The Eeffect of Cronobacter sakazakii on the Brains of Newborn Mice

Main Article Content

Hayder A. Al-Mandalawii adil
Estabraq A. Mahmoud

Abstract

Fifteenth of Cronobacter sakazakii were obtained from previous studies isolates were (infant formula, spinal fluid and bloods). The newborn mice and number was 15 obtaining healthy newborn mice from the Iraqi Center for Cancer and Medical Genetics whose ages ranged between 10-17 days and their weights 8.5 ± 1.25 gm, were divided into 3 groups. The samples were cut and placed in formalin, then placed in stabilizer and concentrations of alcohol (70%, 80%, 90%,100%) to complete dehydration after they were leached with xylene, embedded the samples paraffin wax (58°C) and sectioning the with thickness (5) micrometer and stained with Haematoxylin and Eosin stain. The results of an increase in the weight of the brain organ for the mice compared to the control treatment and this increase was significant at the probability level p≤0.05 and the results showed the inflammatory response of the brain of large number of polymorphnuclear cells and mononuclear cells as well as congested blood vessels with an increase in the size of endothelial cells. The presence of bleeding congestion and shrinking of nerve cells in the area of the cerebral cortex, gliosis (neuroma), was more prominent in the molecular layer in the brain of the newborn mice fed at a concentration of 105 cells and the occurrence of oedema ,the presence of haemorrhage in both concentrations of dosed newborn mice and necrosis of the choroid plexus concentration103 and 105 cells.

Article Details

How to Cite
The Eeffect of Cronobacter sakazakii on the Brains of Newborn Mice. (2023). Ibn AL-Haitham Journal For Pure and Applied Sciences, 36(2), 105-112. https://doi.org/10.30526/36.2.2979
Section
Biology

How to Cite

The Eeffect of Cronobacter sakazakii on the Brains of Newborn Mice. (2023). Ibn AL-Haitham Journal For Pure and Applied Sciences, 36(2), 105-112. https://doi.org/10.30526/36.2.2979

Publication Dates

References

References

Hagan, C.E.; Bolon, B.; Keene, C.D. Nervous system. In: Comparative anatomy and histology

a mouse and human atlas. Treuting, P. M. and Dintzis, S. M. (Eds.). Elsevier Inc., San Diego,

USA, 2012: 339-394.

Ling, N.; Forsythe, S.; Wu, Q.; Ding, Y.; Zhang, J.; Zeng, H. Insights into Cronobacter sakazakii

biofilm formation and control strategies in the food industry. Engineering, 2020, 6, 4, 393-405.

Endersen, L.; Buttimer, C.; Nevin, E.; Coffey, A.; Neve, H.;Oliveira, H.; Lavigne, R.;

O'Mahony, J. Investigating the biocontrol and anti-biofilm potential of a three phage cocktail

against Cronobacter sakazakii in different brands of infant formula. Int. J. Food Microbiol., 2017,

, 1-11.

Singh, N.; Goel1, G.; Raghav, M. Insights into virulence factors determining the pathogenicity

of Cronobacter sakazakii. Virulence, 2015, 6, 5. 433-440.

Franco, A.A.; Kothary, M.H.; Gopinath, G.; Jarvis, K.G.; Grim, C.J.; Hu, L.; Datta, A.R.;

McCardell, B.A.; Tall, B.D. Cpa, the outer membrane protease of Cronobacter sakazakii, activates

plasminogen and mediates resistance to serum bactericidal activity. Infect. Immun., 2011, 79,

–1587.

Al-Zahran, H.A. Protein expression of Human Brain Microvascular Endothelial Cells in

Response to Meningitic C. Sakazakii: in Vitro and in Silico Analyses. Pak. J. Med. Health Sci.,

, 14, 1, 418-424.

Bancroft, J.; Steven, S. A. Theory and practice of histological technique, 2nd ed. Churchill

Livingston, London, 1982, 662.

Bancroft, J. D.; Layton, C. The hematoxylins and eosin. In: Bancroft’s theory and practice of

histological techniques, 7th edn. Suvarna, S.K.; Layton, L. and Bancroft, J.D. (Eds.). Churchill

Livingstone Elsevier Ltd., Shanghai, China, 2013: 173-186.

Emami, CN.; Mittal, R.; Wang, L.; Ford, HR.; Prasadarao, N.V. Role of neutrophils and

macrophages in the pathogenesis of necrotizing enterocolitis caused by Cronobacter sakazakii. J.

Surg. Res., 2012, 172, 1, 18-28.

Mittal, R. Y.; Wang, C. J.; Hunter, I.; Gonzalez-Gomez, N.V.; Prasadarao, A. Brain damage

in newborn rat model of meningitis by Enterobacter sakazakii: a role for outer membrane protein

A. Lab. Invest., 2009, 89, 263–277.

Jaradat, Z.W.; Al Mousa, W.; Elbetieha, A.; Al Nabuls, A.; Tall, B. Cronobacter spp. –

opportunistic food-borne pathogens. A review of their virulence and environmental-adaptive traits.

J. Med. Microbiol., 2014, 63, 1023–1037.

Townsend, S.M.; Hurrell, E.; Gonzalez-Gomez, I.; Lowe, J.; Frye, J.G.; Forsythe, S.; Badger,

J.L. Enterobacter sakazakii invades brain capillary endothelial cells, persists in human

macrophages influencing cytokine secretion and induces severe brain pathology in the neonatal

rat. Microbiology (Reading), 2007, 153(Pt 10), 3538-3547.

Hyun-Lee, H. A.; Hong ,S. ;Park, H.; Kim, H.; Kim. O. Cronobacter sakazakii infection

induced fatal clinical sequels including meningitis in neonatal ICR mice. Lab. Anim. Res., 2011,

, 59–62.

. Kothary, M. H.; McCardell, B.A.; Frazar, C.D.; Deer,D. and Tall , B.D.-(2007).

Characterization of the Zinc-Containing Metalloprotease Encoded by zpx and Development of a

Species-Specific Detection Method for Enterobacter sakazakii. Appl. Environ. Microbiol.,

(13) :4142–4151.

Pagotto, F.; Nazaroec-White, M.; Bidawid, S.; Farber, J.M. (2003). Enterobacter sakazakii

:Infectivity and Enterotoxin Production In vitro and In vivo. J. Food Prot., 2003, 66, 3, 370– 375.

Hunter, C.J.; Bean, J.F. (2013). Cronobacter: an emerging opportunistic pathogen associated