scholarly journals Bovine Bacillus anthracis in Cameroon

2011 ◽  
Vol 77 (16) ◽  
pp. 5818-5821 ◽  
Author(s):  
Paola Pilo ◽  
Alexandra Rossano ◽  
Hamadou Bamamga ◽  
Souley Abdoulkadiri ◽  
Vincent Perreten ◽  
...  

ABSTRACTBovineBacillus anthracisisolates from Cameroon were genetically characterized. They showed a strong homogeneity, and they belong, together with strains from Chad, to cluster Aβ, which appears to be predominant in western Africa. However, one strain that belongs to a newly defined clade (D) and cluster (D1) is penicillin resistant and shows certain phenotypes typical ofBacillus cereus.

2013 ◽  
Vol 79 (12) ◽  
pp. 3860-3863 ◽  
Author(s):  
Jinshui Zheng ◽  
Donghai Peng ◽  
Xiaoling Song ◽  
Lifang Ruan ◽  
Jacques Mahillon ◽  
...  

ABSTRACTcsaBgene analysis clustered 198 strains ofBacillus anthracis,Bacillus cereus, andBacillus thuringiensisinto two groups related to mammalian and insect hosts, respectively. Mammal-related group I strains also have more S-layer homology (SLH) protein genes than group II strains. This indicates thatcsaB-based differentiation reflects selective pressure from animal hosts.


2017 ◽  
Vol 5 (16) ◽  
Author(s):  
Angela Pena-Gonzalez ◽  
Chung K. Marston ◽  
Luis M. Rodriguez-R ◽  
Cari B. Kolton ◽  
Julia Garcia-Diaz ◽  
...  

ABSTRACT We present the genome sequence of Bacillus cereus LA2007, a strain isolated in 2007 from a fatal pneumonia case in Louisiana. Sequence-based genome analysis revealed that LA2007 carries a plasmid highly similar to Bacillus anthracis pXO1, including the genes responsible for the production and regulation of anthrax toxin.


2020 ◽  
Vol 59 (1) ◽  
pp. e02358-20
Author(s):  
Jianchun Wei ◽  
Huijuan Zhang ◽  
Huifang Zhang ◽  
Enmin Zhang ◽  
Binghua Zhang ◽  
...  

ABSTRACTThe objective of this study was to construct a rapid, high-throughput, and biosafety-compatible screening method for Bacillus anthracis and Bacillus cereus based on matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS). MALDI-TOF MS coupled to ClinProTools was used to discover MALDI-TOF MS biomarker peaks and generate a classification model based on a genetic algorithm (GA) to differentiate between different Bacillus anthracis and Bacillus cereus isolates. Thirty Bacillus anthracis and 19 Bacillus cereus strains were used to construct and analyze the model, and 40 Bacillus strains were used for validation. For the GA screening model, the cross-validation values, which reflect the ability of the model to handle variability among the test spectra, and the recognition capability values, which reflect the model’s ability to correctly identify its component spectra, were all 100%. This model contained 10 biomarker peaks (m/z 3,339.9, 3,396.3, 3,682.4, 5,476.7, 6,610.6, 6,680.1, 7,365.3, 7,792.4, 9,475.8, and 10,934.1) used to correctly identify 28 Bacillus anthracis and 12 Bacillus cereus isolates from 40 Bacillus isolates, with a sensitivity and specificity of 100%. With the obvious advantages of being rapid, highly accurate, and highly sensitive and having a low cost and high throughput, MALDI-TOF MS ClinProTools is a powerful and reliable tool for screening Bacillus anthracis and Bacillus cereus strains.


2012 ◽  
Vol 78 (8) ◽  
pp. 3025-3027 ◽  
Author(s):  
Feliza A. Bourguet ◽  
Brian E. Souza ◽  
Angela K. Hinz ◽  
Matthew A. Coleman ◽  
Paul J. Jackson

ABSTRACTLytic proteins encoded by bacterial genomes have been implicated in cell wall biosynthesis and recycling. TheBacillus cereusE33LampDgene encodes a putativeN-acetylmuramoyl-l-alanine amidase. This gene, expressedin vitro, produced a very stable, highly active lytic protein. Very low concentrations rapidly and efficiently lyse vegetativeBacillus anthraciscells.


2019 ◽  
Vol 85 (9) ◽  
Author(s):  
Raymond Schuch ◽  
Adam J. Pelzek ◽  
Daniel C. Nelson ◽  
Vincent A. Fischetti

