\documentclass[11pt,twoside]{article}\makeatletter

\IfFileExists{xcolor.sty}%
  {\RequirePackage{xcolor}}%
  {\RequirePackage{color}}
\usepackage{colortbl}
\usepackage{wrapfig}
\usepackage{ifxetex}
\ifxetex
  \usepackage{fontspec}
  \usepackage{xunicode}
  \catcode`⃥=\active \def⃥{\textbackslash}
  \catcode`❴=\active \def❴{\{}
  \catcode`❵=\active \def❵{\}}
  \def\textJapanese{\fontspec{Noto Sans CJK JP}}
  \def\textChinese{\fontspec{Noto Sans CJK SC}}
  \def\textKorean{\fontspec{Noto Sans CJK KR}}
  \setmonofont{DejaVu Sans Mono}
  
\else
  \IfFileExists{utf8x.def}%
   {\usepackage[utf8x]{inputenc}
      \PrerenderUnicode{–}
    }%
   {\usepackage[utf8]{inputenc}}
  \usepackage[english]{babel}
  \usepackage[T1]{fontenc}
  \usepackage{float}
  \usepackage[]{ucs}
  \uc@dclc{8421}{default}{\textbackslash }
  \uc@dclc{10100}{default}{\{}
  \uc@dclc{10101}{default}{\}}
  \uc@dclc{8491}{default}{\AA{}}
  \uc@dclc{8239}{default}{\,}
  \uc@dclc{20154}{default}{ }
  \uc@dclc{10148}{default}{>}
  \def\textschwa{\rotatebox{-90}{e}}
  \def\textJapanese{}
  \def\textChinese{}
  \IfFileExists{tipa.sty}{\usepackage{tipa}}{}
\fi
\def\exampleFont{\ttfamily\small}
\DeclareTextSymbol{\textpi}{OML}{25}
\usepackage{relsize}
\RequirePackage{array}
\def\@testpach{\@chclass
 \ifnum \@lastchclass=6 \@ne \@chnum \@ne \else
  \ifnum \@lastchclass=7 5 \else
   \ifnum \@lastchclass=8 \tw@ \else
    \ifnum \@lastchclass=9 \thr@@
   \else \z@
   \ifnum \@lastchclass = 10 \else
   \edef\@nextchar{\expandafter\string\@nextchar}%
   \@chnum
   \if \@nextchar c\z@ \else
    \if \@nextchar l\@ne \else
     \if \@nextchar r\tw@ \else
   \z@ \@chclass
   \if\@nextchar |\@ne \else
    \if \@nextchar !6 \else
     \if \@nextchar @7 \else
      \if \@nextchar (8 \else
       \if \@nextchar )9 \else
  10
  \@chnum
  \if \@nextchar m\thr@@\else
   \if \@nextchar p4 \else
    \if \@nextchar b5 \else
   \z@ \@chclass \z@ \@preamerr \z@ \fi \fi \fi \fi
   \fi \fi  \fi  \fi  \fi  \fi  \fi \fi \fi \fi \fi \fi}
\gdef\arraybackslash{\let\\=\@arraycr}
\def\@textsubscript#1{{\m@th\ensuremath{_{\mbox{\fontsize\sf@size\z@#1}}}}}
\def\Panel#1#2#3#4{\multicolumn{#3}{){\columncolor{#2}}#4}{#1}}
\def\abbr{}
\def\corr{}
\def\expan{}
\def\gap{}
\def\orig{}
\def\reg{}
\def\ref{}
\def\sic{}
\def\persName{}\def\name{}
\def\placeName{}
\def\orgName{}
\def\textcal#1{{\fontspec{Lucida Calligraphy}#1}}
\def\textgothic#1{{\fontspec{Lucida Blackletter}#1}}
\def\textlarge#1{{\large #1}}
\def\textoverbar#1{\ensuremath{\overline{#1}}}
\def\textquoted#1{‘#1’}
\def\textsmall#1{{\small #1}}
\def\textsubscript#1{\@textsubscript{\selectfont#1}}
\def\textxi{\ensuremath{\xi}}
\def\titlem{\itshape}
\newenvironment{biblfree}{}{\ifvmode\par\fi }
\newenvironment{bibl}{}{}
\newenvironment{byline}{\vskip6pt\itshape\fontsize{16pt}{18pt}\selectfont}{\par }
\newenvironment{citbibl}{}{\ifvmode\par\fi }
\newenvironment{docAuthor}{\ifvmode\vskip4pt\fontsize{16pt}{18pt}\selectfont\fi\itshape}{\ifvmode\par\fi }
\newenvironment{docDate}{}{\ifvmode\par\fi }
\newenvironment{docImprint}{\vskip 6pt}{\ifvmode\par\fi }
\newenvironment{docTitle}{\vskip6pt\bfseries\fontsize{22pt}{25pt}\selectfont}{\par }
\newenvironment{msHead}{\vskip 6pt}{\par}
\newenvironment{msItem}{\vskip 6pt}{\par}
\newenvironment{rubric}{}{}
\newenvironment{titlePart}{}{\par }

