Isolation and Characterization of Listeria Monocytogenes from Goat Brain

Shivasharanappa Nayakwadi^1*, Vivek Kumar Gupta¹, Rajveer Singh Pawaiya¹, Gundallahallai Bayyappa Manjunatha Reddy², Ashok kumar¹, Sukhadeo B Barbuddhe³

*Corresponding author:drshivasharan@gmail.com

ARTICLE CITATION: Nayakwadi S, Gupta VK, Pawaiya RS, Reddy GBM, kumar A, Barbuddhe SB (2014). Isolation and characterization of listeria monocytogenes from goat brain. Adv. Anim. Vet. Sci. 2 (3S): 12 – 15.
Received: 2013–01–30, Revised: 2013–02–27, Accepted: 2013–02–28
The electronic version of this article is the complete one and can be found online at ( http://dx.doi.org/10.14737/journal.aavs/2014/2.3s.12.15 ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited

ABSTRACT

Caprine listeriosis caused by Listeria monocytogenes is a disease of zoonotic importance. Listeriosis involves central nervous system of goat which is manifested in various clinical signs. A total of 69 brain samples from different breeds of goat collected from the post–mortem cases and slaughter house were examined for the presence of pathogenic Listeria. Twenty one brain samples were found positive for listeria by cultural, biochemical, phenotypic and genotypic characteristics. Among these, nine isolates were characterized as Listeria monocytogenes. The isolates were positive for the hly and actA virulence genes by PCR assay. All the isolates belonged to 4b, 4d and 4e serovar group using multiplex PCR based serotyping. No characteristic pathological lesions of listeriosis have been found in the brain. The isolation of L. monocytogenes is important with regard to food safety and public health, representing a possible link between the animals, environment and human infection.

INTRODUCTION

The neurological disorders of small ruminants are well documented in standard textbooks (Summers et al., 1995; Zachary, 2006; Maxie and Youssef, 2007). The increased movement of live animals and animal products in international trade has increased the risks of spread of trans–boundary diseases of animals as well as zoonotic diseases, particularly those that are food borne. While the international trade in goat and goat products is small relative to the trade in bovine, swine and poultry products, it is still economically important. It includes some unique products such as goat milk cheeses and cashmere fibre, and the goat meat trade plays a large part in sustaining livelihoods in several regions of the world. The trade in small ruminants and their products also merits consideration because goats may transmit zoonotic diseases such as listeriosis (Sherman, 2011). Caprine listeriosis is caused by the serovar Listeria monocytogenes which is characterized by septicaemia, mastitis, meningo–encephalitis and abortion in goats. Besides L. monocytogenes, the infection caused by L. ivanovii is of major veterinary importance in cattle, sheep and goats. (Low and Donachie, 1997) Involvement of the central nervous system is manifested by unilateral ataxia and meningitis with formation of microabscesses (Radostits et al.,1997). These neuropathological changes account for the common name, ‘cirling disease’ of sheep (Barlow and Mc Gorum, 1985). In India, the information available on the occurrence of caprine listeriosis is well evident but isolation and characterization of listeria from brain is not much known. The present study has been undertaken to isolate and characterize the Listeria from goat brains collected from the post mortem house of the Institute and local slaughter house.

MATERIALS AND METHODS

Samples
A total of 69 brain samples were collected from post–mortem cases and local slaughter house and stored at –20oC. Part of the brain samples collected in 10% formalin for histopathology.

Enrichment and Isolation of Listeria
The brain (medulla oblongata, pons and anterior part of spinal cord) samples were processed for isolation of Listeria according to the method of US Department of Agriculture (USDA), as described by McClain and Lee (1988) after making necessary modifications. Briefly, approximately 10g of brain (from hind brain –medulla oblongata, pons and anterior part of spinal cord) samples were directly inoculated into 45ml of University Vermont Medium (UVM) I (Himedia), and incubated overnight at 30◦C. The enriched UVM I inoculum (0.1 ml) was then transferred to UVM II, again incubated overnight at 30◦C. The inoculum from enriched UVM II was streaked directly on PALCAM agar (Himedia) and the inoculated plates were incubated at 37◦C for 48 h. The black, glistening, pointed colonies of about 0.5mm diameter surrounded by a diffuse black zone of esculin hydrolysis were suspected to be of listeria. The presumed colonies of Listeria (at least three per plate) were further confirmed.

