Carbaryl degradation by bacterial isolates from a soil ecosystem of the Gaza Strip.

Carbaryl is an important and widely used insecticide that pollutes soil and water systems. Bacteria from the local soil ecosystem of the Gaza Strip capable of utilizing carbaryl as the sole source of carbon and nitrogen were isolated and identified as belonging to Bacillus, Morganella, Pseudomonas, Aeromonas and Corynebacterium genera. Carbaryl biodegradation by Bacillus, Morganella and Corynebacterium isolates was analyzed in minimal liquid media supplemented with carbaryl as the only source of carbon and nitrogen. Bacillus and Morganella exhibited 94.6% and 87.3% carbaryl degradation, respectively, while Corynebacterium showed only moderate carbaryl degradation at 48.8%. These results indicate that bacterial isolates from a local soil ecosystem in the Gaza Strip are able to degrade carbaryl and can be used to decrease the risk of environmental contamination by this insecticide.

Introduction

Carbamate insecticide (carbaryl) is a broad spectrum insecticide that is used worldwide in the agricultural industry (Hashimoto ). The extensive use of carbamate insecticides results in the pollution of soil and water systems, which in turn increases environmental and human health hazards (Swetha and Phale, 2005). Carbaryl is a cholinesterase inhibitor and is toxic to humans as the inhibition of this enzyme leads to an accumulation of acetylcholine at the synapses resulting in uncontrolled movements, paralysis, convulsions, and possible death (Tomlin, 2000). The United States Environmental Protection Agency (EPA) has classified carbaryl insecticides as probable human carcinogens (EPA, 2008). Human exposure to carbamate insecticides occurs via contaminated food or other routes (Gunasekara ) and because of their potential human risk, many studies have analyzed the presence of carbaryl in fruits and food products (Fana ).

Degradation is one of the most common methods of carbaryl elimination from soil and aqueous systems, which reduces its persistence and the associated risk of environmental contamination (Tam ; Naqvi, 2011). Microorganisms capable of degrading carbamate pesticides have received considerable attention because of their role in pesticide detoxification and elimination from soil and water systems (Naqvi ).

The present study investigated the carbaryl degradation ability of bacteria isolated from unsterilized soils from different areas in the Gaza Strip.

Materials and Methods

Chemicals and devices

All chemicals used in this study were of analytical grade and were obtained from Merck (Darmstadt, Germany), while the nutrients and agar media were purchased from HIMEDIA (Mumbai, India). Carbaryl was obtained from Dr. Ehrenstofer GmbH (Augsburg, Germany). RP-C18 Bakerbond SPE 3 mL, 500 mg cartridges (J. T. Baker, Gross-Gerau, Germany) were used to enrich samples, UV-Spectrophotometer and Dual wavelength flying spot scanning densitometer were from Hitachi (Tokyo, Japan) and the solid phase extraction (SPE) unit was from Supelco (Sigma-Aldrich, Missouri, USA).

Collection of soil samples

Eighteen different soil samples, representative of the soil ecosystem of the Gaza Strip, were locally collected from a depth of 10-20 cm according to the European soil sampling guidelines (Theocharopoulos ). Table 1 lists soil types and geographical location of the samples.

Table 1

Local soil ecosystem: soil types, their geographical location, soil environmental and the value of triplicate bacterial count (cfu/g soil).

No	Soil types	Geographical location	% Moisture	pH	Temp (°C)	(cfu/g soil) 1st	(cfu/g soil) 2nd	(cfu/g soil) 3rd	Mean (cfu/g soil)	Standard deviation
1	Loessial sandy soil	N: 31° 23′ 32.0″	13	7.73	21.7	8.3 × 105	4.2 × 106	2.2 × 106	2.4 × 106	1.7 × 106
		E: 34° 20′ 14.3″
2	Sandy loess soil over loess	N: 31° 20′ 30.1″	12	7.68	21.5	9.0 × 105	4.6 × 106	1.1 × 106	2.2 × 106	2.1 × 106
		E: 34° 19′ 35.3″
3	Dark brown /silty clay	N: 31° 27′ 48.1″	11	8.01	21.0	6.8 × 106	3.0 × 106	4.1 × 106	4.6 × 106	2.0 × 106
		E: 34° 25′ 28.9″
4	Sandy loess soil	N: 31° 27′ 38.7″	7	7.76	21.6	1.3 × 106	1.1 × 106	1.0 × 106	1.1 × 106	1.3 × 105
		E: 34° 24′ 56.2″
5	Loess soils	N: 31° 29′ 24.4″	22	7.8	20.9	4.2 × 106	2.0 × 106	2.5 × 106	2.9 × 106	1.1 × 106
		E: 34° 27′ 40.2″
6	Sandy regosols	N: 31° 30′ 78.8″	6	7.79	21.5	6.9 × 104	1.7 × 105	3.1 × 104	8.9 × 104	7.0 × 104
		E: 34° 26′ 61.8″

Bacterial isolation, identification and total bacterial count

To isolate bacteria from the collected soils, the samples were treated as previously described (Bashir, 2012). Estimation of total bacterial number and subsequent pure culture of bacteria were performed using the standard plate count method and diluted nutrient broth agar (Janssen ). Bacterial isolates were identified using standard morphological, biochemical and culture techniques (Krieg, 1984).