\newcolumntype{L}[1]{){\raggedright\arraybackslash}p{#1}}
\newcolumntype{C}[1]{){\centering\arraybackslash}p{#1}}
\newcolumntype{R}[1]{){\raggedleft\arraybackslash}p{#1}}
\newcolumntype{P}[1]{){\arraybackslash}p{#1}}
\newcolumntype{B}[1]{){\arraybackslash}b{#1}}
\newcolumntype{M}[1]{){\arraybackslash}m{#1}}
\definecolor{label}{gray}{0.75}
\def\unusedattribute#1{\sout{\textcolor{label}{#1}}}
\DeclareRobustCommand*{\xref}{\hyper@normalise\xref@}
\def\xref@#1#2{\hyper@linkurl{#2}{#1}}
\begingroup
\catcode`\_=\active
\gdef_#1{\ensuremath{\sb{\mathrm{#1}}}}
\endgroup
\mathcode`\_=\string"8000
\catcode`\_=12\relax

\usepackage[a4paper,twoside,lmargin=1in,rmargin=1in,tmargin=1in,bmargin=1in,marginparwidth=0.75in]{geometry}
\usepackage{framed}

\definecolor{shadecolor}{gray}{0.95}
\usepackage{longtable}
\usepackage[normalem]{ulem}
\usepackage{fancyvrb}
\usepackage{fancyhdr}
\usepackage{graphicx}
\usepackage{marginnote}

\renewcommand{\@cite}[1]{#1}


\renewcommand*{\marginfont}{\itshape\footnotesize}

\def\Gin@extensions{.pdf,.png,.jpg,.mps,.tif}

  \pagestyle{fancy}

\usepackage[pdftitle={Seroprevalence of Toxoplasma Gondii Infection among Pregnant Women in River Nile State, Sudan, from April to June 2017},
 pdfauthor={}]{hyperref}
\hyperbaseurl{}

	 \paperwidth210mm
	 \paperheight297mm
              
\def\@pnumwidth{1.55em}
\def\@tocrmarg {2.55em}
\def\@dotsep{4.5}
\setcounter{tocdepth}{3}
\clubpenalty=8000
\emergencystretch 3em
\hbadness=4000
\hyphenpenalty=400
\pretolerance=750
\tolerance=2000
\vbadness=4000
\widowpenalty=10000

\renewcommand\section{\@startsection {section}{1}{\z@}%
     {-1.75ex \@plus -0.5ex \@minus -.2ex}%
     {0.5ex \@plus .2ex}%
     {\reset@font\Large\bfseries}}
\renewcommand\subsection{\@startsection{subsection}{2}{\z@}%
     {-1.75ex\@plus -0.5ex \@minus- .2ex}%
     {0.5ex \@plus .2ex}%
     {\reset@font\Large}}
\renewcommand\subsubsection{\@startsection{subsubsection}{3}{\z@}%
     {-1.5ex\@plus -0.35ex \@minus -.2ex}%
     {0.5ex \@plus .2ex}%
     {\reset@font\large}}
\renewcommand\paragraph{\@startsection{paragraph}{4}{\z@}%
     {-1ex \@plus-0.35ex \@minus -0.2ex}%
     {0.5ex \@plus .2ex}%
     {\reset@font\normalsize}}
\renewcommand\subparagraph{\@startsection{subparagraph}{5}{\parindent}%
     {1.5ex \@plus1ex \@minus .2ex}%
     {-1em}%
     {\reset@font\normalsize\bfseries}}


