous test was carried out. This test was positive when the erythema formed had a diameter of more than 9 mm. The evaluation took place 8 to 10 h and 24 h after the injection of leptospirin.
1.
52 humans reacted serologically; out of this group 44 were positive in the leptospirin test. The allergy test was also negative in the 29 serologically negative patients.
2.
Out of the 21 heads of cattle with a positive agglutination test 7 reacted to leptospirin whereas 39 animals which did not react serologically were also negative in the skin test.
3.
Although 10 goats out of 50 reacted serologically, all were negative in the intracutaneous test.
4.
9 out of 40 pigs reacted serologically; however, 8 reacted only to apathogenic leptospires (L. patoc, L. rufino, L.andamana). Out of these 9 animals 4 were positive in the intracutaneous test; among them the pig which reacted serologically to L. autumnalis. Out of 31 serologically negative pigs 2 were allergologically positive.
5.
Out of 21 serologically positive horses 15 exhibited an erythema which was considered positive in the skin test. 4 serologically negative animals also were negative in the intracutaneous test.
6.
Out of 6 serologically positive dogs, 4 reacted to leptospirin. 6 that had not reacted serologically were all negative in the intracutaneous test.
A comparison of the serological and allergological findings judged by the serological standard showed that out of all cases tested, 0.7% had at the same time a serologically negative and allergologically positive reaction and 16.8% had a serologically positive and allergologically negative reaction.
In some cases, the administration of leptospirin caused the formation of antibodies which could only be detected in low dilutions and usually disappeared after 6–8 weeks.
In humans, pigs, and horses the leptospirin also showed positive reactions which serologically could be attributed only to biflexa leptospires. Serotypes not contained in the leptospirin were accounted for to a varying degree in the individual animal species. These reactions and the results of other studies carried out in pig stocks have
在巴伊亚州(巴西),与柏林联邦卫生局兽医研究所合作,将德国生产的钩端螺旋体素用于人类和动物,以诊断钩端螺旋体病。结果与显微凝集反应进行了比较。试验人或动物总数268只;这一组包括81名人类患者、60头牛、50头山羊、40头猪、25匹马和12只狗。所有患者均进行血清学检测,同时进行皮内试验。当形成的红斑直径大于9毫米时,该试验呈阳性。评估分别在注射钩端螺旋体素后8 ~ 10 h和24 h进行。其中44例钩端螺旋体试验呈阳性。29例血清学阴性患者过敏试验均为阴性。在凝集试验呈阳性的21头牛中,有7头对钩端螺旋体有反应,而血清学上没有反应的39头牛在皮肤试验中也呈阴性。50只山羊中有10只血清学反应,但皮内试验均为阴性,40只猪中有4.9只血清学反应;8只对致病性钩体(L. patoc, L. rufino, L.andamana)起反应。9只动物中4只皮内试验呈阳性;其中秋乳杆菌血清学反应的猪。31头血清学阴性猪中2头过敏反应阳性。在21匹血清学阳性的马中,15匹在皮肤试验中表现出红斑,被认为是阳性的。4只血清学阴性动物皮内试验也均为阴性。在6只血清学阳性的狗中,4只对钩端螺旋菌素有反应。6例血清学无反应者皮内试验均为阴性。血清学标准判定的血清学和过敏学结果比较显示,在所有检测病例中,同时出现血清学阴性和过敏学阳性反应的占0.7%,同时出现血清学阳性和过敏学阴性反应的占16.8%。在某些情况下,给药钩端螺旋体引起抗体的形成,抗体只能在低稀释时检测到,通常在6-8周后消失。在人、猪和马中,钩端螺旋体也显示阳性反应,血清学上只能归因于双钩端螺旋体。钩端螺旋体中不含的血清型在个别动物物种中有不同程度的解释。这些反应和在猪群中进行的其他研究的结果是兽医研究所进行研究的基础。这些研究预计将有助于提高钩端螺旋体的敏感性。
{"title":"Leptospirin — An Intradermic Test for the Diagnosis of Leptospirosis","authors":"Arno SchÖnberg , Eulógio Moreira Caldas , Marilena B. Sampaio , Everáldo Costa , Stephen J. Plank","doi":"10.1016/S0172-5599(80)80027-7","DOIUrl":"10.1016/S0172-5599(80)80027-7","url":null,"abstract":"<div><p>In the State of Bahia (Brazil) the leptospirin produced in Germany for experimental use by the Institute for Veterinary Medicine, Federal Health Office, Berlin, was administered to humans and animals in order to diagnose leptospirosis in collaboration with this Institute. The results were compared with the microscopic agglutination reaction. The total number of test persons or animals was 268; this group included 81 human patients, 60 heads of cattle, 50 goats, 40 pigs, 25 horses, and 12 dogs. All were tested serologically and simultaneously the intracutaneous test was carried out. This test was positive when the erythema formed had a diameter of more than 9 mm. The evaluation took place 8 to 10 h and 24 h after the injection of leptospirin.