Pesticide degradation in solid and liquid media

The ability of the bacterial isolates to utilize carbaryl was screened by culturing them at 37 °C for 72 h on minimal agar containing 150 ppm carbaryl as the sole source of carbon and nitrogen. Bacteria capable of utilizing carbaryl were then selected and their pesticide degradation ability was further analyzed in minimal liquid media supplemented with 150 ppm carbaryl as the sole source of carbon and nitrogen. These bacterial cultures were shaken at 37 °C and 220 rpm Bacterial growth and remaining carbaryl concentration were monitored at 600 nm and 360 nm, respectively, as described earlier (Cullington and Walker, 1999).

Solid-phase extraction (SPE) of carbaryl and thin layer chromatography

Bakerbond SPE cartridges were pre-conditioned with 10 mL of methanol and 5 mL of water; the sample solution was introduced in the cartridge at a flow-rate of 2-3 mL/min, washed with 3 mL of distilled water, dried under vacuum for 20 min, and the pesticide was finally eluted with 5 mL of acetonitrile. The effluent was evaporated under nitrogen gas and the residue was re-dissolved in 100 μL acetonitrile (Hamada ). Chromatographic separation was performed on 20 cm × 20 cm TLC plates pre-coated with a 0.2-mm thick layer of silica gel 60 F254 (Macherey-Nagel, Germany). For quantitative analysis equal volumes of standards and samples (2 μL) were applied to the plates as spots using disposable micropipettes with a distance of 2 cm between the spots; else the entire SPE eluate (100 μL) was applied as a band using Linomat IV (Camag). Carbaryl was separated by ascending one-dimensional development in a saturated chamber with ethyl acetate/hexane (3:2, v/v), as the mobile phase. The chromatogram was developed for a distance of 10 cm with a run time of 15 min. The spots or bands were located by viewing under a universal UV lamp (VilberLourmat, France) at λ = 254 nm. Carbaryl concentration was determined using a Shimadzu CS-9301 dual Wavelength, flying-spot scanning densitometer in the reflectance mode using a deuterium lamp (λ = 250 nm). Acquisition parameters were beam size 0.4 mm × 16 mm and deuterium lamp set at zero at start with a 15-point smoothing. Calibration was done by peak area, and the peak find filter was set at 50 with resolution during data collection set at 0. The relative peak area was calculated which is directly proportional to the remaining concentration of the pesticide.

Results and Discussion

Bacteriological, physical and chemical parameters of the soil ecosystem

Bacterial diversity was clearly observed in all five soil types representative of the soil ecosystem in the Gaza Strip. Total bacterial counts (cfu/g soil) for the soil samples are shown in Table 1. Dark brown/silty clay soil had the highest bacterial count (4.64 × 106 cfu g−1) and loessial sandy soil had a total bacterial count of 2.36 × 106 cfu g−1. This soil type is widely distributed in the Gaza Strip and is comparatively less polluted; therefore, we chose bacterial isolates from this sample and analyzed their ability to degrade carbaryl. The total bacterial count of sandy loess over loess soil was 2.21 × 106 cfu g−1 while that of loess soil was 2.92 × 106 cfu g−1. Both sandy loess soil and sandy regosols soil had low bacterial counts of 1.11 × 106 cfu g−1 and 8.9 × 104 cfu g−1, respectively.

The viable bacterial counts reported herein are comparable to those in earlier reports (Bashir 2012). However, these bacterial counts are about a hundred to thousand fold lower than the estimated count reported in other studies (Janssen ; Schoenborn ). The viable bacterial counts in the different soil types of the Gaza Strip were less than the expected bacterial count in one gram of soil. The bacterial isolates were identified via Gram staining, culture and biochemical methods (Krieg, 1984) and belonged to various genera including; Bacillus, Pseudomonas, Staphylococcus, Acinetobacter, Escherichia, and Streptomyces. The physical and chemical parameters (moisture content, pH, and temperature) of the soil ecosystem of the Gaza Strip were found to be similar to those accepted as suitable for bacterial activity (Pietikäinen , Iovieno and Bååth, 2008; Rousk ). Bacteria of the Bacillus genera that were isolated from loessial sandy soil showed the highest rate of biodegradation (Figure 1). While bacteria from all the sampled soil types were capable of carbaryl biodegradation (data not shown), the rate of biodegradation varied among the different soils types and such a marked difference in the ability to degrade different pesticides has been previously observed among the various types of soils (Bending et al., 2004; Kah ).