ABSTRACT Lytic bacteriophages (or phages) drive bacterial mortality by elaborating exquisite abilities to bind, breach, and destroy bacterial cell membranes and subjugate critical bacterial cell functions. These antimicrobial activities make phages ideal candidates to serve as, or provide sources of, biological control measures for bacterial pathogens. In this study, we isolated the Myoviridae phage vB_BanS_Bcp1 (here referred to as Bcp1) from landfill soil, using a Bacillus anthracis host. The antimicrobial activities of both Bcp1 and its encoded endolysin, PlyB, were examined across different B. cereus sensu lato group species, including B. cereus sensu stricto, Bacillus thuringiensis, and Bacillus anthracis, with pathogenic potential in humans and multiple different uses in biotechnological applications. The Bcp1 phage infected only a subset (11 to 66%) of each B. cereus sensu lato species group tested. In contrast, functional analysis of purified PlyB revealed a potent bacteriolytic activity against all B. cereus sensu lato isolates tested (n = 79). PlyB was, furthermore, active across broad temperature, pH, and salt ranges, refractory to the development of resistance, bactericidal as a single agent, and synergistic with a second endolysin, PlyG. To confirm the potential for PlyB as an antimicrobial agent, we demonstrated the efficacy of a single intravenous treatment with PlyB alone or combination with PlyG in a murine model of lethal B. anthracis infection. Overall, our findings show exciting potential for the Bcp1 bacteriophage and the PlyB endolysin as potential new additions to the antimicrobial armamentarium. IMPORTANCE Organisms of the Bacillus cereus sensu lato lineage are ubiquitous in the environment and are responsible for toxin-mediated infections ranging from severe food poisoning (B. cereus sensu stricto) to anthrax (Bacillus anthracis). The increasing incidence of many of these infections, combined with the specter of antibiotic resistance, has created a need for novel antimicrobials with potent activity, including bacteriophages (or phages) and phage-encoded products (i.e., endolysins). In this study, we describe a broadly infective phage, Bcp1, and its encoded endolysin, PlyB, which exhibited a rapidly bacteriolytic effect against all B. cereus sensu lato isolates tested with no evidence of evolving resistance. Importantly, PlyB was highly efficacious in a mouse model of lethal bacteremia with B. anthracis. Both the Bcp1 phage and the PlyB endolysin represent novel mechanisms of action compared to antibiotics, with potential applications to address the evolving problem of antimicrobial resistance.


2020 ◽  
Vol 9 (47) ◽  
Author(s):  
Leonid M. Irenge ◽  
Bertrand Bearzatto ◽  
Jérôme Ambroise ◽  
Jean-Luc Gala

ABSTRACT We report here the complete genome sequence of a Bacillus cereus isolate identified in a soil sample from Namibia. This isolate is closely related to the B. anthracis clade. While the plasmids (500 and 12 kb) carry no detectable B. anthracis virulence gene, the large plasmid shares a 50-kb continuous region similar to plasmid pXO1.


2017 ◽  
Vol 5 (20) ◽  
Author(s):  
Mohamed Seghir Daas ◽  
Albert Remus R. Rosana ◽  
Jeella Z. Acedo ◽  
Farida Nateche ◽  
Salima Kebbouche-Gana ◽  
...  

ABSTRACT Two strains of Bacillus, B. cereus E41 and B. anthracis F34, were isolated from a salt lake in Aïn M’lila-Oum El Bouaghi, eastern Algeria, and Ain Baida-Ouargla, southern Algeria, respectively. Their genomes display genes for the production of several bioactive secondary metabolites, including polyhydroxyalkanoate, iron siderophores, lipopeptides, and bacteriocins.


mSystems ◽  
2018 ◽  
Vol 3 (5) ◽  
Author(s):  
Yoshikazu Furuta ◽  
Hayato Harima ◽  
Emiko Ito ◽  
Fumito Maruyama ◽  
Naomi Ohnishi ◽  
...  

ABSTRACTBacillus anthracisis a Gram-positive endospore-forming bacterial species that causes anthrax in both humans and animals. In Zambia, anthrax cases are frequently reported in both livestock and wildlife, with occasional transmission to humans, causing serious public health problems in the country. To understand the genetic diversity ofB. anthracisstrains in Zambia, we sequenced and compared the genomic DNA ofB. anthracisstrains isolated across the country. Single nucleotide polymorphisms clustered these strains into three groups. Genome sequence comparisons revealed a large deletion in strains belonging to one of the groups, possibly due to unequal crossing over between a pair of rRNA operons. The deleted genomic region included genes conferring resistance to bacitracin, and the strains with the deletion were confirmed with loss of bacitracin resistance. Similar deletions between rRNA operons were also observed in a fewB. anthracisstrains phylogenetically distant from Zambian strains. The structure of bacitracin resistance genes flanked by rRNA operons was conserved only in members of theBacillus cereusgroup. The diversity and genomic characteristics ofB. anthracisstrains determined in this study would help in the development of genetic markers and treatment of anthrax in Zambia.IMPORTANCEAnthrax is caused byBacillus anthracis, an endospore-forming soil bacterium. The genetic diversity ofB. anthracisis known to be low compared with that ofBacillusspecies. In this study, we performed whole-genome sequencing of Zambian isolates ofB. anthracisto understand the genetic diversity between closely related strains. Comparison of genomic sequences revealed that closely related strains were separated into three groups based on single nucleotide polymorphisms distributed throughout the genome. A large genomic deletion was detected in the region containing a bacitracin resistance gene cluster flanked by rRNA operons, resulting in the loss of bacitracin resistance. The structure of the deleted region, which was also conserved among species of theBacillus cereusgroup, has the potential for both deletion and amplification and thus might be enabling the species to flexibly control the level of bacitracin resistance for adaptive evolution.


2017 ◽  
Vol 5 (32) ◽  
Author(s):  
Kasthuri Venkateswaran ◽  
Aleksandra Checinska Sielaff ◽  
Shashikala Ratnayake ◽  
Robert K. Pope ◽  
Thomas E. Blank ◽  
...  

ABSTRACT The draft genome sequences of six Bacillus strains, isolated from the International Space Station and belonging to the Bacillus anthracis-B. cereus-B. thuringiensis group, are presented here. These strains were isolated from the Japanese Experiment Module (one strain), U.S. Harmony Node 2 (three strains), and Russian Segment Zvezda Module (two strains).


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