\def\l@section#1#2{\addpenalty{\@secpenalty} \addvspace{1.0em plus 1pt}
 \@tempdima 1.5em \begingroup
 \parindent \z@ \rightskip \@pnumwidth 
 \parfillskip -\@pnumwidth 
 \bfseries \leavevmode #1\hfil \hbox to\@pnumwidth{\hss #2}\par
 \endgroup}
\def\l@subsection{\@dottedtocline{2}{1.5em}{2.3em}}
\def\l@subsubsection{\@dottedtocline{3}{3.8em}{3.2em}}
\def\l@paragraph{\@dottedtocline{4}{7.0em}{4.1em}}
\def\l@subparagraph{\@dottedtocline{5}{10em}{5em}}
\@ifundefined{c@section}{\newcounter{section}}{}
\@ifundefined{c@chapter}{\newcounter{chapter}}{}
\newif\if@mainmatter 
\@mainmattertrue
\def\chaptername{Chapter}
\def\frontmatter{%
  \pagenumbering{roman}
  \def\thechapter{\@roman\c@chapter}
  \def\theHchapter{\roman{chapter}}
  \def\thesection{\@roman\c@section}
  \def\theHsection{\roman{section}}
  \def\@chapapp{}%
}
\def\mainmatter{%
  \cleardoublepage
  \def\thechapter{\@arabic\c@chapter}
  \setcounter{chapter}{0}
  \setcounter{section}{0}
  \pagenumbering{arabic}
  \setcounter{secnumdepth}{6}
  \def\@chapapp{\chaptername}%
  \def\theHchapter{\arabic{chapter}}
  \def\thesection{\@arabic\c@section}
  \def\theHsection{\arabic{section}}
}
\def\backmatter{%
  \cleardoublepage
  \setcounter{chapter}{0}
  \setcounter{section}{0}
  \setcounter{secnumdepth}{2}
  \def\@chapapp{\appendixname}%
  \def\thechapter{\@Alph\c@chapter}
  \def\theHchapter{\Alph{chapter}}
  \appendix
}
\newenvironment{bibitemlist}[1]{%
   \list{\@biblabel{\@arabic\c@enumiv}}%
       {\settowidth\labelwidth{\@biblabel{#1}}%
        \leftmargin\labelwidth
        \advance\leftmargin\labelsep
        \@openbib@code
        \usecounter{enumiv}%
        \let\p@enumiv\@empty
        \renewcommand\theenumiv{\@arabic\c@enumiv}%
	}%
  \sloppy
  \clubpenalty4000
  \@clubpenalty \clubpenalty
  \widowpenalty4000%
  \sfcode`\.\@m}%
  {\def\@noitemerr
    {\@latex@warning{Empty `bibitemlist' environment}}%
    \endlist}

\def\tableofcontents{\section*{\contentsname}\@starttoc{toc}}
\parskip0pt
\parindent1em
\def\Panel#1#2#3#4{\multicolumn{#3}{){\columncolor{#2}}#4}{#1}}
\newenvironment{reflist}{%
  \begin{raggedright}\begin{list}{}
  {%
   \setlength{\topsep}{0pt}%
   \setlength{\rightmargin}{0.25in}%
   \setlength{\itemsep}{0pt}%
   \setlength{\itemindent}{0pt}%
   \setlength{\parskip}{0pt}%
   \setlength{\parsep}{2pt}%
   \def\makelabel##1{\itshape ##1}}%
  }
  {\end{list}\end{raggedright}}
\newenvironment{sansreflist}{%
  \begin{raggedright}\begin{list}{}
  {%
   \setlength{\topsep}{0pt}%
   \setlength{\rightmargin}{0.25in}%
   \setlength{\itemindent}{0pt}%
   \setlength{\parskip}{0pt}%
   \setlength{\itemsep}{0pt}%
   \setlength{\parsep}{2pt}%
   \def\makelabel##1{\upshape ##1}}%
  }
  {\end{list}\end{raggedright}}
\newenvironment{specHead}[2]%
 {\vspace{20pt}\hrule\vspace{10pt}%
  \phantomsection\label{#1}\markright{#2}%

  \pdfbookmark[2]{#2}{#1}%
  \hspace{-0.75in}{\bfseries\fontsize{16pt}{18pt}\selectfont#2}%
  }{}
      \def\TheFullDate{2017-01-15 (revised: April to June 2017 15 January 2017)}
\def\TheID{\makeatother }
\def\TheDate{2017-01-15}
\title{Seroprevalence of Toxoplasma Gondii Infection among Pregnant Women in River Nile State, Sudan, from April to June 2017}
\author{}\makeatletter 
\makeatletter
\newcommand*{\cleartoleftpage}{%
  \clearpage
    \if@twoside
    \ifodd\c@page
      \hbox{}\newpage
      \if@twocolumn
        \hbox{}\newpage
      \fi
    \fi
  \fi
}
\makeatother
\makeatletter
\thispagestyle{empty}
\markright{\@title}\markboth{\@title}{\@author}
\renewcommand\small{\@setfontsize\small{9pt}{11pt}\abovedisplayskip 8.5\p@ plus3\p@ minus4\p@
\belowdisplayskip \abovedisplayskip
\abovedisplayshortskip \z@ plus2\p@
\belowdisplayshortskip 4\p@ plus2\p@ minus2\p@
\def\@listi{\leftmargin\leftmargini
               \topsep 2\p@ plus1\p@ minus1\p@
               \parsep 2\p@ plus\p@ minus\p@
               \itemsep 1pt}
}
\makeatother
\fvset{frame=single,numberblanklines=false,xleftmargin=5mm,xrightmargin=5mm}
\fancyhf{} 
\setlength{\headheight}{14pt}
\fancyhead[LE]{\bfseries\leftmark} 
\fancyhead[RO]{\bfseries\rightmark} 
\fancyfoot[RO]{}
\fancyfoot[CO]{\thepage}
\fancyfoot[LO]{\TheID}
\fancyfoot[LE]{}
\fancyfoot[CE]{\thepage}
\fancyfoot[RE]{\TheID}
\hypersetup{citebordercolor=0.75 0.75 0.75,linkbordercolor=0.75 0.75 0.75,urlbordercolor=0.75 0.75 0.75,bookmarksnumbered=true}
\fancypagestyle{plain}{\fancyhead{}\renewcommand{\headrulewidth}{0pt}}