</p><p></p><ul><li><span>1.</span><span><p>52 humans reacted serologically; out of this group 44 were positive in the leptospirin test. The allergy test was also negative in the 29 serologically negative patients.</p></span></li><li><span>2.</span><span><p>Out of the 21 heads of cattle with a positive agglutination test 7 reacted to leptospirin whereas 39 animals which did not react serologically were also negative in the skin test.</p></span></li><li><span>3.</span><span><p>Although 10 goats out of 50 reacted serologically, all were negative in the intracutaneous test.</p></span></li><li><span>4.</span><span><p>9 out of 40 pigs reacted serologically; however, 8 reacted only to apathogenic leptospires (<em>L. patoc, L. rufino, L.andamana</em>). Out of these 9 animals 4 were positive in the intracutaneous test; among them the pig which reacted serologically to <em>L. autumnalis</em>. Out of 31 serologically negative pigs 2 were allergologically positive.</p></span></li><li><span>5.</span><span><p>Out of 21 serologically positive horses 15 exhibited an erythema which was considered positive in the skin test. 4 serologically negative animals also were negative in the intracutaneous test.</p></span></li><li><span>6.</span><span><p>Out of 6 serologically positive dogs, 4 reacted to leptospirin. 6 that had not reacted serologically were all negative in the intracutaneous test.</p></span></li></ul><p>A comparison of the serological and allergological findings judged by the serological standard showed that out of all cases tested, 0.7% had at the same time a serologically negative and allergologically positive reaction and 16.8% had a serologically positive and allergologically negative reaction.</p><p>In some cases, the administration of leptospirin caused the formation of antibodies which could only be detected in low dilutions and usually disappeared after 6–8 weeks.</p><p>In humans, pigs, and horses the leptospirin also showed positive reactions which serologically could be attributed only to biflexa leptospires. Serotypes not contained in the leptospirin were accounted for to a varying degree in the individual animal species. These reactions and the results of other studies carried out in pig stocks have ","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 114-123"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80027-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18444110","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80023-X
Ridha Bergaoui , Ilbert Vervaeke
Counting of bacteria, detection of urease-positive bacteria and estimation of bacterial ureolysis influenced by Bacitracin and Flavomycin was done on intestinal contents from different segments of the digestive tract of laying hens.
It was concluded that :
-
the intestinal flora was numerically most important in the caecum and was composed principally of lactobacilli in the crop, gizzard, duodenum, jejunum and ileum, and of lactobacilli and anaerobes in the caecum and colon.
-
17% of the total number of intestinal bacteria were urease-positive.
-
the ureolytic activity was most important in the caecum: 24 mg of urea hydrolysed/g of contents during 4 hours of incubation. The range is between 2 and 4 mg in the other segments.
-
until the level of 500 ppm, Bacitracin and Flavomycin did not influence the in vitro ureolytic activity of fecal and cecal material.