Figure 1

Bacterial growth and percentage of carbaryl remaining in minimal liquid media. Bacterial isolates A) Bacillus B) Morganella and C) Corynebacterium were grown in liquid minimal media at initial concentration equivalent to OD600nm of 0.2 to 0.5. Bacterial growth and percentage of carbaryl remaining in the media were monitored for 10 days.

Carbaryl degradation activity on solid and liquid minimal media

Large variations in growth rate among the bacterial isolates were observed when the ability to metabolize carbaryl was tested in minimal agar media. Some of the tested isolates (25%) were unable to grow with carbaryl as the source of carbon and nitrogen, while the rest (75%) showed varying degrees of growth. Bacterial growth on minimal agar media was monitored for three days and three isolates capable of utilizing carbaryl were selected for further identification. These isolates were identified as belonging to the Bacillus, Corynebacterium and Morganella genera using standard techniques and their carbaryl biodegradation capacity was further tested in liquid media. Table 2 and Figure 1 demonstrate changes in growth and remaining carbaryl percentage in M9 liquid minimal medium for all three isolates. All bacterial isolates reached maximum growth (optical density = 1.5) after 10 days. At this time point, the Bacillus isolate showed greatest carbaryl degradation (98.71%) followed by Corynebacterium (87.37%), while Morganella showed least degradation (47.59%). These results are similar to those reported previously and serve to confirm previous findings that soil bacteria from different genera degrade carbaryl to varying degrees (Rousseaux ; Swetha and Phale, 2005; Uma and Sandhya, 2010).

Table 2

The Spectroscopic measurement of carbaryl degradation in minimal liquid media supplemented with carbaryl as sole source of carbon and nitrogen.

Day	Bacillus			Morganella			Corynebacterium
	OD* 600 nm	Abs360 nm	Remaining* (%)	OD* 600 nm	Abs60 nm	Remaining* (%)	OD* 600 nm	Abs360 nm	Remaining* (%)
0	0.232	0.056	100	0.39	0.024	100	0.43	0.198	100
1	0.318	0.052	92.9	0.70	0.023	96.6	0.60	0.178	90.0
2	0.412	0.048	85.7	0.81	0.023	96.6	0.75	0.15	75.8
3	0.510	0.044	78.6	0.96	0.023	97.1	0.92	0.148	74.8
4	0.623	0.039	69.6	1.13	0.018	76.0	1.11	0.127	64.2
5	0.724	0.034	60.7	1.34	0.017	71.8	1.09	0.114	57.6
6	0.846	0.029	51.8	1.39	0.017	71.8	1.27	0.097	49.1
7	1.125	0.017	30.4	1.51	0.013	55.7	1.33	0.078	39.5
8	1.179	0.009	16.1	1.44	0.013	55.4	1.61	0.033	16.7
9	1.260	0.005	8.9	1.56	0.012	51.7	1.49	0.027	13.7
10	1.246	0.003	5.4	1.59	0.012	51.2	1.55	0.025	12.7

Mean of three measurements.

Table 3 gives the recovery, standard deviation (SD) and relative standard deviation (RSD) of carbaryl degradation by Morganella sp. measured after optimization of SPE conditions for the enrichment of samples spiked with 150 ppm carbaryl. The average recovery for carbaryl using SPE was 92.6% with a relative standard deviation of less than 1%; these values meet the requisite conditions for quantitative determination of pesticide degradation.

Table 3

The standard deviation (SD), relative standard deviation (RSD) and recoveries percentage of the remaining carbaryl after solid phase extraction (SPE).

Degradation time	Relative peak areas	Average	Remaining %	SD	RSD %	Recoveries %
Zero time	891.37	891.11	100.00	0.18	0.020	92.6
	894.74
	887.21
2 days	858.76	858.73	96.36	0.02	0.002
	864.92
	852.52
5 days	651.63	646.90	72.59	3.34	0.51
	646.95
	642.12
7 days	607.72	433.60	48.65	2.51	0.41
	615.16
	610.94

The SPE extracts of days 0, 2, 5 and 7 were also spotted onto the TLC plate and displayed an Rf-value of 0.7. It is important to highlight the fact that the results of carbaryl biodegradation, measured both spectrophotometrically and by SPE, are obviously coincident and in complete agreement with each other.

Conclusion

The results presented herein show that the environmental conditions in the local soil ecosystem of the Gaza Strip are suitable for microbial growth, bacterial isolates from different genera are present, and that they are capable of degrading carbaryl to varying degrees. Bacteria of the genus Bacillus show greatest biodegradation activity. The present study also highlights the need for further studies to identify microbial populations capable of biodegrading organic components, which could efficiently be used in the bioremediation of pesticide-polluted soils. As soil intrinsic factors like organic carbon and composition of clay, silt and sand were not determined in our study; we suggest that a more detailed soil analysis should be conducted. This would provide a wealth of information on pesticide biodegradation in the soil ecosystem of the Gaza Strip, especially when it is compared with bacterial genera isolated from other soil ecosystems.