\date{}
\usepackage{authblk}

\providecommand{\keywords}[1]
{
\footnotesize
  \textbf{\textit{Index terms---}} #1
}

\usepackage{graphicx,xcolor}
\definecolor{GJBlue}{HTML}{273B81}
\definecolor{GJLightBlue}{HTML}{0A9DD9}
\definecolor{GJMediumGrey}{HTML}{6D6E70}
\definecolor{GJLightGrey}{HTML}{929497} 

\renewenvironment{abstract}{%
   \setlength{\parindent}{0pt}\raggedright
   \textcolor{GJMediumGrey}{\rule{\textwidth}{2pt}}
   \vskip16pt
   \textcolor{GJBlue}{\large\bfseries\abstractname\space}
}{%   
   \vskip8pt
   \textcolor{GJMediumGrey}{\rule{\textwidth}{2pt}}
   \vskip16pt
}

\usepackage[absolute,overlay]{textpos}

\makeatother 
      \usepackage{lineno}
      \linenumbers
      
\begin{document}

             \author[1]{Mosab NM  Hamad}

             \affil[1]{  Medical Parasitology Department, Medical Laboratory Sciences Department, Faculty of Health Sciences, Elsheikh Abdallah Elbadri University, Sudan}

\renewcommand\Authands{ and }

\date{\small \em Received: 14 December 2016 Accepted: 1 January 2017 Published: 15 January 2017}

\maketitle


\begin{abstract}
        


Background: Toxoplasmosis is worldwide distribution disease, about 20% to 90% of the adult population in the world are reported with toxoplasmosis.Objectives: To know the prevalence of toxoplasmosis among selected group of pregnant women from Atbara and Aldamer towns, River Nile State ,Sudan by applying Latex agglutination and ELISA serological methods and to compare between these two serological methods Methodology: Blood specimen were collected from 50 pregnant women participated in this studies and then specimens were processed and examined by Latex agglutination and ELISA.Result: 24% were seropositive and 76% were seronegative, 24% positive with latex agglutination and 18% positive with ELISA.Discussion, conclusion and recommendations: ELISA is more specific than latex agglutination method, further studies are required with large sample size and more diagnostic methods.

\end{abstract}


\keywords{}

\begin{textblock*}{18cm}(1cm,1cm) % {block width} (coords) 
\textcolor{GJBlue}{\LARGE Global Journals \LaTeX\ JournalKaleidoscope\texttrademark}
\end{textblock*}

\begin{textblock*}{18cm}(1.4cm,1.5cm) % {block width} (coords) 
\textcolor{GJBlue}{\footnotesize \\ Artificial Intelligence formulated this projection for compatibility purposes from the original article published at Global Journals. However, this technology is currently in beta. \emph{Therefore, kindly ignore odd layouts, missed formulae, text, tables, or figures.}}
\end{textblock*}


