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1
Actinobaculum suis detection using polymerase chain reaction.使用聚合酶链反应检测猪放线杆菌。
ScientificWorldJournal. 2012;2012:572732. doi: 10.1100/2012/572732. Epub 2012 Dec 30.
2
Phenotypic, molecular and genomic characterization of Actinobaculum suis isolated from swine in Brazil.从巴西猪群中分离出的猪放线杆菌的表型、分子和基因组特征
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A case report: Actinobaculum suis infection associated with formation of pyogranuloma, epididymitis and azoospermia in a boar.病例报告:一例公猪感染猪放线杆菌并发脓性肉芽肿、附睾炎及无精子症
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Actinobaculum urinale sp. nov., from human urine.尿道放线杆菌新种,源自人类尿液。
Int J Syst Evol Microbiol. 2003 May;53(Pt 3):679-682. doi: 10.1099/ijs.0.02422-0.
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"Actinobaculum massiliae," a new species causing chronic urinary tract infection.“马赛放线杆菌”,一种引起慢性尿路感染的新菌种。
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Actinobaculum schaalii - invasive pathogen or innocent bystander? A retrospective observational study.沙雷氏 Actinobaculum - 侵袭性病原体还是无辜旁观者?一项回顾性观察研究。
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本文引用的文献

1
Actinobaculum schaalii, a common uropathogen in elderly patients, Denmark.沙雷氏不动杆菌,一种常见的老年尿路感染病原体,丹麦。
Emerg Infect Dis. 2010 Jan;16(1):76-80. doi: 10.3201/eid1601.090761.
2
Characterization of some Actinomyces-like isolates from human clinical specimens: reclassification of Actinomyces suis (Soltys and Spratling) as Actinobaculum suis comb. nov. and description of Actinobaculum schaalii sp. nov.从人类临床标本中分离出的一些类放线菌的鉴定:猪放线菌(Soltys和Spratling)重新分类为猪放线杆菌新组合,以及新种 Schaali 放线杆菌的描述
Int J Syst Bacteriol. 1997 Jul;47(3):899-903. doi: 10.1099/00207713-47-3-899.
3
Studies on the prevalence of Eubacterium suis in boars on farms in Brazil, Portugal and Argentina by indirect immunofluorescence technique.
Dtsch Tierarztl Wochenschr. 1993 Dec;100(12):463-4.
4
Isolation of Corynebacterium suis from the prepuce of boars.从公猪包皮中分离出猪棒状杆菌。
J Am Vet Med Assoc. 1983 Aug 15;183(4):428-9.
5
The carriage of Corynebacterium suis in male pigs.雄性猪体内猪棒状杆菌的携带情况。
J Hyg (Lond). 1984 Oct;93(2):381-8. doi: 10.1017/s0022172400064949.
6
[Comparative studies of the detection of Corynebacterium suis infections in swine by indirect immunofluorescence and culture].
Berl Munch Tierarztl Wochenschr. 1990 Aug 1;103(8):273-6.
7
Evaluation of four commercial anaerobic systems for identification of Eubacterium suis.
J Vet Diagn Invest. 1990 Oct;2(4):318-22. doi: 10.1177/104063879000200412.
8
Rapid and simple method for purification of nucleic acids.快速简便的核酸纯化方法。
J Clin Microbiol. 1990 Mar;28(3):495-503. doi: 10.1128/jcm.28.3.495-503.1990.
9
Phylogenetic evidence for the transfer of Eubacterium suis to the genus Actinomyces as Actinomyces suis comb. nov.猪真杆菌转移至放线菌属并命名为猪放线菌(新组合)的系统发育学证据
Int J Syst Bacteriol. 1992 Jan;42(1):161-5. doi: 10.1099/00207713-42-1-161.

使用聚合酶链反应检测猪放线杆菌。

Actinobaculum suis detection using polymerase chain reaction.

作者信息

Amigo Cristina Román, Sena de Gobbi Debora Dirani, Gomes Vasco Túlio de Moura, Perina Danilo do Prado, Nogueira de Lima Filsner Pedro Henrique, Costa Barbara Letícia Pereira, Spindola Maria Garcia, Ferreira Thais Sebastiana Porfida, Brandão Paulo Eduardo, Moreno Andrea Micke

机构信息

Departamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia (FMVZ), Universidade de São Paulo (USP), Avenida Professor Dr. Orlando Marques de Paiva 87 Cidade Universitária, 05508 270 São Paulo, SP, Brazil.

出版信息

ScientificWorldJournal. 2012;2012:572732. doi: 10.1100/2012/572732. Epub 2012 Dec 30.

DOI:10.1100/2012/572732
PMID:23346017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3544261/
Abstract

Actinobaculum suis is an important agent related to urinary infection in swine females. Due to its fastidious growth characteristics, the isolation of this anaerobic bacterium is difficult, thus impairing the estimation of its prevalence. The purpose of this study was to develop and test a polymerase chain reaction (PCR) for the detection and identification of A. suis and then compare these results with traditional isolation methods. Bacterial isolation and PCR were performed on one hundred and ninety-two urine samples from sows and forty-five preputial swabs from boars. The results indicate that this PCR was specific for A. suis, presenting a detection limit between 1.0 × 10(1) CFU/mL and 1.0 × 10(2) CFU/mL. A. suis frequencies, as measured by PCR, were 8.9% (17/192) in sow urine samples and 82.2% (37/45) in preputial swabs. Assessed using conventional culturing techniques, none of the urine samples were positive for A. suis; however, A. suis was detected in 31.1% (14/45) of the swabs. This PCR technique was shown to be an efficient method for the detection of A. suis in urine and preputial swabs.

摘要

猪放线杆菌是与母猪泌尿系统感染相关的一种重要病原体。由于其苛求的生长特性,分离这种厌氧菌很困难,从而影响了对其流行情况的评估。本研究的目的是开发并测试一种用于检测和鉴定猪放线杆菌的聚合酶链反应(PCR),然后将这些结果与传统分离方法进行比较。对来自母猪的192份尿液样本和来自公猪的45份包皮拭子进行了细菌分离和PCR检测。结果表明,该PCR对猪放线杆菌具有特异性,检测限在1.0×10¹ CFU/mL至1.0×10² CFU/mL之间。通过PCR检测,母猪尿液样本中猪放线杆菌的检出率为8.9%(17/192),包皮拭子中为82.2%(37/45)。采用传统培养技术评估,尿液样本中均未检测到猪放线杆菌阳性;然而,在31.1%(14/45)的拭子中检测到了猪放线杆菌。该PCR技术被证明是检测尿液和包皮拭子中猪放线杆菌的有效方法。