scholarly journals Occurrence and expression of bacterial human virulence gene homologues in natural soil bacteria

2014 ◽  
pp. n/a-n/a ◽  
Author(s):  
Ditte A. Søborg ◽  
Niels Bohse Hendriksen ◽  
Niels Kroer
2019 ◽  
Vol 11 (4) ◽  
pp. 364
Author(s):  
Marcos Gino Fernandes ◽  
Renata Pires de Araújo ◽  
Eduardo Neves Costa ◽  
Ana Claudia Terumi Abe Zangirolymo ◽  
Rodrigo Matheus Pereira

The first record of transgenic cotton cultivation in Brazil was in 2005, of that of the cultivar MON 531, possessing the cry1Ac gene. Since then, no evaluation has been performed to understand whether the cultivation of Bt cotton has caused any interference with the soil microbiota, including bacteria. In this context, our research was aimed to assess whether the cultivation of Bt cotton negatively affects the community of soil bacteria, through quantitative and metagenomic analyses (marker gene 16S rRNA) for phylum identification. Samples of bacterial populations obtained from the soil cultivated with Bt cotton expressing the Cry1Ac toxin were compared with soil samples from the area cultivated with conventional cotton. Significant differences were not observed in the measure of colony-forming units of bacteria between the soils cultivated with Bt and non-Bt cotton; however, differences were detected only when comparing samples from different collection times of the Bt treatment. Cultivation of Bt cotton did not affect the diversity of the soil bacterial population. Overall, our study shows that, similar to most of the works that have been reported worldwide, cultivation of transgenic cotton does not seem to affect the quantity and diversity of natural soil bacteria.


2021 ◽  
Author(s):  
Manami Kato ◽  
Shumpei Asamizu ◽  
Hiroyasu Onaka

Abstract Co-culture is an efficient strategy for natural product discovery. We have used mycolic acid-containing bacteria (MACB) Tsukamurella pumonis TP-B0596 to induce secondary metabolism by actinomycetes and have found several natural products. We also observed that MACB attached to the mycelium of Streptomyces lividans forming coaggregates during combined-culture. This stimulated interest in the interactions among actinomycetes and MACB, and we found that soil isolated cultures contained a mixture of actinomycetes and MACB. Our previously observed interactions were the result of selective screening and combination of bacteria in the lab, which warranted investigation of the existence of these interactions in the natural soil environment. Therefore, in this paper, we report the interaction between a co-isolated natural pair of actinomycetes and MACB in terms of morphology and metabolic changes. A natural pair of actinomycetes and MACB co-aggregated in liquid culture and showed metabolic changes. Interestingly, co-aggregated actinomycetes and MACB were re-isolated from soil with no obvious morphological colony differences from the colony of a single strain. The results demonstrate that there is a stochastic chance of picking colonies containing co-aggregated actinomycetes and MACB, which suggests that the pair can exist in co-aggregate form in the soil environment and interact with each other.


2010 ◽  
Vol 56 (5) ◽  
pp. 716-724 ◽  
Author(s):  
Shintaro HARA ◽  
Yasuyuki HASHIDOKO ◽  
Roman V. DESYATKIN ◽  
Tomoaki MORISHITA ◽  
Ryusuke HATANO

1985 ◽  
Vol 31 (12) ◽  
pp. 1157-1163 ◽  
Author(s):  
Jeffrey J. Byrd ◽  
Lawrence R. Zeph ◽  
L. E. Casida Jr.

Agromyces ramosus occurs in high numbers in many soils. It also is a known predator of various gram-positive and gram-negative soil bacteria, including Azotobacter vinelandii. Based on this, it would seem that, in natural soil, A. ramosus should control the population sizes of these soil bacteria. As a partial test of this assumption, we examined the possibility that soil might contain other bacterial predators that could hold A. ramosus in check. Three gram-negative bacterial predators of A. ramosus were isolated from soil. When one of these predators, strain N-1, was added to natural soil, it exhibited an attack – counter attack phenomenon in its interactions with A. ramosus. The indigenous A. ramosus cells in soil, or added A. ramosus cells, produced mycelium that approached, then lysed, approximately one-third of the N-1 cells. The surviving N-1 cells, however, then proceeded to lyse the A. ramosus mycelium, but not the rod-form cells that had fragmented from the mycelium. Strain N-1 then multiplied. This sequence also occurred if Azotobacter vinelandii was added with A. ramosus to soil, either with or without addition of N-1 cells. N-1 attacked the A. ramosus mycelium that was attacking Azotobacter vinelandii. In soil and with pure cultures in the laboratory, the dormant rod-form cells of A. ramosus that fragmented from the mycelium were not attacked. A growth initiation factor seemed to be involved in the attack – counter attack relationship of N-1 and A. ramosus. Strain N-1 and the other two gram-negative predators mentioned above could attack a variety of bacterial species in soil, in addition to A. ramosus which in itself is a predator. Thus, some sort of hierarchy of bacterial predation seems to exist in soil.


2020 ◽  
Vol 139 ◽  
pp. 153-160
Author(s):  
S Peeralil ◽  
TC Joseph ◽  
V Murugadas ◽  
PG Akhilnath ◽  
VN Sreejith ◽  
...  

Luminescent Vibrio harveyi is common in sea and estuarine waters. It produces several virulence factors and negatively affects larval penaeid shrimp in hatcheries, resulting in severe economic losses to shrimp aquaculture. Although V. harveyi is an important pathogen of shrimp, its pathogenicity mechanisms have yet to be completely elucidated. In the present study, isolates of V. harveyi were isolated and characterized from diseased Penaeus monodon postlarvae from hatcheries in Kerala, India, from September to December 2016. All 23 tested isolates were positive for lipase, phospholipase, caseinase, gelatinase and chitinase activity, and 3 of the isolates (MFB32, MFB71 and MFB68) showed potential for significant biofilm formation. Based on the presence of virulence genes, the isolates of V. harveyi were grouped into 6 genotypes, predominated by vhpA+ flaB+ ser+ vhh1- luxR+ vopD- vcrD+ vscN-. One isolate from each genotype was randomly selected for in vivo virulence experiments, and the LD50 ranged from 1.7 ± 0.5 × 103 to 4.1 ± 0.1 × 105 CFU ml-1. The expression of genes during the infection in postlarvae was high in 2 of the isolates (MFB12 and MFB32), consistent with the result of the challenge test. However, in MFB19, even though all genes tested were present, their expression level was very low and likely contributed to its lack of virulence. Because of the significant variation in gene expression, the presence of virulence genes alone cannot be used as a marker for pathogenicity of V. harveyi.


2017 ◽  
Vol 16 (4) ◽  
pp. 879-889 ◽  
Author(s):  
Florin Daniel Lipsa ◽  
Eugen Ulea ◽  
Andreea Mihaela Balau ◽  
Feodor Filipov ◽  
Evelina Cristina Morari
Keyword(s):  

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