\let\tabcellsep& 	 	 		 
\section[{I. Introduction}]{I. Introduction}\par
oxoplasmosis is worldwide distribution disease, about 20\% to 90\% of the adult population in the world are reported with toxoplasmosis \hyperref[b0]{[1]}.\par
It is third leading infections cause of food-borne death after salmonellosis and listerosis.\par
In Sudan first report of human toxoplasmosis was dated back to 1996 with different prevalence rates \hyperref[b1]{[2]} Toxoplasma gondii is an obligate intracellular protozoan parasite that infects most species of warm blooded animals including humans and causing toxoplasmosis \hyperref[b2]{[3]}  
\section[{a) Morphology}]{a) Morphology}\par
During different period of its life cycle,individual parasites convert into various cellular stages with each stage characterized by a distinct cellular morphology.\par
This stages include tachyzoites, merozoites, bradyzoites and sporozoites. 
\section[{b) Life cycle}]{b) Life cycle}\par
The life cycle of T.gondii can be broadly summarized into two components, sexual part that occur only within cats.\par
The second part isasexual, it is occur within virtually all warm blooded animals include humans, cats and birds \hyperref[b4]{[4]} . because T.gondii can sexually reproduce only within cats, they are called definitive host and other hosts in asexual reproduction are defined as intermediate hosts. 
\section[{c) Sexual reproduction}]{c) Sexual reproduction}\par
When the cat is infected with T.gondii (example by consuming on infected mouse carrying the parasites tissue cyst), the parasite survive passage through the stomach, eventually infecting epithelial cell of the cat's small intestine. \hyperref[b4]{[4]} Inside their intestine cells the parasite undergo sexual development and reproduction, producing millions of thick walled zygote containing cyst called as oocyst.\par
Epithelial cells rupture and release oocysts into intestine's lumen, then shed in cat's feces. Oocysts can spread to soil, water, food and it can survive and remain infective for many months in cold dry climate \hyperref[b5]{[5]} , Ingestion ofoocysts by human or other warm-blooded animals is one of the common routes of infection. \hyperref[b6]{[6]} Other infected stages are tachyzoites of rapid division, and bradyzoites of slow division within tissue cysts, Tissue cysts in brain and muscle tissue formabout 7-10 days after initial infection. \hyperref[b7]{[7]}  
\section[{d) Asexual reproduction}]{d) Asexual reproduction}\par
Inside host cells the tachyzoites replicate inside specialized vacuoles called parasitophorus vacuoles, and multiply inside it until host cells dye and rupture releasing and spreading the tachyzoites via blood stream to all organs and tissues including brain. tachyzoites convert into any organ. Severe toxoplasmosis causing damage to the brain lead to encephalitis and damage in eye and other organs .most severe cases are individuals who have weak immune system.\par
Infant who are infected while still in womb have no symptoms at birth, but they may develop symptoms later in life. 
\section[{II. Stages Toxoplasmosis Infection}]{II. Stages Toxoplasmosis Infection}\par
Tissue cysts can be maintained in host tissue for the life time of the animal. However the presence of cysts appear to be due to periodic process of cyst rupturing and re encysting rather than a perpetual life span of individual cysts or bradyzoites. \hyperref[b8]{[8]} It can passed between intermediate hosts via cycle of consumption of tissue cyst in meat, however parasite's life cycle begins and completes only when passed to host. Infection of T.gondii during third trimester of pregnancy have high risk of congenital transmission, it causing severe damage to the fetus or abortion. Also can cause manifestation such as hydrocephalus, cerebral calcification and chorioretinitisin the new born. \hyperref[b12]{[9,}\hyperref[b9]{10]}  
\section[{c) Diagnosis}]{c) Diagnosis}\par
T.gondii infection can be identified with serologic testing or aminocentesis or presence of abnormal ultra sound findings.\par
Several serological tests are available for detection of T.gondii antibodies such as Sabin field man dye test, Indirect Immune fluorescent test "IFAT", Modified agglutination test "MAT", latex agglutination test and Enzyme -linked Immuno sorbent assay "ELISA".\par
Serologic testing is the first step in diagnosis by using IgG and IgM antibodies ,the diagnostic challenge is differentiating between primary and chronic infection and result of IgG and IgM testing can often be difficult to interpret, for this reason it is important to consult with an expert area when confirming the diagnosis.\par
The presence of IgM cannot be considered reliable for making diagnosis for acute toxoplasmosis infection, its titer rise from five day to week following acute infection and reaching maximum after one to two months and decline rapidly than IgG. \hyperref[b10]{[11]} Also IgM antibodies can decrease to low or undetectable levels in many cases.\par
IgG antibodies appear later than IgM and are usually detectable within one to two weeks after infection, with peak reached within 12 weeks to 6 months after acute infection, but it will be detectable for years after acquired infection and usually present thorough life. \hyperref[b11]{[12]} -If IgG and IgM are both negative this indicate the absence of infection or extremely recent acute infection. \hyperref[b13]{[13]} -If testing reveals positive IgG and negative IgMit indicates an old infection (more than one year ago). -If both IgG and IgM are positive this indicates either a recent infection or false positive test result. \hyperref[b11]{[12]} If acute infection is suspected repeat testing is recommended within two or three weeks [11, 12], rise in IgG antibodies titers between tests indicates a recent infection. \hyperref[b14]{[14]} There for when positive result is appear, it should confirm by confirming test such as ELISA, Sabin Feldman test and IFAT \hyperref[b10]{[11,}\hyperref[b11]{12]} .\par
