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Research Articles
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Influence of biological and chemical fertilisation on rhizosphere bacterial communities of Citrus sinensis L.
Facultad de Ingeniería y Ciencias, Universidad Autónoma de Tamaulipas, Centro Universitario Victoria, Ciudad Victoria, Tamaulipas, México C.P. 87149
Instituto Politécnico Nacional-Centro de Biotecnología Genómica, Blvd. del Maestro esq. Elías Piña, Col. Narciso Mendoza, Reynosa, Tamaulipas, México C.P. 88710
Facultad de Ingeniería y Ciencias, Universidad Autónoma de Tamaulipas, Centro Universitario Victoria, Ciudad Victoria, Tamaulipas, México C.P. 87149
Instituto Politécnico Nacional-Centro de Biotecnología Genómica, Blvd. del Maestro esq. Elías Piña, Col. Narciso Mendoza, Reynosa, Tamaulipas, México C.P. 88710
Abstract
This study evaluated the effects of chemical and biological fertilisation through the application of a fermented product in the rhizosphere of Citrus sinensis L. Olinda. The objective was to examine the relationship between bacterial diversity and plant-microbe interactions. The experiment was conducted from January to July 2025 at the nursery of the Faculty of Engineering and Sciences, Autonomous University of Tamaulipas (23°42′54″ N, 99°09′11″ W). Five nutritional treatments were applied: T1, soil application of a fermented product solution at 6 %; T2, combination of this fermented solution with foliar application; T3, granular fertiliser nitrogen (N), phosphorus (P), potassium (K) and sulfur (S) (NPKS); T4, triple 20 fertiliser and T5, an unfertilised control. Metagenomic DNA was extracted from rhizosphere samples (1 g) using the Quick-DNA kit and the V4 region (~250 bp) of the bacterial 16S rRNA gene was amplified with primer 27F and sequenced on an Illumina MiniSeq platform. All treatments induced changes in bacterial community structure, with beneficial bacterial groups prevailing. The highest diversity was observed in T1 (H′ = 3.35 ± 0.16; observed species = 1631 ± 285), while T2 showed the lowest diversity (H′ = 2.48 ± 0.18; species = 1269 ± 127). Conventional fertilisation (T3 and T4) resulted in intermediate diversity (H′ = 2.82 ± 0.04 and 3.16 ± 0.41, respectively) and the untreated control (T5) showed moderate diversity (H′ = 3.03 ± 0.00). Although sequencing depth varied among treatments, it did not consistently correlate with diversity. Soil nutrient profiles (Ca, Mg, K and P) also varied across treatments, influencing microbial composition. These findings suggest that biological fertilisation promotes greater beneficial bacterial diversity, relevant for improving plant health and developing sustainable citrus management strategies.
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