Enumeration of plant growth-promoting bacteria Herbaspirillum seropedicae viable cells by a propidium monoazide combined with quantitative PCR (PMA-qPCR) assay

被引:2
|
作者
Pedrolo, Ana Marina [1 ]
da Cunha, Elisandra Triches [1 ]
Gnecco, Nicolle [1 ]
Arisi, Ana Carolina Maisonnave [1 ]
机构
[1] Univ Fed Santa Catarina, Agrarian Sci Ctr, Food Sci & Technol Dept, CAL CCA UFSC, Rod Admar Gonzaga 1346, BR-88034001 Florianopolis, SC, Brazil
关键词
Nitrogen-fixing bacteria; Endophyte; Diazotroph; Quantitative PCR; Root colonization; Inoculant; vPCR; LISTERIA-MONOCYTOGENES; QUANTIFICATION; EXPRESSION; VIABILITY; OPTIMIZATION; INOCULATION; RHIZOSPHERE; PRODUCTS; TOMATO; GENES;
D O I
10.1016/j.microc.2023.109820
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The plant growth-promoting bacteria Herbaspirillum seropedicae is an endophytic diazotroph found in several economically important crops. Reliable, high-yield, and cost-effective methods are useful to determine bacterial viability in inoculant formulations or in plant. We developed a PMA-qPCR assay to enumerate viable cells of Herbaspirillum seropedica in pure culture and inoculated maize roots. The results obtained using qPCR, PMA-qPCR and plate counting were compared. The limit of quantification (LOQ) using qPCR was 2 log genome copies. Enumeration obtained in pure cultures by qPCR, PMA-qPCR and plate count were 8.85, 6.51 and 2.25 log CFU. mL(-1), respectively, after 180 min of heat treatment at 48 degrees C. Enumeration obtained in inoculated roots by qPCR, PMA-qPCR and plate count were 6.1, 3.7 and 4.9 log CFU.g(-1), respectively, 7 days after inoculation. These results showed that PMA-qPCR is a powerful approach for quantifying viable and viable but nonculturable cells in inoculants and maize roots. PMA-qPCR allowed reliable obtained results much faster than culture-dependent methods. It is the first PMA-qPCR developed for this important nitrogen-fixing and plant growth-promoting bacteria.
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页数:7
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