Knowing when infection occurred during pregnancy is very important in evaluating the risk of fatal transmission, so initial antibiotic therapy and ensure appropriate prenatal counseling \hyperref[b13]{[13]} . 
\section[{d) Justification}]{d) Justification}\par
Seroprevalence of T.gondii infection particularly in pregnantwomen, are still in conclusive. In River Nile State has no published studies on the seroprevalence of T.gondii infection among pregnant women and this were motivated us to carry out this study to determine the seroprevalence of T.gondii infection among pregnant women in Atbara and ALdamer. 
\section[{e) Objectives i. General objectives}]{e) Objectives i. General objectives}\par
To determine the prevalence of T.gondii infection among pregnant women in Atbara \& ALdamer -River Nile state.  
\section[{g) Sample size}]{g) Sample size}\par
A total of 50 blood samples were drawn from pregnant women who come to Atbara and ALdamer Hospitals. This figure was arrived at using the relation?? = ?? 2 ????(1 ? ??) ?????????? 2\par
Where N= Sample size, Constant set by convention Z= 1.96, P= Previous study's prevalence. P = 92.5\% (0.996). Error was calculated at 5\% (0.05). N= [1.962 X 0.996X (1-0.996)]/0.052 And Questionnaires were administered, completed and returned for analysis. 
\section[{h) Sample Collection}]{h) Sample Collection}\par
The blood samples were collected by venipuncture using 5 ml syringe into plain containers. 
\section[{i) Sample processing}]{i) Sample processing}\par
Serum obtained by centrifugation of the blood at 5000 rpm for 10 minute. Detection by Latex Agglutination test. Then +ve Result Confirmation by ELISA Test.\par
Firstly sample diagnosed with latex agglutination test then confirm with ELISA. Total of 50 pregnant women were enroll in this test from Atbara hospital, data collect by medical field. Take about 5 ml of venous blood by disposable syringes under sterile aseptic technique 2.5 ml in plain tube for latex agglutination test and 2.5 ml also in plain tube for confirming + ve result by detecting IgM and IgG Abs of T.gondii. 
\section[{j) Principle of latex agglutination test}]{j) Principle of latex agglutination test}\par
Latex agglutination is observed when sample containing the specific antigen (or antibody) is mixed with an antibody (or antigen). Which is coated in the surface of latex particles.\par
The reaction between aparticular antigen and an antibody results in visible clumping called agglutination. 
\section[{k) Principle of ELISA Test}]{k) Principle of ELISA Test}\par
Enzyme Linked Immunosorbent Assay Combine the specificity of antibodies with the sensitivity of simple enzyme assays, by using antibodies or antigens coupled to an easily assayed enzyme. ELISAs can be provide useful measurement of antigen or antibody concentration. 
\section[{l) Study variables}]{l) Study variables}\par
-Presence of cats in the house -History of abortion in family -History of delivery -Type of Delivery -Educational level -Raw meat and vegetable habit gestational period blood and organ transfusion -Nature of home ground surface. 
\section[{m) Ethical consideration -Approval from EAEUEC (Elsheikh Abdallah Albadri}]{m) Ethical consideration -Approval from EAEUEC (Elsheikh Abdallah Albadri}\par
University Ethical Committee) -The purpose and procedures involved in this study were explained and written inform consent were obtained from all participants. Blood were collected with the consent of the volunteers n) Data analysis Statistical analysis of data was done by using Statistical package for social science (SPSS). 
\section[{IV. Result}]{IV. Result}\par
Out of 50 samples of serum collected from pregnant women in Atbara and ALdamer Hospitals and screened by using latex agglutination test, the number of positive cases was found to be (22.2\%) Table \hyperref[tab_1]{(1}       The current study is one of the few studies carried out to explore the seroprevalence of T. gondii infection among pregnant women in ALdamer and Atbara Towns and further studies are required with large sample size and various diagnostic methods.   \begin{figure}[htbp]
\noindent\textbf{} \par 
\begin{longtable}{P{0.28465732087227413\textwidth}P{0.00794392523364486\textwidth}P{0.00264797507788162\textwidth}P{0.041043613707165104\textwidth}P{0.5137071651090342\textwidth}}
\multicolumn{5}{l}{Seroprevalence of Toxoplasma Gondii Infection among Pregnant Women in River Nile State, Sudan, from}\\
\tabcellsep \tabcellsep \tabcellsep \multicolumn{2}{l}{April to June 2017}\\
f) Symptoms\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
Most\tabcellsep people\tabcellsep of\tabcellsep toxoplasmosis\tabcellsep are\\
\multicolumn{2}{l}{asymptomatic, some}\tabcellsep \tabcellsep \tabcellsep \\
Year 2017\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
Volume XVII Issue I Version I\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
D D D D ) C\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
(\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
Medical Research\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
Global Journal of\tabcellsep \tabcellsep \tabcellsep \tabcellsep e) Modes of transmission\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Ingestion of undercooked, contaminated meat with\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep infective stage of T.gondii.\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Drinking water contaminated with T.gondii or\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep contact with contaminated soil.\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Accidently swallowing the parasite through contact\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep with cat's feces that contain toxoplasma.\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Vertical (Transplacental) transmission.\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Organs transplantation.\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Sexual transmission.\\
\tabcellsep \tabcellsep \tabcellsep \tabcellsep -Inhalation of infective stage.\end{longtable} \par
 
