Additional file 3: Model calculation for PW-vector 1 2 All the parameters used are detailed in the Additional file 2. 3 4 The probability to introduce a single vector from j to k during the month m which is able to induce an 5 entire transmission cycle in which at least one local host is infected by a local vector is defined as: 6 ๐(๐๐๐ก๐๐๐ต๐๐๐ ) = ๐(๐๐๐๐ต๐๐๐ ) × ๐(๐๐ ๐ก๐ต๐๐๐ ) 7 Where P(relBjkm ) = P (transculijm ) × P (survtrans jkm ) × P(infโก_culijm โก) × ntransjkm 8 And P(estBjkm ) = P (surv๐๐๐๐๐ฃ๐๐jkm ) × bequik × IVH × [1 − [1 − IVH × P(survkm ) × bequik × 9 IHV ] culikm ] 10 With culikm the number of vector feeding on an infected viraemic imported host calculated as: 11 culikm = BRkm x Vir x Ckm 12 13 1. ๐(๐ข๐ง๐โก_๐๐ฎ๐ฅ๐ข๐ฃ๐ฆ ) =โกProbability for a vector to be infected the month m in area j 14 15 P(infโก_culijm ) = POjm × rjm 16 17 2. ๐ (๐ญ๐ซ๐๐ง๐ฌ๐๐ฎ๐ฅ๐ข๐ฃ๐ฆ ) =โกProbability for a vector to be transported after infection from area j 18 Only a vector which is infected and transported poses a risk, therefore we only consider those 19 vectors that are infected and transported during their life time. We assume that an infected vector 20 will be infected at a uniformly distributed time during its life, Dinf. Additionally, we assume that a 21 vector is transported at a uniformly distributed moment during its life time, which is exponentially 22 distributed with mean 1/MRjm. The probability that the moment of transportation occurs after the 23 infection event is equal to the part of the total lifetime of the vector that it is infected. Thus 24 P (transculijm ) is estimated, as made by Napp et al. [1], as: 1 25 P (transculijm ) = (1/MR jm − Dinf ) = 1 − Dinf โกMR jm 1/MR jm 26 27 NB: Temperature in departure area j was assumed to be constant over months and thus MRjm is here 28 also constant over months. 29 30 3. ๐ (๐ฌ๐ฎ๐ซ๐ฏ๐ญ๐ซ๐๐ง๐ฌ๐ฃ๐ค๐ฆ ) =โกProbability for a vector to stay alive from j until the arrival in area k during the month m 31 32 The conditions during travel (e.g. temperature) are assumed to not affect the viability of culicoides 33 except when pest control is applied (worst case scenario). There is no data available on survival rate 34 of culicoides in an unfavorable context as assumed to occur during transport. Moreover the 35 conditions during transports have a high variability and information are impossible to collect. 36 The probability to stay alive until the arrival is the probability to survive until transport and during 37 the time of transport. 38 P (survtransjkm ) = e−MRjm ×(Dtrans +tjk) × (1 − Prot vect ) 39 40 4. ๐ (๐ฌ๐ฎ๐ซ๐ฏ๐๐ซ๐ซ๐ข๐ฏ๐๐ฅ๐ฃ๐ค๐ฆ ) =โกThe vector survives to the transport from j, the EIP and can have at least a blood meal after the end of EIP and when arrives in the area k the month m 41 42 43 If TB < 0 culicoides are assumed to not survive 44 =0 45 46 If (Nm.GCjm) > (Dtransp + tjk) 47 = eMRkm ×(Dtrans +tjk)−Nm ×GCjm 48 49 If (Nm.GCjm) < (Dtransp + tjk) 2 50 If tjk > GCjm 51 we assume that the last GCm is spent half during transport and half in the arrival area k. 52 = e−MRkm × GCjm 2 53 54 If tjk < GCjm 55 we assume that the last GCm is spent half in the departure area j and half in the arrival area k. 56 = e−MRkm × GCjm −๐ก๐๐ 2 57 58 NB : if Tk < T_min (9.5°C), where T_min is the minimal temperature for formulae for MR and GC (if Tk 59 is lower, the formulae are not valid), we will use the T_min in our calculus (worst case scenario). 60 61 62 5. ๐(๐ฌ๐ฎ๐ซ๐ฏ๐ค๐ฆ ) =โกProbability that the local vector survives to the EIP and can have a blood meal during the month m in the area k 63 64 P(survkm ) = โก ๐ −(๐๐๐×๐บ๐ถ๐๐ ×๐๐ ๐๐) 65 66 67 BIBLIOGRAPHIEโก 68 69 70 1. Napp S, García-Bocanegra I, Pagès N, Allepuz A, Alba A, Casal J: Assessment of the risk of a bluetongue outbreak in Europe caused by Culicoides midges introduced through intracontinental transport and trade networks. Med Vet Entomol 2012, 27:19–28. 71 3