Confirmation of the Isolates
Morphologically, typical colonies were verified by Gram's staining, catalase reaction, tumbling motility at 20±250C, methyl red–Voges Proskauer (MR–VP) reactions, nitrate reduction, fermentation of sugars (rhamnose, xylose, mannitol and a–methyle–D–mannopyranoside) and haemolysis on 5% sheep blood agar. One of the virulence genes called Actin gene (actA) with the primer sequence F 5′ CGC CGC GGA AAT TAA AAA AAG A–3′ R 5′–ACG AAG GAA CCG GGC TGC TAG (839bp) (Suarez and Vazquez–Boland, 2001) of L. monocytogens of bovine origin has been amplified in brain samples by polymerase chain reaction (Rawool et al., 2007). The suspected Listeria isolates were confirmed at ICAR Research Complex, Goa as Listeria monocytogenes.

DNA Extraction and PCR Amplification
Bacterial DNA has been isolated by using DNA miniprep kit (MDI, Labs). 50 μl reaction mixture 5.0 μl of 10× PCR buffer, 1 μl of 10 mM dNTP mix (a final concentration of 0.2 mM), 2 μl of 50 mM MgCl2 (a final concentration of 2 mM), 10 μM of a primer set containing forward and reverse primers (a final concentration of 0.1 μM of each primer) 1 U of Taq DNA polymerase, 3 μl of DNA template and nuclease free water to make up the reaction volume. The cycling conditions for PCR included an initial denaturation of DNA at 95°C for 2 min followed by 35 cycles each of 15 s denaturation at 95°C, 30 s annealing at 60 °C and 1 min and 30 s extension at 72 °C, followed by a final extension of 10 min at 72 °C and held at 4°C. The resultant PCR product was further analyzed by agarose gel electrophoresis (1% agarose) stained with ethidium bromide (0.5 μg/ml) and visualized by a UV transilluminator (UVP Gel Seq Software, England).

Twenty one brain samples were processed for histopathology as per standard method (Luna, L.G., 1968) and microscopic lesions at different sub–anatomical sites were examined.

RESULTS AND DISCUSSION

Twenty one brain samples were found positive for Listeria by cultural, biochemical, phenotypic and genotypic characteristics. Among these, 9 were found positive for Listeria monocytogenes. On PALCAM agar, the colonies were gray–green, measuring 1.5–2mm in diameter and had black sunken center (Figure 1). Esculin, ferric iron, D–mannitol and phenol red contribute to this colour formation which is characteristics of Listeria. The cold enrichment has the disadvantage of being a lengthy procedure which can continue for several months and is prone to environmental contamination (Gronstol et al., 1986). Hence, in our opinion, the organism can be readily isolated from brain tissues by enrichment in the selective media UVM I and UVM II and plating on PALCAM agar which is very simple and use full method in isolating Listeria from morbid samples such as brain. Simplified genus identification has been done such as Gram stain (revealed Gram–positive, slim, short rods) (Figure 2), positive catalase (3% hydrogen peroxide solution) methyl red and Voges–Proskauer (V–P) reaction and observation of motility. These isolates were negative for oxidase and nitrate reduction tests. The sugar fermentation tests of Listeria spp. showed negative for Xylose and Mannitol and positive for Ramnose. Antibiogram of these isolates revealed sensitivity to certain antibiotics such as oxytetracycline, ampicillin, gentamycin, amoxycillin, enrofloxacin, ceftriaxone and ciprofloxacin and resistant against cloxacillin. The actA virulence gene (839 bp) of L. monocytogenes was detected by PCR from the nine brain samples. PCR is the only test utilized for rapid detection of L. monocytogenes morbid specimens. Multiplex PCR assay has been used for the detection of Listeria virulence genes (Suarez and Vazquez–Boland, 2001; Rawool et al., 2007). Various test protocols were evaluated for cerebrospinal fluid samples and tissue samples (fresh or in paraffin blocks) (Jaton, et al., 1992)