\caption{\label{tab_0}}\end{figure}
 \begin{figure}[htbp]
\noindent\textbf{1} \par 
\begin{longtable}{P{0.24555555555555553\textwidth}P{0.3022222222222222\textwidth}P{0.3022222222222222\textwidth}}
Sample size\tabcellsep Positive\tabcellsep Negative\\
50\tabcellsep 12(24\%)\tabcellsep 38(76\%)\end{longtable} \par
 
\caption{\label{tab_1}Table 1 :}\end{figure}
 \begin{figure}[htbp]
\noindent\textbf{2} \par 
\begin{longtable}{P{0.36791044776119397\textwidth}P{0.3044776119402985\textwidth}P{0.17761194029850746\textwidth}}
\tabcellsep \multicolumn{2}{l}{T. gondii antibodies(IgG \& IgM)}\\
\multicolumn{3}{l}{among pregnant women}\\
IgG\tabcellsep frequency\tabcellsep Percentage\%\\
positive\tabcellsep 12\tabcellsep 24\%\\
Negative\tabcellsep 38\tabcellsep 76\%\\
IgM\tabcellsep \tabcellsep \\
positive\tabcellsep 9\tabcellsep 18\%\\
Negative\tabcellsep 41\tabcellsep 82\%\end{longtable} \par
 
\caption{\label{tab_2}Table 2 :}\end{figure}
 \begin{figure}[htbp]
\noindent\textbf{3} \par 
\begin{longtable}{P{0.2883928571428572\textwidth}P{0.22767857142857142\textwidth}P{0.3339285714285714\textwidth}}
Age\tabcellsep frequency\tabcellsep Percentage\\
18-20\tabcellsep 13\tabcellsep 26\%\\
21-30\tabcellsep 24\tabcellsep 48\%\\
331-40\tabcellsep 13\tabcellsep 26\%\end{longtable} \par
 
\caption{\label{tab_3}Table 3 :}\end{figure}
 \begin{figure}[htbp]
\noindent\textbf{4} \par 
\begin{longtable}{P{0.85\textwidth}}
Volume XVII Issue I Version I\\
D D D D ) C\\
(\\
Medical Research\\
Global Journal of\end{longtable} \par
 
\caption{\label{tab_4}Table 4 :}\end{figure}
 \begin{figure}[htbp]
\noindent\textbf{5} \par 
\begin{longtable}{P{0.4945454545454545\textwidth}P{0.25242424242424244\textwidth}P{0.10303030303030303\textwidth}}
Toxoplasmosis latex\tabcellsep \multicolumn{2}{l}{ELISA IgG test}\\
agglutination\tabcellsep Positive\tabcellsep Negative\\
Positive\tabcellsep 12\tabcellsep 0\\
Negative\tabcellsep 0\tabcellsep 38\\
Toxoplasmosis latex\tabcellsep \multicolumn{2}{l}{ELISA IgM test}\\
agglutination\tabcellsep Positive\tabcellsep Negative\\
Positive\tabcellsep 9\tabcellsep 3\\
Negative\tabcellsep 0\tabcellsep \end{longtable} \par
 