{"title":"L'activité uréasique de la flore du tractus digestif de la pondeuse, effet de la Bacitracine et de la Flavomycine","authors":"Ridha Bergaoui , Ilbert Vervaeke","doi":"10.1016/S0172-5599(80)80023-X","DOIUrl":"10.1016/S0172-5599(80)80023-X","url":null,"abstract":"<div><p>Counting of bacteria, detection of urease-positive bacteria and estimation of bacterial ureolysis influenced by Bacitracin and Flavomycin was done on intestinal contents from different segments of the digestive tract of laying hens.</p><p>It was concluded that :</p><ul><li><span>-</span><span><p>the intestinal flora was numerically most important in the caecum and was composed principally of lactobacilli in the crop, gizzard, duodenum, jejunum and ileum, and of lactobacilli and anaerobes in the caecum and colon.</p></span></li><li><span>-</span><span><p>17% of the total number of intestinal bacteria were urease-positive.</p></span></li><li><span>-</span><span><p>the ureolytic activity was most important in the caecum: 24 mg of urea hydrolysed/g of contents during 4 hours of incubation. The range is between 2 and 4 mg in the other segments.</p></span></li><li><span>-</span><span><p>until the level of 500 ppm, Bacitracin and Flavomycin did not influence the <em>in vitro</em> ureolytic activity of fecal and cecal material.</p></span></li></ul></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 74-83"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80023-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78474240","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}
Pub Date : 1980-06-01DOI: 10.1016/S0172-5599(80)80018-6
Wolfgang Nimmich , Günter Naumann, Eckhard Budde, Eberhard Straube
E. coli rough strains (as determined by spontaneous agglutination of in boiled saline suspension) isolated in significant amounts (> 105/ml) from patients with urinary tract infections were investigated for some factors possibly related to virulence. The frequencies of capsular antigen, colonization factor antigen (CFA I), dulcitol fermentation, and hemolysin production are summarized in table 1.
270 (66.2%) out of 408 strains were found to be encapsulated as determined by the inagglutinability of the living strains in saline. 180 (44.1%) strains were able to ferment dulcitol, and evidence for hemolysin production could be demonstrated in 146 (35.8%) strains. The CFA I (demonstrated by a mannose resistant hemagglutination of human red blood cells) was detected in 62 (15.2%) of the E. coli rough strains tested. The frequency of single properties in the presence or absence of capsular antigen is shown in table 2 demonstrating no significant differences in both groups.
The most frequent single factor was found to be the capsular antigen with 22.1%, followed by the double combination capsular antigen/dulcitol fermentation (16.7%), dulcitol fermentation alone (10%), and capsular antigen/hemolysin production (9.8%). There were only 5 strains possessing all four factors tested. On the other hand we found 35 (8.6%) rough strains with none of the properties. Some aspects of virulence of E. coli rough strains are discussed.
{"title":"K-Antigen, Adhärenzfaktor, Dulcitol-Abbau und Hämolysin-Bildung bei E. coli-R-Stämmen aus Urin","authors":"Wolfgang Nimmich , Günter Naumann, Eckhard Budde, Eberhard Straube","doi":"10.1016/S0172-5599(80)80018-6","DOIUrl":"10.1016/S0172-5599(80)80018-6","url":null,"abstract":"<div><p><em>E. coli</em> rough strains (as determined by spontaneous agglutination of in boiled saline suspension) isolated in significant amounts (> 10<sup>5</sup>/ml) from patients with urinary tract infections were investigated for some factors possibly related to virulence. The frequencies of capsular antigen, colonization factor antigen (CFA I), dulcitol fermentation, and hemolysin production are summarized in table 1.</p><p>270 (66.2%) out of 408 strains were found to be encapsulated as determined by the inagglutinability of the living strains in saline. 180 (44.1%) strains were able to ferment dulcitol, and evidence for hemolysin production could be demonstrated in 146 (35.8%) strains. The CFA I (demonstrated by a mannose resistant hemagglutination of human red blood cells) was detected in 62 (15.2%) of the <em>E. coli</em> rough strains tested. The frequency of single properties in the presence or absence of capsular antigen is shown in table 2 demonstrating no significant differences in both groups.</p><p>The most frequent single factor was found to be the capsular antigen with 22.1%, followed by the double combination capsular antigen/dulcitol fermentation (16.7%), dulcitol fermentation alone (10%), and capsular antigen/hemolysin production (9.8%). There were only 5 strains possessing all four factors tested. On the other hand we found 35 (8.6%) rough strains with none of the properties. Some aspects of virulence of <em>E. coli</em> rough strains are discussed.</p></div>","PeriodicalId":101293,"journal":{"name":"Zentralblatt für Bakteriologie. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie","volume":"247 1","pages":"Pages 35-42"},"PeriodicalIF":0.0,"publicationDate":"1980-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0172-5599(80)80018-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85219957","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}