\caption{\label{tab_5}Table 5 :}\end{figure}
 			\footnote{© 2017 Global Journals Inc. (US)} 			\footnote{© 2017 Global Journals Inc. (US)Year 2017} 		 		\backmatter  			  				\begin{bibitemlist}{1}
\bibitem[Montoya and Iesen Feldo ()]{b9}\label{b9} 	 		\textit{},  		 			J G Montoya 		,  		 			Iesen Feldo 		.  	 	 		\textit{Toxoplasmosis lancet}  		2004. 363 p. .  	 
\bibitem[Louis et al. ()]{b4}\label{b4} 	 		\textit{},  		 			M Louis 		,  		 			Kami Weiss 		,  		 			Kim 		.  		2011.  	 
\bibitem[Louis et al. ()]{b8}\label{b8} 	 		\textit{},  		 			M Louis 		,  		 			Kami Weiss 		,  		 			Kim 		.  		2011.  	 
\bibitem[Darde et al. ()]{b2}\label{b2} 	 		\textit{3-population structure and epidemiology of toxoplasma gondii in Wess},  		 			Darde 		,  		 			D; Ml; Ajzenberg 		,  		 			Smith 		.  		2011. LM.  	 
\bibitem[Kaboosi et al. ()]{b15}\label{b15} 	 		\textit{A comparative serological study of toxoplasmosis in pregnant women by CLIA and ELISA methods in Chalus City Iran},  		 			H Kaboosi 		,  		 			Faghih Nasiri 		,  		 			A Tabatabaie 		,  		 			S S Golhasani-Keshtan 		,  		 			F Zaboli 		,  		 			F 		.  		2014. Iran Red Crescent Med J. 16 p. e15115.  	 
\bibitem[Robert -Gangneux et al. ()]{b7}\label{b7} 	 		‘Epidemiology and diagnostic strategies for toxoplasmosis’.  		 			Robert -Gangneux 		,  		 			Marie Florence : Darde 		,  		 			Laure 		.  		 22491772.  		 doi:10. 1128\textbackslash CMR.  	 	 		\textit{Clinical Microbiology Reviews}  		2012. 25  (2)  p. .  	 	 (PMC3346298.) 
\bibitem[Dubey ()]{b6}\label{b6} 	 		‘History of the discovery of the life cycle of Toxoplasma gondii’.  		 			Jp Dubey 		.  		 \xref{http://dx.doi.org/10.1645/GE-2774.1}{10.1645/GE-2774.1}.  		 21539466.  	 	 		\textit{International Journal of Parasitology}  		Jul2009. 97  (5)  p. .  	 
\bibitem[Jenum et al. ()]{b14}\label{b14} 	 		‘Improved diagnosis of primary toxoplasma gondii infection in early pregnancy by determination antitoxoplasma immunoglobulin G activity’.  		 			P A Jenum 		,  		 			B Stray-Pedresen 		,  		 			A G Gundersen 		.  	 	 		\textit{J Clinmicrobial}  		1997. 35 p. .  	 
\bibitem[Mc Lead R et al. (ed.) ()]{b12}\label{b12} 	 		 			Remington Js Mc Lead R 		,  		 			P Thulleiz 		,  		 			G Desmonts 		.  		\textit{infectious disease of the fetus and newborn infant},  				 			Js Rimington,  			Klein 		 (ed.)  		2006. p. .  	 	 (WB saunder) 
\bibitem[Thulliez et al. ()]{b13}\label{b13} 	 		‘new agglutination test for the diagnosis of acute and chronic toxoplasma infection’.  		 			P Thulliez 		,  		 			J S Remington 		,  		 			F Santoro 		,  		 			G Ovalque 		,  		 			S Dharma 		,  		 			G Desmonts 		.  	 	 		\textit{pathology Biol}  		1986. 34 p. .  	 
\bibitem[Hedman et al. ()]{b11}\label{b11} 	 		‘recent primary toxoplasma infection indicated by specific IgG’.  		 			K Hedman 		,  		 			M Seppalai 		,  		 			O Makela 		.  	 	 		\textit{J infected Did}  		1989. 159 p. .  	 
\bibitem[Zemene et al. ()]{b0}\label{b0} 	 		‘seroprevalence of T.gondii and associated risk factors among pregnant women in jimma town, south western Ethiopic’.  		 			E Zemene 		,  		 			Abera S Yew Halaw D 		,  		 			T Belay 		,  		 			A Samuel 		.  	 	 		\textit{BMC infect dis}  		2012. 12 p. 337.  	 
\bibitem[Dubey et al. (2011)]{b5}\label{b5} 	 		‘sporulation and survival of Toxoplasma gondiioocycts in different types of commercial cat litter’.  		 			J P Dubey 		,  		 			Ferreira 		,  		 			Lr 		,  		 			J Martins 		,  		 			Jl Jones 		.  		 \xref{http://dx.doi.org/10.1645/GE-2774.1}{10.1645/GE-2774.1}.  	 	 		\textit{The journal of parsitology}  		october 2011. 97  (5)  p. .  	 
\bibitem[Carter and Fleck ()]{b1}\label{b1} 	 		‘the incidence of T.gondii antibodies in Sudanese’.  		 			F S Carter 		,  		 			D G Fleck 		.  	 	 		\textit{Trans Rsoc Trop Med Hyg}  		1966. 60 p. .  	 
\bibitem[Toxoplasmagondii]{b3}\label{b3} 	 		\textit{the model apicomplexan. perspectives and methods. London: Academic Press\textbackslash Elsevier},  		 			K Toxoplasmagondii 		.  		p. .  	 
\bibitem[Stray -Pedresen ()]{b10}\label{b10} 	 		‘Toxoplasmosis in pregnancy’.  		 			B Stray -Pedresen 		.  	 	 		\textit{Baillieres Clin Obstet Gynaecol}  		1993. 7  (1)  p. .  	 
\end{bibitemlist}
 			 		 	 
\end{document}
